Multifunctional surface modification of carbon-based all-inorganic CsPbI2Br solar cells by 3-(trifluoromethyl) phenyltrimethyl ammonium iodide

钙钛矿(结构) 碘化物 热稳定性 化学 能量转换效率 载流子 电负性 溴化铵 材料科学 无机化学 有机化学 化学工程 光电子学 肺表面活性物质 工程类
作者
Lin Gao,Fengli Liu,Ruoshui Li,Qing Yao,Dongbin Jiang,Chenfang Zhong,Wenhui Lin,Miaoliang Huang,Jihuai Wu,Zhang Lan
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:989: 174374-174374 被引量:5
标识
DOI:10.1016/j.jallcom.2024.174374
摘要

The preparation process of carbon-electrode perovskite solar cells (C-PSCs) without hole transport layers (HTLs) is simple, cost-effective, and the as-prepared C-PSCs exhibit excellent thermal stability. However, there are numerous defects at the interfaces of C-PSCs and grain boundaries. Due to the presence of these defect states, non-radiative recombination of charge carriers occurs, ultimately resulting in significant VOC (voltage open circuit) loss and an energy level mismatch between device structures, which seriously affect the photoelectric conversion efficiency (PCE) and stability of C-PSCs. Therefore, this work uses 3-(trifluoromethyl)-phenyltrimethyl-ammonium iodide (TFPTAI) as a surface modifier to modify the surface of CsPbI2Br. Due to the strong electronegativity of fluorine atoms (F), acting as electron-withdrawing groups, they promote the separation of positive and negative charge centers in the molecule. This, in turn, can effectively induce strong binding of ammonium cations (NH+) with negatively charged defects, consequently suppressing the non-radiative recombination of charge carriers. In addition, thanks to the ordered arrangement of F atoms, a hydrophobic protective umbrella is constructed on the perovskite surface layer, effectively improving the stability of the device. The highest PCE of the as-prepared device is 14.02%, surpassing the optimal PCE of the original device at 12.46%. Simultaneously, the surface-modified device exhibits excellent environmental stability.
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