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通过氟化有机铵盐表面钝化提高倒置CsPbIBr钙钛矿太阳能电池的效率和稳定性

Enhanced Efficiency and Stability of Inverted CsPbIBr Perovskite Solar Cells via Fluorinated Organic Ammonium Salt Surface Passivation.

作者信息

Cao Shihan, Wang Lang, She Xingchen, Li Wei, Wei Lin, Xiong Xia, Wang Zhijun, Li Jie, Tian Haibo, Cui Xumei, Zhang Min, Sun Hui, Yang Dingyu, Liu Xin

机构信息

College of Optoelectronic Engineering, Chengdu University of Information Technology, Chengdu 610225, China.

Institute for Advanced Study, Chengdu University, Chengdu 610225, China.

出版信息

Langmuir. 2024 Feb 6. doi: 10.1021/acs.langmuir.3c03437.

DOI:10.1021/acs.langmuir.3c03437
PMID:38320286
Abstract

All-inorganic perovskite solar cells (PSCs) have recently received increasing attention due to their outstanding thermal stability. However, the performance of these devices, especially for the devices with a p-i-n structure, is still inferior to that of the typical organic-inorganic counterparts. In this study, we introduce phenylammonium iodides with different side groups on the surface of the CsPbIBr perovskite film and investigate their passivation effects. Our studies indicate that the 4-trifluoromethyl phenylammonium iodide (CFPA) molecule with the -CF side group effectively decreases the trap density of the perovskite film by forming interactions with the undercoordinated Pb ions and significantly inhibits the nonradiative recombination in the derived PSC, leading to an enhanced open-circuit voltage () from 0.96 to 1.10 V after passivation. Also, the CFPA post-treatment enables better energy-level alignment between the conduction band minimum of CsPbIBr perovskite and [6,6]-phenyl C61 butyric acid methyl ester, thereby enhancing the charge extraction from the perovskite to the charge transport layer. These combined benefits result in a significant enhancement of the power conversion efficiency from 11.22 to 14.37% for inverted CsPbIBr PSCs. The device without encapsulation exhibits a degradation of only ≈4% after 1992 h in a N glovebox.

摘要

全无机钙钛矿太阳能电池(PSCs)因其出色的热稳定性最近受到越来越多的关注。然而,这些器件的性能,特别是对于具有p-i-n结构的器件,仍低于典型的有机-无机同类器件。在本研究中,我们在CsPbIBr钙钛矿薄膜表面引入了具有不同侧基的苯基碘化铵,并研究了它们的钝化效果。我们的研究表明,带有-CF侧基的4-三氟甲基苯基碘化铵(CFPA)分子通过与配位不足的Pb离子形成相互作用,有效降低了钙钛矿薄膜的陷阱密度,并显著抑制了衍生PSC中的非辐射复合,钝化后开路电压()从0.96 V提高到1.10 V。此外,CFPA后处理使CsPbIBr钙钛矿的导带最小值与[6,6]-苯基C61丁酸甲酯之间的能级排列更好,从而增强了从钙钛矿到电荷传输层的电荷提取。这些综合优势使得倒置CsPbIBr PSCs的功率转换效率从11.22%显著提高到14.37%。在N手套箱中,未封装的器件在1992小时后仅表现出约4%的降解。

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