TY - JOUR
T1 - Rubidium Induced Phase Regulation for High-Performance Quasi-2D Perovskite Solar Cells
AU - Xu, Bo
AU - Yang, Rong
AU - Chen, Yu
AU - Zhou, Jinfei
AU - Tan, Wen Liang
AU - Yang, Pinghui
AU - Wang, Fengwei
AU - Wang, Xiliu
AU - Liu, Wenbo
AU - Gao, Xuan
AU - Li, Jingwei
AU - Zhang, Daliang
AU - McNeill, Christopher R.
AU - Li, Renzhi
AU - Huang, Wei
AU - Wang, Jianpu
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/12/13
Y1 - 2024/12/13
N2 - Quasi-two-dimensional (2D) perovskites are notable for their diverse formulations and environmental stability. However, solution-processed quasi-2D perovskites often exhibit inherent multiple-quantum-well structures with broad phase distributions, limiting their efficiency in photovoltaic applications. Here, we demonstrate that incorporating rubidium ions effectively narrows the phase distribution in quasi-2D perovskite by accelerating the formation of the n = 1 2D perovskite phase during the initial crystallization stage. This leads to a decrease in the remaining free organic spacer cations, which in turn limits the transition to medium-n phases (n = 3, 4) and promotes the formation of high-quality 3D-like or large-n perovskites, ultimately enhancing charge transport of quasi-2D perovskite. Consequently, we achieve quasi-2D perovskite solar cells with a champion power conversion efficiency of 21.9%. Furthermore, the thermal stability of the unencapsulated devices containing rubidium is significantly improved, with the T80 lifetime under continuous 60 °C stress increasing from 1150 to over 3000 h.
AB - Quasi-two-dimensional (2D) perovskites are notable for their diverse formulations and environmental stability. However, solution-processed quasi-2D perovskites often exhibit inherent multiple-quantum-well structures with broad phase distributions, limiting their efficiency in photovoltaic applications. Here, we demonstrate that incorporating rubidium ions effectively narrows the phase distribution in quasi-2D perovskite by accelerating the formation of the n = 1 2D perovskite phase during the initial crystallization stage. This leads to a decrease in the remaining free organic spacer cations, which in turn limits the transition to medium-n phases (n = 3, 4) and promotes the formation of high-quality 3D-like or large-n perovskites, ultimately enhancing charge transport of quasi-2D perovskite. Consequently, we achieve quasi-2D perovskite solar cells with a champion power conversion efficiency of 21.9%. Furthermore, the thermal stability of the unencapsulated devices containing rubidium is significantly improved, with the T80 lifetime under continuous 60 °C stress increasing from 1150 to over 3000 h.
UR - http://www.scopus.com/inward/record.url?scp=85210295345&partnerID=8YFLogxK
U2 - 10.1021/acsenergylett.4c02883
DO - 10.1021/acsenergylett.4c02883
M3 - 文章
AN - SCOPUS:85210295345
SN - 2380-8195
VL - 9
SP - 6064
EP - 6071
JO - ACS Energy Letters
JF - ACS Energy Letters
IS - 12
ER -