Combustion Growth of NiFe Layered Double Hydroxide for Efficient and Durable Oxygen Evolution Reaction

被引:6
|
作者
Zhou, Yu [2 ]
Gao, Jinqiang [1 ]
Ju, Min [1 ]
Chen, Yanpeng [3 ]
Yuan, Haifeng [1 ]
Li, Simeng [1 ]
Li, Jinlong [2 ]
Guo, Dongxuan [2 ]
Hong, Mei [1 ]
Yang, Shihe [1 ,4 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Guangdong Prov Key Lab Nanomicro Mat Res, Shenzhen 518055, Peoples R China
[2] Qiqihar Univ, Coll Chem & Chem Engn, Qiqihar 161006, Peoples R China
[3] Harbin Inst Technol Shenzhen, Sch Civil & Environm Engn, State Key Lab Urban Water Resource & Environm, Shenzhen Key Lab Organ Pollut Prevent & Control, Shenzhen 518055, Peoples R China
[4] Inst Biomed Engn, Shenzhen Bay Lab, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
combustion; electrocatalyst; IR camera; FTACV; in situ Raman; HIGH-PERFORMANCE; CATALYSTS; ELECTROCATALYSTS;
D O I
10.1021/acsami.4c03766
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
NiFe layered double hydroxide (LDH) with abundant heterostructures represents a state-of-the-art electrocatalyst for the alkaline oxygen evolution reaction (OER). Herein, NiFe LDH/Fe2O3 nanosheet arrays have been fabricated by facile combustion of corrosion-engineered NiFe foam (NFF). The in situ grown, self-supported electrocatalyst exhibited a low overpotential of 248 mV for the OER at 50 mA cm(-2), a small Tafel slope of 31 mV dec(-1), and excellent durability over 100 h under the industrial benchmarking 500 mA cm(-2) current density. A balanced Ni and Fe composition under optimal corrosion and combustion contributed to the desirable electrochemical properties. Comprehensive ex-situ analyses and operando characterizations including Fourier-transformed alternating current voltammetry (FTACV) and in situ Raman demonstrate the beneficial role of modulated interfacial electron transfer, dynamic atomic structural transformation to NiOOH, and the high-valence active metal sites. This study provides a low-cost and easy-to-expand way to synthesize efficient and durable electrocatalysts.
引用
收藏
页码:28526 / 28536
页数:11
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