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Sunlight-Powered Reverse Water Gas Shift Reaction Catalysed by Plasmonic Au/TiO(2) Nanocatalysts: Effects of Au Particle Size on the Activity and Selectivity
This study reports the low temperature and low pressure conversion (up to 160 °C, p = 3.5 bar) of CO(2) and H(2) to CO using plasmonic Au/TiO(2) nanocatalysts and mildly concentrated artificial sunlight as the sole energy source (up to 13.9 kW·m(−2) = 13.9 suns). To distinguish between photothermal...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738324/ https://www.ncbi.nlm.nih.gov/pubmed/36500776 http://dx.doi.org/10.3390/nano12234153 |
Sumario: | This study reports the low temperature and low pressure conversion (up to 160 °C, p = 3.5 bar) of CO(2) and H(2) to CO using plasmonic Au/TiO(2) nanocatalysts and mildly concentrated artificial sunlight as the sole energy source (up to 13.9 kW·m(−2) = 13.9 suns). To distinguish between photothermal and non-thermal contributors, we investigated the impact of the Au nanoparticle size and light intensity on the activity and selectivity of the catalyst. A comparative study between P25 TiO(2)-supported Au nanocatalysts of a size of 6 nm and 16 nm displayed a 15 times higher activity for the smaller particles, which can only partially be attributed to the higher Au surface area. Other factors that may play a role are e.g., the electronic contact between Au and TiO(2) and the ratio between plasmonic absorption and scattering. Both catalysts displayed ≥84% selectivity for CO (side product is CH(4)). Furthermore, we demonstrated that the catalytic activity of Au/TiO(2) increases exponentially with increasing light intensity, which indicated the presence of a photothermal contributor. In dark, however, both Au/TiO(2) catalysts solely produced CH(4) at the same catalyst bed temperature (160 °C). We propose that the difference in selectivity is caused by the promotion of CO desorption through charge transfer of plasmon generated charges (as a non-thermal contributor). |
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