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
Lin-na 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:6
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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