Dual-doping NiMoO4 with multi-channel structure enable urea-assisted energy-saving H2 production at large current density in alkaline seawater

被引:187
作者
Guo, Lili [1 ]
Chi, Jingqi [1 ,2 ]
Zhu, Jiawei [1 ,2 ]
Cui, Tong [1 ]
Lai, Jianping [1 ]
Wang, Lei [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Ecochem Engn, Minist Educ,Int Sci & Technol Cooperat Base Ecoche, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 320卷
基金
中国国家自然科学基金;
关键词
Ru; P-NiMoO 4 @NF multi -channel nanorods; Seawater splitting; Urea oxidation reaction; Energy -saving hydrogen production; HYDROGEN EVOLUTION; OXYGEN EVOLUTION; EFFICIENT; CATALYST; WATER; LDH;
D O I
10.1016/j.apcatb.2022.121977
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
Seawater electrolysis is an efficient method for producing carbon-neutral hydrogen; however, it is hindered by high energy cost and chlorine evolution reaction. In this study, we report Ru, P dual-doped NiMoO4 multichannel nanorods in-situ grown on nickel foam (Ru/P-NiMoO4 @NF), which can achieve chlorine-free hydrogen production by coupling seawater splitting with thermodynamically favorable urea oxidation. The Ru/P-NiMoO4 @NF exhibits bifunctional activity with working potentials of 0.23 V to deliver 3000 mA cm-2 for HER and 1.46 V to deliver 1000 mA cm-2 for UOR. The overall urea splitting system in the two-electrode electrolyzer require low voltage of 1.73 V to drive 500 mA cm-2, and demonstrate remarkable durability to keep above 100 mA cm-2 for 145 h. Density functional theory calculations reveal that dual-doping modulate the D-band center of catalyst, thus enhancing the adsorption of reactants and intermediates. This work provides information for designing catalysts for combing seawater splitting with urea purification.
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页数:10
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