Resonant vibrational-electronic coupling between photosynthetic excitons is inadequately described by reduced basis sets
Ultrafast internal conversion between excited states of photosynthetic pigments has been a subject of intense spectroscopic interest owing to its near unity quantum yield. Of particular interest is the possibility of strong non-adiabatic mixing between vibrational and electronic degrees of freedom,...
| Auteurs principaux: | , |
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| Format: | Conference Paper |
| Langue: | English |
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2020
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| Accès en ligne: | https://hdl.handle.net/10356/144228 |