In a novel modification of transient differential transmission spectroscopy, the first excited state S-1 is reexcited via a second laser pulse towards a higher lying state S-n. The dynamics of the relaxation of this state S-n as well as the states created from S-n, are revealed by a broad-band probe pulse. We find that the charge carrier generation efficiency from S-n is higher compared to S-1. The push and probe durations below 20 fs enable the temporal resolution of the ultrafast relaxation of the S-n state and enables us to identify the two main contributions to enhanced charge generation from S-n, energy migration towards sites of high dissociation probability, and exciton dissociation during vibrational relaxation.

Double-Excitation Dynamics in m-LPPP probed with sub-20 fs Time Resolution

Cerullo G;Manzoni C;
2003

Abstract

In a novel modification of transient differential transmission spectroscopy, the first excited state S-1 is reexcited via a second laser pulse towards a higher lying state S-n. The dynamics of the relaxation of this state S-n as well as the states created from S-n, are revealed by a broad-band probe pulse. We find that the charge carrier generation efficiency from S-n is higher compared to S-1. The push and probe durations below 20 fs enable the temporal resolution of the ultrafast relaxation of the S-n state and enables us to identify the two main contributions to enhanced charge generation from S-n, energy migration towards sites of high dissociation probability, and exciton dissociation during vibrational relaxation.
2003
1-55899-708-3
POLYMERIC SEMICONDUCTORS
LADDER POLYMER
RELAXATION
STATES
DESIGN
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/215868
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