High-resolution anion photoelectron spectra of TiO2−, ZrO2−, and HfO2− obtained by slow electron velocity-map imaging

2013 ◽  
Vol 15 (48) ◽  
pp. 20973 ◽  
Author(s):  
Jongjin B. Kim ◽  
Marissa L. Weichman ◽  
Daniel M. Neumark
2019 ◽  
Vol 217 ◽  
pp. 235-255 ◽  
Author(s):  
Jessalyn A. DeVine ◽  
Mark C. Babin ◽  
Daniel M. Neumark

High-resolution photoelectron spectroscopy of cryogenically-cooled aluminum oxide anions shows new subtleties in the vibronic structure of Al2O2−/0 and Al3O3−/0.


2006 ◽  
Vol 125 (1) ◽  
pp. 014306 ◽  
Author(s):  
Matthew J. Nee ◽  
Andreas Osterwalder ◽  
Jia Zhou ◽  
Daniel M. Neumark

2016 ◽  
Vol 145 (16) ◽  
pp. 164307 ◽  
Author(s):  
Xiaoxi Fu ◽  
Zhihong Luo ◽  
Xiaolin Chen ◽  
Jiaming Li ◽  
Chuangang Ning

2019 ◽  
Author(s):  
Jessalyn DeVine ◽  
Mark C. Babin ◽  
Katherine Blackford ◽  
Daniel Neumark

Isomer-specific, high-resolution photoelectron spectra of cryogenically-cooled pyridinide anions obtained using slow photoelectron velocity-map imaging are presented. New vibrational structure in the detachment spectrum of para-pyridinide is resolved, and the spectra of meta- and ortho-pyridinide are reported for the first time. These spectra yield electron affinities of 1.4797(5), 1.4473(5), and 0.8669(7) eV for the para-, meta- and ortho-pyridyl radicals, respectively, as well as a number of vibrational frequencies for each neutral isomer. While most of the resolved structure in all three spectra is readily assigned by comparison to B3LYP/6-311+G* Franck-Condon simulations, the para-pyridinide spectrum shows newly-resolved fine structure attributed to anharmonic coupling within the vibrational manifold of the corresponding neutral radical. Isomeric trends in the photoelectron angular distributions are rationalized by approximating the detached anion orbitals as superpositions of s, p, and d-like hydrogenic orbitals, based on an application of Sanov’s generalized mixing model [J. Chem. Phys. 141, 124312 (2014)]. The presented experimental and theoretical results are used to address the relative energies of the anion and neutral isomers, as well as the site-specific bond dissociation energies of pyridine.


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