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Title: CO{sub 2} reduction by group 6 transition metal suboxide cluster anions

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.3455220· OSTI ID:21559878
; ;  [1]
  1. Department of Chemistry, Indiana University, 800 E. Kirkwood Avenue, Bloomington, Indiana 47405 (United States)

Reactions between small group 6 transition metal suboxide clusters, M{sub x}O{sub y}{sup -} (M={sup 98}Mo or {sup 186}W; x=1-4; y{<=}3x) and both CO{sub 2} and CO were studied in gas phase using mass spectrometric analysis of high-pressure, fast flow reaction products. Both Mo{sub 2}O{sub y}{sup -} and W{sub 2}O{sub y}{sup -} show evidence of sequential oxidation by CO{sub 2} of the form, M{sub 2}O{sub y}{sup -}+CO{sub 2}{yields}M{sub 2}O{sub y+1}{sup -}+CO for the more reduced species. Similar evidence is observed for the trimetallic clusters, although Mo{sub 3}O{sub 6}{sup -} appears uniquely unreactive. Lower mass resolution in the M{sub 4}O{sub y}{sup -} range precludes definitive product mass assignments, but intensity patterns suggest the continued trend of sequential oxidation of the more reduced end of the M{sub 4}O{sub y}{sup -} oxide series. Based on thermodynamic arguments, cluster oxidation by CO{sub 2} is possible if D{sub 0}(O-Mo{sub x}O{sub y}{sup -})>5.45 eV. Although simple bond energy analysis suggests that tungsten oxides may be more reactive toward CO{sub 2} compared to molybdenum oxides, this is not born out experimentally, suggesting that the activation barrier for the reduction of CO{sub 2} by tungsten suboxide clusters is very high compared to analogous molybdenum suboxide clusters. In reactions with CO, suboxides of both metal-based oxides show CO addition, with the product distribution being more diverse for Mo{sub x}O{sub y}{sup -} than for W{sub x}O{sub y}{sup -}. No evidence of cluster reduction by CO is observed.

OSTI ID:
21559878
Journal Information:
Journal of Chemical Physics, Vol. 133, Issue 2; Other Information: DOI: 10.1063/1.3455220; (c) 2010 American Institute of Physics; ISSN 0021-9606
Country of Publication:
United States
Language:
English