Enhancement effects of Fe-doped Ni3S2 on efficient electrochemical urea oxidation and mechanism insights

被引:18
作者
Lv, Weixin [1 ]
Zhu, Lin [1 ]
Kong, Xiaoping [1 ]
Shi, Haitao [1 ]
Wang, Chongchong [1 ]
Zhang, Rui [1 ]
Wang, Wei [1 ]
机构
[1] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng 224051, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfide; Doping; One-pot; Hydrothermal; Structure modulation; ELECTROCATALYSTS; COMPOSITES;
D O I
10.1016/j.jallcom.2023.171292
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
The urea oxidation reaction (UOR) can reduce the energy consumption of electrolytic for urea-assisted water splitting to produce hydrogen. Fe(EDTA)-Ni3S2 @NF electrode is prepared by a simple one-step hydrothermal method. The addition of EDTA promotes more Fe atoms doping into Ni3S2. Fe doping regulated the morphology and electronic structure of Ni3S2, and the Fe(EDTA)-Ni3S2 @NF shows excellent UOR activity. The required UOR potentials on Fe(EDTA)-Ni3S2 @NF at 50 mA cm(-2) is 1.363 V (vs. RHE). In addition, the kinetics experiments and DFT calculations of the electrode toward UOR are carried out. It is found that UOR reactions under high current density (760 mA cm(-2)) would be limited. The liquid product of NO2- were detected by ion chromatography for UOR on Fe(EDTA)-Ni3S2 @NF. The faradaic efficiency for the electrooxidation of CO2NH4 to NO2- is 38 %. These findings provide complementary insights for the UOR in water-energy nexus systems.
引用
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页数:8
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