TY - JOUR
T1 - Surface passivation by multifunctional carbon dots toward highly efficient and stable inverted perovskite solar cells
AU - Cao, Qi
AU - Zhang, Yixin
AU - Pu, Xingyu
AU - Zhao, Junsong
AU - Wang, Tong
AU - Zhang, Kui
AU - Chen, Hui
AU - He, Xilai
AU - Yang, Jiabao
AU - Zhang, Cheng
AU - Li, Xuanhua
N1 - Publisher Copyright:
© 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences
PY - 2023/11
Y1 - 2023/11
N2 - Interfacial imperfections between the perovskite layer and the electron transport layer (ETL) in perovskite solar cells (PSCs) can lead to performance loss and negatively influence long-term operational stability. Here, we introduce an interface engineering method to modify the interface between perovskite and ETL by using multifunctional carbon dots (CDs). C = O in the CDs can chelate with the uncoordinated Pb2+ in the perovskite material, inhibit interfacial recombination, and enhance the performance and stability of device. In addition, –OH in CDs forms hydrogen bonds with I− and organic cation in perovskite, inhibiting light-induced I2 release and organic cation volatilization, causing irreversible degradation of perovskite films, thereby enhancing the long-term operational stability of PSCs. Consequently, we achieve the champion inverted device with an efficiency of 24.02%. The CDs-treated PSCs exhibit high operational stability, and the maximum power point tracking only attenuates by 12.5% after 1000 h. Interfacial modification engineering supported by multifunctional quantum dots can accelerate the road to stable PSCs.
AB - Interfacial imperfections between the perovskite layer and the electron transport layer (ETL) in perovskite solar cells (PSCs) can lead to performance loss and negatively influence long-term operational stability. Here, we introduce an interface engineering method to modify the interface between perovskite and ETL by using multifunctional carbon dots (CDs). C = O in the CDs can chelate with the uncoordinated Pb2+ in the perovskite material, inhibit interfacial recombination, and enhance the performance and stability of device. In addition, –OH in CDs forms hydrogen bonds with I− and organic cation in perovskite, inhibiting light-induced I2 release and organic cation volatilization, causing irreversible degradation of perovskite films, thereby enhancing the long-term operational stability of PSCs. Consequently, we achieve the champion inverted device with an efficiency of 24.02%. The CDs-treated PSCs exhibit high operational stability, and the maximum power point tracking only attenuates by 12.5% after 1000 h. Interfacial modification engineering supported by multifunctional quantum dots can accelerate the road to stable PSCs.
KW - Carbon dots
KW - Interfacial engineering
KW - Non-radiative recombination
UR - http://www.scopus.com/inward/record.url?scp=85171671829&partnerID=8YFLogxK
U2 - 10.1016/j.jechem.2023.07.002
DO - 10.1016/j.jechem.2023.07.002
M3 - 文章
AN - SCOPUS:85171671829
SN - 2095-4956
VL - 86
SP - 9
EP - 15
JO - Journal of Energy Chemistry
JF - Journal of Energy Chemistry
ER -