4.8 Article

Sequential Phase Conversion-Induced Phosphides Heteronanorod Arrays for Superior Hydrogen Evolution Performance to Pt in Wide pH Media

期刊

ADVANCED MATERIALS
卷 34, 期 20, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202107548

关键词

heterophase; hydrogen evolution; metal phosphides; pH-universal hydrogen evolution catalysis; sequential phase conversion

资金

  1. National Key R&D Program of China [2020YFA0406204]
  2. National Natural Science Foundation of China [51871060, 52071084, 52071083, 51922031, 51831009]
  3. Collaborative Innovation Center of Suzhou Nano Science Technology
  4. CIC
  5. 111 Project
  6. Shuguang Program by Shanghai Education Development Foundation
  7. Shanghai Municipal Education Commission [20SG03]
  8. Science & Technology Commission of Shanghai Municipality [20XD1420600]
  9. Zhuhai Fudan Innovation Institute

向作者/读者索取更多资源

This study develops a hierarchical structure composed of Ni2P-Ni12P5 nanorod arrays and Ni3S2 film through a unique sequential phase conversion strategy. The structure exhibits excellent catalytic performance and stability for the hydrogen evolution reaction. The findings may provide new insights for the rational design of non-precious electrocatalysts for pH-universal hydrogen production.
Developing an efficient and non-precious pH-universal hydrogen evolution reaction electrocatalyst is highly desirable for hydrogen production by electrochemical water splitting but remains a significant challenge. Herein, a hierarchical structure composed of heterostructured Ni2P-Ni12P5 nanorod arrays rooted on Ni3S2 film (Ni2P-Ni12P5@Ni3S2) via a simultaneous corrosion and sulfidation is built followed by a phosphidation treatment toward the metallic nickel foam. The combination of theoretical calculations with in/ex situ characterizations unveils that such a unique sequential phase conversion strategy ensures the strong interfacial coupling between Ni2P and Ni12P5 as well as the robust stabilization of 1D heteronanorod arrays by Ni3S2 film, resulting in the promoted water adsorption/dissociation energy, the optimized hydrogen adsorption energy, and the enhanced electron/proton transfer ability accompanied with an excellent stability. Consequently, Ni2P-Ni12P5@Ni3S2/NF requires only 32, 46, and 34 mV overpotentials to drive 10 mA cm(-2) in 1.0 m KOH, 0.5 m H2SO4, and 1.0 m phosphate-buffered saline electrolytes, respectively, exceeding almost all the previously reported non-noble metal-based electrocatalysts. This work may pave a new avenue for the rational design of non-precious electrocatalysts toward pH-universal hydrogen evolution catalysis.

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