Abstract
Although solar irradiation has demonstrated beneficial synergy for catalytic CO2 hydrogenation, it has long been debated as to whether the observed photo-assisted catalytic enhancement has a photo-activation component or is driven solely by the heating effect. Here, we confirm that surface adsorbates play a critical role in photo-assisted CO2 activation. We isolate the rate-determining intermediate species in the photo-assisted Sabatier reaction by in situ isotopic spectroscopy. Specifically, we reveal that photo-activation of the formate adsorbate (HCO2*) offers an eightfold photo-enhancement on NiOx/La2O3@TiO2. Concurrently, the active La2O3@TiO2 support facilitates the adsorption of CO2, which may contribute to the sustained HCO2* formation and conversion. The findings are crucial as they provide surface intermediary insights in the design of catalysts for photo-assisted CO2 conversion. Ultimately, the understanding may unlock the solar-driven hydrogenation catalytic pathway for other reactions involving HCO2* such as the synthesis of methanol.
| Original language | English |
|---|---|
| Pages (from-to) | 1034-1043 |
| Journal | Nature Catalysis |
| Volume | 3 |
| Issue number | 12 |
| Online published | 30 Nov 2020 |
| DOIs | |
| Publication status | Published - Dec 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 13 Climate Action
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