Efficient Sb(S,Se) solar cells monitorable chemical bath deposition

The efficiency of Sb 2 (S,Se) 3 solar cells prepared via hydrothermal methods recently broke the bottleneck of 10%. However, limited by the black-box hydrothermal process, important experimental details, such as the real-time chemical reaction process, precursor temperature and pH in the hydrotherma...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-05, Vol.1 (21), p.11625-11635
Hauptverfasser: Li, Sen, Lu, Shuaicheng, Lu, Yue, Xue, Jiayou, Li, Kanghua, Chen, Chao, Tang, Jiang
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Zusammenfassung:The efficiency of Sb 2 (S,Se) 3 solar cells prepared via hydrothermal methods recently broke the bottleneck of 10%. However, limited by the black-box hydrothermal process, important experimental details, such as the real-time chemical reaction process, precursor temperature and pH in the hydrothermal reactor, have not been acquired accurately until now. Moreover, the hydrothermal method is unfavorable for fabricating large-area devices. Herein, we develop a simple and monitorable chemical bath deposition (CBD) method to fabricate an Sb 2 (S,Se) 3 absorber layer. Owing to the open space of CBD, the physical and chemical processes during the whole film deposition could be studied based on the real-time precursor color, pH and temperature. The comprehensive understanding of CBD further guided the optimization of Se/S composition and film thickness. Finally, a champion efficiency of 8.27% with an open-circuit voltage of 0.625 V, a short-circuit current density of 22.98 mA cm −2 and a fill factor of 57.6% were achieved, representing the highest efficiency among all CBD-based antimony chalcogenide solar cells. A monitorable chemical bath deposition is developed to fabricate Sb 2 (S,Se) 3 solar cells. The deposition mechanisms are studied with the aid of real-time solution color, pH and temperature. Finally, a champion efficiency of 8.27% is achieved.
ISSN:2050-7488
2050-7496
DOI:10.1039/d2ta01465c