材料科学
甲脒
钙钛矿(结构)
三碘化物
结晶
能量转换效率
成核
钝化
复合材料
极限抗拉强度
化学工程
光电子学
有机化学
电极
色素敏化染料
图层(电子)
电解质
工程类
物理化学
化学
作者
Hengkai Zhang,Zhiliang Chen,Minchao Qin,Zhiwei Ren,Kuan Liu,Jiaming Huang,Dong Shen,Zehan Wu,Yaokang Zhang,Jianhua Hao,Chun‐Sing Lee,Xinhui Lu,Zijian Zheng,Wei Yu,Gang Li
标识
DOI:10.1002/adma.202008487
摘要
Abstract α‐Formamidinium lead triiodide (α‐FAPbI 3 ) represents the state‐of‐the‐art for perovskite solar cells (PSCs) but experiences intrinsic thermally induced tensile strain due to a higher phase‐converting temperature, which is a critical instability factor. An in situ crosslinking‐enabled strain‐regulating crystallization (CSRC) method with trimethylolpropane triacrylate (TMTA) is introduced to precisely regulate the top section of perovskite film where the largest lattice distortion occurs. In CSRC, crosslinking provides in situ perovskite thermal‐expansion confinement and strain regulation during the annealing crystallization process, which is proven to be much more effective than the conventional strain‐compensation (post‐treatment) method. Moreover, CSRC with TMTA successfully achieves multifunctionality simultaneously: the regulation of tensile strain, perovskite defects passivation with an enhanced open‐circuit voltage ( V OC = 50 mV), and enlarged perovskite grain size. The CSRC approach gives significantly enhanced power conversion efficiency (PCE) of 22.39% in α‐FAPbI 3 ‐based PSC versus 20.29% in the control case. More importantly, the control PSCs’ instability factor—residual tensile strain—is regulated into compression strain in the CSRC perovskite film through TMTA crosslinking, resulting in not only the best PCE but also outstanding device stability in both long‐term storage (over 4000 h with 95% of initial PCE) and light soaking (1248 h with 80% of initial PCE) conditions.
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