FeN4 Sites Embedded into Carbon Nanofiber Integrated with Electrochemically Exfoliated Graphene for Oxygen Evolution in Acidic Medium

Advanced Energy Materials - Tập 8 Số 26 - 2018
Chaojun Lei1, Hengquan Chen2, Junhui Cao1, Jian Yang1, Ming Qiu3, Ying Xia3, Chris Yuan4, Bin Yang1, Zhongjian Li1, Xingwang Zhang1, Lecheng Lei1, Janel Abbott5, Yu Zhong6, Xinhui Xia6, Gang Wu5, Qinggang He2, Yang Hou1
1Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, China
2Zhejiang Provincial Key Laboratory of Advanced Chemical Engineering Manufacture Technology, College of Chemical & Biological Engineering, Zhejiang University, Hangzhou, Zhejiang, 310027 China
3Institute of Nanoscience and Nanotechnology, College of Physical Science and Technology, Central China Normal University, Wuhan 430079, China
4Department of Mechanical and Aerospace Engineering, Case Western Reserve University, 10900 Euclid Ave., Cleveland, OH 44106, USA
5Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY, 14260 USA
6State Key Laboratory of Silicon Materials, Key Laboratory of Advanced Materials and Applications for Batteries of Zhejiang Province, School of Materials Science & Engineering, Zhejiang University, Hangzhou 310027, China

Tóm tắt

Abstract

Development of inexpensive and efficient oxygen evolution reaction (OER) catalysts in acidic environment is very challenging, but it is important for practical proton exchange membrane water electrolyzers. A molecular iron–nitrogen coordinated carbon nanofiber is developed, which is supported on an electrochemically exfoliated graphene (FeN4/NF/EG) electrocatalyst through carbonizing the precursor composed of iron ions absorbed on polyaniline‐electrodeposited EG. Benefitting from the unique 3D structure, the FeN4/NF/EG hybrid exhibits a low overpotential of ≈294 mV at 10 mA cm−2 for the OER in acidic electrolyte, which is much lower than that of commercial Ir/C catalysts (320 mV) as well as all previously reported acid transitional metal‐derived OER electrocatalysts. X‐ray absorption spectroscopy coupled with a designed poisoning experiment reveals that the molecular FeN4 species are identified as active centers for the OER in acid. The first‐principles‐based calculations verify that the FeN4–doped carbon structure is capable of reducing the potential barriers and boosting the electrocatalytic OER activity in acid.

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