串联
钙钛矿(结构)
材料科学
结晶
带隙
卤化物
能量转换效率
钝化
光电流
纳米技术
化学工程
无机化学
光电子学
化学
复合材料
工程类
图层(电子)
作者
Yanxun Li,Yichao Yan,Yuang Fu,Wenlin Jiang,Ming Liu,Mingqian Chen,Xiaofeng Huang,Guanghao Lu,Xinhui Lu,Jun Yin,Shengfan Wu,Alex K.‐Y. Jen
标识
DOI:10.1002/anie.202412515
摘要
Inverted perovskite/organic tandem solar cells (P/O TSCs) suffer from poor long‐term device stability due to halide segregation in organic‐inorganic hybrid wide‐bandgap (WBG) perovskites, which hinders their practical deployment. Therefore, developing all‐inorganic WBG perovskites for incorporation into P/O TSCs is a promising strategy because of their superior stability under continuous illumination. However, these inorganic WBG perovskites also face some critical issues, including rapid crystallization, phase instability, and large energy loss, etc. To tackle these issues, two multifunctional additives based on 9,10‐anthraquinone‐2‐sulfonic acid (AQS) are developed to regulate the perovskite crystallization by mediating the intermediate phases and suppress the halide segregation through the redox‐shuttle effect. By coupling with organic cations having the desirable functional groups and dipole moments, these additives can effectively passivate the defects and adjust the alignment of interface energy levels. Consequently, a record Voc approaching 1.3 V with high power conversion efficiency (PCE) of 18.59% could be achieved in a 1.78 eV bandgap single‐junction inverted all‐inorganic PSC. More importantly, the P/O TSC derived from this cell demonstrates a T90 lifetime of 1000 h under continuous operation, presenting the most stable P/O TSCs reported so far.
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