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用于高效钙钛矿太阳能电池的抗老化PbI的双功能邻苯二甲酰胺调制

Dual-functional phthalamide modulation of aging-resistant PbI for efficient perovskite solar cells.

作者信息

Zhang Qian, Li Yixian, Ma Zhu, Du Hao, Song Mingyu, Gou Fuchun, Lv Zhuo, Xiang Dengqian, Chen Bo, Liu Kai, Mao Maozhu, Cheng Can, Du Zhuowei, Chen Yi, You Wei, Yang Junbo, Chen Leyi, Yin Qiaohuan, Huang Cheng, Xiang Yan, Yu Jian, Sun Kuan, Chen Jiangzhao, Feng Wenyong, Lin Zedong

机构信息

School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China.

School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China; Tianfu Yongxing Laboratory, Chengdu 610213, China.

出版信息

J Colloid Interface Sci. 2025 Sep 4;702(Pt 2):138913. doi: 10.1016/j.jcis.2025.138913.

Abstract

The sequential preparation of perovskite solar cells (PSCs) has received widespread concern for its use in large-scale perovskite modules and perovskite/silicon tandem solar cells. However, the instability of the PbI precursor solution and the incomplete reaction of ammonium salts hinder the industrialization of PSCs. Here, by introducing phthalamide (PA) into PbI solution, the carbonyl oxygen of PA molecules undergoes a bidentate coordination reaction with Pb to form an octahedral coordination structure, and the nitrogen atom in the -NH group exhibits weakly acidic properties due to the conjugation effect. These dual mechanisms synergistically suppress the hydrolysis of PbI. This dual-functional modulation strategy not only inhibits aging of the PbI precursor solution, but also promotes thorough reaction between PbI and organic ammonium salts. Moreover, carbonyl (C=O) and amino (-NH) groups generate van der Waals forces through dipole-dipole interactions, promoting intermolecular interactions within the precursor solution, which facilitates the formation and growth of crystal nuclei. π-electrons in benzene ring further contribute to van der Waals forces via π-π stacking, improving the smoothness and coverage of the perovskite film. Notably, the fabricated PSCs achieved a current density (J) of 26.70 mA cm, and devices retained 95 % of its initial PCE after 1000 h of nitrogen exposure. Aging-resistant PbI precursor tactic enable reproducible, high-efficiency, and low-cost perovskite solar cells.

摘要

钙钛矿太阳能电池(PSCs)的连续制备因其在大规模钙钛矿组件和钙钛矿/硅串联太阳能电池中的应用而受到广泛关注。然而,PbI前驱体溶液的不稳定性和铵盐的不完全反应阻碍了PSCs的工业化进程。在此,通过将邻苯二甲酰胺(PA)引入PbI溶液中,PA分子的羰基氧与Pb发生双齿配位反应形成八面体配位结构,并且由于共轭效应,-NH基团中的氮原子表现出弱酸性。这两种机制协同抑制了PbI的水解。这种双功能调制策略不仅抑制了PbI前驱体溶液的老化,还促进了PbI与有机铵盐之间的充分反应。此外,羰基(C=O)和氨基(-NH)基团通过偶极-偶极相互作用产生范德华力,促进前驱体溶液内的分子间相互作用,这有利于晶核的形成和生长。苯环中的π电子通过π-π堆积进一步增强范德华力,提高了钙钛矿薄膜的平整度和覆盖率。值得注意的是,制备的PSCs实现了26.70 mA cm的电流密度(J),并且在氮气暴露1000小时后,器件保留了其初始光电转换效率(PCE)的95%。抗老化的PbI前驱体策略使得可重复、高效且低成本钙钛矿太阳能电池成为可能。

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