Semiconductor laser device and method of fabricating the laser device.
Abstract
In a buried type semiconductor laser device composed of a II-VI compound semiconductor, a buried layer 9 - 11 is made of a II-VI compound semiconductor having a refraction factor lower than that of an active layer of the laser device. The buried layer has a forbidden band width larger than that of an active layer of the laser device. The buried layer has such a composition that the lattice constant thereof is substantially matched to that of a substrate on which the laser device is grown. The buried layer has an electric resistance high enough not to exert an effect on the operation of the laser composed of an n-type clad-active layer-a p-type clad.

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30 claims: 21 independent, 9 dependent
- 1A buried type semiconductor laser device comprising a II-VI compound semiconductor, wherein a buried layer (9 to 11, 19, 33, 37, 41, 42, 46) is made of a II-VI compound semiconductor having a refraction factor lower than that of an active layer (6, 17, 23, 44) of said laser device.
- 6A method of forming a thin film comprising the steps of:forming sulfur atoms or a layer of sulfur atoms on a II-VI compound semiconductor;introducing said II-VI compound semiconductor in a thin film deposition apparatus;removing said sulfur atoms or a layer of sulfur atoms by a suitable amount using electromagnetic wave, corpuscular beam, heat or solution;and growing or depositing a new material such as a II-VI compound semiconductor, a III-V compound, a IV compound, a IV-VI compound, or a II-VII compound.
- 9A semiconductor laser device composed of a II-VI compound semiconductor, wherein a material, which is used for formation of a protection film or multi-layer reflection film at the end surface of a resonator, contains at least one kind or more of II-VI compounds having a forbidden band width larger than that of an active layer, such as ZnS or MgS.
- 10A semiconductor laser device composed of a II-VI compound semiconductor, wherein a material, which is used for formation of a protection film or multi-layer reflection film at the end surface of a resonator, contains at least one kind or more of IV-VI compounds having a forbidden band width larger than that of an active layer, such as SiO₂ or TiO₂.
- 11A semiconductor laser device composed of a II-VI compound semiconductor, wherein a material, which is used for formation of a protection film or multi-layer reflection film at the end surface of a resonator, contains at least one kind or more of II-VII compounds having a forbidden band width larger than that of an active layer, such as MgF₂ or CaF₂.
- 12A semiconductor laser device composed of a II-VI compound semiconductor, wherein a material, which is used for formation of a protection film or multi-layer reflection film at the end surface of a resonator, contains at least one kind or more of IV compounds having a forbidden band width larger than that of an active layer, such as C, SiCx or SiNx.
- 14A method of forming an electrode to a II-VI compound semiconductor, comprising the steps of:growing a layer including a CdSSe alloy on said II-VI compound semiconductor as a cap layer (8);and depositing a metal film (13) as an electrode on said layer.
- 15A method of forming an electrode to a II-VI compound semiconductor, comprising the steps of:exposing said II-VI compound semiconductor to a molecular beam or a gas containing Cd or Te in a crystal growth apparatus;and depositing a metal film (13) as an electrode on the processed surface.
- 17A semiconductor device composed of a II-VI compound semiconductor, which is epitaxially grown on a substrate (1) made of a IV such as Si or a III-V compound semiconductor such as GaAs or InP, said device having a structure that a strained superlattice (3, 47) including at least one thin film of II-VI compound semiconductor is introduced in the hetero-interface as a region for reducing a strain caused by thermal expansion or contraction.
- 19A double hetero type semiconductor laser device using a II-VI compound semiconductor composed of an alloy of ZnMgCdSSe, comprising an n-type clad layer, a p-type clad layer and an active layer, wherein each of said n-type and p-type clad layers has a lattice constant substantially matched to that of a substrate crystal or a buffer layer formed at the hetero-interface, and which has a forbidden band width larger than that of an active layer;said n-type and p-type clad layers are different in the alloy composition from each other;and the difference ( ΔEv = Ev act - Ev clad ) in the energy of the valency electron band between said n-type clad layer and said active layer is positive, and the difference ( ΔEc = Ec clad - Ec act ) in the energy of the conducting band between said p-type clad layer and said active layer is positive.
- 20A semiconductor laser device having a GRIN-SCH structure using a II-VI compound semiconductor, wherein a light guide layer (16, 18) is made of a superlattice.
- 21A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has at the hetero-interface a superlattice structure (47) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of Zn y Cd 1-y S x' Se 1-x' (0≦x'≦1, 0≦y≦1) having a thickness of 10 nm or less.
- 22A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1) which has at the hetero-interface a superlattice structure (3) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of ZnSe having a thickness of 10 nm or less.
- 23A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has at a portion adjacent to the active layer (44), a superlattice structure (43, 45) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of Zn y Cd 1-y S x' Se 1-x' (0≦x'≦1, 0≦y≦1) having a thickness of 10 nm or less.
