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Ultrafast Molecular Spectroscopy Using a Hollow-Core Photonic Crystal Fiber Light Source.
Kotsina, Nikoleta; Belli, Federico; Gao, Shou-Fei; Wang, Ying-Ying; Wang, Pu; Travers, John C; Townsend, Dave.
Afiliação
  • Kotsina N; Institute of Photonics & Quantum Sciences , Heriot-Watt University , Edinburgh EH14 4AS , U.K.
  • Belli F; Institute of Photonics & Quantum Sciences , Heriot-Watt University , Edinburgh EH14 4AS , U.K.
  • Gao SF; Beijing Engineering Research Centre of Laser Technology, Institute of Laser Engineering , Beijing University of Technology , 100124 Beijing , China.
  • Wang YY; Beijing Engineering Research Centre of Laser Technology, Institute of Laser Engineering , Beijing University of Technology , 100124 Beijing , China.
  • Wang P; Beijing Engineering Research Centre of Laser Technology, Institute of Laser Engineering , Beijing University of Technology , 100124 Beijing , China.
  • Travers JC; Institute of Photonics & Quantum Sciences , Heriot-Watt University , Edinburgh EH14 4AS , U.K.
  • Townsend D; Institute of Photonics & Quantum Sciences , Heriot-Watt University , Edinburgh EH14 4AS , U.K.
J Phys Chem Lett ; 10(4): 715-720, 2019 Feb 21.
Article em En | MEDLINE | ID: mdl-30694062
ABSTRACT
We demonstrate, for the first time, the application of rare-gas-filled hollow-core photonic crystal fibers (HC-PCFs) as tunable ultraviolet light sources in femtosecond pump-probe spectroscopy. A critical requirement here is excellent output stability over extended periods of data acquisition, and we show this can be readily achieved. The time-resolved photoelectron imaging technique reveals nonadiabatic dynamical processes operating on three distinct time scales in the styrene molecule following excitation over the 242-258 nm region. These include ultrafast (<100 fs) internal conversion between the S2(ππ*) and S1(ππ*) electronic states and subsequent intramolecular vibrational energy redistribution within S1(ππ*). Compact, cost-effective, and highly efficient benchtop HC-PCF sources have huge potential to open up many exciting new avenues for ultrafast spectroscopy in the ultraviolet and vacuum ultraviolet spectral regions. We anticipate that our initial validation of this approach will generate important impetus in this area.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido