Light-Enhanced Carbon Dioxide Activation and Conversion by Effective Plasmonic Coupling Effect of Pt and Au Nanoparticles

Hui Song, Xianguang Meng, Thang Duy Dao, Wei Zhou, Huimin Liu, Li Shi, Huabin Zhang, Tadaaki Nagao, Tetsuya Kako, Jinhua Ye

Research output: Contribution to journalArticlepeer-review

172 Scopus citations


Photocatalytic reduction of carbon dioxide (CO2) is attractive for the production of valuable fuels and mitigating the influence of greenhouse gas emission. However, the extreme inertness of CO2 and the sluggish kinetics of photoexcited charge carrier transfer process greatly limit the conversion efficiency of CO2 photoreduction. Herein, we report that the plasmonic coupling effect of Pt and Au nanoparticles (NPs) profoundly enhances the efficiency of CO2 reduction through dry reforming of methane reaction assisted by light illumination, reducing activation energies for CO2 reduction ∼30% below thermal activation energies and achieving a reaction rate 2.4 times higher than that of the thermocatalytic reaction. UV-visible (vis) absorption spectra and wavelength-dependent performances show that not only UV but also visible light play important roles in promoting CO2 reduction due to effective localized surface plasmon resonance (LSPR) coupling between Pt and Au NPs. Finite-difference time-domain simulations and in situ diffuse reflectance infrared Fourier transform spectroscopy further reveal that effective coupling LSPR effect generates strong local electric fields and excites high concentration of hot electrons to activate the reactants and intermediate species, reduce the activation energies, and increase the reaction rate. This work provides a new pathway toward the efficient plasmon-enhanced chemical reactions via reducing the activation energies by utilizing solar energy.
Original languageEnglish (US)
Pages (from-to)408-416
Number of pages9
JournalACS Applied Materials and Interfaces
Issue number1
StatePublished - Jan 10 2018
Externally publishedYes

ASJC Scopus subject areas

  • General Materials Science


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