Trace Cobalt Doping and Defect Engineering of High Surface Area α-Ni(OH)2 for Electrocatalytic Urea Oxidation

被引:17
|
作者
Liu, Yi [1 ]
Yang, Zhihui [1 ]
Zou, Yuqin [2 ]
Wang, Shuangyin [2 ]
He, Junying [1 ]
机构
[1] Cent South Univ, Sch Met & Environm, Changsha 410083, Peoples R China
[2] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chem Biosensing & Chemometr, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
defect engineering; electrocatalysis; small molecule oxidation; NICKEL-HYDROXIDE; NANOSHEETS; CATALYST;
D O I
10.1002/eem2.12576
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Owing to the intrinsically sluggish kinetics of urea oxidation reaction (UOR) involving a six-electron transfer process, developing efficient UOR electrocatalyst is a great challenge remained to be overwhelmed. Herein, by taking advantage of 2-Methylimidazole, of which is a kind of alkali in water and owns strong coordination ability to Co2+ in methanol, trace Co (1.0 mol%) addition was found to induce defect engineering on alpha-Ni(OH)(2) in a dual-solvent system of water and methanol. Physical characterization results revealed that the synthesized electrocatalyst (WM-Ni0.99Co0.01(OH)(2)) was a kind of defective nanosheet with thickness around 5-6 nm, attributing to the synergistic effect of Co doping and defect engineering, its electron structure was finely altered, and its specific surface area was tremendously enlarged from 68 to 172.3 m(2) g(-1). With all these merits, its overpotential to drive 10 mA cm(-2) was reduced by 110 mV. Besides, the interfacial behavior of UOR was also well deciphered by operando electrochemical impedance spectroscopy.
引用
收藏
页数:8
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