TY - JOUR
T1 - Efficient Visible-Light Driven Photothermal Conversion of CO
2
to Methane by Nickel Nanoparticles Supported on Barium Titanate
AU - Mateo, Diego
AU - Morlanes, Natalia Sanchez
AU - Maity, Partha
AU - Shterk, Genrikh
AU - Mohammed, Omar F.
AU - Gascon, Jorge
N1 - KAUST Repository Item: Exported on 2020-12-07
Acknowledgements: Funding for this work was provided by King Abdullah University of Science and Technology (KAUST).
PY - 2020/12/4
Y1 - 2020/12/4
N2 - Solar-driven methanation represents a potentially cost-efficient and environmentally friendly route for the direct hydrogenation of CO2. Recently, photothermal catalysis, which involves the combination of both photochemical and thermochemical pathways, has emerged as a promising strategy for the production of solar fuels. For a photothermal catalyst to efficiently convert CO2 under illumination, in the absence of external heating, effective light harvesting, an excellent photothermal conversion and efficient active sites are required. Here, a new composite catalyst consisting of Ni nanoparticles supported on barium titanate that, under optimal reaction conditions, is able to hydrogenate CO2 to CH4 at nearly 100% selectivity with production rates as high as 103.7 mmol g–1 h–1 under both UV–visible and visible irradiation (production rate: 40.3 mmol g−1 h–1) is reported. Mechanistic studies suggest that reaction mostly proceeds through a nonthermal hot-electron-driven pathway, with a smaller thermal contribution.
AB - Solar-driven methanation represents a potentially cost-efficient and environmentally friendly route for the direct hydrogenation of CO2. Recently, photothermal catalysis, which involves the combination of both photochemical and thermochemical pathways, has emerged as a promising strategy for the production of solar fuels. For a photothermal catalyst to efficiently convert CO2 under illumination, in the absence of external heating, effective light harvesting, an excellent photothermal conversion and efficient active sites are required. Here, a new composite catalyst consisting of Ni nanoparticles supported on barium titanate that, under optimal reaction conditions, is able to hydrogenate CO2 to CH4 at nearly 100% selectivity with production rates as high as 103.7 mmol g–1 h–1 under both UV–visible and visible irradiation (production rate: 40.3 mmol g−1 h–1) is reported. Mechanistic studies suggest that reaction mostly proceeds through a nonthermal hot-electron-driven pathway, with a smaller thermal contribution.
UR - http://hdl.handle.net/10754/666278
UR - https://onlinelibrary.wiley.com/doi/10.1002/adfm.202008244
U2 - 10.1002/adfm.202008244
DO - 10.1002/adfm.202008244
M3 - Article
SN - 1616-301X
SP - 2008244
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -