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纳米多孔银网络对CO还原的韧带尺寸依赖性电催化活性

Ligament size-dependent electrocatalytic activity of nanoporous Ag network for CO reduction.

作者信息

Yang Wanfeng, Ma Wensheng, Zhang Zhonghua, Zhao Chuan

机构信息

School of Chemistry, Faculty of Science, University of New South Wales Sydney, New South Wales 2052, Australia.

出版信息

Faraday Discuss. 2018 Oct 1;210(0):289-299. doi: 10.1039/c8fd00056e.

Abstract

Electrochemical CO2 reduction (ECR) depends significantly on the nanostructures of electrocatalysts. Here we show a nanoporous Ag network catalyst (np-Ag) for efficient electrochemical reduction of CO2. The np-Ag samples with an average ligament size of 21 nm (denoted by np-Ag (21 nm)) and 87 nm (denoted by np-Ag (87 nm)) were fabricated by dealloying the rapidly solidified Mg80Ag20 (wt%) alloy ribbons in 1 wt% citric acid and 5 wt% phosphoric acid, respectively. The ligament size effect on the electrocatalytic activity and selectivity of CO2 conversion into CO is investigated. When catalysing CO2 reduction in 0.1 M KHCO3, the np-Ag (21 nm) catalyst exhibits a significantly enhanced selectivity with a faradaic efficiency for CO formation of 85.0% at -0.8 V versus RHE, about two times that (41.2%) over the np-Ag (87 nm). Additionally, a superior catalytic activity is also achieved over the np-Ag (21 nm), with a >2.5-fold increase in the CO partial current density relative to the np-Ag (87 nm). The improved selectivity and activity of np-Ag (21 nm) are attributed to the enhanced electrochemical surface area, higher local pH derived from ligament size effect, as well as more defect sites (i.e., grain boundaries) in ligaments.

摘要

电化学二氧化碳还原(ECR)在很大程度上取决于电催化剂的纳米结构。在此,我们展示了一种用于高效电化学还原二氧化碳的纳米多孔银网络催化剂(np-Ag)。通过分别在1 wt%柠檬酸和5 wt%磷酸中对快速凝固的Mg80Ag20(wt%)合金带进行脱合金化处理,制备出平均韧带尺寸为21 nm的np-Ag样品(记为np-Ag(21 nm))和87 nm的np-Ag样品(记为np-Ag(87 nm))。研究了韧带尺寸对二氧化碳电催化转化为一氧化碳的活性和选择性的影响。在0.1 M KHCO3中催化二氧化碳还原时,np-Ag(21 nm)催化剂在相对于可逆氢电极(RHE)为-0.8 V时表现出显著提高的选择性,一氧化碳生成的法拉第效率为85.0%,约为np-Ag(87 nm)的两倍(41.2%)。此外,np-Ag(21 nm)还具有优异的催化活性,相对于np-Ag(87 nm),一氧化碳分电流密度增加了2.5倍以上。np-Ag(21 nm)选择性和活性的提高归因于电化学表面积的增加、韧带尺寸效应导致的更高局部pH值以及韧带中更多的缺陷位点(即晶界)。

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