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Updated: Jul 30, 2026

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
Published on: February 19, 2018
FeNi3-modified Fe2O3/NiO/MoO2 heterogeneous nanoparticles immobilized on N, P co-doped CNT as an efficient and stable
Xiaojuan Zhang1, Yuanfu Chen2, Minglong Chen3
1School of Electronic Science and Engineering, and State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, PR China. yfchen@uestc.edu.cn dongxu_y@hotmail.com.
Abstract:
As a rate-determining step, electrocatalytic water oxidation acts a pivotal role in the water splitting process. As a consequence, it is of great significance to explore low-cost, efficient and durable electrocatalysts for the oxygen evolution reaction (OER) to promote electrocatalytic splitting water. Herein, for the first time, FeNi3-modified Fe2O3/NiO/MoO2 heterogeneous nanoparticles immobilized on N, P co-doped CNT matrix materials (FNM/NPCNT) are synthesized via a facile solid-phase grinding of the precursor, composed of nickel hexacyanoferrate/phosphomolybdic acid/CNT, and subsequently pyrolyzing under nitrogen atmosphere without any further post-processing. Due to its significant enhancement of the charge transfer efficiency and prevention of the metallic-based catalysts from being corroded, the as-prepared FNM/NPCNT hybrid electrocatalyst shows a high OER activity with a low overpotential of 282 mV vs. RHE at 10 mA cm-2 and a small Tafel slope of 46.2 mV dec-1 in an alkaline electrolyte. Moreover, the as-prepared FNM/NPCNT hybrid delivers a large mass activity of 327.6 A g-1 at the potential of 1.7 V and excellent stability (more than 20 h). This study opens up a new approach to design and synthesize non-precious transition metal-based composites immobilized N, P co-doped CNT materials as OER catalysts with high efficiency and long-term stability for promoting water splitting.
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