The present disclosure relates to the manufacture of multi junction solar cell substrates, in particular, to the manufacture of multi junction solar cell substrates comprising wafer transfer processes and the manufacture of solar cell devices for terrestrial and space-related applications.
Photovoltaic or solar cells are designed for converting the solar radiation to electrical current. In concentrator solar photovoltaic applications, the incoming sunlight is optically concentrated before it is directed to solar cells. For example, the incoming sunlight is received by a primary mirror that reflects the received radiation toward a secondary mirror that, in turn, reflects the radiation toward a solar cell, which converts the concentrated radiation to electrical current by the generation of electron-hole pairs in III-V semiconductor or single crystal silicon, for example. Alternatively, the sunlight could be concentrated onto solar cells by using transmittive optics like Fresnel lenses.
Since different semiconductor material compositions show optimal absorption for different wavelengths of the incoming solar light, multi junction solar cells have been proposed that comprise, for example, three cells showing optimal absorption in different wavelength ranges. A triple cell structure may comprise a GaInP top cell layer with a gap value of 1.8 eV, a GaAs intermediate cell layer with a gap value of 1.4 eV, and a Ge bottom cell layer with a gap value of 0.7 eV, for instance. In principle, III-V or group IV semiconductors can be used as active cell layers of multi junction solar cell devices manufactured by layer transfer/bonding. Multi-junction solar cells are usually manufactured by monolithic epitaxial growth. The monolithic growth process requires, in general, that any formed layers be substantially lattice matched to previously formed layers or the underlying substrate. However, the epitaxial growth of the solar cell layers on growth substrates still provides a demanding problem in view of lattice mismatches. For example, it is not suitable to epitaxially grow an InP solar cell layer on a Ge substrate, since the crystalline and optical characteristics of the InP solar cell layer would be heavily deteriorated due to crystal mismatch. In addition, in conventionally used transfer processes, intermediate substrates are lost after the transfer of epitaxially grown layers.
Thus, despite the recent engineering progress, there is still a need for an improved manufacturing process for multi junction solar cell devices wherein solar cell layers with a low defect rate are achieved and an intermediate substrate can be recycled.
The present disclosure addresses the above-mentioned need and, accordingly, provides a method for manufacturing a multi junction solar cell device, comprising the steps of:
providing a first substrate;
providing a second substrate;
bonding the first substrate to the second substrate; and
subsequently forming at least one first solar cell layer on the exposed surface of the first substrate and at least one second solar cell layer at the exposed surface of the second substrate.
The resulting structure thus comprises at least one solar cell layer on either side (upper and lower surface, respectively) of bonded first and second substrates. Different from the art, bonding is performed at main surfaces of the first substrate and the second substrate, before any solar cell layer has been formed on the substrates. Since the bonding surfaces of theses substrates can be prepared (for instance, by polishing) before bonding, the bond can be achieved with high quality, in particular, with a better quality as compared to bonding wherein one or two (epitaxially grown) solar cell layers are involved.
Contacting and bonding can be performed at relatively high temperatures of about 400° C. to 600° C. and, more preferably, between 450° C. and 550° C. Preferably, the contacting step is performed at room temperature followed by an annealing step reaching max temperature between 400° C. and 600° C., although it is not excluded to perform the contacting step at a higher temperature. This bonding step is crucial for the quality of the resulting structure and it is favorable to perform a high-temperature bonding anneal in order to achieve a high-quality bonding interface between the two substrates without significant defects.
In case of direct bonding, which forms the preferred approach, the polishing of the surfaces to be bonded may be performed in order to smooth the surface, to 0.5 nm RMS over a field of 5×5 micrometers, for example, to obtain an enhanced bonding strength and improved efficiency and reliability of the subsequent solar cell. Alternatively, an electrically conductive, optically transparent material can be used as a bonding layer and facilitates the adhesion of the two substrates.
The second substrate can be a relatively thin substrate of some 100 micrometers, for example, or from about 100 micrometers to about 300 micrometers, to provide mechanical stability to the resulting structure. In particular, the second substrate can be made of or comprise GaAs.
The first substrate can be provided in the form of an engineered substrate, in particular, comprising sapphire.
The term “engineered substrate” comprises a substrate that is different from a mere pure bulk substrate but rather includes a layer or interface that is formed in the substrate in order to facilitate its removal from the structure resulting from the bonding of the first and second wafer structures. In particular, the “engineered substrate” may comprise a zipper layer between a seed layer and a base substrate. In particular, the engineered substrate may comprise a base substrate that is detached from the seed layer in the step of removal of the engineered substrate.
Detachment by means of the zipper layer allows for recycling the detached substrate.
