材料科学
钙钛矿(结构)
碘化物
相(物质)
抛物线槽
飞秒
动力学
光电子学
分析化学(期刊)
化学工程
能量转换效率
热力学
光学
无机化学
化学
物理
有机化学
工程类
量子力学
热的
激光器
作者
Kai Wang,Zhizai Li,Faguang Zhou,Haoran Wang,Hui Bian,Hong Zhang,Kai Wang,Zhiwen Jin,Liming Ding,Shengzhong Liu
标识
DOI:10.1002/aenm.201902529
摘要
Abstract The highest certified power conversion efficiency (PCE) of black phase based CsPbI 3 perovskite solar cells has exceeded 18%, and become a hotspot in recent progress. However, the black phase of CsPbI 3 rapidly transforms to yellow phase in ambient conditions due to its thermodynamic instability. Here, a Ruddlesden–Popper 2D structure is introduced into γ‐CsPbI 3 film to stabilize the black phase via reducing dimensionality. It is found that a judicious amount of phenylethylammonium iodide can adjust the dimensionality of γ‐CsPbI 3 film from 2D to quasi‐2D and 3D phase. Comprehensive consideration to obtain both the stability and high PCE, quasi‐2D ( n = 40) γ‐CsPbI 3 delivers a reproducible PCE of 13.65% with negligible hysteresis. By utilizing femtosecond transient absorption and time‐resolved PL decay, similar carrier kinetics in n = 40 and ∞ samples are observed, meaning an efficient charge extraction. More importantly, when the device is placed at 80 °C in N 2 condition or in air with RH of 25–30%, its PCE keeps ≈88% and ≈89% of its initial PCE after 12 days, respectively. Such results are better than the 3D one (≈69% and ≈16%, respectively).
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