析氧
催化作用
氢氧化物
过电位
碱性水电解
电催化剂
纳米片
化学工程
材料科学
法拉第效率
电解
电解质
溶解
电解水
无机化学
电化学
化学
纳米技术
有机化学
电极
物理化学
工程类
作者
Yuzhen Chen,Qiuhong Li,Yuxing Lin,Jiao Liu,Jing Pan,Jingguo Hu,Xiaoyong Xu
标识
DOI:10.1038/s41467-024-51521-4
摘要
The oxygen evolution reaction plays a vital role in modern energy conversion and storage, and developing cost-efficient oxygen evolution reaction catalysts with industrially relevant activity and durability is highly desired but still challenging. Here, we report an efficient and durable FeNi hydroxide organic framework nanosheet array catalyst that competently affords long-term oxygen evolution reaction at industrial-grade current densities in alkaline electrolyte. The desirable high-intensity performance is attributed to three aspects as follows. First, two-dimensional nanosheet porous arrays with maximum specific surface facilitate mass/charge transfer to accommodate high-current-density catalysis. Second, in situ derived FeNi hydroxide motifs offer bimetallic synergistic catalysis centers with high intrinsic activity. Third, carboxyl ligands alleviate metal oxidation favorable for charge tolerability against peroxidation dissolution under strong polarization. As a result, this catalyst requires an overpotential of only 280 mV to deliver high current density up to 1 A/cm2 with long durability over 1000 h. Moreover, an alkaline water electrolyzer with this catalyst alternative demonstrates an increased economic effectiveness compared to commercial levels at present. Developing cost-efficient catalysts for oxygen evolution reaction is crucial for various modern energy technologies. Here the authors report an efficient and durable NiFe hydroxide organic framework catalyst for water oxidation at 1 A/cm2 with long durability over 1000 h.
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