Jennifer Miller

420 Chemistry Building
Phone: 517-355-9715 x 107




Research Summary


Absorption of a photon places a molecule in an excited state; the challenge is in understanding the processes that occur subsequent to photoexcitation. One way to investigate the excited states and dynamics of molecules on extremely short timescales is with ultrafast spectroscopy. My research employs femtosecond (fs) time-resolved absorption techniques in order to monitor the excited state evolution of transition metal complexes. This involves studying photoinduced charge separation, where examining the dynamics involved may lead to a better understanding of the relationship between electron transfer and excited-state relaxation to a state that is unable to transfer an electron.

One project I focus on involves the use of time-resolved absorption anisotropy measurements to investigate how solvation dynamics impact photo-induced charge-transfer in complexes such as tris-(2,2’-bipyridine)ruthenium(II). This study aims to resolve a fundamentally interesting question about the evolution of the excited state – whether the excited electron is initially localized or delocalized. A second project focuses on Fe2+-based sensitizers for use in dye-sensitized solar cells (DSSCs). Despite the fact that iron-based sensitizers present new challenges compared to more commonly employed ruthenium-based sensitizers, a better understanding of the dynamics involved will hopefully lead to the development of efficient, low cost dyes.










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Website Updated: 4/5/2012