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Cu-based materials can produce hydrocarbons in CO2 electroreduction (CO2RR), but their stability still needs to be enhanced particularly in acidic media. Metallic Pt is highly stable in both acidic and alkaline media, yet rarely utilized in CO2RR, due to the competitive activity in hydrogen evolution reaction (HER). In this research, abundant thionine (Th) molecules are stably confined within Pt nanocrystals via a molecular doping strategy. The Pt surface is successfully modulated by these Th molecules, and thereby the dominant HER activity is converted to CO2RR activity. CO2 could be electroreduced to CH4 using organic molecule-modified Pt-based catalysts for the first time. Specifically, this composite catalyst maintains more than 100-hour stability in strong acid conditions (pH 1), even comparable to those state-of-the-art CO2RR catalysts. In-situ spectroscopic analysis and theoretical calculations reveal that the molecular modification can decrease the energy barrier for *COOH formation, and guarantee the sufficient local *H near Pt surface. Additionally, the *H derived from H2O dissociation is favorable for the *CO hydrogenation pathway towards *CHO, eventually leading to the formation of CH4. This strategy might be easily applied to microenvironment and interface regulation in other electrocatalytic reactions.
Yang et al. (Thu,) studied this question.