In the document, the expression “detachment of the engineered substrate” should be interpreted as the detachment of the base substrate. This detachment step may be followed by the removal of the possible residue of the zipper layer (if any), and of the removal of the seed layer from the remaining structure.
The zipper layer may be a weakened layer formed, e.g., by an appropriate treatment, for instance, a hydrogen or helium implantation in a substrate, that delimit an upper seed layer and a lower base substrate.
The zipper layer may be formed by a buried porous layer by anodic etching at a surface of the base substrate. Then, epitaxial growth of the seed layer can be performed on top of the porous layer.
The zipper layer may be provided in the form of an absorbing layer for laser lift-off, chemical lift-off or mechanical splitting in an intermediate strained layer during an epitaxy sequence: SiGe in Si matrix, in particular, an intermediate strained layer of SiGe at 20% in an Si substrate. In this alternative, the zipper layer may be formed by the seed layer itself, for instance, the seed layer can be selectively and chemically etched away to detach the engineered substrate.
The zipper layer may also be formed of an SiN absorbing layer for laser lift-off inserted between a seed layer and a transparent base substrate, as known, for example, from WO2010/015878.
Another possibility for an engineered substrate reads as follows: A removable (presenting a low bonding energy of less than 1.5 J/m2, and preferentially less than 1 J/m2) bonding interface is formed between facing surfaces of a seed layer and a base support. In that possibility, the zipper layer is formed by the removable bonding interface. A first solar cell layer may be grown by epitaxy on the seed layer while preserving the removable character of the bonding interface, with the engineered substrate being heated to an epitaxial growth temperature. The low energy bonding is obtained by performing a treatment for augmenting the roughness of the facing surface of one of the seed layer or the substrate, in particular, carried out by chemical attack or etching, by effecting a treatment for decreasing hydrophilicity of the facing surface of one of the seed layer or the substrate (or the bonding layer in SiO2 or Si3N4 on each of them). Moreover, a different material for the bonding layer can be chosen such that weak intrinsic mutual chemical affinity of the interface materials is achieved. The detachment of the base substrate may be performed by application of a thermal treatment or mechanical stresses applied from a jet of fluid or a blade, for example. This is disclosed, for instance, in WO03/063214.
As already mentioned, the engineered substrate may include a seed layer formed at the top of the zipper layer or removable bonding interface. The seed layer is transferred from the seed substrate to a base substrate by layer transfer from wafer to wafer, for example, by the SMARTCUT® process. The seed layer may or may not contain an epitaxial layer that has been formed originally by epitaxy on the seed substrate. Alternatively, the seed layer has been transferred or detached from a bulk seed substrate. In a preferred embodiment of the present disclosure, the seed layer is not used as a solar cell layer, but rather a first solar cell layer is grown on the seed layer.
The first substrate may be provided in the form of an InP bulk substrate comprising H or He implants in some implantation layer at which a part of the InP bulk substrate can be detached after bonding to the second substrate. The first substrate may also be an engineered substrate in the above-described sense. In particular, the first substrate may comprise a zipper layer (see description above) and the method may comprise the step of detaching a part of the first engineered substrate at the zipper layer.
Anyway, thinning at least one of the first and second substrates after bonding and before the formation of the solar cell layers may be comprised in the inventive method according to exemplary embodiments.
According to an example, the first substrate is provided in the form of an InP on sapphire substrate and the InP layer is bonded to the second substrate, followed by detachment of the sapphire base and, optionally, removal of remaining material on the InP layer.
Whatever the method chosen to provide the InP layer, it is preferable that the thickness of this layer be below 10 micrometers and, more preferably, less than 1 micrometer. A solar cell layer can be grown on the InP layer (substrate) with high crystal and electrical quality. For example, a dislocation density of less than 106/cm2 can be achieved.
As already mentioned, the main surfaces of the first and second substrate may be prepared, for instance, by polishing. This not only holds for the bonding surfaces but also for the free surfaces, whereupon the semiconductor layers are grown, since polishing in this case enhances the crystalline quality of the (epitaxially) grown semiconductor layers.
Further, the method may comprise forming a contact on the at least one first solar cell layer. Furthermore, before forming a contact, the corresponding solar cell layer may be patterned to form a mesa, whereupon the contact can be provided.
The structure comprising the (thinned) first and second substrates and at least one solar cell layer on either the main surface of the bonded substrates may be further bonded to a base substrate. The bonding to the base substrate can be performed by means of an electrically conductive (metallic, or with conductor oxides, transparent conductor oxide TCO, silicide or by direct bonding, etc.) bonding layer formed on the first solar cell layer and/or the base substrate. An electrically conductive layer also particularly helps to provide for thermal conductivity to the base substrate that may function as a heat sink or may be connected to a heat sink and preferably is itself thermally and electrically conductive. The conductive bonding may be obtained by forming a eutectic Au/Sn or by thermocompression.
