钙钛矿(结构)
材料科学
纳米技术
矿物学
光电子学
工程物理
结晶学
地质学
化学
物理
作者
Jifei Wang,Guozheng Nie,Wenjin Huang,Yuanyuan Guo,Yongjun Li,Zhangqiang Yang,Runsheng Chen,Kan Ding,Ye Yang,Weike Wang,Le‐Man Kuang,Kaike Yang,Dongsheng Tang,Yaxin Zhai
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-09-03
标识
DOI:10.1021/acs.nanolett.4c03013
摘要
Quasi-two-dimensional (Q-2D) perovskites show great potential in the field of photonic and optoelectronic device applications. However, defects and local lattice dislocation still limit performance and stability improvement by nonradiative recombination, unpreferred phase distribution, and unbonded amines. Here, a low-temperature synergistic strategy for both reconstructing and solidifying the perovskite top and buried interface is developed. By post-treating the 1,4-phenylenedimethanammonium (PDMA) based (PDMA)MA4Pb5I16 films with cesium acetate (CsAc) before thermal annealing, a condensation reaction between R-COO– and -NH2 and ion exchange between Cs+ and MA+ occur. It converts the unbonded amines to amides and passivates uncoordinated Pb2+. Meanwhile, it adjusts film composition and improves the phase distribution without changing the out-of-plane grain orientation. Consequently, performance of 18.1% and much-enhanced stability (e.g., stability for photo-oxygen increased over 10 times, light-thermal for T90 over 4 times, and reverse bias over 3 times) of (PDMA)MA4Pb5I16 perovskite solar cells are demonstrated.
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