Ultrafast electronic relaxations from the S3 state of pyrene

被引:9
|
作者
Noble, Jennifer A. [1 ,4 ]
Aupetit, Christian [1 ]
Descamps, Dominique [2 ]
Petit, Stephane [2 ]
Simon, Aude [3 ]
Mascetti, Joelle [1 ]
Ben Amor, Nadia [3 ]
Blanchet, Valerie [2 ]
机构
[1] Univ Bordeaux, CNRS, ISM, F-33405 Talence, France
[2] Univ Bordeaux, CNRS, CEA, CELIA,UMR5107, F-33405 Talence, France
[3] Univ Toulouse, CNRS UT3, LCPQ IRSAMC, F-31062 Toulouse, France
[4] Aix Marseille Univ, CNRS, PIIM, F-13397 Marseille, France
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; INFRARED-EMISSION SPECTROSCOPY; 2ND-ORDER PERTURBATION-THEORY; ABSORPTION-SPECTRA; BASIS-SETS; RADICAL CATIONS; RYDBERG STATES; EXCITATION; IONIZATION; FRAGMENTATION;
D O I
10.1039/c8cp06895j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ultrafast relaxation occurring in pyrene upon excitation at 4.68 eV was studied in a supersonic gas-jet fs pump-probe experiment. Mass spectrometry and velocity map imaging of photoelectrons produced by probing via multiphoton ionisation at 800 nm reveal that the initially prepared wave packet exhibits a fast relaxation (<80 fs), followed by a slower one of 200 fs. By comparing the propensity rules of photoionisation observed at one color with ab initio calculations, we tentatively assign these two timescales to a first internal conversion to the dark bB(3g) state followed by a second one to the long lived aB(2u) first excited state. Vertical excitation energies determined using ab initio Multi-State Complete Active Space 2nd order Perturbation Theory (MS-CASPT2), as well as oscillator strengths between several electronic states, are reported.
引用
收藏
页码:14111 / 14125
页数:15
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