Bridging The Materials Gap In Catalysis: Reactivity Studies Of Nanostructured Titania

Loading...
Thumbnail Image

Degree type

Doctor of Philosophy (PhD)

Graduate group

Chemical and Biomolecular Engineering

Discipline

Subject

anatase
catalysis
surface science
titanium dioxide
Chemical Engineering
Chemistry

Funder

Grant number

License

Copyright date

2018-02-23T20:15:00-08:00

Distributor

Related resources

Contributor

Abstract

ABSTRACT BRIDGING THE MATERIALS GAP IN CATALYSIS: REACTIVITY STUDIES OF NANOSTRUCTURED TITANIA David A. Bennett John M. Vohs Surface science studies of defect-free, single-crystal model catalysts have provided vital knowledge in the form of structure-activity relationships and elementary reaction mechanisms. However, there is some difficultly in extending this understanding to more complex systems, since these model catalysts typically lack the range of features that occur on the high surface area catalysts used in industry. This project seeks to bridge the gap between these two classes of materials by studying thin films of well-defined TiO2 nanocrystals with tunable size and morphology using traditional surface science techniques. This enables the controlled introduction of features lacking in single-crystal model catalysts, allowing for the formulation of more complex structure-activity relationships. The thermal- and photocatalytic reactions of methanol to produce methane, formaldehyde, dimethyl ether, and methyl formate on these TiO2 nanoparticles were investigated using temperature programmed desorption in ultra high vacuum. Results show clear effects of nanocrystal size and shape on the activity and selectivity of these reactions. This demonstrates the value of studying nanostructured metal-oxide catalysts to better understand the relationship between fundamental catalytic knowledge and the behavior of complex heterogeneous catalysts.

Date of degree

2016-01-01

Date Range for Data Collection (Start Date)

Date Range for Data Collection (End Date)

Digital Object Identifier

Series name and number

Volume number

Issue number

Publisher

Publisher DOI

Journal Issues

Comments

Recommended citation