过电位
塔菲尔方程
电催化剂
材料科学
析氧
化学工程
电化学
多孔性
催化作用
电解质
电解水
纳米孔
比表面积
电解
微观结构
合金
分解水
微尺度化学
介电谱
纳米技术
无机化学
蚀刻(微加工)
作者
YuanYuan Jiang,Yonglin Zhao,Zhen Meng,Haiyan Si,Pan Li,Kaikai Song,Xiaoliang Han,Jinlong Gong,Fubo Wang,Honggang Sun
标识
DOI:10.1021/acsaem.5c02476
摘要
Catalysts with hierarchical porous structures spanning from the microscale to the macroscale can significantly enhance charge-transfer efficiency and active site exposure during the oxygen evolution reaction (OER). Herein, a hierarchical porous electrocatalyst was fabricated by chemically dealloying a phase-separated FeCoNiCuV high-entropy alloy (HEA). Benefiting from the phase-separated microstructure of the FeCoNiCuV HEA, selective etching generated an interconnected multiscale porous network. The dealloyed surface exhibited a hierarchical pore structure with pore sizes of approximately 30–50 μm, 3–5 μm, and 60–80 nm, increasing the electrochemical surface area (ECSA) significantly from 9.4 cm2 to 21.5 cm2 (more than doubling). Electrochemical tests conducted in 1.0 M KOH electrolyte demonstrated that the electrocatalyst exhibited excellent OER performance, with an overpotential of 296.4 mV @10 mA/cm2 and a Tafel slope of 52.2 mV/dec. The ECSA and electrochemical impedance analysis results revealed that the enhancement in catalytic activity originated from both the increased electrochemical surface area and the accelerated charge transfer rate. Furthermore, the catalyst remained stably operational under a constant current of 200 mA/cm2 for 300 h of chronopotentiometry (CP), with negligible performance degradation. These results indicate that the hierarchical porous structure plays a crucial role in enhancing catalytic activity and long-term stability, providing a promising strategy for the development of efficient and durable water oxidation electrocatalysts.
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