Ligament size-dependent electrocatalytic activity of nanoporous Ag network for CO2 reduction

被引:26
|
作者
Yang, Wanfeng [1 ]
Ma, Wensheng [2 ]
Zhang, Zhonghua [2 ]
Zhao, Chuan [1 ]
机构
[1] Univ New South Wales Sydney, Fac Sci, Sch Chem, Sydney, NSW 2052, Australia
[2] Shandong Univ, Sch Mat Sci & Engn, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jingshi Rd 17923, Jinan 250061, Shandong, Peoples R China
基金
澳大利亚研究理事会;
关键词
METAL-ORGANIC FRAMEWORKS; ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; ELECTROREDUCTION ACTIVITY; AU NANOPARTICLES; CATALYSTS; ENERGY; COPPER; NANOWIRES; METHANOL;
D O I
10.1039/c8fd00056e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:289 / 299
页数:11
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