Urea electrooxidation using ZIF-67-derived Co3O4 catalyst

被引:19
|
作者
Sreekanth, T. V. M. [1 ]
Wei, X. [1 ]
Yoo, K. [1 ]
Kim, J. [2 ]
机构
[1] Yeungnam Univ, Sch Mech Engn, Gyongsan 38541, South Korea
[2] Chungnam Natl Univ, Dept Elect Engn, Energy Storage Convers Lab, Daejeon 38534, South Korea
基金
新加坡国家研究基金会;
关键词
ZIF-67; Electrocatalyst; Urea oxidation reaction; METAL-ORGANIC FRAMEWORK; SUPERCAPACITOR; ELECTRODE; ELECTROCATALYST; NANOSHEETS; EFFICIENT;
D O I
10.1016/j.matchemphys.2022.127167
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of highly efficient , inexpensive electrocatalysts exhibiting long-term stability is essential for energy-related applications. In this work, the Co3O4 catalyst was synthesized by annealing ZIF-67. The as-prepared catalysts were characterized by XRD, XPS, SEM , TEM. The electro-oxidation activities were measured by cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). In urea electro-oxidation (UOR), the ZIF-67-derived Co3O4 catalyst showed a lower Tafel-slope value (134 mV dec-1) than ZIF-67. The Co3O4 electrocatalyst had a higher electrochemical active surface area (ECSA) than ZIF-67, and therefore, it exhibited a higher electrocatalytic performance. CA also revealed that the ZIF-67-derived Co3O4 electrocatalyst exhibited a superior current density than ZIF-67 and exhibited consistent elec-trocatalytic activity for UOR.
引用
收藏
页数:6
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