Incorporation of a wave-packet propagation method into theS-matrix framework: Investigation of the effects of excited state dynamics on intense-field ionization

2005 ◽  
Vol 72 (3) ◽  
Author(s):  
Manabu Kanno ◽  
Tsuyoshi Kato ◽  
Hirohiko Kono ◽  
Yuichi Fujimura ◽  
Farhad H. M. Faisal
Keyword(s):  
Excited State ◽  
Wave Packet ◽  
Field Ionization ◽  
Excited State Dynamics ◽  
Intense Field ◽  
Thes Matrix

scholarly journals Identification of an emitting molecular species by time-resolved fluorescence applied to the excited state dynamics of pigment yellow 101

2014 ◽  
Vol 16 (20) ◽  
pp. 9394-9402 ◽  
Author(s):  
Seung Noh Lee ◽  
Jaeheung Park ◽  
Manho Lim ◽  
Taiha Joo
Keyword(s):  
Excited State ◽  
Wave Packet ◽  
Vibrational Spectrum ◽  
Molecular Species ◽  
Time Resolved Fluorescence ◽  
Time Resolved ◽  
Excited State Dynamics ◽  
Emitting Species

Time-resolved fluorescence (TRF) with a resolution higher than the periods of vibrations may provide the vibrational spectrum of an emitting species by directly recording the vibrational wave packet motions in time.

Excited-State Dynamics in the RNA Nucleotide Uridine 5’-Monophosphate Investigated by Femtosecond Broadband Transient Absorption Spectroscopy

2019 ◽  
Author(s):  
Matthew M. Brister ◽  
Carlos Crespo-Hernández
Keyword(s):  
Excited State ◽  
Excited States ◽  
Ground State ◽  
Transient Absorption ◽  
Electronic Energy ◽  
Transient Absorption Spectroscopy ◽  
Electronic Relaxation ◽  
Vibrationally Excited ◽  
Excited State Dynamics ◽  
Π State

<p></p><p> Damage to RNA from ultraviolet radiation induce chemical modifications to the nucleobases. Unraveling the excited states involved in these reactions is essential, but investigations aimed at understanding the electronic-energy relaxation pathways of the RNA nucleotide uridine 5’-monophosphate (UMP) have not received enough attention. In this Letter, the excited-state dynamics of UMP is investigated in aqueous solution. Excitation at 267 nm results in a trifurcation event that leads to the simultaneous population of the vibrationally-excited ground state, a longlived <sup>1</sup>n<sub>O</sub>π* state, and a receiver triplet state within 200 fs. The receiver state internally convert to the long-lived <sup>3</sup>ππ* state in an ultrafast time scale. The results elucidate the electronic relaxation pathways and clarify earlier transient absorption experiments performed for uracil derivatives in solution. This mechanistic information is important because long-lived nπ* and ππ* excited states of both singlet and triplet multiplicities are thought to lead to the formation of harmful photoproducts.</p><p></p>

Modulation of Excited State Dynamics in Lead Halide Perovskite Films with Electrical Bias

2019 ◽  
Author(s):  
Gergely Samu ◽  
R.A. Scheidt ◽  
A. Balog ◽  
C. Janáky ◽  
P.V. Kamat
Keyword(s):  
Excited State ◽  
Excited State Dynamics ◽  
Halide Perovskite ◽  
Electrical Bias ◽  
Lead Halide
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