183 results match your criteria: "Light Technology Institute[Affiliation]"

The molecule 2'--apiosyl-6'--crotonic acid-betanin (called Achkiy) was obtained after an ecofriendly and low-cost purification process of the extract from the ayrampo seed cuticle. Results from EDS give us an idea of the organic elements present in the ayrampo cuticle layer composed of carbon, oxygen and nitrogen. Further characterization analysis of ayrampo extract by Fourier Transform Infrared Spectrophotometry (FTIR) corroborated the presence of characteristic functional groups corresponding to carboxyl, carbonyls, hydroxyls and secondary amines.

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The spatial orientation of chromophores defines the photophysical and optoelectronic properties of a material and serves as the main tunable parameter for tailoring functionality. Controlled assembly for achieving a predefined spatial orientation of chromophores is rather challenging. Metal-organic frameworks (MOFs) are an attractive platform for exploring the virtually unlimited chemical space of organic components and their self-assembly for device optimization.

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Several photophysical properties of chromophores depend crucially on intermolecular interactions. Thermally-activated delayed fluorescence (TADF) is often influenced by close packing of the chromophore assembly. In this context, the metal-organic framework (MOF) approach has several advantages: it can be used to steer aggregation such that the orientation within aggregated structures can be predicted using rational approaches.

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Silicon nanocrystals (SiNCs) are regarded as a green and environmentally friendly material when compared with other semiconductor nanocrystals. Ultra-small SiNCs (with the size 4.6-5.

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The efficiency of photon upconversion via triplet-triplet annihilation is characterized by an upconversion quantum yield (Φ); however, uncertainties remain for its determination. Here, we present a new approach for the relative measurement of Φ for green-to-blue upconversion using BODIPY-pyrene donor-acceptor dyad (BD1) as a heavy-atom-free triplet sensitizer. This new approach exploits broad fluorescence from a charge-transfer (CT) state of BD1, which possesses (i) a significant Stokes shift of 181 nm in dichloromethane and (ii) a comparably high CT-fluorescence quantum yield (Φ = 7.

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Tabanid flies (Diptera: Tabanidae) are attracted to shiny black targets, prefer warmer hosts against colder ones and generally attack them in sunshine. Horizontally polarised light reflected from surfaces means water for water-seeking male and female tabanids. A shiny black target above the ground, reflecting light with high degrees and various directions of linear polarisation is recognised as a host animal by female tabanids seeking for blood.

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Detection of micropollutants such as steroid hormones occurring in the aquatic environment at concentrations between ng/L and µg/L remains a major challenge, in particular when treatment efficiency is to be evaluated. Steroid hormones are typically analysed using mass-spectrometry methods, requiring pre-concentration and/or derivatisation procedures to achieve required detection limits. Free of sample preparation steps, the use of radiolabelled contaminants with liquid scintillation counting is limited to single-compound systems and require a separation of hormone mixtures before detection.

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High-performance Ag-Se-based n-type printed thermoelectric (TE) materials suitable for room-temperature applications have been developed through a new and facile synthesis approach. A high magnitude of the Seebeck coefficient up to 220 μV K and a TE power factor larger than 500 μW m K for an n-type printed film are achieved. A high figure-of-merit ∼0.

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Flexible direct conversion X-ray detectors enable a variety of novel applications in medicine, industry, and science. Hybrid organic-inorganic perovskite semiconductors containing elements of high atomic number combine an efficient X-ray absorption with excellent charge transport properties. Due to their additional cost-effective and low-temperature processability, perovskite semiconductors represent promising candidates to be used as active materials in flexible X-ray detectors.

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Sensitizing TADF Absorption Using Variable Length Oligo(phenylene ethynylene) Antennae.

Front Chem

February 2020

Department of Electrical Engineering and Information Technology, Light Technology Institute, Karlsruhe Institute of Technology, Karlsruhe, Germany.

Beyond their applications in organic light-emitting diodes (OLEDs), thermally activated delayed fluorescence (TADF) materials can also make good photonic markers. Time-gated measurement of their delayed emission enables "background-free" imaging in, for example, biological systems, because no naturally-occurring compounds exhibit such long-lived emission. Attaching a strongly-absorbing antenna, such as a phenylene ethynylene oligomer, to the TADF core would be of interest to increase their brightness as photonic markers.

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The upconversion of near-infrared (NIR) to visible (vis) photons is of interest for display technologies and energy conversion. Although triplet-triplet annihilation (TTA) offers a mechanism for upconversion that works efficiently at low incident irradiance flux densities, current strategies for NIR-vis upconversion based on TTA have fundamental limitations. Herein, we report a strategy for NIR-vis TTA based on lanthanide-containing complexes to sensitize the upconversion.

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Future lightweight, flexible, and wearable electronics will employ visible-light-communication schemes to interact within indoor environments. Organic photodiodes are particularly well suited for such technologies as they enable chemically tailored optoelectronic performance and fabrication by printing techniques on thin and flexible substrates. However, previous methods have failed to address versatile functionality regarding wavelength selectivity without increasing fabrication complexity.

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Achieving efficient devices while maintaining a high fabrication yield is a key challenge in the fabrication of solution-processed, perovskite-based light-emitting diodes (PeLEDs). In this respect, pinholes in the solution-processed perovskite layers are a major obstacle. These are usually mitigated using organic electron-conducting planarization layers.

