Pulsed Electrodeposition of Co3O4 Nanocrystals on One-Dimensional ZnO Scaffolds for Enhanced Electrochemical Water Oxidation

被引:20
作者
Wu, Hao [1 ]
Li, Shangyi [2 ]
Lu, Xinxin [1 ]
Toe, Cui Ying [1 ]
Chung, Hoi Ying [1 ]
Tang, Yiming [2 ]
Lu, Xunyu [1 ]
Amal, Rose [1 ]
Li, Laisheng [2 ]
Ng, Yun Hau [1 ]
机构
[1] Univ New South Wales, Sch Chem Engn, Particles & Catalysis Grp, Syndey, NSW 2052, Australia
[2] South China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
来源
CHEMPLUSCHEM | 2018年 / 83卷 / 10期
基金
澳大利亚研究理事会;
关键词
electrochemistry; hybrid nanostructures; oxygen evolution; pulsed electrodeposition; water splitting; OXYGEN EVOLUTION REACTION; COBALT-OXIDE; CARBON NANOTUBES; NANOWIRE ARRAYS; NEUTRAL PH; TEMPERATURE SYNTHESIS; EVOLVING CATALYST; THIN-FILM; ELECTROCATALYST; GRAPHENE;
D O I
10.1002/cplu.201800218
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pulsed electrodeposition has been introduced to deposit ultrathin flakes of Co3O4 nanocrystals on ZnO nanorods. By fixing the seeding process, the scaffolding function of ZnO nanorods was studied by varying deposition times (30 s, 60 s, and 90 s) of Co3O4 at a nucleation current of -1.0 mA cm(-2). The amount of deposited Co3O4 has a strong influence on the oxygen evolution performance with ZnO scaffolds. To deliver a current density of 10.0 mA cm(-2) in neutral solutions (0.5 M K2SO4), the presence of ZnO scaffold electrodes negatively shifted the overpotential by similar to 200 mV. In particular, the Co3O4/ZnO hybrid nanostructured electrode (60 s) exhibits the lowest onset potential of 1.5 V (vs. reversible hydrogen electrode, RHE). Electrochemical impedance spectra and double layer capacitance showed that the enhanced oxygen evolution activities originated from the improved charge transfer capability and the increased electrochemically active interface between Co3O4 and ZnO.
引用
收藏
页码:934 / 940
页数:7
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