TY - JOUR
T1 - Geometrical Structures of Gas-Phase Cerium Oxide Cluster Cations after Reaction with Nitric Oxide Studied by Ion Mobility Mass Spectrometry
AU - Nagata, Toshiaki
AU - Wu, Jenna W.J.
AU - Nakano, Motoyoshi
AU - Ohshimo, Keijiro
AU - Misaizu, Fuminori
N1 - Funding Information:
This work was supported by Grants-in-Aid for Scientific Research (KAKENHI, nos. JP21H05418 and JP21K14583) from the Japan Society for the Promotion of Science (JSPS); the Institute for Quantum Chemical Exploration; and the Salt Science Research Foundation (nos. 1916 and 2022). The calculations were performed in part using the facilities of the Research Center for Computational Science, Okazaki, Japan.
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/2/24
Y1 - 2022/2/24
N2 - Cerium oxide cluster cations were reacted with nitric oxide molecules and then measured by ion mobility mass spectrometry (IMMS). CenO2n+1N+ species appeared as products of the reaction CenO2n+ + NO → CenO2n+1N+, and their collision cross sections (CCSs) with helium were obtained by IMMS. The experimental CCSs of CenO2n+1N+ were 2-6 Å2 larger than those of CenO2n+ for n = 4-10. Geometrical structures of Ce4O9N+ and Ce5O11N+ were assigned by comparing experimental CCSs with theoretically calculated CCSs of candidate structures. The suggested structures showed that the adsorbed NO molecule is oxidized by the CenO2n+ cluster into a nitrite (NO2-) or nitrate (NO3-). The CenO2n+1N+ species are regarded as intermediates of the NO oxidation reaction CenO2n+ + NO → CenO2n-1+ + NO2, and therefore, the present results are helpful for understanding redox reactions involving gas-phase CenO2n+ cluster ions.
AB - Cerium oxide cluster cations were reacted with nitric oxide molecules and then measured by ion mobility mass spectrometry (IMMS). CenO2n+1N+ species appeared as products of the reaction CenO2n+ + NO → CenO2n+1N+, and their collision cross sections (CCSs) with helium were obtained by IMMS. The experimental CCSs of CenO2n+1N+ were 2-6 Å2 larger than those of CenO2n+ for n = 4-10. Geometrical structures of Ce4O9N+ and Ce5O11N+ were assigned by comparing experimental CCSs with theoretically calculated CCSs of candidate structures. The suggested structures showed that the adsorbed NO molecule is oxidized by the CenO2n+ cluster into a nitrite (NO2-) or nitrate (NO3-). The CenO2n+1N+ species are regarded as intermediates of the NO oxidation reaction CenO2n+ + NO → CenO2n-1+ + NO2, and therefore, the present results are helpful for understanding redox reactions involving gas-phase CenO2n+ cluster ions.
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U2 - 10.1021/acs.jpca.1c10835
DO - 10.1021/acs.jpca.1c10835
M3 - Article
C2 - 35167295
AN - SCOPUS:85125119077
SN - 1089-5639
VL - 126
SP - 1204
EP - 1210
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 7
ER -