In this embodiment, bonding of the first and second substrates is performed while the (final) base substrate is not yet present in the structure. Possibly, no final substrate is necessary since the second substrate is thick enough to provide mechanical stability to the structure. Thus, a risk of metallic contaminations during bonding thermal treatment is avoided such that high temperature may be used. Moreover, the expansion of the base substrate that would be different from the expansion of the first and second substrates at such a temperature due to different coefficients of thermal expansion (CTE) would damage the structure, in particular, it would weaken the bonding interface.
A final base substrate made of tungsten or molybdenum or doped semiconductors like Ge, GaAs or InP may be particularly suitable for receiving the stack of solar cell layers provided on a second substrate made of, for instance, GaAs or GaAsOS (see below). In particular, the difference in CTE of the final base substrate to the CTE of the second substrate should be less than 30% in order to avoid problems related to the bonding to the final substrate.
According to a particular variant, in the above-described examples, the at least one first solar cell layer comprises two layers, a first layer and a second layer, that has been gown by epitaxy on the first layer, and the at least one second solar cell layer also comprises two layers, namely, a third layer and a fourth layer that has been grown by epitaxy on the third layer. According to a particular example, the first layer (bottom cell) comprises or consists of GaInAs and/or the second layer comprises or consists of GaInAsP and/or the fourth layer (top cell in the finished multi junction solar cell device) comprises or consists of GaInP and/or the third layer comprises or consists of GaAs. Thus, a four-cell multi junction solar cell device is achieved (comprising two solar cell layers on one main surface of a first substrate and one main surface of a second substrate) wherein the material of each cell is optimized for a particular wavelength of the incoming solar light. No layer transfer of solar cell layers is necessary during the entire manufacturing process. It should also be noted that in the above-described examples, one single detachment step (detaching the first substrate) only may be involved.
According to another embodiment the inventive method for manufacturing, a multi junction solar cell device further comprises the step of forming a cap layer on the at least one first solar cell layer (formed on the first substrate). The cap layer protects the at least one first solar cell layer during the further processing. In this context, the method may comprise the steps of:
This disclosure also provides an intermediate semiconductor device, comprising:
The intermediate semiconductor substrate may comprise a second solar cell layer foamed on a lower surface of the first substrate, a first solar cell layer formed on the second solar cell layer, a third solar cell layer formed on an upper surface of the second substrate and a fourth solar cell layer formed on the third solar cell layer. In this configuration, according to a particular example, the first layer comprises or consists of GaInAs and/or the second layer comprises or consists of GaInAsP and/or the third layer comprises or consists of GaAs and/or the fourth layer comprises or consists of GaInP.
Furthermore, the intermediate semiconductor substrate may comprise a base substrate, in particular, a base substrate made of Cu, Mo, W or Si or Al, in particular, aluminium sheet bonded to the first solar cell layer, in particular, by a conductive bonding layer.
A final base substrate made of tungsten or molybdenum or doped semiconductors like Ge, GaAs or InP may be particularly suitable for receiving the stack of solar cell layers provided on a second substrate made of, for instance, GaAs or GaAsOS (see below). In particular, the difference in CTE of the final base substrate to the CTE of the second substrate should be less than 30% in order to avoid problems related to the bonding to the final substrate.
In addition, a multi-junction solar cell device is provided that is obtainable by one of the above-described examples of the method for the manufacture of a multi-junction solar cell device according to this disclosure.
Additional features and advantages of the disclosure will be described with reference to the drawings. In the description, reference is made to the accompanying figures that are meant to illustrate an embodiment of the disclosure. It is understood that such an embodiment does not represent the full scope of the disclosure.
An example for the inventive method for the manufacturing of a multi junction solar cell comprising four solar cell layers is shown in
Furthermore, a second substrate 3 is provided. The second substrate 3 may be a thin bulk GaAs, presenting a thickness of 200 micrometers. The main surfaces (upper and lower surfaces) of both the first substrate 1 and the second substrate 3, according to the shown example, are polished in order to facilitate the subsequent processing. The lower surface of the first substrate 1, however, may not be polished before thinning after bonding (see below).
As it is illustrated in
Subsequently, a second 5 and a first 4 solar cell layer are formed on the free surface of the InP layer 1′. Similarly, a third 6 and fourth 7 solar cell layer are formed on the free surface of the second substrate 3. Optionally, a cap layer (not shown in
The four solar cell layers 4, 5, 7, 8 show absorption maxima for incident solar light for different wavelengths. The first solar cell layer 4 becomes the bottom cell and the fourth solar cell layer 7 becomes the top cell in the finished multi junction solar cell device. It is, therefore, important that the material and thicknesses of the second substrate 3 and layer 2 be selected to present a low absorption for incident light in the wavelength absorbed by solar cell layers 4 and 5.
