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Southern Illinois University

FIRST-PRINCIPLES DENSITY FUNCTIONAL THEORY STUDIES OF REACTIVITIES OF HETEROGENEOUS CATALYSTS DETERMINED BY STRUCTURE AND SUBSTRATE

Abstract

dc:description.abstract

<p>In this dissertation, density functional theory (DFT) calculations were used to investigate (1)NO<sub>2</sub> adsorption on BaO in NO<sub>x</sub> Storage Reduction (NSR) catalyst affected by the morphology of BaO and the γ-Al<sub>2</sub>O<sub>3</sub> support, (2) energy barrier of H<sub>2</sub> dissociative adsorption over Mg clusters affected by its electronic structure, and (3) comparison of the activities of CeO<sub>2</sub> clusters affected by two different supports--monoclinic ZrO<sub>2</sub> and non-spinel γ-Al<sub>2</sub>O<sub>3</sub>. Our results showed that the electronic effect caused by the non-stoichiometry of the bare BaO clusters and surfaces improves their reactivities toward NO<sub>2</sub> adsorption greatly, whereas the geometric structure of the catalyst has only minor effect on the activity; we also found that the γ-Al<sub>2</sub>O<sub>3</sub> substrate improves the reactivities of the supported BaO clusters and at the same time the interface between BaO and γ-Al<sub>2</sub>O<sub>3</sub> provided a unique and highly reactive environment for NO<sub>2</sub> adsorption. Hydrogen dissociation barrier over pure Mg clusters is greatly affected by the electronic structure of the clusters--closed shell clusters such as Mg<sub>10</sub> and Mg<sub>9</sub>2- have higher energy barrier toward H<sub>2</sub> dissociation; however, H<sub>2</sub> dissociation over clusters that are two electrons shy from the closed electronic shell are relatively easier. As substrates, neither ZrO<sub>2</sub>(111) nor γ-Al2O3(100) affects the reactivity of the supported Ce<sub>2</sub>O<sub>4</sub> toward CO<sub>2</sub> adsorption and CO physisorption significantly; whereas the reactivity of Ce<sub>2</sub>O<sub>4</sub> toward CO reactive adsorption were found to be affected by the two substrates very differently.</p>

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy
Level thesis:degree_level
Open Access Dissertation
Discipline thesis:degree_discipline
Chemistry
Year dc:date.available
2009

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Cheng, Lei
Contributors dc:contributor
  • Ge, Qingfeng

Subjects

dc:subject × 6

Identifiers

dc:identifier.*
Repository record dc:identifier
https://opensiuc.lib.siu.edu/dissertations/99
OAI identifier oai:identifier
oai:opensiuc.lib.siu.edu:dissertations-1099

Chain of custody

source
Harvested from
Southern Illinois University
Base URL
opensiuc.lib.siu.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Cheng, Lei. FIRST-PRINCIPLES DENSITY FUNCTIONAL THEORY STUDIES OF REACTIVITIES OF HETEROGENEOUS CATALYSTS DETERMINED BY STRUCTURE AND SUBSTRATE. Open Access Dissertation thesis, 2009. https://opensiuc.lib.siu.edu/dissertations/99