材料科学
钙钛矿(结构)
结晶
串联
钝化
氢键
分子
纳米技术
氧化物
光伏
配位复合体
三苯基氧化膦
卤化物
化学工程
纳米晶
晶体工程
析氧
作者
Tao Zhang,Zehang Liu,Yonggui Sun,Taomiao Wang,Qiannan Li,Xiaowei Li,Ruijie Li,Xiaokang Sun,Fei Wang,Xinquan Wang,Yu Bao,Ruoyu Li,Yuzhou Wu,Yaxuan Yang,Pengcheng Wang,Xianfang Zhou,Shicheng Pan,Xiuyuan Chen,Dawei Duan,Guo Yang
摘要
ABSTRACT Molecular additives offer a powerful route to control crystallization kinetics and homogenize component distribution in perovskite semiconductors. However, additives that integrate Pb‐related coordination and hydrogen‐bonding functionalities within a single molecular framework to jointly regulate crystallization evolution and defect chemistry remain largely underexplored. Herein, we introduce 4,4’‐(phenylphosphoryl)dibenzoic acid (PPDBA) as a multifunctional molecular modulator that combines P═O and ─COOH groups within a single framework. Compared with P═O‐only reference molecule triphenylphosphine oxide (TPPO), PPDBA expands the interaction scope by coupling Pb‐related coordination involving P═O/─COOH functionalities with additional ─COOH‐assisted hydrogen bonding toward organic cations. These cooperative interactions facilitate intermediate‐phase evolution modulation, crystallization retardation, and the formation of uniform perovskite films with reduced residual PbI 2 . In addition, PPDBA preferentially enriches near the perovskite surface, where it contributes to defect passivation and improved carrier extraction. Consequently, PPDBA‐treated 1.55 eV PSCs achieve a power conversion efficiency of 26.31% with exceptional stability. The universality of the strategy is further demonstrated by high efficiencies of 23.50% and 19.13% PCEs for 1.68 and 1.84 eV wide‐bandgap PSCs, respectively. Beyond single‐junctions, PPDBA enables high‐performance tandems, delivering 33.05% (certified 32.65%) in perovskite/silicon and 26.11% in perovskite/organic architectures. This work provides a molecular design blueprint for high‐performance, durable perovskite‐based photovoltaics.
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