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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Dirk Wallacher, Götz Schuck, Sukhendu Nath, Nico Grimm et al.
2 citations
Proceedings of the National Academy of Sciences
Catalysts for Methane Reforming
0.78
article

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

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

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.

Proceedings of the National Academy of SciencesVol. 122(49)
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)
Openalex Percentile: Top 26%
Catalysts for Methane Reforming
0.78
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.