Triethanolamine-assisted synthesis of NiFe layered double hydroxide ultrathin nanosheets for efficient oxygen evolution reaction

被引:25
作者
Zheng, Yingqiu [1 ,2 ]
Deng, Haoyuan [2 ]
Feng, Haoran [2 ]
Luo, Guoqiang [1 ,2 ]
Tu, Rong [1 ,2 ]
Zhang, Lianmeng [1 ,2 ]
机构
[1] Chem & Chem Engn Guangdong Lab, Chaozhou Branch, Chaozhou 521000, Peoples R China
[2] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
关键词
Oxygen evolution reaction; NiFe layered double hydroxide; Nanosheets; Triethanolamine; High valence of nickel and iron ions; WATER OXIDATION; IN-SITU; ELECTROCATALYTIC ACTIVITY; ENHANCEMENT; PERFORMANCE; SUPERIOR; ROBUST; OXIDE; IRON; FILM;
D O I
10.1016/j.jcis.2022.09.053
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
Water electrolysis is a promising technique for producing high-quality hydrogen, the application of which is impeded by the sluggish oxygen evolution reaction (OER) process. In this study, ultrathin nickel-iron layered double hydroxide (NiFe LDH) nanosheets were successfully synthesized through a facile hydrothermal reaction with the assistance of triethanolamine (TEA). Morphological and structural characterizations revealed that the presence of TEA modified the morphology of NiFe LDH, facilitated the synthesis of high-purity NiFe LDH, improved the crystallinity of NiFe LDH and resulted in a slight decrease in specific surface area. X-ray photoelectron spectroscopy (XPS) analysis demonstrated the modulation of the electronic structure engendered by the addition of TEA, with nickel and iron appearing in high valence state in the resulting NiFe LDH nanosheets. The as-prepared NiFe LDH nanosheets possessed outstanding OER activity with fast kinetics, exhibiting a low overpotential of 261 mV to achieve a current density of 10 mA cm(-2) and a small Tafel slope of 32.5 mV dec(-1) in 1 M KOH. The excellent OER performance and rapid OER kinetics are mainly attributed to the high-valence Ni and Fe rather than the modification in the morphology and microstructure. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:610 / 619
页数:10
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