Doped photovoltaic semiconductor layers and methods of making
US-2021143288-A1 · May 13, 2021 · US
US11201257B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11201257-B2 |
| Application number | US-201916966424-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 14, 2019 |
| Priority date | Feb 1, 2018 |
| Publication date | Dec 14, 2021 |
| Grant date | Dec 14, 2021 |
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According to the embodiments provided herein, a method for doping an absorber layer can include contacting the absorber layer with an annealing compound. The annealing compound can include cadmium chloride and a group V salt comprising an anion and a cation. The anion, the cation, or both can include a group V element. The method can include annealing the absorber layer, whereby the absorber layer is doped with at least a portion of the group V element of the annealing compound.
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What is claimed is: 1. A method for doping an absorber layer, comprising: contacting the absorber layer with an annealing compound, wherein: the absorber layer comprises cadmium, and tellurium; the annealing compound comprises cadmium chloride and a group V salt comprising an anion and a cation; the anion, the cation, or both comprise a group V element; a ratio of cadmium chloride to group V salt within the annealing compound, on a weight per volume basis, is at least 30 to 1; and annealing the absorber layer, whereby the absorber layer is doped with at least a portion of the group V element of the annealing compound. 2. The method of claim 1 , wherein the annealing compound is a solution, and a proportion of the group V salt to a total amount of the annealing compound is less than 100 grams per liter. 3. The method of claim 2 , wherein the proportion of the group V salt to the total amount of the annealing compound is between 1/25 grams per liter and 20 grams per liter. 4. The method of claim 1 , wherein a grain size of the absorber layer is increased during annealing of the absorber layer. 5. The method of claim 1 , wherein the group V salt is ammonium dihydrogen arsenate. 6. The method of claim 1 , wherein the group V salt is diammonium hydrogen phosphate. 7. The method of claim 1 , wherein the group V element is nitrogen. 8. The method of claim 1 , wherein the group V element is phosphorous. 9. The method of claim 1 , wherein the group V element is arsenic. 10. The method of claim 1 , wherein the group V element is antimony. 11. The method of claim 1 , wherein the group V element is bismuth. 12. The method of claim 1 , comprising exposing an absorber layer to a reducing environment, while the absorber layer is annealed. 13. The method of claim 12 , wherein the reducing environment comprises a forming gas configured to mitigate formation of group V oxides, the forming gas comprising hydrogen, nitrogen, carbon, or combinations thereof. 14. The method of claim 1 , wherein the absorber layer is annealed at a temperature between 350° C. and 500° C. for between 5 minutes and 60 minutes. 15. The method of claim 1 , wherein: the annealing compound comprises an alkali metal chloride; and at least a portion of the group V dopant is activated during annealing of the absorber layer. 16. The method of claim 1 , wherein, after the absorber layer is annealed, an atomic concentration of the group V dopant in a central region of the absorber layer is greater than 1×10 16 cm −3 . 17. The method of claim 1 , wherein the absorber layer comprises selenium. 18. The method of claim 1 , wherein a grain size of the absorber layer is increased during annealing of the absorber layer. 19. The method of claim 1 , wherein the group V salt is ammonium dihydrogen arsenate. 20. The method of claim 1 , wherein the group V salt is diammonium hydrogen phosphate. 21. The method of claim 1 , wherein the group V element is nitrogen. 22. The method of claim 1 , wherein the group V element is phosphorous. 23. The method of claim 1 , wherein the group V element is arsenic. 24. The method of claim 1 , wherein the group V element is antimony. 25. The method of claim 1 , wherein the group V element is bismuth. 26. The method of claim 1 , comprising exposing an absorber layer to a reducing environment, while the absorber layer is annealed. 27. The method of claim 26 , wherein the reducing environment comprises a forming gas configured to mitigate formation of group V oxides, the forming gas comprising hydrogen, nitrogen, carbon, or combinations thereof.
characterised by the semiconductor material · CPC title
within a single semiconductor body or layer in a solid phase; between different semiconductor bodies or layers, both in a solid phase · CPC title
having at least three elements, e.g. HgCdTe · CPC title
characterised by the dopants · CPC title
comprising only Group II-VI materials, e.g. CdS/CdTe photovoltaic cells · CPC title
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