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作 者:Yang Qian Fan Zhang Lingshu Qiu Weiwei Han Zixu Zeng Lecheng Lei Yi He Ping Li Xingwang Zhang
机构地区:[1]Key Laboratory of Biomass Chemical Engineering of Ministry of Education,College of Chemical and Biological Engineering,Zhejiang University,Hangzhou 310027,China [2]Institute of Zhejiang University-Quzhou,Quzhou 324000,China
出 处:《Nano Research》2023年第7期8953-8960,共8页纳米研究(英文版)
摘 要:Alkaline electrolyzers for water splitting under the industrial current densities are always burdened with huge energy consumption due to the high overpotential and poor stability of the anode nanocatalysts for oxygen evolution reaction(OER).Inspired by the interfacial charge transfer for enhancing the performance,a series of in-situ grown interfacial Mn-NiFe lactate dehydrogenase(LDH)was designed on the Fe_(0.64)Ni_(0.36)/NM(nickel mesh)alloy layer.The optimized Mn_(0.15)-NiFe LDH/Fe_(0.64)Ni_(0.36)/NM exhibited an ultralow overpotential of 295 mV to drive 500 mA·cm^(-2)and an incredible stability under large current density.The interfacial space and heteroatom doping synergistically triggered the electronic structure optimization to promote electron transfer and ensure the durability of the high-current reaction.Notably,the designed Mn_(0.15)-NiFe LDH/Fe_(0.64)Ni_(0.36)/NM as an anode in an integral alkaline electrolyzer exhibited a cell voltage of 1.78 V at 500 mA·cm^(-2) with a stability of 366 h.Density functional theory(DFT)calculations further demonstrated the synergistic effect of alloy layer introduction and Mn doping could accelerate electron transfer and stabilize the charged active center to activate the NiFe LDH and reduce the OER energy barrier.Our work offers new insights into developing efficient self-supported catalysts for high-current alkaline water oxidation.
关 键 词:heteroatom doping alloy layer introduction synergistic effect high-current alkaline water oxidation
分 类 号:TG14[一般工业技术—材料科学与工程]
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