Bifunctional catalytic activity of Ni-Co layered double hydroxide for the electro-oxidation of water and methanol

被引:65
作者
Patil, Komal [1 ]
Babar, Pravin [1 ]
Lee, Dong Min [1 ]
Karade, Vijay [1 ]
Jo, Eunae [1 ]
Korade, Sumit [1 ,2 ]
Kim, Jin Hyeok [1 ]
机构
[1] Chonnam Natl Univ, Optoelect Convergence Res Ctr, Dept Mat Sci & Engn, Gwangju 500757, South Korea
[2] Shivaji Univ, Dept Phys, Thin Film Mat Lab, Kolhapur 416004, Maharashtra, India
基金
新加坡国家研究基金会;
关键词
OXYGEN EVOLUTION REACTION; ELECTROCATALYTIC PERFORMANCE; HYDROGEN EVOLUTION; HIGHLY EFFICIENT; OXIDATION; NANOSHEETS; OXIDE; ELECTRODE;
D O I
10.1039/d0se00899k
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 development of nanostructured architectures using low-cost first-row transition metals with high electrocatalytic activity to replace noble-metal-based electrocatalysts has recently gained considerable attention in the field of clean and sustainable energy generation technology. In this study, highly efficient, binder-free, Ni-Co layered double hydroxide (NiCo-LDH) nanowires on a nickel foam (NF) substrate were fabricatedviaa simple, one-step hydrothermal synthesis procedure, and their use as electrocatalysts for the oxygen evolution reaction (OER) and methanol oxidation reaction (MOR) was studied. When NiCo-LDH was used as the OER electrocatalyst, the overpotential required to deliver a current density of 20 and 100 mA cm(-2), was only 270 and 410 mV (without iR correction), and it exhibited a long-term stability of 50 h in 1 M KOH. Moreover, the as-prepared NiCo-LDH nanowire electrocatalyst presented remarkable electrochemical performance for the MOR with a higher current density of 761 mA cm(-2)at 0.7 Vvs.the saturated calomel electrode (SCE) and excellent stability in 1 M KOH with 0.5 M methanol. The vertically aligned NiCo-LDH nanowires presented numerous active sites and open structures and their synergism with the highly conductive NF substrate was responsible for the excellent electrochemical performance of the electrocatalyst.
引用
收藏
页码:5254 / 5263
页数:10
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