化学
催化作用
粒径
纳米颗粒
配体(生物化学)
电催化剂
碳纤维
法拉第效率
粒子(生态学)
银纳米粒子
电化学
无机化学
纳米技术
化学工程
电极
物理化学
有机化学
工程类
复合数
复合材料
受体
生物化学
材料科学
海洋学
地质学
作者
Francesco Mattarozzi,Nienke L. Visser,Jan Willem de Rijk,Peter Ngene,Petra E. de Jongh
标识
DOI:10.1002/ejic.202200365
摘要
Abstract Silver‐based catalysts are attractive for electroreduction of CO 2 to CO. To understand the electrocatalyst properties, a good control over the nanoparticle size is necessary. Herein, we report a strategy to synthesize highly dispersed, ligand‐free silver Ag nanoparticles supported on carbon. We demonstrate that the heat treatment atmosphere and carbon surface chemistry are crucial to control the Ag particle size in the 10–30 nm range. Even at low silver loadings (0.099 m 2 Ag m −2 ), Ag nanoparticles outperforms the bulk silver at low overpotentials, leading to a 23.5 % CO Faradaic efficiency at −1.2 V vs RHE. The Ag weight‐based activity of the catalysts scales with the inverse particle size, while the Ag surface‐specific activity is independent of the particle size in this range. The supported silver nanoparticles can produce a H 2 to CO ratio of 2.9 to 1, interesting for further exploration of this type of catalysts for syngas synthesis.
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