- 24A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has at a portion adjacent to an active layer (44) a superlattice structure (48, 49) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of ZnSe having a thickness of 10 nm or less.
- 25A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1) which has at the heterointerface between a clad layer (22, 24) and a light guide layer (34, 35), a superlattice structure (43, 45) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of Zn y Cd 1-y S x' Se 1-x' (0≦x'≦1, 0≦y≦1) having a thickness of 10 nm or less.
- 26A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate, which has at the hetero-interface between a clad layer (22, 24) and a light guide layer (34, 35), a superlattice structure (48, 49) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of ZnSe having a thickness of 10 nm or less.
- 27A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has in a light guide layer a superlattice structure (43, 45) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of Zn y Cd 1-y S x' Se 1-x' (0≦x'≦1, 0≦y≦1) having a thickness of 10 nm or less.
- 28A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1) which has in a light guide layer a superlattice structure (48, 49) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of ZnSe having a thickness of 10 nm or less.
- 29A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has in a clad layer a superlattice structure (47) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of Zn y Cd 1-y S x' Se 1-x' (0≦x'≦1, 0≦y≦1) having a thickness of 10 nm or less.
- 30A semiconductor laser device composed of a II-VI compound semiconductor fabricated on a IV or a III-V compound semiconductor substrate (1), which has in a clad layer a superlattice structure (47) composed of an alloy layer of ZnS x Se 1-x (0≦x≦1) having a thickness of 10 nm or less and an alloy layer of ZnSe having a thickness of 10 nm or less.
Independent claims21
103 paragraphs, as filed
Background of the Invention
0001The present invention relates to a semiconductor laser device, and particularly to a short wave semiconductor laser device composed of a II-VI compound semiconductor used for information processing terminal equipment such as an optical disk, laser beam printer or laser television, and a method of fabricating the laser device.
0002A conventional semiconductor laser device using a II-VI compound semiconductor has a gain waveguiding type electrode stripe structure in which an alloy of ZnCdSSe or ZnMgSSe is grown on a GaAs substrate. The former structure using ZnCdSSe has been described, for example in Unexamined Japanese Patent Publication No. HEI 3-91270; and the latter structure using ZnMgSSe has been described, for example in Unexamined Japanese Patent Publication No. HEI 5-75217. In these structures, a continuous oscillation at low temperatures or a pulse oscillation at room temperature can be realized at an oscillation wavelength of about 500 nm (ZnCdSSe system) or about 450 nm (ZnMgSSe system).
0003These structures, however, have the following disadvantages. The threshold current is relatively large because of the gain waveguiding type. It is difficult to form an ohmic contact with an electrode material because of the wide gap material. The thermal expansion strain remains in the device because a III-V compound semiconductor is used as a growth substrate. It is difficult to design a laser structure with a large band continuity between a clad layer and an active layer for the ZnCdSSe system being easy in the conducting control compared with the ZnMgSSe system, resulting in the insufficient confinement of injected charge and light. Because of these disadvantages, the above structures are difficult to achieve the continuous oscillation at room temperature and the operation with a high reliability.
Summary of the Invention
0004An object of the present invention is to provide a short wave semiconductor laser device composed of a II-VI compound semiconductor capable of solving the above-described problems.
0005The present invention basically includes a buried type semiconductor laser structure using a II-VI compound semiconductor for reducing the threshold current and improving the reliability, wherein a multi-layer reflection film is provided for achieving the short wave oscillation. Concretely, in a buried type semiconductor laser device composed of a II-VI compound semiconductor, a buried layer is made of a II-VI compound semiconductor having a refraction factor lower than that of an active layer of the laser device. The buried layer has a forbidden band width larger than that of an active layer of the laser device. The buried layer has such a composition that the lattice constant thereof is substantially matched to that of a substrate on which the laser device is grown, and also it has an electric resistance high enough not to exert an effect on the operation of the laser composed of an n-type clad-active layer-a p-type clad. The buried layer is made of a II-VI compound semiconductor having a conducting type opposed to that of a clad layer being horizontally contacted with the surface of a substrate or to that of an active layer. The method of forming a buried layer includes the steps of: forming sulfur atoms or a layer of sulfur atoms on a II-VI compound semiconductor; introducing the II-VI compound semiconductor in a thin film deposition apparatus; removing the sulfur atoms or a layer of sulfur atoms by a suitable amount using electromagnetic wave, corpuscular beam, heat or solution; and growing or depositing a new material of a II-VI compound semiconductor, a III-V compound, a IV compound, a IV-VI compound, or a II-VII compound. At this time, the sulfur atoms or a layer of sulfur atoms formed on the II-VI compound semiconductor are removed at a temperature of 400°C or less, and a new material of a II-VI compound semiconductor, a III-V compound, a IV compound, a IV-VI compound, or a II-VII compound is grown or deposited on the exposed surface. A material, which is used for formation of a protection film or multi-layer reflection film at the end surface of a resonator, contains one kind or more of II-VI compounds having a forbidden band width larger than that of an active layer, such as ZnS or MgS; one kind or more of IV-VI compounds having a forbidden band width larger than that of an active layer, such as SiO₂ or TiO₂; one kind or more of II-VII compounds having a forbidden band width larger than that of an active layer, such as MgF₂ or CaF₂; or one kind or more of IV compounds having a forbidden band width larger than that of an active layer, such as C, SiCx or SiNx.
