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作 者:Ziqi Zhang Zhe Zhang Xiaobo Chen Hanbo Wang Haiyan Lu Zhan Shi Shouhua Feng
机构地区:[1]State Key Laboratory of Inorganic Synthesis and Preparative Chemistry,College of Chemistry,Jilin University,Changchun 130012 [2]School of Engineering,RMIT University,Melbourne,Victoria 3000
出 处:《CCS Chemistry》2024年第5期1324-1337,共14页中国化学会会刊(英文)
基 金:support by the program for JLU Science and Technology Innovative Research Team(JLUSTIRT).
摘 要:Alkaline water electrolysis is an environmentally friendly and promising approach to produce hydrogen.However,high cost,low efficiency,and poor stability are roadblocks to commercialization of electrocatalysts.This work aims to design and develop a highly efficient,durable,and cost-effective electrocatalyst toward water splitting through modifying metal–organic frameworks.The electrocatalytic performance and stability surpass those of noble metal benchmarks at high current density(1–10 A·cm^(−2)).Theoretical calculations and in situ Raman spectra reveal the electronic structure of the synthesized catalyst and the mechanism of the catalytic reaction process,which rationalizes that the high catalytic activity and stability at high current are attributed to the unique electronic structure of cobalt regulated by copper and the protection provided by carbon nanotubes formed in situ,respectively.In addition,this paper proposes that the desorption ability of the catalyst toward the products(H_(2)and O_(2)),rather than the adsorption ability toward the reactants(H^(+)or OH^(−)),is more important to the sustainable and stable electrochemical water splitting progress at high current density,which is a kinetic rather than thermodynamic dominating process.The findings provide alternative insights to design and employ high performance catalysts to fuel hydrogen production as a clean energy source to tackle the global energy crisis.
关 键 词:metal-organic frameworks non-noble metal catalyst hydrogen evolution reaction oxygen evolution reaction electrocatalytic water splitting
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