Abstract
Coupling the concept of photo-thermal catalysis is a promising strategy for solar driven DRM reaction. However, highly efficient photo-thermal catalyst and its catalytic reaction mechanism are still barren. Therefore, a highly efficient Pt/mesoporous TiO2 photo-thermal catalyst is reported in this work, and reaction mechanism is investigated through XRD, XPS, Raman, UV–vis–nir, PL and in situ DRIFTS. It is found that Pt active sites and semiconductor TiO2 could work together with SPR and photoelectric effects to enhance adsorption and activation of CH4 and CO2, as well as the conversions of intermediate products (CHx, COO–, –OH etc.). Besides, the formation rates of CO and H2 are 281.0 and 178.6 mmol·gcat−1·h−1 respectively under 500 °C and 3.1 W·m−2 light irradiation intensity, which are 1.58 and 1.74 times higher than those under dark conditions. The activities of the prepared Pt/mesoporous-TiO2 catalyst performs better than recently published reports, showing great potential in photo-thermal chemical conversions.
| Original language | English |
|---|---|
| Article number | 115496 |
| Journal | Energy Conversion and Management |
| Volume | 258 |
| DOIs | |
| State | Published - 15 Apr 2022 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Dry reforming of methane
- Improved conversion performance
- Photo-thermal catalysis
- Reaction mechanism
- Solar fuel
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