According to the present example, all of the four monocrystal solar cell layers 4, 5, 7, 8 are formed by epitaxial growth. In principle, the material of the solar cell layers can be selected from III-V semiconductors of the group consisting of InGaAs, GaAS, AlGaAs, InGaP, InP and InGaAsP. For example, the first solar cell layer 4 may be comprised of InGaAs, the second solar cell layer 5 may be comprised of InGaP, InGaAsP or InP, the third solar cell layer 7 may be comprised of GaAsP or GaAs, and the fourth solar cell layer 8 may be comprised of InGaP or InAlAs. Appropriate tunnel junction layers may be provided between particular ones of the solar cell layers by deposition or growth on a respective solar cell layer.
In the next step illustrated in
In a possible but not necessary approach, the thus obtained structure can be bonded to a base substrate (not shown in
A final base substrate made of tungsten or molybdenum or doped semiconductors like Ge, GaAs or InP may be particularly suitable for receiving the stack of solar cell layers provided on a second substrate made of, for instance, GaAs or GaAsOS (see below). In particular, the difference in CTE of the final base substrate to the CTE of the second substrate should be less than 30% in order to avoid problems related to the bonding to the final substrate.
Sapphire may preferably be chosen in view of its coefficient of thermal expansion, which is of importance for the temperature change (up and down) during epitaxy and for the further processing, in particular, bonding step (see below). Moreover, sapphire is transparent to laser light and can, thus, allow for laser lift-off in a later processing step (see below).
The first substrate 1 and the second engineered substrate are bonded at the upper surface of the first substrate 1 and the GaAs layer 50 of the second engineered substrate. After the bonding, the major part of the bulk InP of the first substrate 1 is detached by means of the weakened layer 20. Moreover, the sapphire base 30 is detached from the GaAs layer 50 by means of the zipper layer 40, for example, the second engineered substrate is cleaved at the zipper layer 40, allowing the detachment of the sapphire base 30. For instance, the zipper layer 40 may be provided in the form of a weakened layer (similar to the one formed in the first substrate 1) formed by the implantation of ionic species, for example, hydrogen or helium ions.
The detachment of the sapphire base substrate 30 can be mediated by the application of mechanical forces to delaminate at the weakened layer formed by hydrogen or helium ions. Residue of the base substrate may be removed by etching and/or polishing, for example. It is noted that the detached sapphire base substrate 30 can be recycled to faint a new engineered substrate for the re-usage in the manufacture of further multi junction solar cells.
Then, a second solar cell layer 70 and a first solar cell layer 60 are subsequently formed on the InP layer 10′ that is bonded to the GaAs layer 50. On the other hand, a third solar cell layer 80 and a fourth solar cell layer 90 are formed on the GaAs layer 50. In addition, in the shown example, a cap layer 100 is provided for the protection of the first and second solar cell layers 60 and 70 during the further processing.
The third and fourth solar cell layers 80 and 90 are then patterned to form mesas 80′ and 90′. A contact 110 is formed atop of the mesa 90′ of the fourth solar cell layer 90. Subsequently, the cap layer 100 is removed from the second solar cell layer 70 and the first 60 and second 70 solar cell layers are also patterned to obtain mesas 70′ and 60′. After the patterning is completed, a base substrate 120 is bonded to the mesa 60′ resulting from the second solar cell layer 60.
All previously discussed embodiments are not intended as limitations but serve as examples illustrating features and advantages of the disclosure. It has to be understood that some or all of the above-described features can also be combined in different ways. It has to be understood that some or all of the above-described features can also be combined in different ways. In particular, it is possible, according to the invention, to form multi junction solar cells not only composed of four junctions (as generally disclosed in the previous embodiments), but also 2, 3, 5 or more.
Number | Date | Country | Kind |
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12290108.5 | Mar 2012 | EP | regional |
This application is a national phase entry under 35 U.S.C. §371 of International Patent Application PCT/EP2013/055138, filed Mar. 13, 2013, designating the United States of America and published in English as International Patent Publication WO 2013/143852 A1 on Oct. 3, 2013, which claims the benefit under Article 8 of the Patent Cooperation Treaty and under 35 U.S.C. §119(e) to European Patent Application Serial No. 12290108.5, filed Mar. 28, 2012, the disclosure of each of which is hereby incorporated herein in its entirety by this reference.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2013/055138 | 3/13/2013 | WO | 00 |