A molecular theory for two-photon and three-photon fluorescence polarization

In the analysis of molecular structure and local order in heterogeneous samples, multiphoton excitation of fluorescence affords chemically specific information and high-resolution imaging. This report presents the results of an investigation that secures a detailed theoretical representation of the fluorescence polarization produced by one-, two-, and three-photon excitations, with orientational averaging procedures being deployed to deliver the fully disordered limits. The equations determining multiphoton fluorescence response prove to be expressible in a relatively simple, generic form, and graphs exhibit the functional form of the multiphoton fluorescence polarization. Amongst other features, the results lead to the identification of a condition under which the fluorescence produced through the concerted absorption of any number of photons becomes completely unpolarized. It is also shown that the angular variation of fluorescence intensities is reliable indicator of orientational disorder

An insight into polarization states of solid-state organic lasers

The polarization states of lasers are crucial issues both for practical applications and fundamental research. In general, they depend in a combined manner on the properties of the gain material and on the structure of the electromagnetic modes. In this paper, we address this issue in the case of solid-state organic lasers, a technology which enables to vary independently gain and mode properties. Different kinds of resonators are investigated: in-plane micro-resonators with Fabry-Perot, square, pentagon, stadium, disk, and kite shapes, and external vertical resonators. The degree of polarization P is measured in each case. It is shown that although TE modes prevail generally (P>0), kite-shaped micro-laser generates negative values for P, i.e. a flip of the dominant polarization which becomes mostly TM polarized. We at last investigated two degrees of freedom that are available to tailor the polarization of organic lasers, in addition to the pump polarization and the resonator geometry: upon using resonant energy transfer (RET) or upon pumping the laser dye to an higher excited state. We then demonstrate that significantly lower P factors can be obtained.Comment: 12 pages, 12 figure

Efficient energy transfer in layered hybrid organic/inorganic nanocomposites: A dual function of semiconductor nanocrystals

The efficiency of energy transfer in hybrid organic/inorganic nanocomposites based on conjugated polymers and semiconductor nanocrystals is strongly dependent on both the energy transfer rate and the rate of the nonradiative recombination of the polymer. We demonstrate that the polymer nonradiative recombination can be reduced by the suppression of exciton diffusion via proper morphology engineering of a hybrid structure. In the layer-by-layer assembled nanocomposite of a conjugated polymer and CdTe nanocrystals the latter have a dual role: first, they are efficient exciton acceptors and, second, they reduce nonradiative recombination in the polymer by suppressing exciton diffusion across the layers.Fil: Lutich, Andrey A.. Ludwig Maximilians Universitat; AlemaniaFil: Pöschl, Andreas. Ludwig Maximilians Universitat; AlemaniaFil: Jiang, Guoxin. Ludwig Maximilians Universitat; AlemaniaFil: Stefani, Fernando Daniel. Ludwig Maximilians Universitat; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Susha, Andrei S.. City University of Hong Kong; ChinaFil: Rogach, Andrey L.. City University of Hong Kong; ChinaFil: Feldmann, Jochen. Ludwig Maximilians Universitat; Alemani

Size dependent exciton dynamics in one-dimensional perylene bisimide aggregates

The size dependent exciton dynamics of one-dimensional aggregates of substituted perylene bisimides are studied by ultrafast transient absorption spectroscopy and kinetic Monte-Carlo simulations in dependence on the temperature and the excitation density. For low temperatures the aggregates can be treated as infinite chains and the dynamics is dominated by diffusion driven exciton-exciton annihilation. With increasing temperature the aggregates decompose into small fragments consisting of very few monomers. This scenario is also supported by the time dependent anisotropy deduced from polarization dependent experiments

Photoluminescence Activation of Organic Dyes via Optically Trapped Quantum Dots

This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Nano, copyright © American Chemical Society after peer review and technical editing by the publisher.[EN] Laser tweezers afford quantum dot (QD) manipulation for use as localized emitters. Here, we demonstrate fluorescence by radiative energy transfer from optically trapped colloidal QDs (donors) to fluorescent dyes (acceptors). To this end, we synthesized silica-coated QDs of different compositions and triggered their luminescence by simultaneous trapping and two-photon excitation in a microfluidic chamber filled with dyes. This strategy produces a near-field light source with great spatial maneuverability, which can be exploited to scan nanostructures. In this regard, we demonstrate induced photoluminescence of dye-labeled cells via optically trapped silica-coated colloidal QDs placed at their vicinity. Allocating nanoscale donors at controlled distances from a cell is an attractive concept in fluorescence microscopy because it dramatically reduces the number of excited dyes, which improves resolution by preventing interferences from the whole sample, while prolonging dye luminescence lifetime due to the lower power absorbed from the QDs.H.R.-R. is supported by an FPI-UAM 2015 fellowship (BES-2009-027909). Authors acknowledge funding from the Spanish Ministry of Economy and Competitiveness through MAT2017-85617-R and MAT2015-71806-R. B.H.J. acknowledges financial support from the Spanish Ministry of Economy and Competitiveness, through the Maria de Maeztu (IFIMAC) and Severo Ochoa (IMDEA Nanoscience) Programmes for Units of Excellence in R&D.Rodríguez-Rodríguez, H.; Acebrón, M.; Iborra, F.; Arias-Gonzalez, JR.; Juárez, B. (2019). Photoluminescence Activation of Organic Dyes via Optically Trapped Quantum Dots. ACS Nano. 13(6):7223-7230. https://doi.org/10.1021/acsnano.9b02835S7223723013

Dermatological cancer screening: Evaluation of a new community pharmacy service

Background: Skin cancer accounts for one third of all cancers. Prognosis is inversely related to identification stage. Objectives: To describe a novel service, mole scans, performed in community pharmacy, the findings from the first 3.5 years it was in place, and to explore patient acceptability of the service. Methods: Norwegian Boots' pharmacies offer a mole scanning service in cooperation with ScreenCancer. Scans are undertaken within pharmacy consultation rooms. Image interpretation is undertaken remotely by a specialist. Number and result of scans performed from 2010 to 2014 are reported. A satisfaction questionnaire was returned by 10% of participants. Results: A total of 25836 scans were performed on 15777 individuals. Of these, 83.6% had normal scans, 1% had melanoma, and 15.4% had another skin condition. In 2014 the service identified 4.1% of melanoma cases registered in the Norwegian Cancer Registry. Most responders (88%) would use a similar service again. Nearly all (99%) felt the pharmacy was a suitable venue, and 95% would recommend the service to others. In total, 99% of respondents scored their overall satisfaction as “good” or higher. Conclusions: This approach was acceptable among participants who provided feedback. Providing mole scanning through pharmacies enables individuals to obtain a rapid check of moles causing concern, in an acceptable environment with a high level of satisfaction