Peifang Guo , Lingxia Shi , Da Liu , Xinqiang Wang , Fan Gao , Yuan Ha , Jie Yin , Miao Liu , Hongge Pan , Renbing Wu
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引用次数: 2
Abstract
Water electrolysis is a green technology for hydrogen fuel production, but greatly hampered by the slow kinetics of the anodic oxygen evolution reaction (OER) and the cathodic hydrogen evolution reaction (HER). In this work, we report an efficient strategy to simultaneously promote OER and HER performance on Co3O4 hexagonal nanosheets via Fe-doping-induced cation substitution and anion vacancies. Benefiting from the integrated advantages of well-defined ultrathin nanosheets, abundant vacancies, and unique three-dimensional electrode configuration, the optimized Fe-doped Co3O4 hexagonal nanosheets/nickel foam (Fe0.4Co2.6O4 HNSs/NF) can achieve overpotentials of 328 mV at 100 mA cm−2 for OER and 315 mV at 500 mA cm−2 for HER, respectively, which is comparable to those of the benchmark noble electrocatalysts. More importantly, the Fe0.4Co2.6O4 HNSs/NF-assembled electrolyzer for overall water splitting can deliver a current density of 100 mA cm−2 at a cell voltage as low as 1.66 V and work steadily at 50 mA cm−2 with a negligible fading up to 140 h.
水电解是一种用于氢燃料生产的绿色技术,但阳极析氧反应(OER)和阴极析氢反应(HER)的缓慢动力学大大阻碍了其发展。在这项工作中,我们报道了一种有效的策略,通过Fe掺杂诱导的阳离子取代和阴离子空位,同时提高Co3O4六边形纳米片上的OER和HER性能。得益于定义明确的超薄纳米片、丰富的空位和独特的三维电极配置的综合优势,优化的Fe掺杂Co3O4六角纳米片/泡沫镍(Fe0.4Co2.6O4 HNSs/NF)在100 mA cm−2时OER可实现328 mV的过电势,在500 mA cm−2中HER可实现315 mV的过电位,其可与基准贵金属电催化剂的那些相比较。更重要的是,用于整体水分解的Fe0.4Co2.6O4 HNSs/NF组装电解槽可以在低至1.66 V的电池电压下提供100 mA cm−2的电流密度,并在50 mA cm−2中稳定工作,在140小时内可忽略不计的衰减。