Preparation of NiCo-LDH@NiCoV-LDH interconnected nanosheets as high-performance electrocatalysts for overall water splitting

被引:43
|
作者
Xu, Li [1 ,2 ]
Yuan, Bo [1 ,2 ]
Min, Luofu [1 ,2 ]
Xu, Wei [3 ]
Zhang, Wen [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Tianjin Key Lab Membrane Sci & Desalinat Technol, Tianjin 300350, Peoples R China
[3] Tianjin Mainland Hydrogen Equipment Co Ltd, Tianjin 301609, Peoples R China
关键词
Layered double hydroxide; Oxygen evolution; Hydrogen evolution; Nickel foam; Alkaline water electrolysis; LAYERED DOUBLE HYDROXIDE; HYDROGEN EVOLUTION REACTION; BIFUNCTIONAL ELECTROCATALYSTS; NICKEL FOAM; EFFICIENT; ARRAYS; HETEROSTRUCTURES; CATALYST;
D O I
10.1016/j.ijhydene.2022.03.062
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
Alkaline water electrolysis is a promising strategy for the production of hydrogen and oxygen. However, developing high-efficiency non-precious electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is still a big chal-lenge. Here, we report a nickel foam-based electrode coated with NiCoV-LDH and NiCo-LDH nanosheets (denoted as NiCo-LDH@NiCoV-LDH/NF) by a two-step method for effi-cient water splitting performance. The NiCo-LDH@NiCoV-LDH/NF with unique nanosheet-on-nanosheet construction can enlarge the electrochemical active specific surface area greatly, and thus accelerate the charge transfer of electrocatalytic reactions. Besides, the doping of vanadium could also improve the OER performance. The electrode only requires a low overpotential for OER (260 mV at 100 mA cm-2), and HER (80 mV at 10 mA cm-2) reactions in 1.0 mol/L KOH solution at room temperature. Furthermore, in the two-electrode water splitting test, a current density of 10 mA cm-2 was achieved at 1.55 V using 1.0 mol/L KOH solution, with excellent durability of 40 h. This work provided a facile method for developing new bifunctional catalysts. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:15583 / 15592
页数:10
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