Ligand-assisted cation-exchange engineering for high-efficiency colloidal Cs1−xFAxPbI3 quantum dot solar cells with reduced phase segregation

RIS ID

141164

Publication Details

Hao, M., Bai, Y., Zeiske, S., Ren, L., Liu, J., Yuan, Y., Zarrabi, N., Cheng, N., Ghasemi, M., Chen, P., Lyu, M., He, D., Yun, J., Du, Y., Wang, Y., Ding, S., Armin, A., Meredith, P., Liu, G., Cheng, H. & Wang, L. (2020). Ligand-assisted cation-exchange engineering for high-efficiency colloidal Cs1−xFAxPbI3 quantum dot solar cells with reduced phase segregation. Nature Energy, 5 (1), 79-88.

Abstract

2020, The Author(s), under exclusive licence to Springer Nature Limited. The mixed caesium and formamidinium lead triiodide perovskite system (Cs1−xFAxPbI3) in the form of quantum dots (QDs) offers a pathway towards stable perovskite-based photovoltaics and optoelectronics. However, it remains challenging to synthesize such multinary QDs with desirable properties for high-performance QD solar cells (QDSCs). Here we report an effective oleic acid (OA) ligand-assisted cation-exchange strategy that allows controllable synthesis of Cs1−xFAxPbI3 QDs across the whole composition range (x = 0-1), which is inaccessible in large-grain polycrystalline thin films. In an OA-rich environment, the cross-exchange of cations is facilitated, enabling rapid formation of Cs1−xFAxPbI3 QDs with reduced defect density. The hero Cs0.5FA0.5PbI3 QDSC achieves a certified record power conversion efficiency (PCE) of 16.6% with negligible hysteresis. We further demonstrate that the QD devices exhibit substantially enhanced photostability compared with their thin-film counterparts because of suppressed phase segregation, and they retain 94% of the original PCE under continuous 1-sun illumination for 600 h.

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Link to publisher version (DOI)

http://dx.doi.org/10.1038/s41560-019-0535-7