多硫化物
光伏
催化作用
氧化还原
量子点
纳米技术
化学
Atom(片上系统)
材料科学
光化学
无机化学
电极
物理化学
光伏系统
有机化学
嵌入式系统
生物
电解质
计算机科学
生态学
作者
Linna Li,Yu Lin,Yongming Xia,Di Lin,Yang Xiang,Jiaqi Fang,Xuehui Liu,Jiawen Chen,Xiong Yin,Chenyan Ma,Xiaoying Yan,Peng Xu,Rui Xu,Lipeng Zhang,Zhihai Cheng,Leyu Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-06-05
卷期号:23 (11): 5123-5130
被引量:12
标识
DOI:10.1021/acs.nanolett.3c01064
摘要
Developing cost-effective and highly efficient photocathodes toward polysulfide redox reduction is highly desirable for advanced quantum dot (QD) photovoltaics. Herein, we demonstrate nitrogen doped carbon (N-C) shell-supported iron single atom catalysts (Fe-SACs) capable of catalyzing polysulfide reduction in QD photovoltaics for the first time. Specifically, Fe-SACs with FeN4 active sites feature a power conversion efficiency of 13.7% for ZnCuInSe-QD photovoltaics (AM1.5G, 100 mW/cm2), which is the highest value for ZnCuInSe QD-based photovoltaics, outperforming those of Cu-SACs and N-C catalysts. Compared with N-C, Fe-SACs exhibit suitable energy level matching with polysulfide redox couples, revealed by the Kelvin probe force microscope, which accelerates the charge transferring at the interfaces of catalyst/polysulfide redox couple. Density functional theory calculations demonstrate that the outstanding catalytic activity of Fe-SACs originates from the preferable adsorption of S42- on the FeN4 active sites and the high activation degree of the S-S bonds in S42- initiated by the FeN4 active sites.
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