钝化
钙钛矿(结构)
甲脒
载流子寿命
材料科学
能量转换效率
钙钛矿太阳能电池
光电子学
化学工程
纳米技术
硅
工程类
图层(电子)
作者
Jun Li,Lisha Xie,Guanhao Liu,Zhenwei Pu,Xili Tong,Shuncheng Yang,Mengjin Yang,Jian Liu,Jiujiang Chen,Yuanyuan Meng,Ying Wang,Tao Wang,Ziyi Ge
标识
DOI:10.1002/anie.202316898
摘要
Abstract The main obstacles to promoting the commercialization of perovskite solar cells (PSCs) include their record power conversion efficiency (PCE), which still remains below the Shockley–Queisser limit, and poor long‐term stability, attributable to crystallographic defects in perovskite films and open‐circuit voltage ( V oc ) loss in devices. In this study, potassium (4‐tert‐butoxycarbonylpiperazin‐1‐yl) methyl trifluoroborate (PTFBK) was employed as a multifunctional additive to target and modulate bulk perovskite defects and carrier dynamics of PSCs. Apart from simultaneously passivating anionic and cationic defects, PTFBK could also optimize the energy‐level alignment of devices and weaken the interaction between carriers and longitudinal optical phonons, resulting in a carrier lifetime of greater than 3 μs. Furthermore, it inhibited non‐radiative recombination and improved the crystallization capacity in the target perovskite film. Hence, the target rigid and flexible p‐i‐n PSCs yielded champion PCEs of 24.99 % and 23.48 %, respectively. More importantly, due to hydrogen bonding between formamidinium and fluorine, the target devices exhibited remarkable thermal, humidity, and operational tracking at maximum power point stabilities. The reduced Young's modulus and residual stress in the perovskite layer also provided excellent bending stability for flexible target devices.
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