材料科学
结晶度
结晶
能量转换效率
钙钛矿(结构)
钝化
化学工程
卤化物
相对湿度
离子
纳米技术
光电子学
复合材料
无机化学
化学
热力学
有机化学
工程类
物理
图层(电子)
作者
Min Ju Jeong,Soo Woong Jeon,Sung Yong Kim,Jun Hong Noh
标识
DOI:10.1002/aenm.202300698
摘要
Abstract Inorganic CsPbI 2 Br perovskite has a substantial potential for triple‐junction tandem solar cells as a top subcell, however it exhibits relative instability in the air compared with organic‐inorganic perovskites as well as significantly lower efficiency than the theoretical efficiency limit. To further enhance the air‐stability and efficiency of CsPbI 2 Br‐based perovskite solar cells (PSCs), it is vitally crucial to improve the crystallinity and passivate the defects within films that accelerate the phase transformation to the photo‐inactive phase in the air. Here, it is reported that crystallization management via incorporating sodium formate (NaFo) in a CsPbI 2 Br perovskite solution effectively leads to enlarged grain size and the reduced trap density. The Na + cation and HOOC − anion produce a synergistic effect for engineering the defects by acting as cation and pseudo‐halide anion passivators, respectively. As a result, the NaFo‐incorporating device shows an improved power conversion efficiency (PCE) of 17.7% with a fill factor (FF) of 84.5%. To the best of the authors' knowledge, this progressive FF value is the highest value among CsPbI 2 Br‐based PSCs reported thus far. In addition, the NaFo‐incorporated device shows improved air stability compared to the control device, retaining over 95% of its initial PCE for 1000 hours under 10% relative humidity at room temperature without any encapsulation.
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