Probing the Synergistic Effects of Mg2+on CO2 Reduction Reaction on CoPc by In Situ Electrochemical Scanning Tunneling Microscopy

We report herein the in situ electrochemical scanning tunneling microscopy (ECSTM) study on the synergistic effect of Mg2+ in CO2 reduction reaction (CO2RR) catalyzed by cobalt phthalocyanine (CoPc). ECSTM measurement molecularly resolves the self-assembled CoPc monolayer on the Au(111) substrate. In the CO2 environment, high-contrast species are observed in the adlayer and assigned to the CO2 adsorption on CoPc. Furthermore, the contrast of the CO2-bound complex is higher in Mg2+-containing electrolytes than in Mg2+-free electrolytes, indicating the formation of the CoPc-CO2-Mg2+ complex. The surface coverage of adsorbed CO2 is positively correlated with the Mg2+ concentration as the additive in electrolytes up to a plateau of 30.8 +/- 2.7% when c(Mg2+) > 30 mM. The potential step experiment indicates the higher CO2 adsorption dynamics in Mg2+-containing electrolytes than without Mg2+. The rate constants of CO2 adsorption and dissociation in different electrolytes are extracted from the data fitting of statistical results from in situ ECSTM experiments.

Automated summary

We report an in situ electrochemical scanning tunneling microscopy (ECSTM) study on the synergistic effect of Mg2+ in the CO2 reduction reaction (CO2RR) catalyzed by cobalt phthalocyanine (CoPc). Our study reveals that Mg2+ enhances the adsorption of CO2 on CoPc, resulting in the formation of CoPc-CO2-Mg2+ complexes.