Cao Junhui, Wang Kexin, Chen Jiayi, Lei Chaojun, Yang Bin, Li Zhongjian, Lei Lecheng, Hou Yang, Ostrikov Kostya
Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310058, People's Republic of China.
Ningbo Research Institute, Zhejiang University, Ningbo, 315100, People's Republic of China.
Nanomicro Lett. 2019 Aug 8;11(1):67. doi: 10.1007/s40820-019-0299-4.
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)Se-NC) hybrid is developed and synthesized by a vapor-phase hydrothermal strategy and subsequent selenization process. The as-prepared EG/(Co, Ni)Se-NC hybrid exhibits a core-shell structure where the particle diameter of (Co, Ni)Se 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)Se-NC hybrid shows remarkable electrocatalytic activity toward OER with a comparatively low overpotential of 258 mV at an current density of 10 mA cm and a small Tafel slope of 73.3 mV dec. The excellent OER catalysis performance of EG/(Co, Ni)Se-NC hybrid is much better than that of commercial Ir/C (343 mV at 10 mA cm and 98.1 mV dec), 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.
对于高效的、以地球上储量丰富的过渡金属为基础的电催化剂来替代贵金属材料以促进析氧反应(OER)的需求正在迅速增长。在此,通过气相水热策略和随后的硒化过程,开发并合成了一种包裹在氮掺杂碳中的电化学剥离石墨(EG)箔负载双金属硒化物(EG/(Co, Ni)Se-NC)杂化物。所制备的EG/(Co, Ni)Se-NC杂化物呈现核壳结构,其中(Co, Ni)Se核的粒径约为70nm,氮掺杂碳壳的厚度约为5nm。受益于高活性Co物种的组合以及Ni物种和氮掺杂碳改善的电子转移之间的协同效应,EG/(Co, Ni)Se-NC杂化物对OER表现出显著的电催化活性,在电流密度为10mA cm时具有相对较低的过电位258mV和较小的塔菲尔斜率73.3mV dec。EG/(Co, Ni)Se-NC杂化物优异的OER催化性能远优于商业Ir/C(在10mA cm时为343mV和98.1mV dec),甚至在所有先前报道的基于二元CoNi硒化物的OER电催化剂中几乎是最好的。此外,原位电化学拉曼光谱结合非原位X射线光电子能谱分析表明,出色的OER催化活性可归因于高活性的Co-OOH物种和来自Ni元素的改性电子转移过程。