{"id":{"repo_id":"kennesaw","oai_identifier":"oai:digitalcommons.kennesaw.edu:mscs_etd-1001"},"canonical_url":"https://search.dev.ndltd.org/etd/kennesaw/oai:digitalcommons.kennesaw.edu:mscs_etd-1001","repository":{"repo_id":"kennesaw","name":"Kennesaw State University","base_url":"https://digitalcommons.kennesaw.edu/do/oai/"},"display":{"title":"Analysis and Comparison of the Photodecomposition Reaction of Methanol on CeO2 Impregnated TiO2 Surfaces Versus Bare TiO2 Surfaces","abstract":"<p>Titanium dioxide (TiO<sub>2</sub>) has been well-studied primarily due to its unique photocatalytic activity. Different preparation techniques have been developed to increase its photocatalytic activity by various means, including simply increasing the surface area, changing the makeup of the framework, and modifying the surface with a dopant. This study focuses on the effect cerium oxide (CeO<sub>2</sub>) has on the photocatalytic activity of TiO<sub>2</sub> by depositing CeO<sub>2</sub> on the TiO<sub>2</sub> surface. Methanol is used as a probe reactant for these experiments due to its wide use in heterogeneous catalysis research and the limited products that can form. Three-dimensional CeO<sub>2</sub> crystallites form on the 1 and 2 monolayer CeO<sub>2</sub>-TiO<sub>2</sub> samples while crystals are not observed for the 0.5 or 0.25 monolayer samples. Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) was used to characterize the surface chemistry occurring on these samples while a flow reactor was used to characterize the reaction products using a long path gas cell in a Fourier transform infrared spectrometer (FTIR). Except for the 1 monolayer sample, CeO<sub>2</sub> seems to increase the reaction and decomposition of organic compounds, especially chemisorbed methoxy groups, on the surface. The CeO<sub>2</sub> modified samples appear to adsorb molecular methanol less strongly than TiO<sub>2</sub>. Upon UV irradiation, the CeO<sub>2</sub> modified samples desorb methoxy as methanol more so than TiO<sub>2</sub>. All samples consistently produce carbon dioxide, water, formaldehyde, dimethyl ether, and methanol in the presence of ultraviolet light and oxygen.</p>","abstract_html":"&lt;p&gt;Titanium dioxide (TiO&lt;sub&gt;2&lt;/sub&gt;) has been well-studied primarily due to its unique photocatalytic activity. Different preparation techniques have been developed to increase its photocatalytic activity by various means, including simply increasing the surface area, changing the makeup of the framework, and modifying the surface with a dopant. This study focuses on the effect cerium oxide (CeO&lt;sub&gt;2&lt;/sub&gt;) has on the photocatalytic activity of TiO&lt;sub&gt;2&lt;/sub&gt; by depositing CeO&lt;sub&gt;2&lt;/sub&gt; on the TiO&lt;sub&gt;2&lt;/sub&gt; surface. Methanol is used as a probe reactant for these experiments due to its wide use in heterogeneous catalysis research and the limited products that can form. Three-dimensional CeO&lt;sub&gt;2&lt;/sub&gt; crystallites form on the 1 and 2 monolayer CeO&lt;sub&gt;2&lt;/sub&gt;-TiO&lt;sub&gt;2&lt;/sub&gt; samples while crystals are not observed for the 0.5 or 0.25 monolayer samples. Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) was used to characterize the surface chemistry occurring on these samples while a flow reactor was used to characterize the reaction products using a long path gas cell in a Fourier transform infrared spectrometer (FTIR). Except for the 1 monolayer sample, CeO&lt;sub&gt;2&lt;/sub&gt; seems to increase the reaction and decomposition of organic compounds, especially chemisorbed methoxy groups, on the surface. The CeO&lt;sub&gt;2&lt;/sub&gt; modified samples appear to adsorb molecular methanol less strongly than TiO&lt;sub&gt;2&lt;/sub&gt;. Upon UV irradiation, the CeO&lt;sub&gt;2&lt;/sub&gt; modified samples desorb methoxy as methanol more so than TiO&lt;sub&gt;2&lt;/sub&gt;. All samples consistently produce carbon dioxide, water, formaldehyde, dimethyl ether, and methanol in the presence of ultraviolet light and oxygen.&lt;/p&gt;","abstract_has_math":false,"creators":["Estes, Christopher A"],"institution":null,"degree_name":"Master of Science in Chemical Sciences (MSCB)","degree_level":"Thesis","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Mark B. Mitchell","Heather Abbott-Lyon","Michael Van Dyke"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-05-01T07:00:00Z","date_published":"2015-05-01T07:00:00Z","updated_at":"2026-07-24T02:43:00Z","subjects":["TiO2","titanium dioxide","CeO2","cerium oxide","photocatalysis","methanol","Chemistry","Physical Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.kennesaw.edu/mscs_etd/3","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Mark B. Mitchell","Heather Abbott-Lyon","Michael