An In Situ Polymerization-Assisted Grain Growth Strategy for Efficient and Stable Sb2S3 Solar Cells
Source abstract
Abstract
Antimony sulfide (Sb 2 S 3 ) stands out as an exemplary material for the light-absorbing layer in solar cells, attributed to its favorable light absorption properties, eco-friendliness, and robust stability. However, undesirable [ hk 0] crystal orientation and the presence of pinholes will degrade film quality and device performance. Here, an in situ polymerization-assisted grain growth strategy was introduced by adding monomer acrylic acid (AA) to the growth solution during the chemical bath deposition (CBD) process of Sb 2 S 3 . At the initial stage, AA serves as a complexing agent, coordinating with Sb 3+ ions to mitigate particle agglomeration in the solution, which not only enhances the film quality but also ensures a more desirable [ hk 1] crystal orientation. During the reaction, in situ synthesized poly(acrylic acid) (PAA) builds coordination bonds with Sb 3+ through the carboxyl groups, inducing the cross-linking of Sb 2 S 3 grains. This cross-linking yields compressive constraints and reduces the number of pinholes in the Sb 2 S 3 films, culminating in improved film quality and reinforced device steadiness. Consequently, the best power conversion efficiency (PCE) of the AA-modified Sb 2 S 3 solar cell reached 7.12% (compared to 6.70% for the control), Furthermore, incorporating an additional SnO 2 electron transport layer and a BTR-TPA interfacial layer bolstered the efficiency to 7.51%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei 230009, P. R. China
Funding
National Natural Science Foundation of China
References (27)
Show source-provided references
1. 10.1002/adfm.20210026510.1002/adfm.202100265 ↗
2. 10.1016/j.joule.2018.04.00310.1016/j.joule.2018.04.003 ↗
3. 10.1016/j.solener.2016.02.01510.1016/j.solener.2016.02.015 ↗
4. 10.1002/anie.20231295110.1002/anie.202312951 ↗
5. 10.1038/s41560-020-0652-310.1038/s41560-020-0652-3 ↗
6. 10.1002/solr.20190050310.1002/solr.201900503 ↗
7. 10.1063/1.509077310.1063/1.5090773 ↗
8. 10.1002/adfm.20200288710.1002/adfm.202002887 ↗
9. 10.1002/adfm.20220960110.1002/adfm.202209601 ↗
10. 10.1016/j.jechem.2021.08.02910.1016/j.jechem.2021.08.029 ↗
11. 10.1016/0025-5408(75)90042-210.1016/0025-5408(75)90042-2 ↗
12. 10.1038/nenergy.2017.4610.1038/nenergy.2017.46 ↗
13. 10.1002/adfm.20231157710.1002/adfm.202311577 ↗
14. 10.1002/adma.20220624210.1002/adma.202206242 ↗
15. 10.1039/D3TA00678F10.1039/D3TA00678F ↗
16. 10.1002/aenm.20230274310.1002/aenm.202302743 ↗
17. 10.1002/adma.20200061710.1002/adma.202000617 ↗
18. 10.1002/aenm.20200234110.1002/aenm.202002341 ↗
19. 10.1021/acsaem.1c0366010.1021/acsaem.1c03660 ↗
20. 10.1016/j.optmat.2023.11388110.1016/j.optmat.2023.113881 ↗
21. 10.1021/acscatal.2c0138410.1021/acscatal.2c01384 ↗
22. 10.1002/adma.20200848710.1002/adma.202008487 ↗
23. 10.1039/C8TA07545J10.1039/C8TA07545J ↗
24. 10.1002/advs.20220235610.1002/advs.202202356 ↗
25. 10.1039/C4RA11739E10.1039/C4RA11739E ↗
26. 10.1021/nl202618410.1021/nl2026184 ↗
27. 10.1063/1.280255310.1063/1.2802553 ↗