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Highly selective electrocatalytic Cl− oxidation reaction by oxygen-modified cobalt nanoparticles immobilized carbon nanofibers for coupling with brine water remediation and H2 production 被引量:1

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摘要 Combining the H2 production with brine remediation is regarded as a sustainable approach to achieving clean H2 energy. However, designing stable Cl− oxidation reaction (COR) electrocatalyst is the key to realize this route. Herein, a type of oxygen-modified Co nanoparticles anchored graphitic carbon nanofibers catalyst (Co/GCFs) was synthesized through a two-step strategy of adsorption and pyrolysis. The Co/GCFs-2.4 exhibits high selectivity and stability for COR at neutral electrolyte. It is worth noting that unlike the water oxidation, the chemical valence of cobalt has not changed during the COR. Further results demonstrated that the oxygen-modified Co nanoparticles provide active sites for selective COR, meanwhile, the graphitic carbon gives rise to strong catalytic stability. Thanks to the superior COR and H2 production activity of Co/GCFs-2.4, a two-electrode brine electrocatalysis system employing Co/GCFs-2.4 as both cathode and anode for H2 production exhibited robust stability, efficient and high Faraday efficiency (98%-100%). We propose that this work provides a novel strategy for designing efficient and stable catalysts with electrocatalytic COR and HER activities at neutral brine water for practically coupling with H2 production by water electrolysis and brine water remediation.
出处 《Nano Research》 SCIE EI CAS CSCD 2021年第5期1443-1449,共7页 纳米研究(英文版)
基金 This work was financially supported by the National Natural Science Foundation of China(No.51902312) Natural Science Foundation of Anhui Province(Nos.1908085QC139 and 1908085QB83) the Youth Science Fund of Anhui Agricultural University(No.2018zd25) the Science Foundation for Distinguished Young Scholars of Anhui Province(No.2008085J13) the Key research and development Project of Anhui Province(No.1804h07020148) the Fundamental Research Funds for the Central Universities(Nos.JZ2019HGBH0204 and PA2019GDPK0061) The authors thank the 1W1B station for XAFS measurement in Beijing Synchrotron Radiation Facility.
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