银和铜银合金上二氧化碳电化学还原的温度依赖性

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Catalysis Pub Date : 2024-06-18 DOI:10.1016/j.jcat.2024.115613
Rafaël E. Vos, Jeroen P. Smaak, Marc T.M. Koper
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引用次数: 0

摘要

由于银对一氧化碳具有高选择性,且容易与铜合金化以提高铜银催化剂的性能,因此经常被研究用作电化学二氧化碳还原催化剂。在本研究中,我们研究了温度对银和铜银催化剂的影响,并将其与之前对金和铜催化剂的研究结果进行了比较。我们发现,温度效应非常复杂,因为它与二氧化碳浓度、电势和质量传输相互影响。因此,对这些参数进行解构并研究温度在不同条件下的影响至关重要。此外,我们还发现,将银与铜进行合金化可以抑制纯铜在高温下产生的一些失活效应。CuAg 合金可以防止氢气在高温下的主要演化,尽管仍然可以观察到 C2+ 产物随温度变化的最佳值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The temperature dependence of electrochemical CO2 reduction on Ag and CuAg alloys

Ag is often studied as catalyst for electrochemical CO2 reduction as it shows high selectivity towards CO and is easily alloyed with Cu to enhance performance using CuAg catalysts. In this study, we investigated the effect of temperature on Ag and CuAg catalysts and compare these with previous results on Au and Cu catalysts. We show that the temperature effect is complicated as it shows an interplay with CO2 concentration, potential and mass transport. It is therefore crucial to deconvolute these parameters and study the effect of temperature under different conditions. Moreover, we show that alloying Ag with Cu can inhibit some of the deactivation effects observed at high temperatures on pure Cu. CuAg alloys can prevent the dominance of hydrogen evolution at elevated temperatures, although an optimum of C2+ products with temperature is still observed.

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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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