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School of Chemistry - Research Publications
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ItemHighly Efficient Luminescent Solar Concentrators by Selective Alignment of Donor-Emitter FluorophoresZhang, 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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ItemFRET-enhanced photoluminescence of perylene diimides by combining molecular aggregation and insulationZhang, B ; Lyskov, I ; Wilson, LJ ; Sabatini, RP ; Manian, A ; Soleimaninejad, H ; White, JM ; Smith, TA ; Lakhwani, G ; Jones, DJ ; Ghiggino, KP ; Russo, SP ; Wong, WWH (Royal Society of Chemistry, 2020-07-14)The photoluminescence quantum yield (ϕPL) of perylene diimide derivatives (PDIs) is often limited by aggregation caused quenching (ACQ) at high concentration or in the neat solid-state. Energy transfer in high dye concentration systems is also a key factor in determining ϕPL as a result of energy funneling to trap sites in the sample. By tuning the substituents, we present two classes of PDIs with aggregation and insulation of the PDI core. By combining these fluorophores in a polymer film, we demonstrate highly emissive samples (85% ϕPL) at high concentration (140 mM or 20% w/w). Experimental and theoretical studies provide insight into why such a combination is necessary to achieve high ϕPL. While insulated fluorophores maintain respectable ϕPL at high concentration, an improved ϕPL can be achieved in the presence of appropriately oriented fluorophore aggregates as emissive traps. The theoretical calculations show that the relative orientation of aggregated monomers can result in energetic separation of localized states from the charge-transfer and bi-excitonic states thereby enabling high ϕPL.
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ItemSingle Isomer of Indene-C70 Bisadduct-Isolation and Performance in Bulk Heterojunction Solar CellsWong, WWH ; Subbiah, J ; White, JM ; Seyler, H ; Zhang, B ; Jones, DJ ; Holmes, AB (AMER CHEMICAL SOC, 2014-02-25)
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ItemOrganic Photovoltaic MaterialsDesign, Synthesis and Scale-UpWong, WWH ; Banal, JL ; Geraghty, PB ; Hong, Q ; Zhang, B ; Holmes, AB ; Jones, DJ (WILEY-V C H VERLAG GMBH, 2015-12)This account describes the work of our group in the area of organic photovoltaics in the past six years. The emphasis is on our experiences in the development of the organic materials, their characterization, scale-up and application in devices. We share our insight into the relationship between synthetic methods, molecular properties, bulk material properties and device performance.
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ItemRegioselective synthesis of fullerene multiadducts via tether-directed 1,3-dipolar cycloadditionZhang, B ; White, JM ; Jones, DJ ; Wong, WWH (ROYAL SOC CHEMISTRY, 2015)The regioselective synthesis of fullerene multiadducts was achieved from commercially available reagents in one pot over two steps. The configuration of the isolated regioisomers was determined using various NMR methods, UV-vis spectroscopy and electrochemical analysis with the structure of one isomer confirmed by single crystal X-ray analysis. Interesting variation in regioselectivity was observed when different amino acid reagents were used in the reactions. Theoretical calculations and additional experiments, such as deuterium exchange, led to a proposed mechanism for the regioselective product formation.
