Electron transfer dynamics of triphenylamine dyes bound to TiO2 nanoparticles from femtosecond stimulated Raman spectroscopy
AuthorsHoffman, David P.
Lee, Olivia P.
Millstone, Jill E.
Chen, Mark S.
Su, Timothy A.
Mathies, Richard A.
KAUST DepartmentChemical Science Program
Office of the VP
Physical Science and Engineering (PSE) Division
Online Publication Date2013-03-27
Print Publication Date2013-04-11
Permanent link to this recordhttp://hdl.handle.net/10754/562720
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AbstractInterfacial electron transfer between sensitizers and semiconducting nanoparticles is a crucial yet poorly understood process. To address this problem, we have used transient absorption (TA) and femtosecond stimulated Raman spectroscopy (FSRS) to investigate the photoexcited dynamics of a series of triphenylamine-coumarin dye/TiO2 conjugates. The TA decay is multiexponential, spanning time scales from 100 fs to 100 ps, while the characteristic transient Raman spectrum of the radical cation decays biexponentially with a dominant ∼3 ps component. To explain these observations, we propose a model in which the decay of the TA is due to hot electrons migrating from surface trap states to the conduction band of TiO 2 while the decay of the Raman signature is due to internal conversion of the dye molecule. Furthermore, the S1 Raman spectrum of TPAC3, a dye wherein a vinyl group separates the triphenylamine and coumarin moieties, is similar to the S1 Raman spectrum of trans-stilbene; we conclude that their S1 potential energy surfaces and reactivity are also similar. This correlation suggests that dyes containing vinyl linkers undergo photoisomerization that competes with electron injection. © 2013 American Chemical Society.
CitationHoffman, D. P., Lee, O. P., Millstone, J. E., Chen, M. S., Su, T. A., Creelman, M., … Mathies, R. A. (2013). Electron Transfer Dynamics of Triphenylamine Dyes Bound to TiO2 Nanoparticles from Femtosecond Stimulated Raman Spectroscopy. The Journal of Physical Chemistry C, 117(14), 6990–6997. doi:10.1021/jp400369b
SponsorsThis work was supported the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering, under Contract DE-ACO2-05CH11231 and in part by the Mathies Royalty fund. DFT calculations were carried out with the support of the National Science Foundation Grant CHE-0840505, and M.S.C. thanks the Camille and Henry Dreyfus Postdoctoral Program in Environmental Chemistry for a fellowship.
PublisherAmerican Chemical Society (ACS)