钝化
钙钛矿(结构)
异质结
材料科学
光伏
制作
基质(水族馆)
光电子学
结晶
光伏系统
能量转换效率
纳米技术
化学工程
图层(电子)
电气工程
地质学
工程类
病理
海洋学
替代医学
医学
作者
Ning Wei,Yanfeng Miao,Xingtao Wang,Zhixiao Qin,Xiaomin Liu,Hao Chen,Haifei Wang,Yugang Liang,Shaowei Wang,Yixin Zhao,Yuetian Chen
出处
期刊:JACS Au
[American Chemical Society]
日期:2023-11-21
卷期号:3 (12): 3324-3332
被引量:14
标识
DOI:10.1021/jacsau.3c00469
摘要
High Resolution Image Download MS PowerPoint Slide For achieving high-efficiency perovskite solar cells, it is almost always necessary to substantially passivate defects and protect the perovskite structure at its interfaces with charge transport layers. Such a modification generally involves the post-treatment of the deposited perovskite film by spin coating, which cannot meet the technical demands of scaling up the production of perovskite photovoltaics. In this work, we demonstrate one-step construction of buried and capped double 1D/3D heterojunctions without the need for any post-treatment, which is achieved through facile tetraethylammonium trifluoroacetate (TEATFA) prefunctionalization on the SnO 2 substrate. The functional TEATFA salt is first deposited onto the SnO 2 substrate and reacts on this buried interface. Once the FAPbI 3 perovskite precursor solution is dripped, a portion of the TEA + cations spontaneously diffuse to the top surface over film crystallization. The TEATFA-based water-resistant 1D/3D TEAPbI 3 /FAPbI 3 heterojunctions at both the buried and capped interfaces lead to much better photovoltaic performance and higher operational stability. Since this approach saves the need for any postsynthesis passivation, its feasibility for the fabrication of large-area perovskite photovoltaics is also showcased. Compared to ∼15% for a pristine 5 cm × 5 cm FAPbI 3 mini-module without postsynthesis passivation, over 20% efficiency is achieved following the proposed route, demonstrating its great potential for larger-scale fabrication with fewer processing steps.
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