| Title: |
Sunlight-Powered Reverse Water Gas Shift Reaction Catalysed by Plasmonic Au/TiO2 Nanocatalysts: Effects of Au Particle Size on the Activity and Selectivity |
| Authors: |
VOLDERS, Jordi; ELEN, Ken; Raes, Arno; Ninakanti, Rajeshreddy; KELCHTERMANS, An-Sofie; Sastre, Francesc; HARDY, An; Cool, Pegie; Verbruggen, Sammy W.; BUSKENS, Pascal; VAN BAEL, Marlies |
| Contributors: |
Sastre, Francesc/0000-0002-9266-0561; KELCHTERMANS; An-Sofie/0000-0001-6957-2216; VOLDERS, Jordi; ELEN, Ken; Raes, Arno; Ninakanti, Rajeshreddy; KELCHTERMANS, An-Sofie; Sastre, Francesc; HARDY, An; Cool, Pegie; Verbruggen, Sammy W.; BUSKENS, Pascal; VAN BAEL, Marlies |
| Publisher Information: |
MDPI |
| Publication Year: |
2023 |
| Collection: |
Document Server@UHasselt (Universiteit Hasselt) |
| Subject Terms: |
plasmonic; nanoparticle; gold; titania; catalysis; CCU; carbon dioxide; syngas; solar fuel |
| Description: |
This study reports the low temperature and low pressure conversion (up to 160 degrees C, p = 3.5 bar) of CO2 and H-2 to CO using plasmonic Au/TiO2 nanocatalysts and mildly concentrated artificial sunlight as the sole energy source (up to 13.9 kW center dot 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 TiO2-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 TiO2 and the ratio between plasmonic absorption and scattering. Both catalysts displayed >= 84% selectivity for CO (side product is CH4). Furthermore, we demonstrated that the catalytic activity of Au/TiO2 increases exponentially with increasing light intensity, which indicated the presence of a photothermal contributor. In dark, however, both Au/TiO2 catalysts solely produced CH4 at the same catalyst bed temperature (160 degrees 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). ; We acknowledge financial support from the Flanders Innovation & Entrepeneurship (Vlaio) network through the Moonshot project D2M. We thank Jan D’Haen from Hasselt University for SEM-EDX measurement. |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
English |
| Relation: |
Nanomaterials, 12 (23) (Art N° 4153); https://hdl.handle.net/1942/39120; 23; 12; 000896093900001 |
| DOI: |
10.3390/nano12234153 |
| Availability: |
https://hdl.handle.net/1942/39120; https://doi.org/10.3390/nano12234153 |
| Accession Number: |
edsbas.8A8F726 |
| Database: |
BASE |