Structures and CO-Adsorption Reactivities of Nickel Oxide Cluster Cations Studied by Ion Mobility Mass Spectrometry

  • Keijiro Ohshimo
    Department of Chemistry, Graduate School of Science, Tohoku University, 6−3 Aoba, Aramaki, Aoba-ku, Sendai 980−8578, Japan
  • Shohei Azuma
    Department of Chemistry, Graduate School of Science, Tohoku University, 6−3 Aoba, Aramaki, Aoba-ku, Sendai 980−8578, Japan
  • Tatsuya Komukai
    Department of Chemistry, Graduate School of Science, Tohoku University, 6−3 Aoba, Aramaki, Aoba-ku, Sendai 980−8578, Japan
  • Ryoichi Moriyama
    Department of Chemistry, Graduate School of Science, Tohoku University, 6−3 Aoba, Aramaki, Aoba-ku, Sendai 980−8578, Japan
  • Fuminori Misaizu
    Department of Chemistry, Graduate School of Science, Tohoku University, 6−3 Aoba, Aramaki, Aoba-ku, Sendai 980−8578, Japan

書誌事項

公開日
2015-01-09
資源種別
journal article
DOI
  • 10.1021/jp5115674
公開者
American Chemical Society (ACS)

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説明

Structures and CO-adsorption reactivities of nickel oxide cluster cations were investigated by ion mobility mass spectrometry. The series of NinOn–2+, NinOn–1+ and NinOn+ cluster cations were predominantly observed in a mass spectrum at high ion-injection energy into an ion-drift cell. From the arrival time distributions of NinOn+ and NinOn–1+ in the ion mobility spectrometry, structural transition from two-dimensional (2D) ring to three-dimensional (3D) compact structures was found at n = 5. In addition, 2D and 3D structural isomers were found to coexist for Ni5O5+, Ni6O5+ and Ni7O6+. By adding CO gas to buffer gas in the ion-drift cell, Ni4O3+ and Ni5O4+ cluster cations were found to be more reactive for the CO adsorption reactions than Ni4O4+ and Ni5O5+. Under the pseudo-first-order approximation, rate constants for CO-adsorption were determined to be (8.4 ± 0.7) × 10–11 cm3 molecule–1 s–1 for Ni4O3+ and (9.6 ± 0.8) × 10–11 cm3 molecule–1 s–1 for Ni5O4+. These rate constants are 2 orders of magnitude f...

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