School of Chemistry - Research Publications

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    Light losses from scattering in luminescent solar concentrator waveguides
    Breukers, RD ; Smith, GJ ; Stirrat, HL ; Swanson, AJ ; Smith, TA ; Ghiggino, KP ; Raymond, SG ; Winch, NM ; Clarke, DJ ; Kay, AJ (OPTICAL SOC AMER, 2017-04-01)
    The reductions in the transmission of emission originating from a fluorophore dissolved in a polymer matrix due to light scattering were compared in two forms of planar waveguides used as luminescent solar concentrators: a thin film of poly(methylmethacrylate) (PMMA) spin-coated on a glass plate and a solid PMMA plate of the same dimensions. The losses attributable to light scattering encountered in the waveguide consisting of the thin film of polymer coated on a glass plate were not detectable within experimental uncertainty, whereas the losses in the solid polymer plate were significant. The losses in the solid plate are interpreted as arising from light-scattering centers comprising minute bubbles of vapor/gas, incomplete polymerization or water clusters that are introduced during or after the thermally induced polymerization process.
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    Resolving the Mechanisms of Photocurrent Improvement in Ternary Organic Solar Cells
    Bi, PQ ; Hall, CR ; Yin, H ; So, SK ; Smith, TA ; Ghiggino, KP ; Hao, XT (AMER CHEMICAL SOC, 2019-08-01)
    The ultralow band gap small-molecule IEICO-4F has been employed as a secondary acceptor in both fullerene-based (PTB7-Th:PC71BM) and nonfullerene-based (PBDB-T:ITIC) ternary organic solar cells (OSCs). Structural characterization methods combined with ultrafast spectroscopy have been applied to resolve the mechanisms, leading to the observed improvement in device efficiency upon addition of IEICO-4F. It is shown that IEICO-4F forms ternary mixed domains in the host systems and improves the device efficiency by broadening the absorption spectral range and enhancing both charge separation and charge transport. The enhanced crystallinity of the semiconductor polymer electron donors in the presence of the EIECO-4 provides additional channels for ultrafast charge transfer and transport compared to binary systems. The optimum ternary blend formulations required to improve device efficiencies are reported. This work provides new insights into the fabrication of high-performance ternary OSCs.
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    Optimizing the Crystallinity and Phase Separation of PTB7:PC71BM Films by Modified Graphene Oxide
    Lv, C-K ; Zheng, F ; Yang, X-Y ; Bi, P-Q ; Niu, M-S ; Wang, Y-Z ; Smith, TA ; Ghiggino, KP ; Hao, X-T (American Chemical Society, 2018-02-08)
    A facile method is proposed to obtain modified shorn graphene oxide (DDAB-sGO) with improved dispersion in organic solvents. Didodecyl dimethylammonium bromide (DDAB)-sGO, which exhibits good dispersibility in the nonpolar solvent o-dichlorobenzene, was obtained via the sono-Fenton reaction and DDAB ionic functionalization. DDAB-sGO was used in the preparation of conjugated polymer:fullerene blend composites. UV–visible absorption spectra, steady-state photoluminescence spectra, fluorescence decay, and grazing incidence X-ray scattering measurements were applied to characterize morphologies, structural features, and charge-transport characteristics of the composites. Doped into poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl]] (PTB7):[6,6]-phenyl C71 butyric acid methyl ester (PC71BM) conjugated polymer blends, DDAB-sGO is shown to facilitate increased crystallinity and phase separation of PTB7 and PC71BM to achieve a more optimal morphology for bulk heterojunction solar cells, resulting in a ∼12% enhancement in power conversion efficiency over the undoped PTB7:PC71BM blend.
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    Spatially Resolved Photophysical Dynamics in Perovskite Microplates Fabricated Using an Antisolvent Treatment
    Xu, W-L ; Niu, M-S ; Yang, X-Y ; Bi, P-Q ; Zhang, K-N ; Xiong, C ; Yuan, H-C ; Smith, TA ; Ghiggino, KP ; Hao, X-T (American Chemical Society, 2017-11-30)
    Perovskite microplates have important implications in the fields of functional electronics and optoelectronics. We report a facile strategy, antisolvent treatment for the growth of perovskite microplates. The morphology and crystalline quality of the microplates could be controlled by the amount of the chlorobenzene antisolvent used. An appropriate amount of antisolvent facilitates the formation of high-quality perovskite microplates with no residual precursor remaining. Spatially and temporally resolved fluorescence measurements demonstrate the heterogeneity of defect-state density and recombination processes in various perovskite microplate regions. The body center shows higher defect state density when compared with that at the edge or the corner of the microplate. Excessive antisolvent degrades the microplates into smaller particles. The results of this study reveal the factors that influence the crystallization process and photophysical dynamics of perovskite microplates.
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    Highly Efficient Luminescent Solar Concentrators by Selective Alignment of Donor-Emitter Fluorophores
    Zhang, B ; Gao, C ; Soleimaninejad, H ; White, JM ; Smith, TA ; Jones, DJ ; Ghiggino, KP ; Wong, WWH (AMER CHEMICAL SOC, 2019-04-23)
    Vertically aligning fluorophores to the surface of a waveguide is known to be an effective approach to improve the optical quantum efficiency (OQE) of luminescent solar concentrators (LSCs). While the chromophore alignment assists waveguiding of the emitted photons to the LSC edges, it also significantly reduces the light-harvesting properties of the LSC. We report here a fluorophore pair consisting of a sphere-shaped energy donor and a rod-shaped emitter that was incorporated in LSCs to provide selective fluorophore alignment to address the reduced incident-light absorption issue. A liquid-crystal polymer matrix was used to perpendicularly align the rod-shaped acceptors to a favorable orientation for light guiding, while the sphere-shaped donor was randomly oriented to maintain its light-absorbing properties. The OQE of LSC devices with this selectively aligned donor-acceptor fluorophore system is 78% without significant loss of light-harvesting capability.
