Issue 2, 2020

FexNiy/CeO2 loaded on N-doped nanocarbon as an advanced bifunctional electrocatalyst for the overall water splitting

Abstract

Developing a highly efficient and cost-effective electrocatalyst for catalyzing the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is fundamentally important for the practical application of the overall water splitting technique. Herein, a bifunctional electrocatalyst constituted by FexNiy and CeO2 nanoparticles supported on the N-doped nanocarbon (NC) is fabricated by a simple one-pot pyrolysis of the homogeneous mixture of Fe, Ni, Ce nitrates and melamine. The synergistic effect of each component in the FexNiy/CeO2/NC gives rise to outstanding electrocatalytic activities and stability toward the HER and OER. For hydrogen evolution, the FexNiy/CeO2/NC shows a smaller overpotential of 260 mV to achieve a current density of 50 mA cm−2 in a 1 M KOH electrolyte. More significantly, a small overpotential of 240 mV for FexNiy/CeO2/NC affords an oxygen evolution current density of 10 mA cm−2, far lower than that of the benchmark IrO2. The practicability and electrocatalytic activity of the prepared FexNiy/CeO2/NC under practical operation conditions are also investigated. In particular, the FexNiy/CeO2/NC-based overall water splitting cell only needs a cell voltage of 1.70 V to output 10 mA cm−2 in alkaline electrolytes, comparable to that of the IrO2∥Pt/C cell. The present study may pioneer a new avenue for developing novel bifunctional electrocatalysts with high-performance and low cost for water splitting.

Graphical abstract: FexNiy/CeO2 loaded on N-doped nanocarbon as an advanced bifunctional electrocatalyst for the overall water splitting

Supplementary files

Article information

Article type
Research Article
Submitted
27 Sep 2019
Accepted
06 Nov 2019
First published
07 Nov 2019

Inorg. Chem. Front., 2020,7, 470-476

FexNiy/CeO2 loaded on N-doped nanocarbon as an advanced bifunctional electrocatalyst for the overall water splitting

L. Chen, H. Jang, M. G. Kim, Q. Qin, X. Liu and J. Cho, Inorg. Chem. Front., 2020, 7, 470 DOI: 10.1039/C9QI01251F

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