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ItemEmissive Molecular Aggregates and Energy Migration in Luminescent Solar ConcentratorsBanal, JL ; Zhang, B ; Jones, DJ ; Ghiggino, KP ; Wong, WWH (American Chemical Society, 2017-01-17)Luminescent solar concentrators (LSCs) are light harvesting devices that are ideally suited to light collection in the urban environment where direct sunlight is often not available. LSCs consist of highly luminescent compounds embedded or coated on a transparent substrate that absorb diffuse or direct solar radiation over a large area. The resulting luminescence is trapped in the waveguide by total internal reflection to the thin edges of the substrate where the concentrated light can be used to improve the performance of photovoltaic devices. The concept of LSCs has been around for several decades, and yet the efficiencies of current devices are still below expectations for commercial viability. There are two primary challenges when designing new chromophores for LSC applications. Reabsorption of dye emission by chromophores within the waveguide is a significant loss mechanism attenuating the light output of LSCs. Concentration quenching, particularly in organic dye systems, restricts the quantity of chromophores that can be incorporated in the waveguide thus limiting the light absorbed by the LSC. Frequently, a compromise between increased light harvesting of the incident light and decreasing emission quantum yield is required for most organic chromophore-based systems due to concentration quenching. The low Stokes shift of common organic dyes used in current LSCs also imposes another optimization problem. Increasing light absorption of LSCs based on organic dyes to achieve efficient light harvesting also enhances reabsorption. Ideally, a design strategy to simultaneously optimize light harvesting, concentration quenching, and reabsorption of LSC chromophores is clearly needed to address the significant losses in LSCs. Over the past few years, research in our group has targeted novel dye structures that address these primary challenges. There is a common perception that dye aggregates are to be avoided in LSCs. It became apparent in our studies that aggregates of chromophores exhibiting aggregation-induced emission (AIE) behavior are attractive candidates for LSC applications. Strategic application of AIE chromophores has led to the development of the first organic-based transparent solar concentrator that harvests UV light as well as the demonstration of reabsorption reduction by taking advantage of energy migration processes between chromophores. Further developments led us to the application of perylene diimides using an energy migration/energy transfer approach. To prevent concentration quenching, a molecularly insulated perylene diimide with bulky substituents attached to the imide positions was designed and synthesized. By combining the insulated perylene diimide with a commercial perylene dye as an energy donor–acceptor emitter pair, detrimental luminescence reabsorption was reduced while achieving a high chromophore concentration for efficient light absorption. This Account reviews and reinspects some of our recent work and the improvements in the field of LSCs.
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ItemHighly Fluorescent Molecularly Insulated Perylene Diimides: Effect of Concentration on Photophysical PropertiesZhang, B ; Soleimaninejad, H ; Jones, DJ ; White, JM ; Ghiggino, KP ; Smith, TA ; Wong, WWH (AMER CHEMICAL SOC, 2017-10-10)
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ItemAggregation-induced emission-mediated spectral downconversion in luminescent solar concentratorsZhang, B ; Banal, JL ; Jones, DJ ; Tang, BZ ; Ghiggino, KP ; Wong, WWH (Royal Society of Chemistry, 2018-03-01)The light-harvesting efficiency of luminescent solar concentrators (LSCs) is encumbered by reabsorption of emission and concentration quenching. Energy transfer from a high-concentration donor to a low-concentration energy trap can reduce reabsorption losses while maintaining efficient light collection. Emissive aggregates enable this approach by reducing the impact of concentration quenching, which is detrimental to the entire energy transfer process. Here we describe a LSC that utilizes emissive aggregates as energy-transfer pairs for downconversion. We characterize the photophysics of a benzothiadiazole-based emissive aggregate, PITBT-TPE, that complements a highly emissive donor, DPATPAN, and functions as a highly emissive energy-transfer acceptor even at high concentrations in excess of 180 mM in the PMMA matrix. Monte Carlo simulations of LSCs that leverage these emissive aggregates as energy-transfer pairs predicted notable optical efficiencies at large concentrator dimensions. We demonstrate for the first time a LSC that utilizes donor and acceptor AIE chromophores to reduce reabsorption.
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ItemSeparation and identification of indene-C70 bisadduct isomersZhang, B ; Subbiah, J ; Jones, DJ ; Wong, WWH (BEILSTEIN-INSTITUT, 2016-05-06)Following an initial work on the isolation of a single geometric isomer from an indene-C70 bisadduct (IC70BA) mixture, we report the full fractionation and identification of the bisadduct species in the material. Eleven fractions of IC70BA isomers were separated by high-performance liquid chromatography. A number of fractions contained relatively pure isomer species and their configuration were deduced using a variety of analytical techniques including (1)H and (13)C NMR and UV-vis spectroscopy. The electrochemical properties and the organic solar cell device performance were investigated for fractions where a reasonable quantity of sample could be isolated.
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ItemOne-pot selective synthesis of a fullerene bisadduct for organic solar cell applicationsZhang, B ; Subbiah, J ; Lai, Y-Y ; White, JM ; Jones, DJ ; Wong, WWH (ROYAL SOC CHEMISTRY, 2015)A single isomer of fullerene bisadduct, PC61PF, was obtained from commercially available fullerene derivative, PC61BM, in one pot over two steps. The tether-directed remote functionalization approach provided a very simple and fast method to produce a single isomer of fullerene bisadduct with good yield and easy purification. Bulk heterojunction organic solar cells containing the bisadduct was fabricated and tested.