Journal of Materials Chemistry2022,Vol.10Issue(30) :9.DOI:10.1039/d2ta04042e

Enhanced oxygen evolution catalyzed by in situ formed Fe-doped Ni oxyhydroxides in carbon nanotubes

Chen Dandan Sun Qiuhong Han Cheng Guo Yuanyuan Huang Qi Goddard William A. Qian Jinjie
Journal of Materials Chemistry2022,Vol.10Issue(30) :9.DOI:10.1039/d2ta04042e

Enhanced oxygen evolution catalyzed by in situ formed Fe-doped Ni oxyhydroxides in carbon nanotubes

Chen Dandan 1Sun Qiuhong 1Han Cheng 1Guo Yuanyuan 1Huang Qi 1Goddard William A. 2Qian Jinjie1
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作者信息

  • 1. Wenzhou University
  • 2. California Institute of Technology
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Abstract

The rational design and preparation of cost-effective, efficient and durable metal carbon nanomaterials for the oxygen evolution reaction (OER) is of great urgency. Herein, we report a high-performance OER electrocatalyst consisting of bimetallic FeNi3 nanoparticles encapsulated in hierarchical carbon nanomaterial, denoted as FeNi3@NCNT. Through a stepwise strategy, hollow carbon nanorods with abundant carbon nanotubes can be successfully calcined from rod-like NiOF-1-Fe, which are hydrolyzed to the initial NiOF-1 by Fe(iii) ions. The optimal FeNi3@NCNT catalyst exhibits an excellent electrochemical performance with a low overpotential of 264 mV at 10 mA cm−2, a Tafel slope of 58.5 mV dec−1, and a robust stability over 10 hours compared to the control samples. This enhanced OER arises from the unique hollow nanorod modified with a nanotube structure, a large surface area, a rich nitrogen content, and the synergistic effect between Ni and Fe species. Indeed, it is catalyzed by in situ generated Fe coupling with NiOOH in carbon nanotubes, which is validated by the subsequent theoretical calculations. This work enables insights into the mechanism of Fe-doped Ni oxyhydroxides for efficient OER and adds to the increasing understanding of the design and synthesis of novel catalysts for efficient energy conversion and storage.

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出版年

2022
Journal of Materials Chemistry

Journal of Materials Chemistry

ISSN:2050-7488
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