共 4 条
Achieving low-energy consumption water-to-hydrogen conversion via urea electrolysis over a bifunctional electrode of hierarchical cuprous sulfide@nickel selenide nanoarrays
被引:29
|作者:
Lv, Lin
[1
,2
]
Li, Zhishan
[2
,3
]
Wan, Houzhao
[4
]
Wang, Chundong
[2
]
机构:
[1] Cent China Normal Univ, Coll Chem, Wuhan 430079, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Opt & Elect Informat, Wuhan Natl Lab Optoelect, Wuhan 430074, Peoples R China
[3] Kunming Univ Sci & Technol, Fac Met & Energy Engn, State Key Lab Complex Nonferrous Met Resources Cl, Kunming 650093, Yunnan, Peoples R China
[4] Hubei Univ, Fac Phys & Elect Sci, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430092, Peoples R China
基金:
中国国家自然科学基金;
国家重点研发计划;
中国博士后科学基金;
关键词:
Hydrogen evolution;
Urea electrocatalysis;
Electrocatalyst;
Full-cell;
Bifunctionality;
LAYERED-DOUBLE-HYDROXIDE;
ELECTROCATALYTIC OXYGEN EVOLUTION;
IN-SITU GROWTH;
ORGANIC FRAMEWORKS;
EFFICIENT;
NI;
OXIDATION;
CATALYSTS;
NANOHYBRIDS;
D O I:
10.1016/j.jcis.2021.02.038
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:
Replacing sluggish oxygen evolution reaction with thermodynamically favorable urea oxidation reaction is a promising strategy for hydrogen-generation from water with low-energy consumption. However, the involved six-electron transfer process makes it formidable and seems critical. Hence, exploring high-efficient and low-cost bifunctional catalysts toward urea electrolysis is highly desirable. Herein, hierarchical cuprous sulfide@nickel selenide nanowire arrays were grown on copper foam (termed as Cu2S@Ni3Se2) via a developed method composed of in situ chemical deposition, ion exchange and electrodeposition. The as-prepared bifunctional Cu2S@Ni3Se2 not only shows remarkable hydrogen evolution reaction (HER) activity but also affords excellent urea oxidation reaction (UOR) activity. A subsequently configured Cu2S@Ni3Se2//Cu2S@Ni3Se2 full-cell (Cu2S@Ni3Se2 working as both anode and cathode) only requires a low voltage of 1.48 V to launch a current density of 10 mA cm(-2), not only surpassing the routine water electrolysis (1.70 V), but also outperforming the state-of-the-art Pt/C//IrO2 for urea electrolysis (1.65 V). Moreover, the performance is superior to most recently reported ones that configured with other catalysts. This work presents a solid step for hydrogen-generation from water with low-energy consumption. (C) 2021 Elsevier Inc. All rights reserved.
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页码:13 / 21
页数:9
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