Van Dyke"]},{"key":"dc:creator","label":"Author","values":["Estes, Christopher A"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2015-05-08T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science in Chemical Sciences (MSCB)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["TiO2","titanium dioxide","CeO2","cerium oxide","photocatalysis","methanol","Chemistry","Physical Chemistry"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.kennesaw.edu/mscs_etd/3"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["<p>Titanium dioxide (TiO<sub>2</sub>) has been well-studied primarily due to its unique photocatalytic activity. Different preparation techniques have been developed to increase its photocatalytic activity by various means, including simply increasing the surface area, changing the makeup of the framework, and modifying the surface with a dopant. This study focuses on the effect cerium oxide (CeO<sub>2</sub>) has on the photocatalytic activity of TiO<sub>2</sub> by depositing CeO<sub>2</sub> on the TiO<sub>2</sub> surface. Methanol is used as a probe reactant for these experiments due to its wide use in heterogeneous catalysis research and the limited products that can form. Three-dimensional CeO<sub>2</sub> crystallites form on the 1 and 2 monolayer CeO<sub>2</sub>-TiO<sub>2</sub> samples while crystals are not observed for the 0.5 or 0.25 monolayer samples. Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) was used to characterize the surface chemistry occurring on these samples while a flow reactor was used to characterize the reaction products using a long path gas cell in a Fourier transform infrared spectrometer (FTIR). Except for the 1 monolayer sample, CeO<sub>2</sub> seems to increase the reaction and decomposition of organic compounds, especially chemisorbed methoxy groups, on the surface. The CeO<sub>2</sub> modified samples appear to adsorb molecular methanol less strongly than TiO<sub>2</sub>. Upon UV irradiation, the CeO<sub>2</sub> modified samples desorb methoxy as methanol more so than TiO<sub>2</sub>. All samples consistently produce carbon dioxide, water, formaldehyde, dimethyl ether, and methanol in the presence of ultraviolet light and oxygen.</p>"]},{"key":"dc:title","label":"Title","values":["Analysis and Comparison of the Photodecomposition Reaction of Methanol on CeO2 Impregnated TiO2 Surfaces Versus Bare TiO2 Surfaces"]}]}],"canonical_facts":{"dc:contributor":["Mark B. Mitchell","Heather Abbott-Lyon","Michael Van Dyke"],"dc:creator":["Estes, Christopher A"],"dc:date.available":["2015-05-08T07:00:00Z"],"dc:description.abstract":["<p>Titanium dioxide (TiO<sub>2</sub>) has been well-studied primarily due to its unique photocatalytic activity. Different preparation techniques have been developed to increase its photocatalytic activity by various means, including simply increasing the surface area, changing the makeup of the framework, and modifying the surface with a dopant. This study focuses on the effect cerium oxide (CeO<sub>2</sub>) has on the photocatalytic activity of TiO<sub>2</sub> by depositing CeO<sub>2</sub> on the TiO<sub>2</sub> surface. Methanol is used as a probe reactant for these experiments due to its wide use in heterogeneous catalysis research and the limited products that can form. Three-dimensional CeO<sub>2</sub> crystallites form on the 1 and 2 monolayer CeO<sub>2</sub>-TiO<sub>2</sub> samples while crystals are not observed for the 0.5 or 0.25 monolayer samples. Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) was used to characterize the surface chemistry occurring on these samples while a flow reactor was used to characterize the reaction products using a long path gas cell in a Fourier transform infrared spectrometer (FTIR). Except for the 1 monolayer sample, CeO<sub>2</sub> seems to increase the reaction and decomposition of organic compounds, especially chemisorbed methoxy groups, on the surface. The CeO<sub>2</sub> modified samples appear to adsorb molecular methanol less strongly than TiO<sub>2</sub>. Upon UV irradiation, the CeO<sub>2</sub> modified samples desorb methoxy as methanol more so than TiO<sub>2</sub>. All samples consistently produce carbon dioxide, water, formaldehyde, dimethyl ether, and methanol in the presence of ultraviolet light and oxygen.</p>"],"dc:identifier":["https://digitalcommons.kennesaw.edu/mscs_etd/3"],"dc:subject":["TiO2","titanium dioxide","CeO2","cerium oxide","photocatalysis","methanol","Chemistry","Physical Chemistry"],"dc:title":["Analysis and Comparison of the Photodecomposition Reaction of Methanol on CeO2 Impregnated TiO2 Surfaces Versus Bare TiO2 Surfaces"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science in Chemical Sciences (MSCB)"]},"updated_at":"2026-07-24T02:43:00Z"}