4.8 Article

General Synergistic Capture-Bonding Superassembly of Atomically Dispersed Catalysts on Micropore-Vacancy Frameworks

期刊

NANO LETTERS
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.2c00042

关键词

KEYWORDS; atomically dispersed catalysts; metal; organic frameworks; mild temperature; general strategy; hydrogen evolution

资金

  1. National Key Research and Development Program of China [2019YFC1604601, 2019YFC1604600, 2017YFA0206901, 2017YFA0206900, 2018YFC1602301]
  2. National Natural Science Foundation of China [21705027, 21974029]
  3. Natural Science Foundation of Shanghai [18ZR1404700]
  4. Construction project of Shanghai Key Laboratory of Molecular Imaging [18DZ2260400]
  5. Shanghai Municipal Education Commission (Class II Plateau Disciplinary Construction Program of Medical Technology of SUMHS)

向作者/读者索取更多资源

This study presents a new method for the large-scale synthesis of atomically dispersed catalysts under mild conditions. By utilizing the precise capture via narrow pores and stable bonding of vacancies, the synthesis process of catalysts is simplified, and high electrocatalytic activity and long-term stability are achieved.
Atomically dispersed catalysts are a new type of material in the field of catalysis science, yet their large-scale synthesis under mild conditions remains challenging. Here, a general synergistic capture-bonding superassembly strategy to obtain atomically dispersed Pt (Ru, Au, Pd, Ir, and Rh)-based catalysts on micropore-vacancy frameworks at a mild temperature of 60 degrees C is reported. The precise capture via narrow pores and the stable bonding of vacancies not only simplify the synthesis process of atomically dispersed catalysts but also realize their large-scale preparation at mild temperature. The prepared atomically dispersed Pt-based catalyst possesses a promising electrocatalytic activity for hydrogen evolution, showing an activity (at overpotential of 50 mV) about 21.4 and 20.8 times higher than that of commercial Pt/C catalyst in 1.0 M KOH and 0.5 M H2SO4, respectively. Besides, the extremely long operational stability of more than 100 h provides more potential for its practical application.

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