By applying femtosecond pump–probe spectroscopy to a substituted quinquethiophene molecule in solution, we observe in the time domain the coherent torsional dynamics that drives planarization of the excited state. Our interpretation is based on numerical modeling of the ground and excited state potential energy surfaces and simulation of wavepacket dynamics, which reveals two symmetric excited state deactivation pathways per oscillation period. We use the acquired knowledge on torsional dynamics to coherently control the excited state population with a pump-dump scheme, exploiting the non-stationary Franck–Condon overlap between ground and excited states.

Observation and control of coherent torsional dynamics in a quinquethiophene molecule

Piacenza M;Della Sala F;Favaretto L;
2010

Abstract

By applying femtosecond pump–probe spectroscopy to a substituted quinquethiophene molecule in solution, we observe in the time domain the coherent torsional dynamics that drives planarization of the excited state. Our interpretation is based on numerical modeling of the ground and excited state potential energy surfaces and simulation of wavepacket dynamics, which reveals two symmetric excited state deactivation pathways per oscillation period. We use the acquired knowledge on torsional dynamics to coherently control the excited state population with a pump-dump scheme, exploiting the non-stationary Franck–Condon overlap between ground and excited states.
2010
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Istituto Nanoscienze - NANO
QUANTUM CONTROL; EXCITATION-ENERGIES; POPULATION TRANSFER; THIOPHENE; DENSITY; PULSES; PHASE; HEXAMETHYLSEXITHIOPHENE; PHOTOLUMINESCENCE; SPECTROSCOPY
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/150379
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