journal article·2024-11Open access

Innovative In Situ Passivation Strategy for High‐Efficiency Sb2(S,Se)3 Solar Cells

Yuqi Zhao, Wentao Xu, Jing Wen, Xiaomin Wang, Xueling Chen, Bo Che, Haolin Wang, Junbo Gong, Tao Chen, Xudong Xiao, Jianmin Li

Advanced Materials· Volume 36· Issue 46

Abstract

Abstract An effective defect passivation strategy is crucial for enhancing the performance of antimony selenosulfide (Sb2(S,Se)3) solar cells, as it significantly influences charge transport and extraction efficiency. Herein, a convenient and novel in situ passivation (ISP) technique is successfully introduced to enhance the performance of Sb2(S,Se)3 solar cells, achieving a champion efficiency of 10.81%, which is among the highest recorded for Sb2(S,Se)3 solar cells to date. The first principles calculations and the experimental data reveal that incorporating sodium selenosulfate in the ISP strategy effectively functions as an in situ selenization, effectively passivating deep‐level cation antisite SbSe defect within the Sb2(S,Se)3 films and significantly suppressing non‐radiative recombination in the devices. Space‐charge‐limited current (SCLC), photoluminescence (PL), and transient absorption spectroscopy (TAS) measurements verify the high quality of the passivated films, showing fewer traps and defects. Moreover, the ISP strategy improved the overall quality of the Sb2(S,Se)3 films, and fine‐tuned the energy levels, thereby facilitating enhanced carrier transport. This study thus provides a straightforward and effective method for passivating deep‐level defects in Sb2(S,Se)3 solar cells.
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Research context

OpenAlex topics: Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties · Phase-change materials and chalcogenides

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory of Artificial Micro‐ and Nano‐structures of Ministry of Education and School of Physics and Technology Wuhan University Wuhan 430072 China

Hubei Key Laboratory of Plasma Chemistry and Advanced Materials Hubei Engineering Technology Research Center of Optoelectronic and New Energy Materials Wuhan Institute of Technology Wuhan 430205 China

Hefei National Research Center for Physical Science at the Microscale CAS Key Laboratory of Materials for Energy Conversion Department of Materials Science and Engineering School of Chemistry and Materials Science University of Science and Technology of China Hefei 230026 China

Funding

National Natural Science Foundation of China

References (63)

Show source-provided references
1. 10.1038/nphoton.2015.7810.1038/nphoton.2015.78 ↗
2. 10.1038/nenergy.2017.4610.1038/nenergy.2017.46 ↗
3. 10.1002/adfm.20190172010.1002/adfm.201901720 ↗
4. 10.1038/s41560-020-0652-310.1038/s41560-020-0652-3 ↗
5. 10.1002/adfm.20231367610.1002/adfm.202313676 ↗
6. 10.1002/adfm.20210026510.1002/adfm.202100265 ↗
7. Ayala‐Mató F. · Appl. Phys. Lett. · 2021 · 118
8. 10.1016/j.joule.2018.04.00310.1016/j.joule.2018.04.003 ↗
9. 10.1021/acsami.9b0122010.1021/acsami.9b01220 ↗
10. 10.1002/solr.20190050310.1002/solr.201900503 ↗
11. 10.1021/acsami.0c0367410.1021/acsami.0c03674 ↗
12. 10.1063/5.009409110.1063/5.0094091 ↗
13. 10.1002/adfm.20130423810.1002/adfm.201304238 ↗
14. 10.1002/solr.20220111510.1002/solr.202201115 ↗
15. 10.1063/1.489417010.1063/1.4894170 ↗
16. 10.1021/acsami.2c0680510.1021/acsami.2c06805 ↗
17. 10.1016/j.nanoen.2019.10392910.1016/j.nanoen.2019.103929 ↗
18. 10.1016/j.solmat.2021.11152010.1016/j.solmat.2021.111520 ↗
19. 10.1039/D1FD00056J10.1039/D1FD00056J ↗
20. 10.1039/D2TA00893A10.1039/D2TA00893A ↗
21. 10.1002/solr.20190058210.1002/solr.201900582 ↗
22. 10.1007/s40843-022-2066-510.1007/s40843-022-2066-5 ↗
23. 10.1002/adma.20220624210.1002/adma.202206242 ↗
24. 10.1002/aenm.20230039110.1002/aenm.202300391 ↗
25. 10.1038/s41467-018-04634-610.1038/s41467-018-04634-6 ↗
26. 10.1002/adma.20220296910.1002/adma.202202969 ↗
27. 10.1002/pip.290010.1002/pip.2900 ↗
28. 10.1002/ente.20180023810.1002/ente.201800238 ↗
29. 10.1021/acsami.1c0239310.1021/acsami.1c02393 ↗
30. 10.1039/D2TA00893A10.1039/D2TA00893A ↗
31. 10.1039/D2EE02261C10.1039/D2EE02261C ↗
32. 10.1021/acsami.2c1791210.1021/acsami.2c17912 ↗
33. 10.1002/smll.20220617510.1002/smll.202206175 ↗
34. 10.1002/adfm.20231497410.1002/adfm.202314974 ↗
35. 10.1002/adma.20210907810.1002/adma.202109078 ↗
36. 10.1016/j.solmat.2020.11050210.1016/j.solmat.2020.110502 ↗
37. 10.1021/acsami.1c1912210.1021/acsami.1c19122 ↗
38. 10.1002/adfm.20230976410.1002/adfm.202309764 ↗
39. 10.1002/adma.20220624210.1002/adma.202206242 ↗
40. 10.1002/nano.20200028810.1002/nano.202000288 ↗
41. 10.1021/acsenergylett.0c0094010.1021/acsenergylett.0c00940 ↗
42. 10.1002/advs.20210526810.1002/advs.202105268 ↗
43. 10.1002/smll.20210242910.1002/smll.202102429 ↗
44. 10.1039/C9TA02022E10.1039/C9TA02022E ↗
45. 10.1002/solr.20200069310.1002/solr.202000693 ↗
46. 10.1007/s12200-017-0702-z10.1007/s12200-017-0702-z ↗
47. 10.1021/acsenergylett.2c0146410.1021/acsenergylett.2c01464 ↗
48. 10.1016/j.jcis.2018.10.01510.1016/j.jcis.2018.10.015 ↗
49. 10.1021/acsami.0c1155010.1021/acsami.0c11550 ↗
50. 10.1002/aenm.20200234110.1002/aenm.202002341 ↗
51. 10.1039/D1TA02356J10.1039/D1TA02356J ↗
52. 10.1002/anie.20230250710.1002/anie.202302507 ↗
53. 10.7498/aps.70.2020201610.7498/aps.70.20202016 ↗
54. 10.1002/aenm.20210301510.1002/aenm.202103015 ↗
55. 10.1021/acsenergylett.6b0050910.1021/acsenergylett.6b00509 ↗
56. 10.1016/0379-6787(82)90057-610.1016/0379-6787(82)90057-6 ↗
57. 10.1021/acsenergylett.1c0181110.1021/acsenergylett.1c01811 ↗
58. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
59. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
60. 10.1103/PhysRevB.28.180910.1103/PhysRevB.28.1809 ↗
61. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗
62. 10.1002/solr.20180012810.1002/solr.201800128 ↗
63. 10.1063/1.509077310.1063/1.5090773 ↗