电化学
催化作用
阳极
电解质
阴极
氧化还原
阴极保护
析氧
电极
材料科学
分解水
化学工程
制作
沉积(地质)
纳米技术
无机化学
化学
物理化学
有机化学
古生物学
沉积物
替代医学
光催化
病理
工程类
生物
医学
作者
Zhirong Zhang,Feng Chen,Chunxiao Liu,Ming J. Zuo,Lang Qin,Xupeng Yan,Yulin Xing,Hongliang Li,Rui Si,Shiming Zhou,Jie Zeng
标识
DOI:10.1038/s41467-020-14917-6
摘要
Abstract Single-atom catalysts (SACs) exhibit intriguing catalytic performance owing to their maximized atom utilizations and unique electronic structures. However, the reported strategies for synthesizing SACs generally have special requirements for either the anchored metals or the supports. Herein, we report a universal approach of electrochemical deposition that is applicable to a wide range of metals and supports for the fabrication of SACs. The depositions were conducted on both cathode and anode, where the different redox reactions endowed the SACs with distinct electronic states. The SACs from cathodic deposition exhibited high activities towards hydrogen evolution reaction, while those from anodic deposition were highly active towards oxygen evolution reaction. When cathodically- and anodically-deposited Ir single atoms on Co 0.8 Fe 0.2 Se 2 @Ni foam were integrated into a two-electrode cell for overall water splitting, a voltage of 1.39 V was required at 10 mA cm −2 in alkaline electrolyte.
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