磷化物
材料科学
电催化剂
催化作用
化学工程
无定形固体
联氨(抗抑郁剂)
镍
电化学
无机化学
冶金
电极
有机化学
化学
物理化学
色谱法
工程类
作者
Jin Zhang,Xinyue Cao,Min Guo,Haining Wang,Martin Saunders,Yan Xiang,San Ping Jiang,Shanfu Lu
标识
DOI:10.1021/acsami.9b00878
摘要
It is highly attractive but challenging to develop transition-metal electrocatalysts for direct hydrazine fuel cells (DHzFCs). In this work, a nickel crystalline core@nickel phosphide amorphous shell heterostructured electrocatalyst supported by active carbon (Ni@NiP/C) is developed. Ni@NiP/C with a P/Ni molar ratio of 3:100, Ni@NiP3.0/C, exhibits outstanding catalytic activity for the hydrazine oxidation reaction (HzOR) in alkaline solution, achieving a much better catalytic activity (2675.1 A gNi–1@0.25 V vs RHE) and high stability, as compared to Ni nanoparticles supported on carbon (Ni/C) and Pt/C catalysts. The results indicate that formation of the NiP amorphous shell effectively inhibits the passivation of the Ni core active sites and enhances the adsorption of hydrazine on Ni by improving the adsorption energy, leading to high electrochemical activity and stability of the Ni@NiP3.0/C catalysts for HzOR. The density functional theory calculation confirms the structural and electrocatalytic effect of the core–shell heterostructure on the stability and activity of Ni active sites for HzOR. The unique crystalline core/amorphous shell-structured Ni@NiP/C demonstrates promising potential as an effective electrocatalyst for DHzFCs.
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