材料科学
串联
钙钛矿(结构)
润湿
单层
能量转换效率
复合数
氧化物
结晶
化学工程
纳米技术
光伏系统
光电子学
分子
表面工程
表面能
自组装单层膜
卤化物
表面粗糙度
作者
Qingquan He,Xinquan Wang,Gang Xu,Tao Zhang,Ruoyu Li,Zehang Liu,Yu Bao,Yaxuan Yang,Jijin Qiao,Jing Li,Jun Pan
标识
DOI:10.1021/acsami.5c21997
摘要
Wide-bandgap (WBG) perovskite solar cells (PSCs) based on self-assembled monolayers (SAMs) have demonstrated impressive efficiencies, though their performance and longevity remain substantially compromised by poor wettability during film formation, defects, and energy-level misalignment at the interfaces. Herein, we develop an interface regulation strategy employing a tris(4-carboxyphenyl)phosphine oxide (TC) modified [4-(7 H -benzimidazol-7-yl)butyl]phosphonic acid (4PADCB) to construct a multifunctional composite SAM (Co-SAM). The incorporation of TC molecules significantly enhances the interfacial wetting characteristics and crystallization quality of WBG perovskites, effectively passivating defects, optimizing energy-level alignment, and facilitating selective charge transport. This Co-SAM strategy yields impressive device performance: 1.68 eV WBG PSCs achieve a champion power conversion efficiency (PCE) of 22.40% while maintaining >90% of initial efficiency after 1440 h of ambient storage. Furthermore, perovskite/silicon tandem solar cells fabricated using this approach reach a PCE of 30.74%. Our work establishes a new paradigm in interfacial molecular engineering for highly efficient and operationally stable tandem photovoltaics.
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