Surface reconstruction of cobalt phosphide nanosheets by electrochemical activation for enhanced hydrogen evolution in alkaline solution

被引:199
作者
Su, Liang [1 ]
Cui, Xiangzhi [2 ]
He, Ting [1 ]
Zeng, Liming [2 ,3 ]
Tian, Han [2 ,3 ]
Song, Yiling [2 ,3 ]
Qi, Kai [1 ]
Xia, Bao Yu [1 ]
机构
[1] HUST, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Chem & Serv Failure,Minist Educ, Wuhan Natl Lab Optoelect,Sch Chem & Chem Engn, 1037 Luoyu Rd, Wuhan 430074, Hubei, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
EFFICIENT ELECTROCATALYST; NANOWIRE ARRAYS; VOLMER STEP; COP; OXYGEN; NANOPARTICLES; HYDROXIDE; CATALYSTS; CARBON; SITES;
D O I
10.1039/c8sc04589e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal phosphides exhibit promising catalytic performance for the hydrogen evolution reaction (HER); however their surface structure evolution during electrochemical operation has rarely been studied. In this work, we investigate the surface reconstruction of CoP nanosheets by an in situ electrochemical activation method. After remodeling, CoP nanosheets experience an irreversible and significant evolution of the morphology and composition, and low-valence Co complexes consisting of Co(OH)(x) species are formed on the surface of CoP nanosheets, and they largely accelerate the dissociation of water. Benefiting from the synergistic effect of CoP and Co(OH)(x), the working electrode shows a remarkably enhanced HER activity of 100 mV at 10 mA cm(-2) with a Tafel slope of 76 mV dec(-1), which is better than that of most transition metal phosphide catalysts. This work would provide a deep understanding of surface reconstruction and a novel perspective for rational design of high performance transition metal phosphide electrocatalysts for water related electrolysis.
引用
收藏
页码:2019 / 2024
页数:6
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