Operando Infrared Spectroscopy Insights into Methane C–H Bond Activation and Conversion on Platinum

作者：Jiafeng Du, Jinyu Ye, Chao Yang, Tian Sheng, Zhi‐You Zhou, Shi‐Gang Sun · 发表于：Journal of the American Chemical Society · 年份：2025 · DOI：10.1021/jacs.5c14879 · 被引用次数：5 · 研究领域：Electrocatalysts for Energy Conversion、Catalytic Processes in Materials Science、CO2 Reduction Techniques and Catalysts

Elucidating the mechanistic pathways of methane (CH 4 ) electrooxidation is crucial for advancing sustainable C 1 chemical synthesis. Herein, we report a comprehensive mechanistic picture of CH 4 activation and conversion on Pt/C membrane electrode assemblies (MEAs), through highly sensitive operando infrared spectroscopy and density functional theory (DFT) calculations. A characteristic vibrational band at ∼2916 cm –1, assigned to a key intermediate of *CH species formed via CH 4 dehydrogenation, was detected across a wide potential window from −0.4 to 0.3 V vs RHE. This activation step is thermodynamically favorable and nearly potential independent. In contrast, the subsequent oxidation of *CH to *CO, *COOH, and ultimately, CO 2 is strongly governed by applied potentials and competitive *OH adsorption. DFT calculations validate the energetics and site-specific interactions of these intermediates, highlighting the critical role of surface coverage and adsorbate migration in controlling reaction selectivity. These findings provide direct spectroscopic evidence for CH 4 activation on Pt surfaces and suggest that stabilizing and selectively oxidizing *CH intermediates represent key challenges for catalyst design. This study establishes a mechanistic foundation for the rational design of catalysts capable of selective CH 4 electrooxidation.