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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