Hot electron–driven tandem CO <sub>2</sub> reduction and propane dehydrogenation over plasmonic black gold nanoreactors
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.
Authors
- Dirk Wallacher (ORCID: https://orcid.org/0000-0002-3391-7048)
- Götz Schuck (ORCID: https://orcid.org/0000-0002-0624-2719)
- Sukhendu Nath (ORCID: https://orcid.org/0000-0001-9976-7719)
- Nico Grimm
- Pavan Nukala (ORCID: https://orcid.org/0000-0002-3988-4224)
- Amitabha Nandi (ORCID: https://orcid.org/0000-0002-6688-0237)
- Abhishek Kumar (ORCID: https://orcid.org/0000-0003-3718-5654)
- Vivek Polshettiwar (ORCID: https://orcid.org/0000-0003-1375-9668)
- Soumya Ghosh (ORCID: https://orcid.org/0000-0002-9429-5238)
- Gunjan Sharma (ORCID: https://orcid.org/0000-0002-4683-8488)
- Charvi Singhvi (ORCID: https://orcid.org/0009-0003-3800-3522)
- Girish Mishra (ORCID: https://orcid.org/0009-0001-4526-5956)
Institutions
- Tata Institute of Fundamental Research (IN)
- Homi Bhabha National Institute (IN)
- Helmholtz-Zentrum Berlin für Materialien und Energie (DE)
- Center for NanoScience (DE)
- Indian Institute of Science Bangalore (IN)
Publication Details
- Journal
- Proceedings of the National Academy of Sciences
- Published
- 2025-12-02
- DOI
- https://doi.org/10.1073/pnas.2520317122
- Citations
- 2
- Primary Topic
- Catalysts for Methane Reforming
- Type
- article
- Field-Weighted Citation Impact
- 0.78