Real-Time In Situ Monitoring of CO(2) Electroreduction in the Liquid and Gas Phases by Coupled Mass Spectrometry and Localized Electrochemistry

[Image: see text] The mechanism and dynamics of the CO(2) reduction reaction (CO(2)RR) 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 CO(2)RR behavior of Au and Au−Cu catalysts. The platform achieves high reduction currents (∼ – 50 mA cm(–2) 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(2). 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(–1)), ethene (160/170 mV decade(–1)), and methane (96/100 mV decade(–1)) evolution reactions. Moreover, the UME is used to simultaneously measure the local pH shift during CO(2)RR 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(–2) during the CO(2)RR.