2026-09-22T07:43:56Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/1000622022-01-13T07:55:22Zcom_1721.1_7582com_1721.1_7581col_1721.1_131023
Alexie M. Kolpak and Jeffrey C. Grossman.
Alawode, Babatunde
Massachusetts Institute of Technology. Department of Materials Science and Engineering.
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Massachusetts Institute of Technology. Department of Mechanical Engineering
2015-12-03T18:46:38Z
2015-12-03T18:46:38Z
2015
2015
http://hdl.handle.net/1721.1/100062
930153745
Thesis: S.M., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2015.
Thesis: S.M., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2015.
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 119-126).
Due to its role in climate change, there is great interest in finding ways to take advantage of the vast amount of waste CO₂ we produce by its conversion to useful substances. This approach is currently impractical due to the high temperatures and pressures generally required for the synthesis of compounds using CO₂ as a precursor. To make direct CO₂ capture and conversion economically viable, new materials able to catalyze the conversion reactions at significantly milder conditions will be essential. In this thesis, we use DFT computations to begin the design of a dynamically tunable ferroelectric oxide-supported thin film catalyst that can capture CO₂ directly from the emission stream and convert it into methanol or cyclic carbonates. Promising candidates for a dynamically tunable catalyst of this type are the different combinations of ZnO directions grown on the perovskite PbTiO₃. For the non-polar ZnO(112̄0) grown on the perovskite, we demonstrate that the surface chemistry is dependent on both the polarization direction of the PbTiO₃ substrate and on the number of ZnO(112̄0) layers n. Growing the ZnO in the (0001) direction on the perovskite showed even more interesting results. We found that this process is sufficient to obtain a ZnO ferroelectric and is superior to previous attempts to make ferroelectric phase changes possible in the oxide, namely Li-doping. We demonstrate that switching the polarization direction of the perovskite substrate is sufficient to switch the polarity at the ZnO surface. This is an excellent basis for a dynamically tunable catalyst.
by Babatunde Alawode.
S.M.
126 pages
eng
Massachusetts Institute of Technology
M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
http://dspace.mit.edu/handle/1721.1/7582
Mechanical Engineering.
Materials Science and Engineering.
A first principles computational study of ZnO/PbTiO₃ as a tunable catalyst for CO₂ conversion
Thesis
application/pdf
Publication
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<Abstract>Due to its role in climate change, there is great interest in finding ways to take advantage of the vast amount of waste CO₂ we produce by its conversion to useful substances. This approach is currently impractical due to the high temperatures and pressures generally required for the synthesis of compounds using CO₂ as a precursor. To make direct CO₂ capture and conversion economically viable, new materials able to catalyze the conversion reactions at significantly milder conditions will be essential. In this thesis, we use DFT computations to begin the design of a dynamically tunable ferroelectric oxide-supported thin film catalyst that can capture CO₂ directly from the emission stream and convert it into methanol or cyclic carbonates. Promising candidates for a dynamically tunable catalyst of this type are the different combinations of ZnO directions grown on the perovskite PbTiO₃. For the non-polar ZnO(112̄0) grown on the perovskite, we demonstrate that the surface chemistry is dependent on both the polarization direction of the PbTiO₃ substrate and on the number of ZnO(112̄0) layers n. Growing the ZnO in the (0001) direction on the perovskite showed even more interesting results. We found that this process is sufficient to obtain a ZnO ferroelectric and is superior to previous attempts to make ferroelectric phase changes possible in the oxide, namely Li-doping. We demonstrate that switching the polarization direction of the perovskite substrate is sufficient to switch the polarity at the ZnO surface. This is an excellent basis for a dynamically tunable catalyst.</Abstract>
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