Silicon photovoltaic element and fabrication method
Abstract
A method of forming a photovoltaic device that includes providing an absorption layer of a first crystalline semiconductor material having a first conductivity type, and epitaxially growing a second crystalline semiconductor layer of a second conductivity type that is opposite the first conductivity type. The first conductivity type may be p-type and the second conductivity type may be n-type, or the first conductivity type may be n-type and the second conductivity type may be p-type. The temperature of the epitaxially growing the second crystalline semiconductor layer does not exceed 500° C. Contacts are formed in electrical communication with the absorption layer and the second crystalline semiconductor layer.
Claims
exact text as granted — not AI-modified1 . A photovoltaic device comprising:
an absorption layer comprised of a crystalline semiconductor material, wherein the crystalline semiconductor material is doped to a first conductivity type; an epitaxial semiconductor material in direct contact with the absorption layer, wherein the epitaxial semiconductor material is doped to a second conductivity type opposite the first conductivity type; and a passivation layer comprises an intrinsic amorphous semiconductor material is in direct contact with the epitaxial semiconductor material.
2 . The photovoltaic device of claim 1 , wherein the crystalline semiconductor material of the absorption layer comprises a single crystal crystalline structure.
3 . The photovoltaic device of claim 1 , wherein the crystalline semiconductor material of the absorption layer comprises a poly-crystalline or multi-crystalline structure.
4 . The photovoltaic device of claim 1 , wherein the crystalline semiconductor material is a silicon-containing material.
5 . The photovoltaic device of claim 4 , wherein the first conductivity type is n-type and the second conductivity type is p-type, or the first conductivity type is p-type and the second conductivity type is n-type.
6 . The photovoltaic device of claim 5 , wherein the absorption layer has a thickness ranging from 50 nm to 1 mm, and the first conductivity type is provided by a dopant present in a concentration ranging from 10 9 atoms/cm 3 to 10 20 atoms/cm 3 .
7 . The photovoltaic device of claim 1 , wherein the epitaxial semiconductor material is comprises a single crystal crystalline structure.
8 . The photovoltaic device of claim 1 , wherein the epitaxial semiconductor material is a poly-crystalline or multi-crystalline structure.
9 . The photovoltaic device of claim 1 , wherein the epitaxial semiconductor material is a silicon-containing material.
10 . The photovoltaic device of claim 9 , wherein the epitaxial semiconductor material has a thickness ranging from 2 nm to 2 μm, and the first conductivity type is provided by a dopant present in a concentration ranging from 10 16 atoms/cm 3 to 5 10 20 atoms/cm 3 .
11 . The photovoltaic device of claim 1 , further comprising a transparent conductive material layer present in direct contact with the passivation layer.
12 . The photovoltaic device of claim 11 , further comprising an emitter contact in direct contact with the transparent conductive material layer, and a back contact to the absorption layer.
13 . The photovoltaic device of claim 12 , further comprising a back surface field layer between and in direct contact with the absorption layer and the back contact, wherein at least a portion of the back surface field layer comprises a semiconductor material doped to provide a same conductivity type as the absorption layer.
14 . The photovoltaic device of claim 13 , wherein the back surface field layer comprises single or multi-layers of crystalline, or non-crystalline semiconductor material, having a thickness ranging from 2 nm to 10 μm, wherein a dopant to provide the same conductivity type as the absorption layer is present in the back surface field layer in a concentration ranging from 10 17 atoms/cm 3 to 10 21 atoms/cm 3 .
15 . The photovoltaic device of claim 1 , wherein the passivation layer is comprised of intrinsic amorphous hydrogenated silicon (a-Si:H).
16 . A method of forming a photovoltaic device comprising:
providing an absorption layer comprised of a first crystalline semiconductor material having a first conductivity type; epitaxially growing a second crystalline semiconductor layer having a second conductivity type that is opposite the first conductivity type, wherein temperature of the epitaxially growing the second crystalline semiconductor layer is 500° C. or less; and forming contacts in electrical communication with the absorption layer and the second crystalline semiconductor layer.
17 . A method of claim 16 , wherein the temperature of the epitaxially growing the second crystalline semiconductor layer is 200° C. or less.
18 . The method of claim 16 , wherein the first conductivity type is p-type and the second conductivity type is n-type, or the first conductivity type is n-type and the second conductivity type is p-type.
19 . The method of claim 16 , wherein the absorption layer is provided by a semiconductor substrate having a single crystal crystalline structure, the absorption layer having a thickness ranging from 50 nm to 1 mm, and having a dopant concentration that provides the first conductivity type of the absorption layer that ranges from 10 9 atoms/cm 3 to 10 20 atoms/cm 3 .
20 . The method of claim 16 , wherein the absorption layer has a single crystal crystalline structure, and the epitaxially growing of the second crystalline semiconductor layer produces a single crystal crystalline structure for the second crystalline semiconductor layer, wherein the second crystalline semiconductor layer has a thickness ranging from 2 nm to 2 um, and the second crystalline semiconductor layer has a dopant concentration that ranges from 10 16 atoms/cm 3 to 5×10 20 atoms/cm 3 .
21 . The method of claim 16 , wherein the epitaxially growing of the second crystalline semiconductor layer comprises plasma enhanced chemical vapor deposition (PECVD) from a mixture of silane (SiH 4 ), hydrogen (H 2 ) and dopant gasses.
22 . The method of claim 21 , wherein the ratio of silane (SiH 4 ) to hydrogen (H 2 ) is greater than 5:1.
23 . The method of claim 22 , wherein the ration of silane (SiH 4 ) to hydrogen (H 2 ) ranges from 5:1 to 1000:1.
24 . The method of claim 22 , wherein the second conductivity type dopant is n-type, the dopant gasses comprise phosphine gas (PH 3 ) present in a ratio to silane (SiH 4 ) ranging from 0.01% to 10%, or the dopant gasses comprise arsenic gas (AsH 3 ) present in a ratio to silane (SiH 4 ) ranging from 0.01% to 10%.
25 . The method of claim 22 , wherein the second conductivity type dopant is p-type, the dopant gasses comprise diborane gas (B 2 H 6 ) present in a ratio to silane (SiH 4 ) ranging from 0.01% to 10%, or the dopant gasses comprise trimethylboron gas (TMB) present in a ratio to silane (SiH 4 ) ranging from 0.01% to 10%.Join the waitlist — get patent alerts
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