硼
相(物质)
化学工程
化学
无机化学
材料科学
有机化学
工程类
作者
Yu Ma,J. Wang,Xiaohan Liu,Na Xu,Xin Li,Youhe Wang,Lianming Zhao,Yong‐Ming Chai,Bin Dong
标识
DOI:10.1016/j.cej.2024.151490
摘要
Self-supported NiFe-based oxygen evolution reaction (OER) catalysts with high activity and durability are essential for the industrialization of green hydrogen. Herein, Boron-interfered NiFe LDH nanosheets (B2-NiFe-(a-10)) with abundant wrinkle structure are prepared by introducing nonmetallic sources into the surface reconstruction of layered double hydroxide (NiFe LDH) through a novel short-time potential constant activation strategy. It enhances interactions with the electrolyte, decreases Arrhenius activation energy (Ea), accelerates efficient charge transfer and O2 escape rate. The as-reconstructed B2-NiFe-(a-10) exhibits outstanding alkaline OER activity with an ultralow overpotential of 290 mV at 100 mA cm−2 and excellent durability (100 h). Additionally, density functional theory calculations further reveal that the interaction optimizes the adsorption of oxygenated intermediates (*OH→*O), induces the center of the d-band toward the Fermi energy level, and lowers the dissociation barrier of H2O. Moreover, the anion-exchange membrane water electrolyzer (AEMWE) achieves a current density of 1 A cm−2 at 1.97 V.
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