0006To form an electrode having a small contact resistance on a p-type clad layer having a wide forbidden band width, a cap layer is made of a P-type CdSSe alloy having a small energy difference on the valency electron side to the clad layer and a relatively narrow forbidden band width. The cap layer made of an alloy with a gradient composition can be easily fabricated by exposing the surface of a clad layer to a molecular beam of Cd or Te. Namely, in forming an electrode to the II-VI compound semiconductor, a layer including an alloy of CdSSe is grown on the II-VI compound semiconductor as a cap layer, and then a metal film as an electrode is deposited on this layer. In this case, the II-VI compound semiconductor is exposed to a molecular beam or a gas containing Cd or Te in a crystal deposition apparatus, and a metal film as an electrode is deposited on the surface thereof.
0007For reducing a strain generated in the device due to a large difference in a linear thermal expansion coefficient between a substrate of GaAs, that is, a III-V compound and a II-VI compound, a strain superlattice is introduced in the hetero-interface. Namely, in epitaxially growing a device composed of a II-VI compound semiconductor on a substrate made of a IV such as Si or a III-V compound semiconductor such as GaAs or InP, a strained supperlattice including at least one thin film of II-VI compound semiconductor is introduced in the hetero-interface as a region for reducing a strain caused by thermal expansion or contraction.
0008To realize the sufficient confinement of injected charge in the ZnCdSSe based laser structure, there is provided an asymmetric double hetero structure in which the ZnSSe layer is used as the p-type clad layer and the ZnCdSSe layer is used as the n-type clad layer. Moreover, to sufficient confine a light, the ZnCdSSe based laser structure adopts a GRIN-SCH structure using a supperlattice with the film thickness gradually changed as a light confinement layer. Namely, a double hetero type semiconductor laser device using a II-VI compound semiconductor composed of an alloy of ZnMgCdSSe, includes an n-type clad layer, a p-type clad layer and an active layer, wherein each of said n-type and p-type clad layers has a lattice constant substantially matched to that of a substrate crystal or a buffer layer formed at the hetero-interface, and which has a forbidden band width larger than that of an active layer; said n-type and p-type clad layers are different in the alloy composition from each other; and the difference ( <maths id="math0001"><math display="inline"><mrow><msub><mrow><mtext>ΔEv = Ev</mtext></mrow><mrow><mtext>act</mtext></mrow></msub><msub><mrow><mtext> - Ev</mtext></mrow><mrow><mtext>clad</mtext></mrow></msub></mrow></math><img file="EP0637862A2_D0001.tif" /></maths> ) in the energy of the valency electron band between said n-type clad layer and said active layer is positive, and the difference ( <maths id="math0002"><math display="inline"><mrow><msub><mrow><mtext>ΔEc = Ec</mtext></mrow><mrow><mtext>clad</mtext></mrow></msub><msub><mrow><mtext> - Ec</mtext></mrow><mrow><mtext>act</mtext></mrow></msub></mrow></math><img file="EP0637862A2_D0002.tif" /></maths> ) in the energy of the conducting band between said p-type clad layer and said active layer is positive. Moreover, in the semiconductor laser device having a GRIN-SCH structure using a II-VI compound semiconductor, the light guide layer is made of a superlattice.
0009In the present invention, a buried type laser structure enables the effective current constriction. Moreover, by provision of a refraction factor waveguiding type structure for waveguide of a light, it is possible to reduce the threshold current, and to improve the laser light characteristics. To fabricate the buried structure, the re-growth technique of the buried layer is required. However, by processing the surface of a II-VI compound forming the mesa structure with sulfur, it becomes possible to obtain the cleaned surface through heating at a temperature near the growth temperature of II-VI compound (400°C or less).
0010Moreover, by forming a reflection multi-layer film or protection film not to absorb a short wave light on the end surface of the resonator, it is possible to reduce the threshold current, and to suppress the breakage of the end surface. In this case, by use of a thin film of ZnS or MgS excellent in adhesiveness, or a diamond based (poly-C, SiC) thin film having a high refraction factor and a resistance to deterioration, and by processing the end surface with sulfur prior to formation of these thin films, it becomes possible to obtain a high reliability.
