Zhou Qiuxia, Xu Caixia, Hou Jiagang, Ma Wenqing, Jian Tianzhen, Yan Shishen, Liu Hong
Institute for Advanced Interdisciplinary Research (iAIR), Spintronics Institute, Collaborative Innovation Center of Technology and Equipment for Biological Diagnosis and Therapy in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022, People's Republic of China.
School of Medical Information and Engineering, Southwest Medical University, Luzhou, 646000, People's Republic of China.
Nanomicro Lett. 2023 Apr 10;15(1):95. doi: 10.1007/s40820-023-01066-w.
The sluggish kinetics of both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) generate the large overpotential in water electrolysis and thus high-cost hydrogen production. Here, multidimensional nanoporous interpenetrating-phase FeNiZn alloy and FeNi intermetallic heterostructure is in situ constructed on NiFe foam (FeNiZn/FeNi@NiFe) by dealloying protocol. Coupling with the eminent synergism among specific constituents and the highly efficient mass transport from integrated porous backbone, FeNiZn/FeNi@NiFe depicts exceptional bifunctional activities for water splitting with extremely low overpotentials toward OER and HER (η = 367/245 mV) as well as the robust durability during the 400 h testing in alkaline solution. The as-built water electrolyzer with FeNiZn/FeNi@NiFe as both anode and cathode exhibits record-high performances for sustainable hydrogen output in terms of much lower cell voltage of 1.759 and 1.919 V to deliver the current density of 500 and 1000 mA cm as well long working lives. Density functional theory calculations disclose that the interface interaction between FeNiZn alloy and FeNi intermetallic generates the modulated electron structure state and optimized intermediate chemisorption, thus diminishing the energy barriers for hydrogen production in water splitting. With the merits of fine performances, scalable fabrication, and low cost, FeNiZn/FeNi@NiFe holds prospective application potential as the bifunctional electrocatalyst for water splitting.
析氢反应(HER)和析氧反应(OER)缓慢的动力学过程在水电解中产生了较大的过电位,从而导致制氢成本高昂。在此,通过脱合金法在泡沫镍铁(FeNiZn/FeNi@NiFe)上原位构建了多维纳米多孔互穿相FeNiZn合金和FeNi金属间化合物异质结构。FeNiZn/FeNi@NiFe结合了特定成分之间显著的协同作用以及集成多孔骨架的高效质量传输,展现出卓越的双功能析水活性,对OER和HER具有极低的过电位(η = 367/245 mV),并且在碱性溶液中400小时的测试过程中具有强大的耐久性。以FeNiZn/FeNi@NiFe作为阳极和阴极构建的水电解槽,在可持续产氢方面表现出创纪录的高性能,在500和1000 mA cm的电流密度下,电池电压低至1.759和1.919 V,且工作寿命长。密度泛函理论计算表明,FeNiZn合金与FeNi金属间化合物之间的界面相互作用产生了调制的电子结构状态并优化了中间化学吸附,从而降低了析水中制氢的能垒。凭借优异的性能、可扩展的制造工艺和低成本,FeNiZn/FeNi@NiFe作为析水双功能电催化剂具有广阔的应用前景。