Abstract

The excited-state dynamics of β-carotene in hexane was studied with dispersed ultrafast transient absorption techniques. A new excited state is produced after blue-edge excitation. Pump–repump–probe and pump–dump–probe measurements identified and characterized this state, termed S ‡ , which exhibits a blue-shifted spectrum with a longer lifetime than S 1. We establish the independent co-existence of the S ‡ and S 1 states following the relaxation of S 2 and demonstrate that S ‡ is an electronically excited state and not a vibrationally excited ground-state species. Our data support the premise that S ‡ is formed directly from S 2 and not via preferential excitation of ground-state sub-populations.

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