4.8 Article

Engineering defect-rich Fe-doped NiO coupled Ni cluster nanotube arrays with excellent oxygen evolution activity

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 285, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2020.119809

关键词

Hollow nanotube arrays; Fe-doped NiO; Oxygen evolution reaction; d-band; Nonconcerted; Proton-electron transfer

资金

  1. Shenzhen Basic Research Project [JCYJ20170818092720054, JCYJ20190808145203535, JCYJ20190808144413257]
  2. National Natural Science Foundation of China [21671136]
  3. Postdoctoral Science Foundation of China [2019M663085]
  4. Shenzhen Technology Development Program [JSGG20160328151657828, XCL201110060]
  5. Major Industrial Projects of Shenzhen [s2017001850011]
  6. Project of Natural Science Foundation of Guangdong Province [2020A1515010380]

向作者/读者索取更多资源

The Fe-doped NiO CHNAs exhibit excellent catalytic performance and outstanding durability in the oxygen evolution reaction due to their large specific area for catalytic reaction and the downshift of the d band of metal sites caused by Fe doping, as confirmed by X-ray absorption fine structure. The OER of Fe-NiO-Ni CHNAs follows the adsorbate evolution mechanism with a nonconcerted proton-electron transfer pathway as a rate-determining step.
Herein we present a novel multi-level structure of Fe-doped NiO coupled Ni cluster hollow nanotube arrays (FeNiO-Ni CHNAs) grown on carbon fiber cloth as an efficient catalyst for oxygen evolution reaction. In this multilevel structure, rocksalt-type Fe-doped NiO phase hybrids with Ni clusters coupled into the nanospheres anchored to the outside of nanotube, forming a unique 3D corn-like structure. This novel multi-level structure represents a large specific area for catalytic reaction. X-ray absorption fine structure indicates that the defect-rich Fe-doped NiO phase has abundant coordinative unsaturated sites as active sites, and Fe doping downshifts the d band of metal sites, which is the main contribution to the improved oxygen evolution reaction catalytic activity. The OER of Fe-NiO-Ni CHNAs obeys the adsorbate evolution mechanism with the nonconcerted proton-electron transfer pathway as a rate-determining step. Thus Fe-doped NiO CHNAs exhibits excellent OER performance and outstanding durability that surpasses most of transition metal oxides.

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