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用于准单晶钙钛矿薄膜和稳定太阳能电池的桥连溶剂策略

Bridging-Solvent Strategy for Quasi-Single-Crystal Perovskite Films and Stable Solar Cells.

作者信息

Zhang Yao, Sun Xiangyu, Guan Zhen, Li Dongni, Wang Qingya, Yue Yansong, Liu Fangze, Wei Jing, Li Hongbo

机构信息

Beijing Key Laboratory of Construction-Tailorable Advanced Functional Materials and Green Applications, Experimental Center of Advanced Materials, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, China.

Advanced Research Institute of Multidisciplinary Sciences, Beijing Institute of Technology, Zhuhai, 519088, China.

出版信息

Small Methods. 2025 Jan;9(1):e2400214. doi: 10.1002/smtd.202400214. Epub 2024 Jun 18.

Abstract

Controllable fabrication of formamidinium (FA)-based perovskite solar cells (PSCs) with both high efficiency and long-term stability is the key to their further commercialization. However, the diversity of PbI complexes and perovskite compositions usually leads to light sensitive PbI residues and phase impurities in the film, which can accelerate the device degradation. Here, the crystallization kinetics of FA-based perovskite films are studied and a bridging-solvent strategy is proposed to modulate the reaction kinetics between PbI and ammonium salts by prohibiting the formation of undesired intermediates. N-methylpyrrolidone (NMP) solvent is introduced into the PbI precursor solution to obtain stable and homogeneous PbI-NMP complex films. The strong interaction between NMP and formamidinium iodide (FAI) molecules promotes the conversion from PbI-NMP into (001)-oriented quasi-single-crystal perovskite films with negligible impurities, long carrier lifetime of 1.5 µs and a large grain size of 3 µm. The optimized PSCs exhibit a high power conversion efficiency of 24.1%, as well as superior shelf stability which maintains 95% initial efficiency after storage in air for 1200 h (T = 1200 h), and operating stability with T = 300 h under continuous working at the maximum power point. This work offers a simple and reproducible method for fabricating phase-pure and uniaxially oriented perovskite films.

摘要

可控制备兼具高效率和长期稳定性的甲脒基(FA)钙钛矿太阳能电池(PSC)是其进一步商业化的关键。然而,PbI络合物和钙钛矿组成的多样性通常会导致薄膜中出现光敏性PbI残留物和相杂质,从而加速器件退化。在此,研究了基于FA的钙钛矿薄膜的结晶动力学,并提出了一种桥连溶剂策略,通过禁止不需要的中间体的形成来调节PbI与铵盐之间的反应动力学。将N-甲基吡咯烷酮(NMP)溶剂引入PbI前驱体溶液中,以获得稳定且均匀的PbI-NMP络合物薄膜。NMP与碘化甲脒(FAI)分子之间的强相互作用促进了从PbI-NMP向(001)取向的准单晶钙钛矿薄膜的转变,杂质可忽略不计,载流子寿命长达1.5 μs,晶粒尺寸达3 μm。优化后的PSC表现出24.1%的高功率转换效率,以及优异的储存稳定性,在空气中储存1200小时(T = 1200小时)后仍保持95%的初始效率,在最大功率点连续工作300小时(T = 300小时)具有工作稳定性。这项工作提供了一种简单且可重复的方法来制备相纯且单轴取向的钙钛矿薄膜。

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