Time-Resolved Coincidence Imaging Spectroscopy of Molecular Photodissociation

2005 ◽  
Author(s):  
O. GeβnerAZ ◽  
A.M.D. Lee ◽  
J.P. Shaffer ◽  
C.C. Hayden ◽  
A. Stolow
Keyword(s):  
Imaging Spectroscopy ◽  
Time Resolved ◽  
Coincidence Imaging ◽  
Molecular Photodissociation

Photodissociation dynamics studied via Time-Resolved Coincidence Imaging Spectroscopy

2005 ◽  
pp. 496-498
Author(s):  
O. Geßner ◽  
E.t-H. Chrysostom ◽  
A.M.D. Lee ◽  
J.P. Shaffer ◽  
C.C. Hayden ◽  
...  
Keyword(s):  
Imaging Spectroscopy ◽  
Time Resolved ◽  
Coincidence Imaging

Non-adiabatic intramolecular and photodissociation dynamics studied by femtosecond time-resolved photoelectron and coincidence imaging spectroscopy

2004 ◽  
Vol 127 ◽  
pp. 193-212 ◽  
Author(s):  
O. Geßner ◽  
E. t.-H. Chrysostom ◽  
A. M. D. Lee ◽  
D. M. Wardlaw ◽  
M.-L. Ho ◽  
...  
Keyword(s):  
Imaging Spectroscopy ◽  
Time Resolved ◽  
Coincidence Imaging

scholarly journals Ultrafast F2− photodissociation by intense laser pulses: a time-resolved fragment imaging study

2019 ◽  
Vol 205 ◽  
pp. 09012
Author(s):  
Abhishek Shahi ◽  
Yishai Albeck ◽  
Daniel Strasser
Keyword(s):  
Single Photon ◽  
Imaging Study ◽  
Laser Pulses ◽  
Intense Laser ◽  
Time Resolved ◽  
Intense Field ◽  
Intense Laser Pulses ◽  
Ultrafast Pulses ◽  
Coincidence Imaging ◽  
Field Dissociation

We present time-resolved coincidence imaging of F2− photodissociation by 400nm and intense 800nm ultrafast pulses. Coincidence fragment imaging reveals parallel and perpendicular single photon dissociation on 2Σg+ and 2πg states, and additional intense-field dissociation features.

scholarly journals Femtosecond time-resolved photoelectron-photoion coincidence imaging of multiphoton multichannel photodynamics in NO2

2008 ◽  
Vol 128 (20) ◽  
pp. 204311 ◽  
Author(s):  
Arno Vredenborg ◽  
Willem G. Roeterdink ◽  
Maurice H. M. Janssen
Keyword(s):  
Time Resolved ◽  
Coincidence Imaging

scholarly journals TIME-RESOLVED IMAGING SPECTROSCOPY OF PLANT ADAPTATIONS TO CHANGES IN THE LIGHT ENVIRONMENT AND APPLICABILITY TO SCREENING MUTANTS

HortScience ◽  
1994 ◽  
Vol 29 (4) ◽  
pp. 249b-249
Author(s):  
Sylvain L. Dubé ◽  
John F. Allen
Keyword(s):  
Energy Balance ◽  
Physiological State ◽  
Imaging Spectroscopy ◽  
State Transitions ◽  
Time Resolved ◽  
Growth And Survival ◽  
Plant Adaptations ◽  
Physico Chemical ◽  
Time Resolved Imaging ◽  
Kinetics Of

Photosynthesis, a major determinant in growth and survival of plants, is very sensitive to the energy balance of the processes triggered by the physico-chemical environment. It is, therefore, an excellent indicator of the plants' physiological state. Fundamental events in photosynthesis can be studied non-invasively and non-destructively by examining there-emission of absorbed light energy as chlorophyll a fluorescence. In this study we present digitized consecutive images of fluorescence of intact leaves of Arabidopsis sp. The relative intensity and kinetics of fluorescence of several AOI (areas of interests) of each image have been analyzed and compared. We demonstrate the feasibility of this technique for studying the physiology of light adaptations (state-transitions) of several organisms simultaneously and its applicability in indentifying mutants. Implications of this technique to the horticulture industry will be discussed.

scholarly journals Ultrafast Relaxation Dynamics of the S1 (nπ*) State and the 3p and 3d Rydberg States in Cyclohexanone by Femtosecond Photoelectron Imaging

2019 ◽  
Author(s):  
Ole Hüter ◽  
Niklas Helle ◽  
Friedrich Temps
Keyword(s):  
Imaging Spectroscopy ◽  
Rydberg States ◽  
Population Transfer ◽  
Relaxation Dynamics ◽  
Photoelectron Imaging ◽  
Time Resolved ◽  
Flight Mass Spectrometry ◽  
Vibronic Interactions ◽  
Photon Excitation ◽  
Photoelectron Imaging Spectroscopy

<div>The radiationless decay dynamics of the S1 (nπ*) state and the 3p and 3d Rydberg states of cyclohexanone are investigated using femtosecond time-resolved time-of- flight mass spectrometry and photoelectron imaging spectroscopy. After two-photon excitation of the 3p and 3d states, an ultrafast population transfer to the 3s state is observed within < 120 fs. We ascribe this behavior to strong vibronic interactions of the excited Rydberg states with the <sup>1</sup>ππ* valence state that enable an ultrafast population transfer via an avoided crossing and the subsequent passage of a conical intersection between the respective electronic states. Eventually, the 3s state deactivates by internal conversion to the S<sub>1</sub> (nπ*) state, which in turn is found to be long-lived with a decay time of ~ 300 - 800 ps.</div>

Visualization of the formation of cyclopentylcarbene using time-resolved photoelectron imaging spectroscopy

2017 ◽  
Vol 14 (10) ◽  
pp. 105301 ◽  
Author(s):  
Yuzhu Liu ◽  
Wenyi Yin ◽  
Thomas Gerber ◽  
Feng Jin ◽  
Gregor Knopp
Keyword(s):  
Imaging Spectroscopy ◽  
Photoelectron Imaging ◽  
Time Resolved ◽  
Photoelectron Imaging Spectroscopy

Time-resolved photoion imaging spectroscopy: Determining energy distribution in multiphoton absorption experiments

2018 ◽  
Vol 148 (13) ◽  
pp. 134303 ◽  
Author(s):  
D. B. Qian ◽  
F. D. Shi ◽  
L. Chen ◽  
S. Martin ◽  
J. Bernard ◽  
...  
Keyword(s):  
Energy Distribution ◽  
Imaging Spectroscopy ◽  
Multiphoton Absorption ◽  
Time Resolved
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