Sugar Blowing‐Induced Porous Cobalt Phosphide/Nitrogen‐Doped Carbon Nanostructures with Enhanced Electrochemical Oxidation Performance toward Water and Other Small Molecules

过电位 催化作用 材料科学 析氧 化学工程 电化学 分解水 无机化学 贵金属 过渡金属 碳纤维 化学 有机化学 电极 复合材料 冶金 物理化学 光催化 复合数 工程类
作者
Chengzhou Zhu,Shaofang Fu,Bo Xu,Junhua Song,Qiurong Shi,Mark Engelhard,Xiaolin Li,Scott P. Beckman,Junming Sun,Dan Du,Yuehe Lin
出处
期刊:Small [Wiley]
卷期号:13 (33) 被引量:71
标识
DOI:10.1002/smll.201700796
摘要

Rational design of high active and robust nonprecious metal catalysts with excellent catalytic efficiency in oxygen evolution reaction (OER) is extremely vital for making the water splitting process more energy efficient and economical. Among these noble metal-free catalysts, transition-metal-based nanomaterials are considered as one of the most promising OER catalysts due to their relatively low-cost intrinsic activities, high abundance, and diversity in terms of structure and morphology. Herein, a facile sugar-blowing technique and low-temperature phosphorization are reported to generate 3D self-supported metal involved carbon nanostructures, which are termed as Co2 P@Co/nitrogen-doped carbon (Co2 P@Co/N-C). By capitalizing on the 3D porous nanostructures with high surface area, homogeneously dispersed active sites, the intimate interaction between active sites, and 3D N-doped carbon, the resultant Co2 P@Co/N-C exhibits satisfying OER performance superior to CoO@Co/N-C, delivering 10 mA cm-2 at overpotential of 0.32 V. It is worth noting that in contrast to the substantial current density loss of RuO2 , Co2 P@Co/N-C shows much enhanced catalytic activity during the stability test and a 1.8-fold increase in current density is observed after stability test. Furthermore, the obtained Co2 P@Co/N-C can also be served as an excellent nonprecious metal catalyst for methanol and glucose electrooxidation in alkaline media, further extending their potential applications.
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