4.8 Article

Electrochemical deposition as a universal route for fabricating single-atom catalysts

期刊

NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-14917-6

关键词

-

资金

  1. National Science Fund for Distinguished Young Scholars [21925204]
  2. NSFC [21972132, U1732149, U19A2015]
  3. National Key Research and Development Program of China [2019YFA0405600]
  4. Key Research Program of Frontier Sciences of the CAS [QYZDB-SSW-SLH017]
  5. Major Program of Development Foundation of Hefei Center for Physical Science and Technology [2017FXZY002]
  6. Fundamental Research Funds for the Central Universities
  7. USTC Research Funds of the Double First-Class Initiative [YD2340002002]

向作者/读者索取更多资源

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 Co0.8Fe0.2Se2@Ni foam were integrated into a two-electrode cell for overall water splitting, a voltage of 1.39V was required at 10mAcm(-2) in alkaline electrolyte. While single-atom catalysts exhibit intriguing catalytic performances and electronic structures, syntheses are often tailored to a particular system. Here, authors report electrochemical deposition as a universal approach for the fabrication of single-atom catalysts over range of metals and supports.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据