钙钛矿(结构)
材料科学
串联
带隙
能量转换效率
光电子学
卤化物
纳米技术
结晶学
无机化学
化学
复合材料
作者
Hongling Guan,Shun Zhou,Shiqiang Fu,Dexin Pu,Xuepeng Chen,Yansong Ge,Shuxin Wang,Chen Wang,Hongsen Cui,Jiwei Liang,Xuzhi Hu,Weiwei Meng,Guojia Fang,Weijun Ke
标识
DOI:10.1002/adma.202307987
摘要
Abstract Wide‐bandgap (WBG) perovskite solar cells have attracted considerable interest for their potential applications in tandem solar cells. However, the predominant obstacles impeding their widespread adoption are substantial open‐circuit voltage ( V OC ) deficit and severe photo‐induced halide segregation. To tackle these challenges, a crystal orientation regulation strategy by introducing dodecyl‐benzene‐sulfonic‐acid as an additive in perovskite precursors is proposed. This method significantly promotes the desired crystal orientation, passivates defects, and mitigates photo‐induced halide phase segregation in perovskite films, leading to substantially reduced nonradiative recombination, minimized V OC deficits, and enhanced operational stability of the devices. The resulting 1.66 eV bandgap methylamine‐free perovskite solar cells achieve a remarkable power conversion efficiency (PCE) of 22.40% (certified at 21.97%), with the smallest V OC deficit recorded at 0.39 V. Furthermore, the fabricated semitransparent WBG devices exhibit a competitive PCE of 20.13%. Consequently, four‐terminal tandem cells comprising WBG perovskite top cells and 1.25 eV bandgap perovskite bottom cells showcase an impressive PCE of 28.06% (stabilized 27.92%), demonstrating great potential for efficient multijunction tandem solar cell applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI