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在源自氧化铜的铜纳米线上将二氧化碳选择性电化学还原为一氧化碳

Selective electrochemical reduction of CO2 to CO on CuO-derived Cu nanowires.

作者信息

Ma Ming, Djanashvili Kristina, Smith Wilson A

机构信息

Materials for Energy Conversion and Storage, Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, P.O. Box 5045, 2600 GA Delft, The Netherlands.

出版信息

Phys Chem Chem Phys. 2015 Aug 28;17(32):20861-7. doi: 10.1039/c5cp03559g. Epub 2015 Jul 27.

Abstract

In this work, we report a new synthesis method to prepare a Cu nanowire electrocatalyst for selective CO2 reduction at room temperature and atmospheric pressure. Cu nanowire array electrodes were prepared through a two-step synthesis of Cu(OH)2 and CuO nanowire arrays on Cu foil substrates and a subsequent electrochemical reduction of the CuO nanowire arrays. The Cu nanowire arrays are able to electrochemically reduce CO2 to CO with a faradaic efficiency of ∼50% at a moderate overpotential of 490 mV, which is significantly higher than that of polycrystalline Cu foil catalysts at identical conditions. The improved faradaic efficiency for the reduction of CO2 to CO is ascribed to the enhanced stabilization for the CO2˙(-) intermediate on the high surface area Cu nanowire arrays.

摘要

在本工作中,我们报道了一种新的合成方法,用于制备在室温及大气压下选择性还原CO₂的铜纳米线电催化剂。通过在铜箔基底上两步合成Cu(OH)₂和CuO纳米线阵列,随后对CuO纳米线阵列进行电化学还原,制备了铜纳米线阵列电极。铜纳米线阵列能够在490 mV的中等过电位下将CO₂电化学还原为CO,法拉第效率约为50%,这显著高于相同条件下多晶铜箔催化剂的效率。将CO₂还原为CO的法拉第效率提高归因于高表面积铜纳米线阵列上CO₂˙(-)中间体的稳定性增强。

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