A cryogenic octopole accumulation trap (COAT) has been coupled to a photoelectron-photofragment coincidence (PPC) spectrometer allowing for improved control over anion vibrational excitation. The anions are heated and cooled via collisions with buffer gas <17 K. Shorter trapping times (500 μs) prevent thermalization and result in anions with high internal excitation while longer trapping times (80 ms) at cryogenic temperatures thermalize the ions to the temperature of the buffer gas. The capabilities of the COAT are demonstrated using PPC spectroscopy of at 388 nm (E = 3.20 eV). Cooling the precursor anions with COAT resulted in the elimination of the autodetachment of vibrationally excited produced by the photodissociation + hν → O + (v ≥ 4). Under heating conditions, a lower limit temperature for the anions was determined to be 1,500 K through Franck-Condon simulations of the photodetachment spectrum of , considering a significant fraction of the ions undergo photodissociation in competition with photodetachment. The ability to cool or heat ions by varying ion injection and trapping duration in COAT provides a new flexibility for studying the spectroscopy of cold ions as well as thermally activated processes.
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http://dx.doi.org/10.3389/fchem.2019.00295 | DOI Listing |
ACS Phys Chem Au
January 2023
Department of Chemistry, Indiana University, 800 East Kirkwood, Avenue Bloomington, Indiana47405, United States.
Bimolecular reaction and collision complexes that drive atmospheric chemistry and contribute to the absorption of solar radiation are fleeting and therefore inherently challenging to study experimentally. Furthermore, primary anions in the troposphere are short lived because of a complicated web of reactions and complex formation they undergo, making details of their early fate elusive. In this perspective, the experimental approach of photodetaching mass-selected anion-molecule complexes or complex anions, which prepares neutrals in various vibronic states, is surveyed.
View Article and Find Full Text PDFRSC Adv
October 2021
Department of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Dr La Jolla Ca 92093-0340 USA
Photoelectron-photofragment coincidence (PPC) spectroscopy is a powerful technique for studying the decarboxylation dynamics of carboxyl radicals. Measurement of photoelectron and photofragment kinetic energies in coincidence provides a kinematically complete measure of the dissociative photodetachment (DPD) dynamics of carboxylate anions. PPC spectroscopy studies of methanoate, ethanoate, propanoate, 2-butenoate, benzoate, -coumarate and the oxalate monoanion are reviewed.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2022
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0340, United States.
Transition state dynamics of bimolecular reactions can be probed by photodetachment of a precursor anion when the Franck-Condon region of the corresponding neutral potential energy surface is near a saddle point. In this study, photodetachment of anions at / = 49 enabled investigation of the exit channel of the OH + CHOH → HO + CHO reaction using photoelectron-photofragment coincidence spectroscopy. High-level coupled-cluster calculations of the stationary points on the anion surface show that the methoxide-water cluster CHO(HO) is the stable minimum on the anion surface.
View Article and Find Full Text PDFMolecules
November 2021
Department of Chemistry, Saitama University, Shimo-Okubo 255, Sakura-ku, Saitama 338-8570, Japan.
The dissociative photodetachment dynamics of the oxalate anion, COH + → CO + 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.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2021
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Dr, La Jolla, CA 92093-0340, USA.
Photoelectron-photofragment coincidence spectroscopy was used to study the dissociation dynamics of the conjugate bases of benzoic acid and p-coumaric acid. Upon photodetachment at 266 nm (4.66 eV) both aromatic carboxylates undergo decarboxylation, as well as the formation of stable carboxyl radicals.
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