Electronic structure regulation of nickel-iron layered double hydroxides by tuning ternary component for overall water splitting

被引:18
作者
Lyu, X. [1 ]
Zhang, Y. [1 ]
Wang, X. [2 ]
Chen, H. [1 ]
Li, S. [1 ]
Zhang, W. [3 ]
Hu, Y. [1 ]
Li, F. [1 ]
Li, D. [2 ]
Yang, D. [2 ]
机构
[1] Shenyang Ligong Univ, Sch Mat Sci & Engn, 6 Nanping Cent Rd, Shenyang 110159, Peoples R China
[2] Qingdao Univ, Sch Environm Sci & Engn, State Key Lab Biofibers & Ecotext, Collaborat Innovat Ctr Marine Biomass Fibers Mat &, Qingdao 266071, Peoples R China
[3] Northeastern Univ, Key Lab Electromagnet Proc Mat, 3 Wenhua Rd, Shenyang 110819, Peoples R China
基金
中国国家自然科学基金;
关键词
Transition metal; Electrocatalyst; Oxygen evolution reaction; Hydrogen evolution reaction; Water splitting; OXYGEN; EFFICIENT; NANOSHEETS; ELECTROCATALYSTS; OXIDATION;
D O I
10.1016/j.mtsust.2022.100295
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
NiFe layer double hydroxide (LDH) preserves high electrocatalytic activities for oxygen evolution reaction (OER); however, the catalytic performance on hydrogen evolution reaction (HER) is still suffering from poor catalytic activities. In this work, zinc (Zn)-doped NiFe LDH was synthesized as an excellent bifunctional electrocatalysts in alkaline electrolyte. For OER performance, the NiFeZn LDH achieves a Tafel slope of 35.2 mV/dec, which is much lower than that of commercial IrO2 catalysts (124.3 mV/dec). Expected, NiFeZn LDH also remains enhanced HER activity with an overpotential of 236 mV at 50 mA/ cm2, superior to most of reported transition metal LDHs. The density functional theory results demonstrated that the Zn dopants could effectively manipulate the electronic structure of NiFeZn LDH, which is responsible to the enhanced active sites for HER.
引用
收藏
页数:9
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