Geoffrey B. Piland
University of California, Riverside
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Publication
Featured researches published by Geoffrey B. Piland.
Journal of the American Chemical Society | 2013
Robert J. Dillon; Geoffrey B. Piland; Christopher J. Bardeen
The dynamics of singlet fission (SF) are studied in monoclinic and orthorhombic crystals of 1,6-diphenyl-1,3,5-hexatriene. Picosecond time-resolved fluorescence measurements and the presence of a strong magnetic field effect indicate that up to 90% of the initially excited singlets undergo SF in both forms. The initial SF and subsequent triplet pair dissociation rates are found to be more rapid in the monoclinic crystal by factors of 1.5 and 3.5, respectively. These results provide clear evidence that molecular organization affects the rates of triplet pair formation and separation, both important parameters for determining the ultimate utility of a SF material.
Journal of Physical Chemistry Letters | 2015
Geoffrey B. Piland; Christopher J. Bardeen
The dependence of exciton dynamics on the crystalline morphology of tetracene is investigated using time-resolved photoluminescence. Single crystals exhibit relatively slow singlet decays with times that range from 130 to 300 ps depending on the sample. This decay has an activation energy of ∼450 cm(-1) over the temperature range of 200-400 K. Single-crystal samples also exhibit more pronounced quantum beats due to the triplet pair spin coherences. Polycrystalline thin films grown by thermal evaporation have singlet decay times on the order of 70-90 ps with a much weaker temperature dependence. Many thin-film samples also exhibit a red-shifted excimer-like emission. When a polycrystalline thin film is thermally annealed to produce larger crystal domains, single-crystal behavior is recovered. We hypothesize that the different dynamics arise from the ability of singlet excitons in the thin films to sample regions with defects or packing motifs that accelerate singlet fission.
Journal of Physical Chemistry Letters | 2014
Geoffrey B. Piland; Jonathan J. Burdett; Robert J. Dillon; Christopher J. Bardeen
Singlet fission, in which an initially excited singlet state spontaneously splits into a pair of triplet excitons, is a process that can potentially boost the efficiency of solar energy conversion. The separate electronic bands in organic semiconductors make them especially useful for dividing a high-energy singlet exciton into a pair of lower-energy triplet excitons. Recent experiments illustrate the role of spin coherence in fission, while kinetic models are used to describe how triplet and singlet states interact on longer time scales. Despite insights gained from recent experiments, the detailed structure and dynamics of the electronic states involved in the initial step of singlet fission remain active areas of investigation. On longer time scales, finding ways to efficiently harvest the triplet excitons will be an important challenge for making devices based on this phenomenon. A full understanding of singlet fission requires consideration of a sequence of photophysical events (decoherence, relaxation, and diffusion) occurring on different time scales.
Journal of Physical Chemistry C | 2013
Geoffrey B. Piland; Jonathan J. Burdett; Dharmalingam Kurunthu; Christopher J. Bardeen
Chemical Physics Letters | 2013
Jonathan J. Burdett; Geoffrey B. Piland; Christopher J. Bardeen
Journal of Physical Chemistry C | 2013
Valerie M. Nichols; Marco T. Rodriguez; Geoffrey B. Piland; Fook S. Tham; Vladimir N. Nesterov; W. Justin Youngblood; Christopher J. Bardeen
Journal of Physical Chemistry C | 2016
Geoffrey B. Piland; Zhiyuan Huang; Ming Lee Tang; Christopher J. Bardeen
Chemical Physics Letters | 2014
Geoffrey B. Piland; Jonathan J. Burdett; Tzu-Yao Hung; Po-Hsun Chen; Chi-Feng Lin; Tien-Lung Chiu; Jiun-Haw Lee; Christopher J. Bardeen
Journal of Luminescence | 2012
Xiaoquan Zhou; Geoffrey B. Piland; Dharmalingam Kurunthu; Robert J. Dillon; Jonathan J. Burdett; Christopher J. Bardeen
Chemical Physics Letters | 2017
Geoffrey B. Piland; Christopher J. Bardeen