Understanding Interfacial Kinetics of Catalytic Carbon Dioxide Transformations from Multiscale Simulations

Carbon dioxide (CO2), as a greenhouse gas, has shown to achieve the highest level in history, causes the global warming issue, leading to a 1.2 ℃ increase of the global average temperature. The consumption of fossil fuels is one of the main reasons that cause CO2 emission. Current industrial production of chemicals accounts for 29% of total fossil fuels consumption, which can be the feedstock or raw materials for carbon source, or act as the fuel to generate heat and power. CO2 conversion technologies, e.g., thermo-catalytic reaction and electrochemical reduction, have drawn researchers' attention, since they have the potential to resolve the feedstock and fuel consumption sectors of chemical production at the same time. CO2 conversion technologies use CO2 as the direct carbon source of chemicals and store the intermittent renewable energies as the energy source, which can ultimately achieve a net-zero CO2 emission and produce value-added chemical products. However, there are challenges for a practical application of CO2 conversion technologies. For instance, electrochemical CO2 reduction reaction (ECO2RR) suffers from the low activity and selectivity, while thermocatalytic CO2 conversion, or the CO2 hydrogenation reaction, usually requires harsh reaction conditions and has a low selectivity. Nonetheless, the improvement of developing new promising catalysts remains limited, due to the lack of insights of the reactions. The complex reaction networks and kinetics lead to an elusive reaction mechanism, and various effects, e.g., solvation, potential, structure, and coverage, hinder our fundamental understanding of catalytic processes. Herein, we report the efforts that we have been put in to gain insights of reaction mechanism of CO2 reduction reactions. Bi has shown to reduce CO2 to formic acid (HCOOH), while we have found that, by constituting a Bi-Cu2S heterostructure catalyst, a better catalytic performance was achieved, due to the structural effect of the interface (Chapter 2). However, it is shown that the CO2 electrochemical reduction mechanism on Bi has changed when switching the electrolyte from water to aprotic media, e.g., ionic liquids, and CO was obtained as the main product instead of HCOOH, showing a shift of reaction pathway due to the electrolyte effect (Chapter 3). However, the fundamental understanding of reaction mechanism requires not only the reaction pathways, but the reaction kinetics under reaction conditions, where the lateral or adsorbate-adsorbate interactions play an important role. In this case, we summarized recent advances of applications of machine learning (ML) algorithms for adsorbate-adsorbate interaction model developments to deal with the realistic reaction kinetics (Chapter 4). The lattice based Kinetic Monte Carlo (KMC) has shown promising performances for considering the lateral interactions of surface reactions. We report the mechanistic and KMC kinetic study of CO2 hydrogenation on Cesium promoted Au(111) surface, to gain insights of alkali metal promoting effects under reaction conditions (Chapter 5). To expand the scope, the integration of CO2 reduction with the C-N bond formation provides a promising strategy to produce more value-added product such as urea. Recent studies show that urea can be produced by reducing CO2 and nitrate (NO3-) from wastewater, which mitigate both global warming and nitrate pollution issue. However, the reaction mechanism remains elusive due to the complicated reaction network. Therefore, we employed the first-principles molecular dynamics to reveal the reaction mechanism of C-N coupling and the effect of different reaction conditions including applied potential and electrolyte (Chapter 6). Although recent advances in the computational catalysis field have significantly push forward the understanding of the chemistry nature of heterogeneous catalysis, the gap between theory and experiment remains far beyond bridged due to the complexity nature of the problem in a wide range of time and length scales, hinders the development and discovery of active catalytic materials. Recent advances of narrowing and bridging the complexity gap between theory and experiment with machine learning have been summarized to emphasize the importance of utilizing machine learning for rational catalyst design (Chapter 7).

Name thesis:degree_name

Doctor of Philosophy

Level thesis:degree_level

doctoral

Discipline thesis:degree_discipline

Chemical Engineering

Department dc:contributor.department

Chemical Engineering

Grantor dc:publisher

Virginia Tech

Year dc:date.issued

2023

Author dc:creator

• Mou, Tianyou

Chair dc:contributor.committeechair

• Xin, Hongliang

Committee members dc:contributor.committeemember

• Achenie, Luke E. K.
• Zhu, Huiyuan
• Valeyev, Eduard Faritovich

• Computational catalysis
• reaction kinetics
• multiscale simulations
• machine learning

Statement dc:rights

• In Copyright

Licence dc:rights.uri

• http://rightsstatements.org/vocab/InC/1.0/

Language dc:language.iso

en

Dc Identifier Other

vt_gsexam:37762

OAI identifier oai:identifier

oai:vtechworks.lib.vt.edu:10919/115796