This invention relates generally to a multi-junction solar cell device and, more particularly, it relates to a multi-junction solar cell device containing III-V layers grown lattice-matched on silicon substrates.
Solar photovoltaic devices, i.e., solar cells, are devices capable of converting solar radiation into usable electrical energy. The energy conversion occurs as the result of what is known as the photovoltaic-effect which occurs in a cell composed of a p-type semiconductor layer adjacent to an n-type semiconductor layer, hereafter referred to as a p-n junction cell. Solar radiation impinging on a solar cell and absorbed by an active region of semiconductor material generates electricity.
Multi-junction solar cells may be more efficient than single-junction solar cells if properly designed. One such design is described in U.S. Pat. No. 5,223,043 issued to Olson et al. Important considerations to achieve high efficiency energy conversion include the following: a) high quality crystalline layers; b) appropriate choice of junction band-gaps based on the impinging solar spectrum; c) tunnel junction interconnects between p-n junctions; d) appropriate choice of layer thicknesses to achieve a current-matched structure; and e) passivating layers, such as back-surface-field layers or window layers, to reduce losses. In the past, high-efficiency III-V semiconductor multi-junction solar cells have been grown on GaAs, InP, and Ge substrates, but silicon substrates have been found advantageous for cost and mechanical robustness reasons.
Alloys containing the atoms (AlGaIn)(PAsSb) are examples of III-V semiconductors, so named because their constituent elements come from the columns IIIb and Vb of the periodic table. In the past, solar cells consisting of high-quality, single-crystal layers of (AlGaIn)(PAsSb) semiconductor alloys with a large range of optical properties have been grown on GaAs, InP, and Ge substrates because these alloys can be fabricated with compositions such that the crystal lattice parameter and crystal symmetry match that of the underlying substrate. This “lattice-matching” condition results in epitaxial layers with minimal strain, few defects and thus superior electrical properties. Unfortunately, the set of semiconductors alloys (AlGaIn)(PAsSb) cannot be lattice-matched to silicon for any composition.
In the past, many investigators have attempted to grow III-v solar cells on single-crystal silicon substrates. Blakeslee et al. (U.S. Pat. No. 4,278,474), Umeno et al. (U.S. Pat. No. 4,963,508), and Ringel et al. (U.S. Pat. No. 5,571,339) have all disclosed lattice-mismatched III-V solar cell devices grown on silicon substrates using strain-relieving buffer layers. But because these III-V solar cell designs are not lattice-matched to the underlying silicon, problems with high defect densities in the III-V semiconductor layers have prevented such solar cell designs from achieving efficiencies as high as those on GaAs or Ge substrates.
The addition of small amounts of boron (B) and/or nitrogen (N) to the more standard III-V alloys does allow for compositions lattice-matched to silicon to be reached. For example, GaNxP1-x-yAsy is lattice-matched to silicon for 0.022<x<0.194 and y=4.6x−0.09. The ability to fabricate these semiconductor alloys with nitrogen or boron concentrations greater than about 0.1% has only recently been discovered and the achievable compositions and their properties are under current investigation.
In the recent past, GaNxP1-x, GaInyNxP1-x, and GaNxP1-x-yAsy have been grown on Gap and Si substrates for light emitting applications. GaNxP1-x has also been shown to have a direct (or direct-like) band gap. BxGa1-x-yInyAs has been grown on GaAs, but would require considerably greater concentrations of boron to be lattice-matched to silicon. BxGa1-xP has not been attempted but would have a much better chance to be lattice-matched with silicon than BxGa1-x-yInyAs. All of these III-V semiconductors have typically been grown using metal-organic vapor phase epitaxy (MOVPE), molecular beam epitaxy (MBE), and similar techniques.
The present invention is a multi-junction solar cell device. The multi-junction solar cell device comprises either two or three active solar cells connected in series in a monolithic structure. The multi-junction device comprises a bottom active cell having a single-crystal silicon substrate base and an emitter layer. The multi-junction device further comprises one or two subsequent active cells, each of which has a base layer and an emitter layer and wherein there is an interconnecting tunnel junction between two adjacent active cells. At least one layer that forms each of the top and middle active cells comprises a single-crystal III-V semiconductor alloy that is substantially lattice-matched to the silicon substrate. The polarity of the active p-n junction cells in the multi-junction device can be either p-on-n or n-on-p.
The present invention further includes a method for substantially lattice matching an active III-V solar cell or cells with an active silicon solar cell formed from a silicon substrate in a multi-junction solar cell device. The method comprises forming the bottom active cell from a silicon substrate, and forming the top active cell or cells with at least one III-V semiconductor layer which contains boron and/or nitrogen. The general composition of the III-V semiconductor layer, BxAlyGa1-x-y-zInzNsP1-s-t-wAstSbw, hereafter referred to as (BAlGaIn)(NPAsSb), can be lattice matched to a silicon substrate only when boron and/or nitrogen compositions are greater than zero. The quatemary alloys:
The lattice matching condition is temperature dependent because the thermal expansion coefficient of silicon is different from that of III-V semiconductors. Since these III-V semiconductor layers are typically grown at elevated temperatures, it may be more beneficial to lattice match the III-V semiconductor layers to silicon substrates at growth temperature rather than room temperature. When cooled to room temperature, III-V semiconductor layers that have been lattice matched at growth temperature will be slightly lattice mismatched, but should also be considered “substantially lattice matched.”
