合金
材料科学
电化学
催化作用
铜
纳米颗粒
钯
还原(数学)
过渡金属
电催化剂
冶金
无机化学
化学工程
纳米技术
物理化学
电极
化学
几何学
工程类
生物化学
数学
作者
Andreas Dueholm Bertelsen,Rebekka Klemmt,Kirstine Nygaard Kolding,Espen D. Bøjesen,Bo B. Iversen
标识
DOI:10.1021/acs.chemmater.5c01148
摘要
Copper is uniquely able to catalyze the formation of hydrocarbon-derived molecules through the electrochemical carbon dioxide reduction reaction (CO2RR) in aqueous media. Here, we investigate the change of selectivity and/or activity in CO2RR by alloying Cu with palladium by using PdxCu1–xnanoparticles as electrocatalysts. In situ powder X-ray diffraction reveals a much lowered reduction temperature of the Cu-precursor upon alloying and establishes the importance of high heating rates during synthesis to ensure homogeneous Pd alloying into copper-rich PdxCu1–xnanoparticles. Two different synthetic approaches were used to obtain PdxCu1–xnanoparticles with a composition range of x = 0.025–0.20, and the complex nanostructures of the particles were highlighted using four-dimensional Scanning Transmission Electron Microscopy (4D-STEM). The activity and selectivity toward electrochemical CO2RR in 0.1 M KHCO3were assessed for increasing Pd contents, and a systematic decrease in faradaic efficiency toward hydrocarbon products was found coupled with an increase in faradaic efficiency toward primarily H2. The results do not support PdxCu1–xalloying as a viable method for increasing selectivity toward specific hydrocarbon products in electrochemical CO2RR.
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