Abstract
AbstractThe mechanistic understanding of electrochemical CO2 reduction reaction (CO2RR) requires a rapid and accurate characterisation of product distribution to unravel the activity and selectivity, which is yet hampered by the lack of advanced correlative approaches. Here, we present the time‐resolved identification of CO2RR products by using the synchronised electrochemistry‐mass spectrometry (sEC‐MS). Transients in product formation can be readily captured in relation to electrochemical conditions. Moreover, a soft ionisation (SI) strategy is developed in MS for the direct observation of CO, immune to the interference of CO2 fragments. With the sEC‐MS‐SI, the kinetic information, such as Tafel slopes and onset potentials, for a myriad of CO2RR products are revealed and we show the hysteresis seen for the evolution of some species may originate from the potential‐driven changes in surface coverage of intermediates. This work provides a real‐time picture of the dynamic formation of CO2RR products.
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