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This thesis investigates ethylbenzene dehydrogenation to styrene on rutile TiO₂(110) using DFT-PBE-D3 for geometry optimization and SA-CASSCF for excited state electronic structure. The study finds that on stoichiometric surfaces, both thermal and photochemical pathways proceed via proton-coupled electron transfer (PCET), with wavelength dependence explained by excited state lifetimes. Surface oxidation shifts the mechanism to direct hydrogen atom transfer (HAT) facilitated by pre-adsorbed oxygen radicals, explaining increased styrene yield.
Photocatalysis can bypass kinetic bottlenecks in styrene production, but only if you tune the wavelength to match the excited state landscape of the TiO2 catalyst.
This master's thesis investigates the thermal and photochemical dehydrogenation of ethylbenzene (EB) to styrene on the rutile TiO$_{2}$(110) surface. A dual-methodological quantum chemical approach is used for this investigation. While industrial styrene production is energy-intensive, photocatalysis on semiconductor materials offers a promising alternative under significantly milder conditions. To elucidate the underlying mechanisms, this study employs density functional theory (DFT-PBE-D3) for geometry optimization and high-level multi-reference methods (SA-CASSCF) to accurately describe the electronic complexity of excited states and radical intermediates. The investigation reveals that, on the stoichiometric surface, both thermal and photochemical pathways are dominated by proton-coupled electron transfer (PCET). The wavelength dependence observed in the literature is explained by how the system navigates electronic manifolds. 343 nm irradiation leads to rapid relaxation into the ground state, where high kinetic barriers persist. In contrast, 257 nm excitation enables the system to persist in higher excited states (S1/T2). This allows the reaction to bypass the rate-determining ground-state barrier. Furthermore, the study demonstrates that surface oxidation causes a fundamental mechanistic shift. On oxidized surfaces, pre-adsorbed oxygen radicals (O$_{Ti}$) enable direct hydrogen atom transfer (HAT), which is more efficient than PCET on reduced surfaces. This "hydrogen scavenger" effect explains the significant increase in styrene yield. This work underscores the necessity of multi-reference treatments for complex surface reactions and provides a fundamental understanding of how surface stoichiometry and photon energy govern photocatalytic efficiency.
