Journal
SUSTAINABLE ENERGY & FUELS
Volume 4, Issue 9, Pages 4688-4693Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0se00582g
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Funding
- German Science Foundation DFG [TRR234, 364549901]
- Deutscher Akademischer Austauschdienst DAAD
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Understanding the complex photophysics of covalent photosensitizer-catalyst (PS-CAT) dyads is the basis for advanced structure and reactivity design. Here, we compare the light-induced processes of two PS-CAT hydrogen evolution dyads which differ in the chemical linkage between the Ir photosensitizer and the polyoxometalate catalyst. Variation of the linkage structure results in major changes of the photophysical properties and deactivation pathways which could be one of the factors controlling the catalytic activity.
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