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    Fluorescence anisotropy imaging of a polydiacetylene photopolymer film
    Soleimaninejad, H ; Ghiggino, KP ; Smith, TA ; Paige, MF (CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS, 2019-06)
    UV-illumination of phase-separated surfactant films prepared from mixtures of photopolymerizable 10,12-pentacosadiynoic acid and perfluorotetradecanoic acid results in the formation of fluorescent polydiacetylene fibers and aggregates. In this work, the orientation of polymer strands that comprise the resulting photopolymer structures has been probed using fluorescence anisotropy imaging in combination with defocused single-molecule fluorescence imaging. Imaging experiments indicate the presence of significant fiber-to-fiber heterogeneity, as well as anisotropy within each fiber (or aggregate), with both of these properties changing as a function of film preparation conditions. This anisotropy can be attributed to various alignments of the constituent polymer strands that comprise the larger fibers and aggregates. Intriguingly, when using defocused imaging, fiber images consisted of a series of discrete “doughnut” fluorescence emission patterns, which exhibited intermittent on–off blinking behavior; both of these properties are characteristic of individual emission transition dipoles (single molecules). Further, all of the individual emission transition dipoles had a uniform orientation with respect to the axis of the fiber, indicating a common orientation of discrete emitters in the larger polymer fiber. The implications of these results for future studies of the electronic properties of conjugated polymers in larger macroscopic systems are noted.
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    Liquid Crystallinity as a Self-Assembly Motif for High-Efficiency, Solution-Processed, Solid-State Singlet Fission Materials
    Masoomi-Godarzi, S ; Liu, M ; Tachibana, Y ; Mitchell, VD ; Goerigk, L ; Ghiggino, KP ; Smith, TA ; Jones, DJ (WILEY-V C H VERLAG GMBH, 2019-08)
    Abstract Solution and solution‐deposited thin films of the discotic liquid crystalline electron acceptor–donor–acceptor (A‐D‐A) p‐type organic semiconductor FHBC(TDPP)2, synthesized by coupling thienyl substituted diketopyrrolopyrrole (TDPP) onto a fluorenyl substituted hexa‐peri‐hexabenzocoronene (FHBC) core, are examined by ultrafast and nanosecond transient absorption spectroscopy, and time‐resolved photoluminescence studies to examine their ability to support singlet fission (SF). Grazing incidence wide‐angle X‐ray (GIWAX) studies indicate that as‐cast thin films of FHBC(TDPP)2 are “amorphous,” while hexagonal packed discotic liquid crystalline films evolve during thermal annealing. SF in as‐cast thin films is observed with an ≈150% triplet generation yield. Thermally annealing the thin films improves SF yields up to 170%. The as‐cast thin films show no long‐range order, indicating a new class of SF material where the requirement for local order and strong near neighbor coupling has been removed. Generation of long‐lived triplets (µs) suggests that these materials may also be suitable for inclusion in organic solar cells to enhance performance.
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    Solution-Processable, Solid State Donor-Acceptor Materials for Singlet Fission
    Masoomi-Godarzi, S ; Liu, M ; Tachibana, Y ; Goerigk, L ; Ghiggino, KP ; Smith, TA ; Jones, DJ (WILEY-V C H VERLAG GMBH, 2018-10-25)
    Abstract The exploitation of singlet fission (SF) materials in optoelectronic devices is restricted by the limited number of SF materials available and developing new organic materials that undergo singlet fission is a significant challenge. Using a new strategy based on conjugating strong donor and acceptor building blocks, the small molecule (BDT(DPP)2) and polymer (p‐BDT‐DPP) systems are designed and synthesized knowing that bisthiophene‐2,5‐dihydropyrrolo[3,4‐c]pyrrole‐1,4‐dione (DPP) has a low lying triplet energy level, which is further confirmed by time‐dependent density functional theory (TD‐DFT) calculations. TD‐DFT and natural transition orbital (NTO) analysis are conducted to gain insight into the photophysical properties and features of excited states in BDT(DPP)2, respectively. Femtosecond and nanosecond transient absorption spectroscopies are used to investigate the excited state kinetics in the synthesized compounds. Fast formation of triplet pairs in thin film of p‐BDT‐DPP and BDT(DPP)2 and the equilibrium formation of correlated triplet pairs and S1 from triplet–triplet annihilation in solution of BDT(DPP)2 are further evidence of SF in these compounds. The short triplet lifetime, as a result of fast biexcitonic recombination, provides additional support for triplet pair formation through singlet fission.
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    Energy Migration in Organic Solar Concentrators with a Molecularly Insulated Perylene Diimide
    Banal, JL ; Soleimaninejad, H ; Jradi, FM ; Liu, M ; White, JM ; Blakers, AW ; Cooper, MW ; Jones, DJ ; Ghiggino, KP ; Marder, SR ; Smith, TA ; Wong, WWH (AMER CHEMICAL SOC, 2016-06-23)
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    Highly Fluorescent Molecularly Insulated Perylene Diimides: Effect of Concentration on Photophysical Properties
    Zhang, B ; Soleimaninejad, H ; Jones, DJ ; White, JM ; Ghiggino, KP ; Smith, TA ; Wong, WWH (AMER CHEMICAL SOC, 2017-10-10)