113 research outputs found
Recommended from our members
PCDTBT: From Polymer Photovoltaics to Light-Emitting Diodes by Side-Chain-Controlled Luminescence
Poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole) (PCDTBT) is a copolymer composed of alternating thiophene-benzothiadiazole-thiophene (TBT) and carbazole (Cbz) repeat units widely used for stable organic photovoltaics. However, the solubility of PCDTBT is limited, which decreases polymer yield and makes synthesis and purification tedious. Here, we introduce a strategy to increase both solubility and luminescence by the statistical incorporation of additional hexyl side chains at the TBT unit (hex-TBT). An increasing amount of hex-TBT as comonomer from 0 to 100% enhances solubility, leads to backbone torsion, and causes a blue-shift in the absorption and emission spectra. While photovoltaic performance of both PCDTBT:P3HT blends and PCDTBT:PCBM blends decreases with increasing content of hex-TBT due to weaker and blue-shifted absorption, the luminescence properties can be systematically improved. Both photo- and electroluminescence (PL and EL) quantum efficiencies increase with increasing hex-TBT content. We further demonstrate solution-processed red polymer light-emitting diodes based on fully hexylated PCDTBT showing an EL quantum efficiency enhancement of up to 7 times and 2 orders of magnitude enhancement of brightness compared to standard PCDTBT. Fully hexylated PCDTBT shows a peak external quantum efficiency of 1.1% and a peak brightness of 2500 cd/m2Financial support from the Fonds der Chemischen Industrie (FCI), the Research Innovation Fund of the University of Freiburg and the DFG (SPP1355) is greatly acknowledged. F.L. greatly acknowledges the EPSRC for funding. D.D. acknowledges the Department of Physics (University of Cambridge) and the KACST-Cambridge University Joint Centre of Excellence for support
Recommended from our members
Efficient Triplet Exciton Fusion in Molecularly Doped Polymer Light-Emitting Diodes.
Solution-processed polymer organic light-emitting diodes (OLEDs) doped with triplet-triplet annihilation (TTA)-upconversion molecules, including 9,10-diphenylanthracene, perylene, rubrene and TIPS-pentacene, are reported. The fraction of triplet-generated electroluminescence approaches the theoretical limit. Record-high efficiencies in solution-processed OLEDs based on these materials are achieved. Unprecedented solid-state TTA-upconversion quantum yield of 23% (TTA-upconversion reaction efficiency of 70%) at electrical excitation well below one-sun equivalent is observed.D.D. acknowledges the Department of Physics (University of Cambridge) and the KACST–Cambridge University Joint Centre of Excellence for financial support. L.Y. thanks the Singapore Agency for Science, Technology and Research (A*STAR) for a PhD studentship. The authors thank the Engineering and Physical Sciences Research Council (EPSRC) for financial support
Star-shaped fluorene-BODIPY oligomers: versatile donor-acceptor systems for luminescent solar concentrators
Energy transfer in star-shaped donor–acceptor molecules reduces self-absorption in luminescent solar concentrators.N. J. L. K. D. is supported by the Cambridge Commonwealth European and International Trust, Cambridge Australian Scholarships and Mr Charles K Allen. R. W. M. acknowledges funding from the Initiative and Networking Fund of the Helmholtz Association. S. T. E. J. is supported by the Royal society. RGDT is supported by the EPSRC. D. C. thanks the Royal Society. PJS thanks the Royal Society for a Wolfson Research Merit Award. This work as supported by the EPSRC [EP/M005143/1, EP/M014797/1, EP/L012200/1]
Strong Photocurrent from Two-Dimensional Excitons in Solution-Processed Stacked Perovskite Semiconductor Sheets
Room-temperature photocurrent measurements in two-dimensional (2D) inorganic-organic perovskite devices reveal that excitons strongly contribute to the photocurrents despite possessing binding energies over 10 times larger than the thermal energies. The p-type (C₆H₉C₂H₄NH₃)₂PbI₄ liberates photocarriers at metallic Schottky aluminum contacts, but incorporating electron- and hole-transport layers enhances the extracted photocurrents by 100-fold. A further 10-fold gain is found when TiO₂ nanoparticles are directly integrated into the perovskite layers, although the 2D exciton semiconducting layers are not significantly disrupted. These results show that strong excitonic materials may be useful as photovoltaic materials despite high exciton binding energies and suggest mechanisms to better understand the photovoltaic properties of the related three-dimensional perovskites.This work was supported by EPSRC Grants EP/K028510/1, EP/G060649/1, EP/G037221/1, EP/H007024/1, EP/L027151/1, and EP/L015978/1, the Cambridge NanoDTC, and ERC LINASS 320503
Fractional Levy motion through path integrals
Fractional Levy motion (fLm) is the natural generalization of fractional
Brownian motion in the context of self-similar stochastic processes and stable
probability distributions. In this paper we give an explicit derivation of the
propagator of fLm by using path integral methods. The propagators of Brownian
motion and fractional Brownian motion are recovered as particular cases. The
fractional diffusion equation corresponding to fLm is also obtained.Comment: 9 pages, minor changes, published versio
Recommended from our members
Short hydrogen bonds enhance nonaromatic protein-related fluorescence.
