Chen Yuzhen, Li Qiuhong, Lin Yuxing, Liu Jiao, Pan Jing, Hu Jingguo, Xu Xiaoyong
School of Physics Science & Technology, and Chemistry Interdisciplinary Research Center, Yangzhou University, Yangzhou, China.
Department of Physics, Xiamen University, Xiamen, China.
Nat Commun. 2024 Aug 23;15(1):7278. doi: 10.1038/s41467-024-51521-4.
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/cm 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.
析氧反应在现代能量转换和存储中起着至关重要的作用,开发具有工业相关活性和耐久性的低成本析氧反应催化剂是非常必要的,但仍然具有挑战性。在此,我们报道了一种高效且耐用的氢氧化铁镍有机框架纳米片阵列催化剂,该催化剂能够在碱性电解质中以工业级电流密度胜任长期析氧反应。这种理想的高强度性能归因于以下三个方面。首先,具有最大比表面积的二维纳米片多孔阵列有助于质量/电荷转移,以适应高电流密度催化。其次,原位衍生的氢氧化铁镍基序提供具有高本征活性的双金属协同催化中心。第三,羧基配体减轻了金属氧化,有利于在强极化下对过氧化溶解的电荷耐受性。因此,这种催化剂仅需280 mV的过电位就能提供高达1 A/cm²的高电流密度,并具有超过1000小时的长期耐久性。此外,与目前的商业水平相比,使用这种催化剂替代品的碱性水电解槽显示出更高的经济效益。