Photoinduced electron transfer at the tetrapyrrole-TiO2 interface: effect of the energy alignment
| Author(s) | Nieto-Pescador, Jesus | |
| Date Accessioned | 2017-04-20T12:23:54Z | |
| Date Available | 2017-04-20T12:23:54Z | |
| Publication Date | 2017 | |
| Abstract | Photoinduced electron transfer is a ubiquitous process behind several physical, chemical, and biological processes. Its potential applications, ranging from solar cell technologies to photodynamic cancer therapy, require a thorough understanding of the basics of the reaction. This dissertation addresses open questions for a particular case of electron transfer processes: Heterogeneous Electron Transfer (HET). In this process, an electron is transferred between a localized donor and a multitude of delocalized acceptor states. HET between photoexcited tetrapyrroles and colloidal TiO2 has been investigated using femtosecond transient absorption spectroscopy. Specifically, this work explores the not well-understood influence of the availability of states on the HET reaction. This problem is addressed by measuring electron injection times as a function of the energy difference between the LUMO and the conduction band of TiO2. The change in the energy alignment was done using two experimental strategies. The first one employs a recently synthesized phlorin with two different excited states above the conduction band of TiO2. This molecule allows comparing HET rates from two different excited states. The phlorin presents the rare case in which electron transfer process can be measured from various excited states with the same experimental condition. The second strategy measures the electron injection rates after exciting the same electronic state of a set of specially designed porphyrins. The novelty of the approach is that the difference in energy alignment is attained by the introduction of dipole groups within the bridge group of the molecule. This strategy generates a difference in energy alignment of up to 200 meV. The reported measurements were carried in a high vacuum environment with an apparatus capable of resolving sub 30 fs processes. Disentanglement of the electron transfer processes was done, after careful study of the relaxation dynamics of the molecules in solution, by monitoring the decay of the excited state absorption and the rise of the cation spectral signatures. Within our time resolution, our results show that the increase in the availability of acceptor states does not influence the electron injection dynamics. The results suggest that the injection process takes place into a spectrum of states different from those obtained by steady state calculations. | en_US |
| Advisor | Gundlach, Lars | |
| Degree | Ph.D. | |
| Department | University of Delaware, Department of Physics and Astronomy | |
| Unique Identifier | 983202419 | |
| URL | http://udspace.udel.edu/handle/19716/21242 | |
| Publisher | University of Delaware | en_US |
| URI | https://search.proquest.com/docview/1884769785?accountid=10457 | |
| Title | Photoinduced electron transfer at the tetrapyrrole-TiO2 interface: effect of the energy alignment | en_US |
| Type | Thesis | en_US |