A multi-step induced strategy to fabricate core-shell Pt-Ni alloy as symmetric electrocatalysts for overall water splitting

分解水 电催化剂 析氧 过电位 双功能 氧化物 化学工程 材料科学 电解 石墨烯 电解水 阳极 催化作用 电解质 无机化学 纳米技术 化学 电化学 电极 冶金 光催化 物理化学 工程类 生物化学
作者
Wenjuan Xu,Jinfa Chang,Yinggang Cheng,Hongqi Liu,Jifan Li,Yongjian Ai,Zenan Hu,Xinyue Zhang,Yiming Wang,Qionglin Liang,Yang Yang,Hongbin Sun
出处
期刊:Nano Research [Springer Science+Business Media]
卷期号:15 (2): 965-971 被引量:75
标识
DOI:10.1007/s12274-021-3582-x
摘要

Devising an electrocatalyst with brilliant efficiency and satisfactory durability for hydrogen production is of considerable demand, especially for large-scale application. Herein, we adopt a multi-step consequential induced strategy to construct a bifunctional electrocatalyst for the overall water splitting. Graphene oxide (GO) was used as a carbon matrix and in situ oxygen source, which was supported by the octahedral PtNi alloy to form the PtxNiy-GO precursor. When calcinating in Ar atmosphere, the oxygen in GO induced the surface segregation of Ni from the PtNi octahedron to form a core-shell structure of Ptx@Niy. Then, the surface-enriched Ni continuously induced the reformation of C in reduced graphene oxide (rGO) to enhance the degree of graphitization. This multi-step induction formed a nanocatalyst Ptx@Niy-rGO which has very high catalytic efficiency and stability. By optimizing the feeding ratio of PtNi (Pt:Ni = 1:2), the electrolytic overall water splitting at 10 mA·cm−2 can be driven by an electrolytic voltage of as low as 1.485 V, and hydrogen evolution reaction (HER) only needs an overpotential of 37 mV in 1.0 M KOH aqueous solution. Additionally, the catalyst exhibited consistent existence form in both HER and oxygen evolution reaction (OER), which was verified by switching the anode and cathode of the cell in the electrolysis of water. This work provides a new idea for the synthesis and evaluation of the bifunctional catalysts for water splitting.
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