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通过耦合质谱和局部电化学对液相和气相中CO电还原进行实时原位监测

Real-Time In Situ Monitoring of CO Electroreduction in the Liquid and Gas Phases by Coupled Mass Spectrometry and Localized Electrochemistry.

作者信息

Zhang Guohui, Cui Youxin, Kucernak Anthony

机构信息

Department of Chemistry, Imperial College London, London SW7 2AZ, United Kingdom.

出版信息

ACS Catal. 2022 May 20;12(10):6180-6190. doi: 10.1021/acscatal.2c00609. Epub 2022 May 10.

Abstract

The mechanism and dynamics of the CO reduction reaction (CORR) remain poorly understood, which is largely caused by mass transport limitations and lack of time-correlated product analysis tools. In this work, a custom-built gas accessible membrane electrode (GAME) system is used to comparatively assess the CORR behavior of Au and Au-Cu catalysts. The platform achieves high reduction currents (∼ - 50 mA cm at 1.1 V vs RHE) by creating a three-phase boundary interface equipped with an efficient gas-circulation pathway, facilitating rapid mass transport of CO. The GAME system can also be easily coupled with many other analytical techniques as exemplified by mass spectrometry (MS) and localized ultramicroelectrode (UME) voltammetry to enable real-time and in situ product characterization in the gas and liquid phases, respectively. The gaseous product distribution is explicitly and quantitatively elucidated with high time resolution (on the scale of seconds), allowing for the independent assessment of Tafel slope estimates for the hydrogen (159/168 mV decade), ethene (160/170 mV decade), and methane (96/100 mV decade) evolution reactions. Moreover, the UME is used to simultaneously measure the local pH shift during CORR and assess the production of liquid phase species including formate. A positive shift of 0.8 pH unit is observed at a current density of -11 mA cm during the CORR.

摘要

一氧化碳还原反应(CORR)的机理和动力学仍未得到很好的理解,这在很大程度上是由传质限制和缺乏与时间相关的产物分析工具所致。在这项工作中,使用定制的气体可及膜电极(GAME)系统来比较评估金和金 - 铜催化剂的CORR行为。该平台通过创建配备高效气体循环途径的三相边界界面实现了高还原电流(在相对于可逆氢电极1.1 V时约为 - 50 mA cm),促进了一氧化碳的快速传质。GAME系统还可以很容易地与许多其他分析技术联用,例如质谱(MS)和局部超微电极(UME)伏安法,分别实现气相和液相产物的实时原位表征。以高时间分辨率(秒级)明确且定量地阐明了气态产物分布,从而能够独立评估氢气(159/168 mV/十倍电流变化)、乙烯(160/170 mV/十倍电流变化)和甲烷(96/100 mV/十倍电流变化)析出反应的塔菲尔斜率估计值。此外,UME用于在CORR期间同时测量局部pH变化,并评估包括甲酸盐在内的液相物种的生成。在CORR期间,在电流密度为 - 11 mA cm时观察到pH值正向偏移0.8个单位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2966/9127967/c636234dd417/cs2c00609_0002.jpg

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