In addition, GaP and AlxGa1-xP are only slightly lattice mismatched with silicon substrates, but it may be argued that they are not “substantially lattice-matched with silicon.” While their high band gaps and slight lattice mismatch with silicon do not allow them to be useful as thicker light absorbing layers in the present invention, relatively thin layers of GaP and AlGaP within the structure of the present invention do not significantly affect the degree to which the relatively thick active solar cells on silicon substrates are strained. Thus, the active cell which contains a relatively thin GaP or AlGaP layer does not develop strain-related defects and the entire active cell is considered substantially lattice-matched with silicon.
The accompanying drawings, which are incorporated in and form a part of the specification, illustrate the preferred embodiments of the present invention, and together with the descriptions serve to explain the principles of the invention.
In the Drawings:
As illustrated in
As illustrated in
In a preferred embodiment of the present invention described above, the compositions of (BAlGaIn)(NPAsSb) substantially lattice matched to the silicon substrate would be chosen from the group of quaternary alloys; GaNPAs, GaInNP, or BGaPAs specified previously. The following is a detailed description of a preferred embodiment to illustrate the spirit of the two-junction device 10 of the present invention as illustrated in
In this example, III-V semiconductors are grown on a single-crystal p-type silicon wafer 22 by MOVPE. Source materials would include triethylgallium, phosphine, tertiary-butyl arsine, and dimethylhydrazine. Growth temperatures would be between 600°-700° C.
The first layer deposited on the silicon substrate 22 would be a window layer of 0.1 μm GaP doped highly n-type with Se from hydrogen selenide. Some of the phosphorus from this layer would diffuse into the silicon substrate 22 during growth forming a thin n-type emitter layer 23 within the silicon substrate 22 Next a 0.05 μm thick GaP layer doped highly p-type with carbon from CCl4 together with the n-type GaP window layer would form the tunnel junction 50. A p-type Zn-doped back-surface-field for the top active cell 30 composed of 0.1 μm GaP would then be deposited on the tunnel junction 50. A 1.0 μm GaN0.07As0.23P0.70 top base layer 32 with a band gap of approximately 1.65 eV would serve as the primary absorbing layer of the top active cell 30. The GaN0.07As0.23P0.70 base 32 is not intentionally doped but has a background p-type doping level of approximately 1×1016 cm−3. The top emitter 33 is composed of 0.1 μm Se-doped GaP. A 0.1 μm thick highly Se-doped GaAs contact layer is deposited on the top emitter 33. This GaAs contact layer is removed except beneath the metal grid 70 after the Au/Sn/Au metal grids 70 are deposited by vacuum evaporation and standard photolithography techniques. A gold back-side contact 72 is also evaporated on the back of the device 10. A broadband two layer anti-reflective coating is finally deposited on the front of the device 10. The thickness and composition of the GaN0.07As0.23P0.70 top base layer 32 would be adjusted slightly to achieve a current-matched structure to optimize the efficiency of the entire device 10.
As illustrated in
In an example embodiment of the three-junction version of the solar cell device 100 of the present invention, the compositions of (BAlGaIn)(NPAsSb) substantially lattice matched to the silicon substrate may be chosen from the group of quatemary alloys; GaNPAs, GaInNP, or BGaPAs previously discussed above.
The foregoing exemplary descriptions and the illustrative preferred embodiments of the present invention have been explained in the drawings and described in detail, with varying modifications and alternative embodiments being taught. While the invention has been so shown, described and illustrated, it should be understood by those skilled in the art that equivalent changes in form and detail may be made therein without departing from the true spirit and scope of the invention, and that the scope of the present invention is to be limited only to the claims except as precluded by the prior art. Moreover, the invention as disclosed herein, may be suitably practiced in the absence of the specific elements which are disclosed herein.
The United States Government has rights in this invention under Contract No. DE-AC36-99GO10337 between the U.S. Department of Energy and the National Renewable Energy Laboratory, a Division of Midwest Research Institute.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US01/48183 | 12/14/2001 | WO | 00 | 5/27/2004 |
Publishing Document | Publishing Date | Country | Kind |
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WO03/052836 | 6/26/2003 | WO | A |
Number | Name | Date | Kind |
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4278474 | Blakeslee et al. | Jul 1981 | A |
4681982 | Yoshida | Jul 1987 | A |
4963508 | Umeno et al. | Oct 1990 | A |
5002618 | Kanai et al. | Mar 1991 | A |
5009719 | Yoshida | Apr 1991 | A |
5571339 | Ringel et al. | Nov 1996 | A |
5944913 | Hou et al. | Aug 1999 | A |
6100546 | Major et al. | Aug 2000 | A |
6281426 | Olson et al. | Aug 2001 | B1 |
6300558 | Takamoto et al. | Oct 2001 | B1 |
6815736 | Mascarenhas | Nov 2004 | B2 |
Number | Date | Country |
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63217672 | Sep 1988 | JP |
09237909 | Sep 1997 | JP |
Number | Date | Country | |
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20040261837 A1 | Dec 2004 | US |