0011In the formation of an electrode on the p-type crystal, by coating the p-type crystal with the material of an alloy of CdSSe being small in the energy difference on the valency electron band side with respect to the p-type crystal, it becomes possible to effectively inject positive holes. On the other hand, when ZnTe being large in the energy difference on the valency electron band side and being easy to obtain the p-type conduction is used, an alloy with a gradient composition must be fabricated. According to the present invention, it becomes possible to easily fabricate such an alloy with a gradient composition.
0012As a typical example, between a substrate of GaAs (III-V compound) and ZnSe or ZnS (II-VI compound), there is a mismatch in the thermal expansion coefficient of about 40%. Accordingly, even when the lattice constant of the ZnSSe alloy is matched to that of the GaAs substrate at the growth temperature of about 300°C, there is generated a lattice strain at room temperature where the device is used. To reduce the strain, by introducing, for example a ZnSe-ZnSSe strained superlattice in the hetero-interface, it becomes possible to suppress the propagation of the expansion or contraction of the substrate to the device, and hence to improve the reliability of the semiconductor laser.
0013In a semiconductor laser of a ZnCdSSe system using clad layers having different alloy compositions, it is possible to achieve the lattice match to the substrate, and to effectively confine the injected charge. For example, when a ZnSSe alloy is used as the p-type clad layer, a ZnCdSe alloy is used as an active layer, and a ZnCdSSe alloy is used as an n-type clad layer, electrons can be confined by the electrical field formed in ZnSSe and positive holes can be confined by the electrical field formed in ZnCdSSe. Moreover, an asymmetric SCH structure is used to achieve the light confinement, wherein a ZnCdSSe n-type clad layer is used as a light guide layer, and an n-type ZnCdS alloy is used as a clad layer.
0014On the other hand, in the recent structure including a clad layer of ZnSSe, an active layer of ZnCdSe, and a light guide layer of ZnSe, the film thickness of the light guide layer is required to be more than the critical film thickness of ZnSe for effectively confining a light. In this regard, lattice defects in ZnSe present a problem. To cope with this problem, a superlattice composed of ZnSe-ZnSSe with the film thickness gradually changed is used as the light guide layer. This makes it possible to obtain a film thickness enough to confine a light without any generation of lattice defects, and to easily fabricate a GRIN-SCH type semiconductor device using molecular beam epitaxy which is difficult to fabricate an alloy having a gradient composition.
Brief Description of the Drawings
0015<ul id="ul0001" list-style="none"><li>Fig. 1 is a semiconductor laser structure of a first embodiment of the present invention;</li><li>Fig. 2 is a bad structure of the semiconductor laser of the first embodiment of the present invention;</li><li>Fig. 3 is a semiconductor laser structure of a second embodiment of the present invention;</li><li>Fig. 4 is a structure of a supperlattice light guide layer of the second embodiment of the present invention;</li><li>Fig. 5 is a band structure of the semiconductor laser of the second embodiment of the present invention;</li><li>Fig. 6 is a semiconductor laser structure of a third embodiment of the present invention;</li><li>Fig. 7 is a semiconductor laser structure of a fourth embodiment of the present invention;</li><li>Fig. 8 is a semiconductor laser structure of a fifth embodiment of the present invention;</li><li>Fig. 9 is a semiconductor laser structure of a sixth embodiment of the present invention;</li><li>Fig. 10 is a semiconductor laser structure of a seventh embodiment of the present invention;</li><li>Fig. 11 is a semiconductor laser structure of an eighth embodiment of the present invention;</li><li>Fig. 12 is a semiconductor laser structure of a ninth embodiment of the present invention;</li><li>Fig. 13 is a semiconductor laser structure of a tenth embodiment of the present invention;</li><li>Fig. 14 is a semiconductor laser structure of an eleventh embodiment of the present invention;</li><li>Fig. 15 is a semiconductor laser structure of a twelfth embodiment; and</li><li>Fig. 16 is a semiconductor laser structure of a thirteenth embodiment of the present invention.</li></ul>
Description of the Preferred Embodiments
(Embodiment 1)
0016A first embodiment of the present invention will be described with reference to Fig. 1. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnSe-ZnS<sub>0.2</sub>Se<sub>0.8</sub> strained superlattice 3 (n = 5El8, 0.5 µm), a Cℓ doped Zn<sub>0.5</sub>Cd<sub>0.5</sub>S<sub>0.9</sub>Se<sub>0.1</sub> clad layer 4 (n = 5El8, 1.5 µm), a Cℓ doped Zn<sub>0.8</sub>Cd<sub>0.2</sub>S<sub>0.4</sub>Se<sub>0.6</sub> light guide layer 5 (n = 5El7, 0.5 µm), an undoped Zn<sub>0.8</sub>Cd<sub>0.2</sub>S<sub>0.1</sub>Se<sub>0.9</sub> active layer 6 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 1El8, 1.0 µm), and an N₂ doped CdSe cap layer 8 (p = 1El9, 0.01 µm).
