Ultrarapid in Situ Synthesis of Cu2S Nanosheet Arrays on Copper Foam with Room-Temperature-Active Iodine Plasma for Efficient and Cost-Effective Oxygen Evolution

被引:139
|
作者
He, Liangbo [1 ]
Zhou, Dan [1 ]
Lin, Yao [1 ]
Ge, Ruixiang [1 ]
Hou, Xiandeng [2 ]
Sun, Xuping [1 ]
Zheng, Chengbin [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, Analyt & Test Ctr, Chengdu 610064, Sichuan, Peoples R China
来源
ACS CATALYSIS | 2018年 / 8卷 / 05期
基金
中国国家自然科学基金;
关键词
active iodine plasma; Cu2S nanosheet arrays; electrocatalysts; oxygen evolution; DIELECTRIC-BARRIER DISCHARGE; WATER OXIDATION CATALYST; POROUS NANOWIRE ARRAYS; HYDROGEN EVOLUTION; OXIDE ELECTROCATALYST; ASSISTED SYNTHESIS; VAPOR GENERATION; HIGHLY EFFICIENT; COBALT-SULFIDE; ELECTRODEPOSITION;
D O I
10.1021/acscatal.8b00032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing simple and cost-effective methods for the rapid synthesis of oxygen evolution reaction (OER) electrocatalysts from earth-abundant elements is a highly desired yet challenging task. Herein we report a two-step strategy based on the use of a room-temperature- and atmospheric-pressure active iodine DBD plasma and an anion exchange reaction for the in situ generation of 3D Cu2S nanosheet arrays on Cu foam (Cu2S/CF). Owing to the advantages of this plasma-based approach, and the extremely rapid anion exchange reaction between the generated CuI and S2-, synthesis of the Cu2S/CF OER catalyst can be accomplished within 6 min. The porous 3D catalyst exhibited prominent electrocatalytic activity and persistent stability (>10 h) for OER with an overpotential of 336 mV to drive a geometrical current density of 20 mA cm(-2) in 1.0 M KOH, comparable to the performance of a noble-metal IrO2/CF electrode.
引用
收藏
页码:3859 / 3864
页数:11
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