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Single-walled carbon nanotubes as emerging quantum-light sources may fill a technological gap in silicon photonics due to their potential use as near-infrared, electrically driven, classical or nonclassical emitters. Unlike in photoluminescence, where nanotubes are excited with light, electrical excitation of single tubes is challenging and heavily influenced by device fabrication, architecture, and biasing conditions. Here we present electroluminescence spectroscopy data of ultra-short-channel devices made from (9,8) carbon nanotubes emitting in the telecom band.

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We demonstrate modular modifications of the widely employed emitter 2,4,5,6-tetra(9-carbazol-9-yl)isophthalonitrile (4CzIPN) by replacing one or both nitrile acceptors with oxadiazole groups via a tetrazole intermediate. This allows the introduction of various functional groups including halides, alkynes, alkenes, nitriles, esters, ethers and a protected amino acid while preserving the thermally activated delayed fluorescence (TADF) properties. The substituents control the emission maximum of the corresponding emitters, ranging between 472-527 nm, and show high solid-state photoluminescence quantum yields up to 85 %.

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Perovskite solar cells (PSCs) are one of the most promising emerging energy-conversion technologies because of their high power conversion efficiencies (PCEs) and potentially low fabrication cost. To improve PCE, it is necessary to develop PSCs with good interfacial engineering to reduce the trap states and carrier transport barriers present at the various interfaces of the PSCs' architecture. This work reports a facile method to improve the interface between the perovskite absorber layer and the hole transport layer (HTL) by adding a small amount of acetonitrile (ACN) in the Spiro-OMeTAD precursor solution.

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Liquid Glass for Photovoltaics: Multifunctional Front Cover Glass for Solar Modules.

ACS Appl Mater Interfaces

September 2019

Institute of Microstructure Technology , Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen , Germany.

Advanced optical concepts, making use of tailored microstructured front cover glasses, promise to reduce the losses encountered with encapsulated solar modules. However, implementing optical concepts into the conventional architecture of encapsulated solar modules and simultaneously maintaining high durability represent a severe technological challenge. The liquid glass technique offers a route to meet this challenge by enabling the implementation of these optical concepts directly into the durable front cover glass of solar modules.

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A novel combination of a poly(vinylidene fluoride) (PVDF) membrane with pore size 0.2 μm and a photosensitizer 5,10,15,20-tetrakis (pentafluorophenyl)-21,23-porphine palladium(II) (PdTFPP) makes a promising hybrid material for the generation of singlet oxygen (O) and, thus, water treatment applications. The fabricated photocatalytic membrane exhibits permeability of 4280 ± 250 L·m·h·bar and stable photocatalytic degradation performance over a 90 h period, when illuminated with green light (528 ± 20 nm) and operated in a dead-end, single-pass configuration.

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Organophosphorus-B(CF) adducts: towards new solid-state emitting materials.

Dalton Trans

September 2019

Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany. and Faculty of Pharmacy, University of Castilla-La Mancha, Calle Almansa 14 - Edif. Bioincubadora, 02008, Albacete, Spain.

The coordination of B(CF) to materials based on six-membered phosphorus heterocycles via P[double bond, length as m-dash]O bonds tunes their physicochemical properties both in solution and in the solid state, remarkably improving their performances in light-emitting layers.

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In photon upconversion (UC) based on triplet-triplet annihilation, the upconversion photoluminescent quantum yield (UC-PLQY) depends on the excitation power density in a way that can be described by a single figure of merit. This figure of merit, the threshold value, allows the excitation power density required for efficient UC-PLQY to be compared between different triplet-triplet annihilation systems. Here, we investigate the excitation power density dependence of two-photon UC processes in a series of four lanthanide-doped inorganic host materials (oxides, fluorides, and chlorides) all doped with 18 mol % Yb sensitizer ions and 2 mol % Er activator ions.

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Imaging the phase distribution of amorphous or partially crystalline organic materials at the nanoscale and analyzing the local atomic structure of individual phases has been a long-time challenge. We propose a new approach for imaging the phase distribution and for analyzing the local structure of organic materials based on scanning transmission electron diffraction (4D-STEM) pair distribution function analysis (PDF). We show that electron diffraction based PDF analysis can be used to characterize the short- and medium-range order in aperiodically packed organic molecules.

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The remarkable recent progress in perovskite photovoltaics affords a novel opportunity to advance the power conversion efficiency of market-dominating crystalline silicon (c-Si) solar cells. A severe limiting factor in the development of perovskite/c-Si tandems to date has been their inferior light-harvesting ability compared to single-junction c-Si solar cells, but recent innovations have made impressive headway on this front. Here, we provide a quantitative perspective on future steps to advance perovskite/c-Si tandem photovoltaics from a light-management point of view, addressing key challenges and available strategies relevant to both the 2-terminal and 4-terminal perovskite/c-Si tandem architectures.

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A de novo strategy for predictive crystal engineering to tune excitonic coupling.

Nat Commun

May 2019

Karlsruhe Institute of Technology (KIT), Institute of Functional Interfaces (IFG), Hermann-von-Helmholtz Platz-1, 76344, Eggenstein-Leopoldshafen, Germany.

In molecular solids, the intense photoluminescence (PL) observed for solvated dye molecules is often suppressed by nonradiative decay processes introduced by excitonic coupling to adjacent chromophores. We have developed a strategy to avoid this undesirable PL quenching by optimizing the chromophore packing. We integrated the photoactive compounds into metal-organic frameworks (MOFs) and tuned the molecular alignment by introducing adjustable "steric control units" (SCUs).

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