0017Next, an SiO₂ film was formed on the above layers by vacuum vapor deposition. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 2.5 µm was then formed using a phosphoric acid based etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the molecular beam epitaxy system again.
0018This sample was heated at about 300°C to remove excessive sulfur. On this sample, there were sequentially grown, as buried layers, an N₂ doped Zn<sub>0.5</sub>Cd<sub>0.5</sub>S<sub>0.9</sub>Se<sub>0.1</sub> block layer 9 (p = 1El6, 1.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> block layer 10 (n = 1El6, 1.0 µm), and an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> block layer 11 (p = 1El6, 0.5 µm). The SiO₂ film was then removed using a fluoric acid based etching solution, and an SiO₂ film 12 was formed on the sample by vacuum vapor deposition.
0019Next, a striped hole having a width of about 5 µm was opened in the SiO₂ film 12 to the above stripe using the known photolithography. The sample was then dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. After that, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure having a length of 400 µm.
0020The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. A ZnS-SiO₂ multi-layer reflection film was then formed at the end surface of the resonator by sputtering.
0021The band structure of this structure in the laser oscillation state is shown in Fig. 2. Numeral 26 designates the Fermi level. Positive holes injected by the p-type semiconductor layer are confined by an electric potential formed on the valency electron band side by the p-n junction and the junction between the Zn<sub>0.8</sub>Cd<sub>0.2</sub>S<sub>0.4</sub>Se<sub>0.6</sub> light guide layer and the Zn<sub>0.8</sub>Cd<sub>0.2</sub>S<sub>0.1</sub>Se<sub>0.9</sub> active layer. On the other hand, electrons injected from the n-type semiconductor are confined by an electric potential formed on the conducting band side by the p-n junction and the junction between the ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer and the Zn<sub>0.8</sub>Cd<sub>0.2</sub>S<sub>0.1</sub>Se<sub>0.9</sub> active layer. Thus, this structure enables the laser oscillation at a wavelength of 490 nm.
(Embodiment 2)
0022A second embodiment of the present invention will be described with reference to Fig. 3. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnSe-ZnS<sub>0.2</sub>Se<sub>0.8</sub> strained superlattice 3 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 1.5 µm), a Cℓ doped ZnSe-Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se supperlattice light guide layer 16 (n = 5El7, 0.5 µm), an undoped Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se active layer 17 (0.01 µm), an N₂ doped ZnSe-Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se supperlattice light guide layer 18 (p = 5El7, 0.5 µm), and an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 1El8, 1.5 µm). The surface of the sample was then irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature. By this processing, a p-type ZnSeTe alloy having a gradient composition was formed on the surface of the sample.
0023An SiO₂ film was formed on the sample by vacuum vapor deposition. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 3.0 µm was then formed using a phosphoric acid based etching solution. The sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the molecular beam epitaxy system again.
0024The sample was heated at about 300°C to remove excessive sulfur. On the sample, there were sequentially grown, as buried layers, an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> block layer 19 (p = 1El6, 1.0 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> block layer 10 (n = 1El6, 1.5 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> block layer 11 (p = 1El6, 0.5 µm). The SiO₂ film was then removed using a fluoric acid based etching solution, and an SiO₂ film 12 was formed on the surface of the sample by vacuum vapor deposition.
0025Next, a striped hole having a width of about 5 µm was opened in the SiO₂ film 12 to the above stripe using the known photolithography. The sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. After that, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure having a length of 400 µm.
0026The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. An SiNx-SiCx multi-layer reflection film was then formed at the end surface of the resonator by plasma CVD.
0027The ZnSe-Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se supperlattice light guide layer used in this structure is shown in Fig. 4. In this figure, numeral 27 designates ZnSe, 28 is Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se, 29 is the lower end of an apparent conducting band, and 30 is the upper end of an apparent valency electron band. As shown in the figure, the structure in which the film thickness is gradually changed has the same effect as that of the alloy having the gradient composition. The laser of this structure has a band structure shown in Fig. 5. In this figure, numeral 26 designates the Fermi level. By provision such a GRIN-SCH type semiconductor laser, it is possible to eliminate lattice defects of the light guide layer which has conventionally presented a problem, and hence to improve the reliability of the device.
