电合成
铜
催化作用
法拉第效率
纳米晶
纳米技术
胶体
选择性
丙醇
化学工程
材料科学
过渡金属
电化学
化学
冶金
电极
甲醇
有机化学
物理化学
工程类
作者
Min Wang,Anna Loiudice,Enric Ibáñez Alé,Krishna Kumar,Dragos Stoian,Zan Lian,Petru P. Albertini,Ludovic Zaza,Jari Leemans,Núria López,Raffaella Buonsanti
标识
DOI:10.21203/rs.3.rs-4544481/v1
摘要
Abstract Achieving a carbon neutral manufacturing of chemicals is imperative to accelerate the transition towards a sustainable future. Propanol electrosynthesis from CO electroreduction represents a promising alternative to the current manufacturing of this chemical. Yet, the catalyst features driving propanol formation are poorly understood, which limits further advancement in the performance. Herein, we report on a comprehensive mapping of the sensitivity of the CO electroreduction to the catalyst structure exploiting well-defined copper nanocrystals (NCs) with tunable shape and size synthesized via colloidal chemistry. In addition to clarify the dependence from the exposed surfaces, we discover that spheres uniquely promote n-propanol selectivity, which we explain mostly with strain effects. Driven by this novel insight, we achieve unprecedent n-propanol production via electrosynthesis with a copper catalyst. We demonstrate that colloidal copper nanospheres with a diameter of 4 nm deliver n-propanol faradaic efficiency of 39.6±1.4% at 119±4.2 mA/cm2 production rate, the latter being ten times the current state of the art for copper catalysts.
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