Fluorescence in biological systems is usually associated with the presence of aromatic groups. Here, by employing a combined experimental and computational approach, we show that specific hydrogen bond networks can significantly affect fluorescence. In particular, we reveal that the single amino acid L-glutamine, by undergoing a chemical transformation leading to the formation of a short hydrogen bond, displays optical properties that are significantly enhanced compared with L-glutamine itself. Ab initio molecular dynamics simulations highlight that these short hydrogen bonds prevent the appearance of a conical intersection between the excited and the ground states and thereby significantly decrease nonradiative transition probabilities. Our findings open the door to the design of new photoactive materials with biophotonic applications
Short hydrogen bonds enhance nonaromatic protein-related fluorescence.
Fluorescence in biological systems is usually associated with the presence of aromatic groups. Here, by employing a combined experimental and computational approach, we show that specific hydrogen bond networks can significantly affect fluorescence. In particular, we reveal that the single amino acid L-glutamine, by undergoing a chemical transformation leading to the formation of a short hydrogen bond, displays optical properties that are significantly enhanced compared with L-glutamine itself. Ab initio molecular dynamics simulations highlight that these short hydrogen bonds prevent the appearance of a conical intersection between the excited and the ground states and thereby significantly decrease nonradiative transition probabilities. Our findings open the door to the design of new photoactive materials with biophotonic applications
Polaron pair mediated triplet generation in polymer/fullerene blends
Electron spin is a key consideration for the function of organic semiconductors in light-emitting diodes and solar cells, as well as spintronic applications relying on organic magnetoresistance. A mechanism for triplet excited state generation in such systems is by recombination of electron-hole pairs. However, the exact charge recombination mechanism, whether geminate or nongeminate and whether it involves spin-state mixing is not well understood. In this work, the dynamics of free charge separation competing with recombination to polymer triplet states is studied in two closely related polymer-fullerene blends with differing polymer fluorination and photovoltaic performance. Using time-resolved laser spectroscopic techniques and quantum chemical calculations, we show that lower charge separation in the fluorinated system is associated with the formation of bound electron-hole pairs, which undergo spin-state mixing on the nanosecond timescale and subsequent geminate recombination to triplet excitons. We find that these bound electron-hole pairs can be dissociated by electric fields
Best practices for measuring emerging light-emitting diode technologies
The arrival of light-emitting diodes based on new materials is posing challenges for the characterization and comparison of devices in a trusted and consistent manner. Here we provide some advice and guidelines that we hope will benefit the community
High-performance light-emitting diodes based on carbene-metal-amides
Organic light-emitting diodes (OLEDs) promise highly efficient lighting and display technologies. We introduce a new class of linear donor-bridge-acceptor light-emitting molecules, which enable solution-processed OLEDs with near-100% internal quantum efficiency at high brightness. Key to this performance is their rapid and efficient utilization of triplet states. Using time-resolved spectroscopy, we establish that luminescence via triplets occurs within 350 nanoseconds at ambient temperature, after reverse intersystem crossing to singlets. We find that molecular geometries exist at which the singlet-triplet energy gap (exchange energy) is close to zero, so that rapid interconversion is possible. Calculations indicate that exchange energy is tuned by relative rotation of the donor and acceptor moieties about the bridge. Unlike other systems with low exchange energy, substantial oscillator strength is sustained at the singlet-triplet degeneracy point.D.D. and R.H.F. acknowledge support from the Department of Physics (Cambridge) and the King Abdulaziz City for Science and Technology–Cambridge University Joint Centre of Excellence. L.Y. thanks the Singapore Agency for Science, Technology and Research (A*STAR) for a Ph.D. studentship. J.M.R. acknowledges support from the Winton Program for the Physics of Sustainability. J.P.H.R. acknowledges the Cambridge NanoDTC (grant EP/L015978/1). M.L. acknowledges support by the Academy of Finland (project 251448). The computations were made possible by use of the Finnish Grid and Cloud Infrastructure. This work was supported by the Engineering and Physical Sciences Research Council (grant no. EP/M005143/1) and the European Research Council (ERC). M.B. is an ERC Advanced Investigator Award holder (grant no. 338944-GOCAT). D.C. and S.J. acknowledge support from the Royal Society (grant nos. UF130278 and RG140472)
- …