(Embodiment 3)
0028A third embodiment of the present invention will be described with reference to Fig. 6. On an n-type ZnSe substrate 20, there were sequentially grown by molecular beam epitaxy, a Cℓ doped ZnSe buffer layer 21 (n = 1El8, 0.5 µm), a Cℓ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> clad layer 39 (n = 1El8, 1.0 µm), a Cℓ doped Zn<sub>0.9</sub>Cd<sub>0.1</sub>S<sub>0.2</sub>Se<sub>0.8</sub> light guide layer 31 (n = 5El7, 0.5 µm), an undoped ZnSe active layer 23 (0.2 µm), an N₂ doped ZnS<sub>0.9</sub>Cd<sub>0.1</sub>S<sub>0.2</sub>Se<sub>0.8</sub> light guide layer 32 (p = 5El7, 0.5 µm), an N₂ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> clad layer 40 (p = 1El8, 1.0 µm), and an N₂ doped CdSe cap layer 8 (p = 1El9, 0.01 µm).
0029An SiO₂ film was formed on the above layers by vacuum vapor deposition. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 2.0 µm was then formed using a sulfuric acid based etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the molecular beam epitaxy system again.
0030This sample was heated at about 300°C to remove excessive sulfur. On this sample, an undoped MgS<sub>0.9</sub>Se<sub>0.1</sub> block layer 33 (n/p < 1 El5, 2.0 µm) was grown as a buried layer. The SiO₂ film was then removed using a fluoric acid based etching solution, and an SiO₂ film 12 was formed on the surface of the sample by vacuum vapor deposition.
0031Next, a striped hole having a width of about 5 µm was opened in the SiO₂ film 12 to the above stripe using the known photolithography. The sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. After that, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 25 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure having a length of 500 µm.
0032The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and a SiO₂-TiO₂ multi-layer reflection film was formed at the end surface of the resonator by vacuum vapor deposition.
0033The semiconductor laser device of this structure is capable of continuously oscillating a blue laser of a single vertical mode with an oscillation wavelength of about 450 nm at room temperature.
(Embodiment 4)
0034A fourth embodiment of the present invention will be described with reference to Fig. 7. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnSe-ZnS<sub>0.2</sub>Se<sub>0.8</sub> strained superlattice 3 (n = 1El8, 0.5 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.3 µm), an undoped Zn<sub>0.8</sub>Cd<sub>0.2</sub>Se active layer 17 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.3 µm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El8, 1.0 µm), and an N₂ doped ZnSe cap layer 38 (p = 5El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and then was cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy having a gradient composition was formed on the surface of the sample.
0035Next, an SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 2 µm was then formed using a sulfuric acid based etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0036This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, there were sequentially grown, as buried layers, an N₂ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 36 (p = 1El6, 1.0 µm), a Cℓ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 37 (n = 1El6, 1.0 µm), an N₂ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 42 (p = 1El6, 0.5 µm). The SiO₂ film was then removed using a fluoric acid based etching solution, and an SiO₂ film 12 was formed on the sample by plasma CVD.
0037Next, a striped hole having a width of about 5 µm was opened in the SiO₂ film 12 to the above stripe using the known photolithography. The sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent. After that, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 400 µm.
0038The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and a CaF₂-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0039The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 50 mA, a drive voltage 4V, and an oscillation wavelength of 510 nm.
(Embodiment 5)
0040A fifth embodiment of the present invention will be described with reference to Fig. 8. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnSe-ZnS<sub>0.2</sub>Se<sub>0.8</sub> strained superlattice 3 (n = 1El8, 0.5 µm), a Cℓ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> clad layer 39 (n=1El8, 1.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.3 µm), an undoped ZnSe active layer 23 (0.1 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El8, 0.3 µm), an N₂ doped Mg<sub>0.2</sub>Zn<sub>0.8</sub>S<sub>0.3</sub>Se<sub>0.7</sub> clad layer 40 (p = 1El8, 1.0 µm), and an N₂ doped ZnSe cap layer 38 (p = 5El8, 0.05 µm). Next, an SiO₂ film was formed on the above layers by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1 µm was formed using a sulfuric acid based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0041The sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, a Cℓ doped Mg<sub>0.3</sub>Zn<sub>0.7</sub>S<sub>0.4</sub>Se<sub>0.6</sub> block layer 41 (n = 1El6, 1.0 µm) was grown as a buried layer. The SiO₂ film was then removed using a fluoric acid based etching solution, and the sample was dipped in a (NH₄)₂Sx solution for several minutes and cleaned using an alcohol solvent, and it was put in the molecular beam epitaxy system.
0042The sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur, and an N₂ doped ZnSe cap layer 38 (p = 5El8, 0.1 µm) was grown on the this sample. The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy having a gradient composition was formed on the surface of the sample.
0043Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure having a length of 400 µm.
0044The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and a ZnS-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0045The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 60 mA, a drive voltage 5V, and an oscillation wavelength of 450 nm.
(Embodiment 6)
0046A sixth embodiment of the present invention will be described with reference to Fig. 9. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a strained supperlattice 47 (n = 1El8, 0.03 µm) of five cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (5 nm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a supperlattice light guide layer 43 (n = 5El7, 0.1 µm) of seven cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), a supperlattice light guide layer 45 (p = 5El7, 0.1 µm) of seven cycles of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm), and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. Next, an SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was then formed using a bromine based selective etching solution. The sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0047This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed in the SiO₂ film using the known photolithography.
