Zhang Liujiang, Fu Meirong, Jiang Xianyuan, Zhang Ziheng, Wang Chenyue, Su Zhenhuang, He Bingchen, Tang Lin, Zheng Guanhaojie, Gao Xingyu, He Jianhua
The Institute for Advanced Studies, Wuhan University, Wuhan, 430072, China.
Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201204, China.
Adv Sci (Weinh). 2025 Dec;12(45):e12117. doi: 10.1002/advs.202512117. Epub 2025 Sep 25.
While [4-(3,6-Dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) self-assembled monolayers (SAMs) enable high-performance inverted perovskite solar cells (PSCs), their sparse coverage on nickel oxide (NiOx) induces heterogeneous interfacial charge distribution at the buried perovskite interface. This increases non-radiative recombination, ultimately limiting device performance. Herein, benzylphosphonic acid (BPPA) is added, a small molecule featuring a phosphonic acid group, into Me-4PACz to construct a co-assembled monolayer (Co-SAM) with enhanced molecular ordering on NiOx. The resulting compact Co-SAM hole transport layer (HTL) simultaneously improves electrical conductivity, hole mobility, and interfacial energy level alignment, facilitating efficient hole injection. Moreover, BPPA's phosphonic acid groups enable bifacial passivation: coordinating NiOx surface defects while chelating uncoordinated Pb at the perovskite interface, significantly suppressing non-radiative recombination. Optimized Me-4PACz/BPPA-based PSCs achieve a champion power conversion efficiency (PCE) of 26.35%, while retaining 90% of the initial efficiency after 3000 h in a nitrogen atmosphere without encapsulation. This molecular co-assembly strategy concurrently refines HTL properties and buried interface passivation, providing a generalized approach for high-efficiency, stable PSCs.
虽然[4-(3,6-二甲基-9H-咔唑-9-基)丁基]膦酸(Me-4PACz)自组装单分子层(SAMs)可实现高性能倒置钙钛矿太阳能电池(PSC),但其在氧化镍(NiOx)上的稀疏覆盖会在掩埋的钙钛矿界面处引发异质界面电荷分布。这会增加非辐射复合,最终限制器件性能。在此,将具有膦酸基团的小分子苄基膦酸(BPPA)添加到Me-4PACz中,以在NiOx上构建具有增强分子有序性的共组装单分子层(Co-SAM)。由此形成的致密Co-SAM空穴传输层(HTL)同时提高了电导率、空穴迁移率和界面能级对准,促进了高效空穴注入。此外,BPPA的膦酸基团可实现双面钝化:配位NiOx表面缺陷,同时螯合钙钛矿界面处未配位的Pb,显著抑制非辐射复合。基于优化的Me-4PACz/BPPA的PSC实现了26.35%的最佳功率转换效率(PCE),并且在无封装的氮气气氛中3000小时后仍保留初始效率的90%。这种分子共组装策略同时优化了HTL性能和掩埋界面钝化,为高效、稳定的PSC提供了一种通用方法。