Photoelectron–neutral–neutral coincidence studies of dissociative photodetachment

1995 ◽  
Vol 103 (22) ◽  
pp. 9876-9879 ◽  
Author(s):  
K. A. Hanold ◽  
C. R. Sherwood ◽  
R. E. Continetti
Keyword(s):  
Dissociative Photodetachment

Dissociative Photodetachment Dynamics of the OH–(C2H4) Anion Complex

2021 ◽  
Author(s):  
Yanice Benitez ◽  
Austin J. Parsons ◽  
Katharine G. Lunny ◽  
Robert E. Continetti
Keyword(s):  
Anion Complex ◽  
Dissociative Photodetachment

scholarly journals On-the-Fly Ring-Polymer Molecular Dynamics Calculations of the Dissociative Photodetachment Process of the Oxalate Anion

Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7250
Author(s):  
Yukinobu Takahashi ◽  
Yu Hashimoto ◽  
Kohei Saito ◽  
Toshiyuki Takayanagi
Keyword(s):  
Molecular Dynamics ◽  
Potential Energy ◽  
Quantum Effects ◽  
Experimental Spectrum ◽  
Computational Time ◽  
Oxalate Anion ◽  
Dissociative Photodetachment ◽  
Ring Polymer ◽  
Ring Polymer Molecular Dynamics ◽  
Nuclear Quantum Effects

The dissociative photodetachment dynamics of the oxalate anion, C2O4H− + hν → CO2 + HOCO + e−, were theoretically studied using the on-the-fly path-integral and ring-polymer molecular dynamics methods, which can account for nuclear quantum effects at the density-functional theory level in order to compare with the recent experimental study using photoelectron–photofragment coincidence spectroscopy. To reduce computational time, the force acting on each bead of ring-polymer was approximately calculated from the first and second derivatives of the potential energy at the centroid position of the nuclei beads. We find that the calculated photoelectron spectrum qualitatively reproduces the experimental spectrum and that nuclear quantum effects are playing a role in determining spectral widths. The calculated coincidence spectrum is found to reasonably reproduce the experimental spectrum, indicating that a relatively large energy is partitioned into the relative kinetic energy between the CO2 and HOCO fragments. This is because photodetachment of the parent anion leads to Franck–Condon transition to the repulsive region of the neutral potential energy surface. We also find that the dissociation dynamics are slightly different between the two isomers of the C2O4H− anion with closed- and open-form structures.

Dissociative photodetachment of H3O2−: a full-dimensional quantum dynamics study

2021 ◽  
Vol 23 (39) ◽  
pp. 22298-22304
Author(s):  
Hongwei Song ◽  
Yongfa Zhu ◽  
Mengyi Pan ◽  
Minghui Yang
Keyword(s):  
Quantum Dynamics ◽  
Dissociative Photodetachment ◽  
Good Agreement

Good agreement between experimental and theoretical PPC spectra for the pentatomic anion H3O2−.

Transition state dynamics of the OH+OH→O+H2O reaction studied by dissociative photodetachment of H2O2−

2001 ◽  
Vol 115 (15) ◽  
pp. 6931-6940 ◽  
Author(s):  
Hans-Jürgen Deyerl ◽  
Todd G. Clements ◽  
A. Khai Luong ◽  
Robert E. Continetti
Keyword(s):  
Transition State ◽  
Dissociative Photodetachment

Dissociative photodetachment studies of O−(H2O)2, OH−(H2O)2, and the deuterated isotopomers: Energetics and three-body dissociation dynamics

2001 ◽  
Vol 114 (19) ◽  
pp. 8436-8444 ◽  
Author(s):  
Todd G. Clements ◽  
A. Khai Luong ◽  
Hans-Jürgen Deyerl ◽  
Robert E. Continetti
Keyword(s):  
Dissociation Dynamics ◽  
Dissociative Photodetachment ◽  
Three Body

Dissociative photodetachment dynamics of O2− · (H2O)

1996 ◽  
Vol 258 (1-2) ◽  
pp. 171-179 ◽  
Author(s):  
C.R. Sherwood ◽  
R.E. Continetti
Keyword(s):  
Dissociative Photodetachment

Dissociative Photodetachment Dynamics of S2O2-

2002 ◽  
Vol 106 (2) ◽  
pp. 279-284 ◽  
Author(s):  
Todd G. Clements ◽  
Hans-Jürgen Deyerl ◽  
Robert E. Continetti
Keyword(s):  
Dissociative Photodetachment
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