0048Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure having a length of 1000 µm.
0049The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0050The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 7)
0051A seventh embodiment of the present invention will be described with reference to Fig. 10. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1 El8, 0.5 µm), a strained supperlattice 3 (n = 1El8, 0.03 µm) of five cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a supperlattice light guide layer 48 (n = 5El7, 0.1 µm) of ten cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), a supperlattice light guide layer 49 (p = 5El7, 0.1 µm) of ten cycles of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>S<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm), and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature of at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. Next, an SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0052This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed in the SiO₂ film using the known photolithography.
0053Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0054The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0055The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 8)
0056A eighth embodiment of the present invention will be described with reference to Fig. 11. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1 El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a supperlattice light guide layer 43 (n = 5El7, 0.1 µm) of seven cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.1 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.1 µm), a supperlattice light guide layer 45 (n = 5El7, 0.1 µm) of seven cycles of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm), and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. Next, an SiO₂ film was formed on the above layers by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned with an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0057This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed on the SiO₂ film using the known photolithography.
0058Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0059The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0060The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 9)
0061A ninth embodiment of the present invention will be described with reference to Fig. 12. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a strained supperlattice light guide layer 48 (n = 5El7, 0.1 µm) of ten cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.1 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 43 (p = 5El7, 0.1 µm), a supperlattice light guide layer 49 (p = 5El7, 0.1 µm) of ten cycles of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm), and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. Next, an SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0062The sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On this sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed in the SiO₂ film using the known photolithography.
0063Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0064The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with an alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0065The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 10)
0066A tenth embodiment of the present invention will be described with reference to Fig. 13. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 0.5 µm), a strained supperlattice 47 (n = 5El7, 0.07 µm) of five cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.0 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5 El7, 0.1 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.1 µm), an undoped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7, and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. An SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0067This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On the sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed on the SiO₂ film using the known photolithography.
0068Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0069The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0070The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 11)
0071An eleventh embodiment of the present invention will be described with reference to Fig. 14. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 0.5 µm), a strained supperlattice 3 (n = 5El7, 0.05 µm) of five cycles of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.1 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 43 (p = 5El7, 0.1 µm), an undoped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm) and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. An SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0072This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On the sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed on the SiO₂ film using the known photolithography.
0073Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0074The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0075The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 12)
0076A twelfth embodiment of the present invention will be described with reference to Fig. 15. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.5 µm), a supperlattice light guide 43 (n = 5El7, 0.01 µm) of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.5 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.05 µm), a supperlattice light guide 45 (n = 5El7, 0.01 µm) of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (10 nm) - Zn<sub>0.7</sub>Cd<sub>0.3</sub>S<sub>0.1</sub>Se<sub>0.9</sub> (3 nm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.05 µm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm) and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. An SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0077This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On the sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed on the SiO₂ film using the known photolithography.
0078Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0079The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0080The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
(Embodiment 13)
0081A thirteenth embodiment of the present invention will be described with reference to Fig. 16. On an n-type GaAs substrate 1, there were sequentially grown by molecular beam epitaxy, an Se doped GaAs buffer layer 2 (n = 1El8, 0.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 15 (n = 1El8, 0.1 µm), a Cℓ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 22 (n = 1El8, 1.5 µm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.5 µm), a supperlattice light guide 48 (n = 5El7, 0.01 µm) of Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), a Cℓ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 34 (n = 5El7, 0.5 µm), an undoped Zn<sub>0.7</sub>Cd<sub>0.3</sub>Se active layer 44 (0.01 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.05 µm), a supperlattice light guide 49 (p = 5El7, 0.01 µm) of N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> (5 nm) - ZnSe (5 nm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> light guide layer 35 (p = 5El7, 0.05 µm), an N₂ doped Mg<sub>0.1</sub>Zn<sub>0.9</sub>S<sub>0.2</sub>Se<sub>0.8</sub> clad layer 24 (p = 1El7, 1.0 µm), an N₂ doped ZnS<sub>0.1</sub>Se<sub>0.9</sub> clad layer 7 (p = 5El7, 0.5 µm) and a ZnSe cap layer 38 (p = 1El8, 0.1 µm). The surface of the sample was irradiated with molecular beams of Te for several tens min while keeping the sample temperature at the crystal growth temperature, and was then cooled to a temperature near room temperature. By this processing, a p-type ZnSeTe alloy with a gradient composition was formed on the surface of the sample. An SiO₂ film was formed on the sample by plasma CVD. The SiO₂ film was made in the form of a stripe having a width of about 5 µm using the known photolithography. A reverse mesa structure having a depth of about 1.5 µm was formed using a bromine based selective etching solution. This sample was then dipped in a (NH₄)₂Sx solution for several min and cleaned by an alcohol based solvent, and it was put in the metal-organic vapor deposition system.
