过电位
材料科学
双金属片
硒化物
塔菲尔方程
X射线光电子能谱
析氧
化学工程
催化作用
分解水
磷化物
无机化学
电化学
金属
化学
光催化
电极
物理化学
冶金
硒
工程类
生物化学
作者
Junhui Cao,Kexin Wang,Jiayi Chen,Chaojun Lei,Bin Yang,Zhongjian Li,Lecheng Lei,Yang Hou,Kostya Ostrikov
出处
期刊:Nano-micro Letters
[Springer Science+Business Media]
日期:2019-08-08
卷期号:11 (1)
被引量:81
标识
DOI:10.1007/s40820-019-0299-4
摘要
Demand of highly efficient earth-abundant transition metal-based electrocatalysts to replace noble metal materials for boosting oxygen evolution reaction (OER) is rapidly growing. Herein, an electrochemically exfoliated graphite (EG) foil supported bimetallic selenide encased in N-doped carbon (EG/(Co, Ni)Se2–NC) hybrid is developed and synthesized by a vapor-phase hydrothermal strategy and subsequent selenization process. The as-prepared EG/(Co, Ni)Se2–NC hybrid exhibits a core–shell structure where the particle diameter of (Co, Ni)Se2 core is about 70 nm and the thickness of N-doped carbon shell is approximately 5 nm. Benefitting from the synergistic effects between the combination of highly active Co species and improved electron transfer from Ni species, and N-doped carbon, the EG/(Co, Ni)Se2–NC hybrid shows remarkable electrocatalytic activity toward OER with a comparatively low overpotential of 258 mV at an current density of 10 mA cm−2 and a small Tafel slope of 73.3 mV dec−1. The excellent OER catalysis performance of EG/(Co, Ni)Se2–NC hybrid is much better than that of commercial Ir/C (343 mV at 10 mA cm−2 and 98.1 mV dec−1), and even almost the best among all previously reported binary CoNi selenide-based OER electrocatalysts. Furthermore, in situ electrochemical Raman spectroscopy combined with ex situ X-ray photoelectron spectroscopy analysis indicates that the superb OER catalysis activity can be attributed to the highly active Co–OOH species and modified electron transfer process from Ni element.
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