Synergistic effect of defect engineering and crystalline/amorphous interfaces in NiFe layered double hydroxides for efficient oxygen evolution

被引:0
作者
Zhang, Dai [1 ]
Ou, Shiting [2 ]
Chang, Xijiang [1 ]
机构
[1] Donghua Univ, Coll Phys, Shanghai 201620, Peoples R China
[2] Xinjiang Univ, Sch Mat Sci & Engn, Urumqi 830000, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Layered double hydroxide; Plasma modification; Oxygen evolution reaction; Electrocatalyst; Density functional theory; TOTAL-ENERGY CALCULATIONS; BIFUNCTIONAL ELECTROCATALYSTS; NANOSHEETS;
D O I
10.1016/j.jallcom.2025.182010
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 efficient and durable oxygen evolution reaction (OER) catalysts is pivotal for sustainable hydrogen production via water electrolysis. Herein, a hybrid crystalline/amorphous NiFe-layered double hydroxides (c/a-NiFe-LDHs) catalyst with tailored defects is synthesized via rapid electrodeposition followed by plasma post-treatment. The c/a heterostructure was constructed via rapid electrodeposition, followed by introducing cationic and oxygen vacancies via Ar/H2 plasma. Optimizing plasma power (300 W) and duration (1 min) yielded c/a-NiFe-LDHs-P@300:1 with abundant defects and preserved structural integrity. The optimal catalyst exhibited exceptional OER activity, requiring an overpotential of only 290 mV to achieve 100 mA cm-2, along with a low Tafel slope of 32.3 mV dec-1 and robust stability over 48 h. Density functional theory calculations revealed that plasma-induced vacancies reduced the energy barrier of the rate-determining step (*O -> *OOH) by optimizing intermediate adsorption and electronic structure. This work highlights the synergistic effect of crystalline/amorphous interfaces and defect engineering in designing high-performance OER catalysts for efficient water oxidation.
引用
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页数:9
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