0082This sample was irradiated with hydrogen radicals while being heated at about 300°C to remove excessive sulfur. On the sample, an undoped Mg<sub>0.2</sub>Zn<sub>0.7</sub>S<sub>0.3</sub>Se<sub>0.7</sub> block layer 46 (n = 1El4, 1.5 µm) was grown as a buried layer. Next, an SiO₂ film 12 was formed on the buried layer by plasma CVD, and a striped hole having a width of about 5 µm was formed on the SiO₂ film using the known photolithography.
0083Next, a Ti-Pt-Au multi-layer electrode 13 was deposited to a thickness of about 1 µm by vacuum vapor deposition. Moreover, an AuGe-Ni-Au multi-layer electrode 14 was deposited on the rear surface of the GaAs substrate which was polished to a thickness of 100 µm, after which the sample was cleaved to form a laser structure with a length of 1000 µm.
0084The device thus obtained was dipped in the (NH₄)₂Sx solution for several min and cleaned with alcohol based solvent, and an SiNx-SiO₂ multi-layer reflection film was formed at the end surface of the resonator by sputtering.
0085The semiconductor laser of this structure is capable of continuously oscillating at room temperature a marine blue laser of a single vertical mode having a characteristic of a threshold current of 2 mA, a drive voltage 4V, and an oscillation wavelength of 500 nm.
0086According to the present invention, there can be provided a short wave II-VI compound semiconductor laser with a high reliability, which is capable of reducing the threshold current, lowering the contact resistance of an electrode, and reducing the lattice strain due to thermal expansion; and which is capable of continuously oscillating a laser at room temperature by the improvement in the confinement of injected charge and light.
13 sheets
Sheet 1 Sheet 2 Sheet 3 Sheet 4 Sheet 5 Sheet 6 Sheet 7 Sheet 8 Sheet 9 Sheet 10 Sheet 11 Sheet 12 Sheet 13
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| Document | Relation | Office | Cited during |
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| WO9707536A3 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| WO9707536A3 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP1622207A4 | Cited by | European Patent Office (EPO) | Examiner |
| US5619518A | Cited by | United States of America | Search report |
| EP0661784A2 | Cited by | European Patent Office (EPO) | Search report |
| EP2290766A3 | Cited by | European Patent Office (EPO) | Search report |
| WO9939413A3 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP1622207A1 | Cited by | European Patent Office (EPO) | Examiner |
| WO9939413A2 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP0661784A3 | Cited by | European Patent Office (EPO) | Search report |
| WO9707536A2 | Cited by | World Intellectual Property Organization (WIPO) | International search |
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| US9450375B2 | Cited by | United States of America | Applicant |
| WO03096498A2 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| EP0284031A2 | Cites | European Patent Office (EPO) | Search report |
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| FR2651605A1 | Cites | France | Search report |
| US4866489A | Cites | United States of America | Search report |
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4 priority claims, no other members on record
Priority claims4
| Document | Office | Kind | Date |
|---|---|---|---|
| 19447193 | Japan | – | |
| 19447193 | Japan | A | |
| 6238494 | Japan | – | |
| 6238494 | Japan | A |
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Numbers
- Publication
- 0637862
- Application
- 941118929
Titles3
- German
- Halbleiterlaservorrichtung und Herstellungsverfahren
- English
- Semiconductor laser device and method of fabricating the laser device
- French
- Dispositif laser à semi-conducteur et méthode de fabrication
Classification
- CPC, 35
- H01S5/327
- H10H20/832
- B82Y20/00
- H01S5/028
- H01S5/0281
- H01S5/0282
- H01S5/0421
- H01S5/20
- H01S5/2004
- H01S5/2009
- H01S5/2211
- H01S5/2231
- H01S5/227
- H01S5/2275
- H01S5/3201
- H01S5/3211
- H01S5/3213
- H01S5/3215
- H01S5/3216
- H01S5/3218
- H01S5/3406
- H01S5/3409
- H01S5/3422
- H01S5/347
- H10H20/0125
- H10H20/823
- H10P14/3221
- H10P14/3228
- H10P14/3231
- H10P14/2911
- H10P14/3252
- H10P14/3428
- H10P14/3431
- H10P14/3442
- H10P14/3444
- IPC, 14
- H01L21 36
- H01L33 00
- H01L33 28
- H01L33 40
- H01S5 028
- H01S5 042
- H01S5 20
- H01S5 22
- H01S5 223
- H01S5 227
- H01S5 32
- H01S5 327
- H01S5 34
- H01S5 347
Designated states3
- Contracting states, 3
- Germany
- United Kingdom
- Netherlands (Kingdom of the)