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Effects of metal oxide surface doping with phosphonic acid monolayers on alcohol dehydration activity and selectivity

Journal Article · · Applied Catalysis. A, General
 [1];  [2];  [2];  [2]
  1. Univ. of Colorado, Boulder, CO (United States); University of Colorado Boulder
  2. Univ. of Colorado, Boulder, CO (United States)

Controlling the near-surface environment of heterogeneous catalysts is of fundamental importance for high selectivity and activity. Self-assembled monolayers (SAMs) are effective tools to control reaction selectivity and activity for both supported noble metal and metal oxide catalysts. In prior work, we demonstrated tunable dehydration activity of alcohols on phosphonic acid-modified, anatase-phase TiO2. In this work, we investigated the generality of this approach by studying the modification of other metal oxides including Al2O3, CeO2, CuO, Fe2O3, MgO, rutile-TiO2, SnO2, V2O5, WO3, ZrO2, and ZnO. Modification of these materials with phosphonic acids results in the formation of SAMs on the surface, as determined by infrared spectroscopy; studies of the thermal stability on selected catalysts indicated that the SAMs remained intact up to approximately 400 °C in inert environments. Decomposition of alcohols on these native materials resulted in dehydration, dehydrogenation, and condensation. Upon functionalization with phosphonic acid modifiers, the activity of all pathways decreased significantly, except for dehydration on CeO2, anatase-TiO2, and SnO2. We explored the properties of these oxides that may be responsible for this increase in dehydration activity using correlations to bulk properties. This analysis supported the hypothesis that phosphonic acid monolayers act as surface-level dopants for metal oxides of specific metal-oxygen bond strength and oxidation state.

Research Organization:
Univ. of Colorado, Boulder, CO (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences & Biosciences Division; USDA; National Institute of Food and Agriculture (NIFA)
Grant/Contract Number:
SC0005239
OSTI ID:
1658630
Alternate ID(s):
OSTI ID: 1610817
Journal Information:
Applied Catalysis. A, General, Journal Name: Applied Catalysis. A, General Vol. 571; ISSN 0926-860X
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English

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