Harunobu Tedzuka, Hikaru Saito, Nobuki Matsumoto, Masanari Nagasaka, Hiromasa Sato, Yasushi Sekine, Toshiki Sugimoto
Here, we unveil the nonthermal catalytic origin of DC-applied DRM over Pd/CeO 2 through multimodal operando analyses.
Catalytic dry reforming of methane (DRM) is a key reaction for the sustainable utilization of major greenhouse gases, CO 2 and CH 4 . However, conventional DRM often suffers from severe catalyst deactivation due to high temperature requirements. Applying direct current (DC) to catalysts has emerged as a promising strategy to overcome these limitations, yet the underlying DC-enhanced catalytic mechanisms remain elusive. Here, we unveil the nonthermal catalytic origin of DC-applied DRM over Pd/CeO 2 through multimodal operando analyses. Spatially resolved operando infrared measurements revealed that key reaction intermediates specific to nonthermal DRM exclusively emerge on current-carrying regions of the catalyst surface under DC bias. Furthermore, operando infrared and visible absorption spectroscopy detected the trapped electrons and holes generated in CeO 2 during DC application and revealed a clear correlation between the density of injected charges and the DRM activity. Soft X-ray spectroscopic analysis uncovers an unconventional pathway of hole generation in nominally n-type CeO 2 under DC bias. These observations demonstrate that DC application induces distinct molecular and electronic species that promote CO 2 reduction and CH 4 oxidation in DRM via nonthermal pathways.