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

Sharma, Gunjan; Singhvi, Charvi; Mishra, Girish; Nandi, Amitabha; Schuck, Götz; Grimm, Nico; Wallacher, Dirk; Kumar, Abhishek et al. · Proc Natl Acad Sci U S A · 2025

basic_science · Level V

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Abstract

Catalytic CO<sub>2</sub> reduction into value-added products is an energy-intensive process and typically relies on molecular hydrogen as reductant. Coupling CO<sub>2</sub> 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<sub>2</sub> reduction and propane dehydrogenation under visible-light irradiation. The catalyst consistently produces equimolar amounts (~1,600 µmol g<sup>-1</sup> h<sup>-1</sup>) 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<sub>2</sub> and propane. This study establishes hot electron-driven plasmonic catalysis as a distinctive strategy for tandem propane dehydrogenation and circular CO<sub>2</sub> utilization under mild conditions.