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◆ Proceedings of the National Academy of Sciences2025-12-02· Dehydrogenation

Hot electron–driven tandem CO <sub>2</sub> reduction and propane dehydrogenation over plasmonic black gold nanoreactors

Gunjan Sharma, Charvi Singhvi, Girish Mishra, Amitabha Nandi, Götz Schuck, Nico Grimm, Dirk Wallacher, Abhishek Kumar, Pavan Nukala, Sukhendu Nath, Soumya Ghosh, Vivek Polshettiwar

原始摘要(英文原文)· Original abstract
Catalytic CO 2 reduction into value-added products is an energy-intensive process and typically relies on molecular hydrogen as reductant. Coupling CO 2 reduction with propane dehydrogenation for in situ hydrogen generation presents a sustainable alternative but conventionally demands high temperatures, causing undesirable side reactions such as cracking and coke formation. Here, we demonstrate a nonthermal catalytic pathway driven by hot electrons generated via localized surface plasmon resonance. Using a plasmonic catalyst comprising Ga–Ni–Mn active sites anchored on broadband plasmonic “black gold,” we achieve tandem CO 2 reduction and propane dehydrogenation under visible-light irradiation. The catalyst consistently produces equimolar amounts (~1,600 µmol g −1 h −1 ) of CO and propene under flow conditions, maintaining exceptional stability even after 500 h. Notably, light illumination suppresses undesired side reactions, such as dry reforming of propane, cracking, and coking, preserving a stable stoichiometric ratio of CO and propene. Mechanistic studies, including controlled thermal experiments, Arrhenius analysis, and finite-difference time-domain simulations, confirm that catalytic selectivity and stability originate specifically from plasmon-induced hot electrons rather than photothermal effects. Comprehensive structural characterization using X-ray absorption near-edge structure and extended X-ray absorption fine structure, in situ diffuse reflectance infrared Fourier transform spectroscopy, ultrafast transient absorption spectroscopy, and density functional theory calculations elucidate that plasmonic excitation promotes advantageous charge-transfer states within Ga–Ni–Mn ensembles, facilitating selective activation of CO 2 and propane. This study establishes hot electron–driven plasmonic catalysis as a distinctive strategy for tandem propane dehydrogenation and circular CO 2 utilization under mild conditions.
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Hot electron–driven tandem CO <sub>2</sub> reduction and propane dehydrogenation over plasmonic black gold nanoreactors — 科研速览 Science Skim