TY - CONF A1 - Würth, Christian T1 - Time resolved spectroscopy of upconverting lanthanide based upconversion nanocrystals N2 - The optical properties of these materials strongly depend on the excitation power density, i.e., the number of photons absorbed per time interval. The upconversion quantum efficiencies (ΦUC) of these materials, the excitation power dependent population i.e. the emission characteristics, and the deactivation dynamics are influenced by nanoparticle architecture, doping concentration, and the microenvironment. We will discuss how time resolved measurements can help to understand the fundamental photophysical mechanisms and discuss differences to other nanocrystals like quantum dots. T2 - 19th International Course on “Principles and Applications of Time-resolved Fluorescence Spectroscopy” CY - Berlin, Germany DA - 16.11.2022 KW - Nanoparticle KW - Lanthanide KW - Upconversion KW - Energy transfer PY - 2022 AN - OPUS4-57000 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Relative and absolute determination of the quantum efficiency of transparent and scattering luminescent materials T2 - Institutsseminar Werkstoffwissenschaften Universität Erlangen CY - Erlangen, Germany DA - 2014-06-23 PY - 2014 AN - OPUS4-30919 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Scattering of Particles N2 - Introduction to theory and applications of light scattering T2 - Cost-action Training school CY - Turku, Finland DA - 03.04.2017 KW - Light scattering PY - 2017 AN - OPUS4-40010 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Spektroskopie mit der Ulbrichtkugel: Streuende und floureszierende Systeme in der Bioanalytik T2 - PTB-Institutsseminar CY - Braunschweig, Germany DA - 2013-01-23 PY - 2013 AN - OPUS4-27806 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Time resolved spectroscopy of upconverting lanthanide based upconversion nanocrystals N2 - This presentation gives an overview of time correlated population and depopulation processes of the electronic states of lanthanide doped nanoparticles. The fundamental principles of sensitized photon upconversion are explained. Theoretical principles and the correlation to experimental results are shown. Examples are given for particle growth, dissolution as well as influences of size, doping concentration and microenvironment. T2 - Principles and Applications of Time-resolved Fluorescence Spectroscopy CY - Berlin, Germany DA - 12.11.2024 KW - Upconversion KW - Time domain PY - 2024 AN - OPUS4-61652 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grauel, Bettina A1 - Würth, Christian A1 - Homann, C. A1 - Krukewitt, Lisa A1 - Andresen, Elina A1 - Roik, Janina A1 - Recknagel, Sebastian A1 - Haase, M. A1 - Resch-Genger, Ute T1 - Volume and surface effects on two-photonic and three-photonic processes in dry co-doped upconversion nanocrystals N2 - Despite considerable advances in synthesizing high-quality core/shell upconversion (UC) nanocrystals (NC; UCNC) and UCNC photophysics, the application of near-infrared (NIR)-excitable lanthanide-doped UCNC in the life and material sciences is still hampered by the relatively low upconversion luminescence (UCL) of UCNC of small size or thin protecting shell. To obtain deeper insights into energy transfer and surface quenching processes involving Yb3+ and Er3+ ions, we examined energy loss processes in differently sized solid core NaYF4 nanocrystals doped with either Yb3+ (YbNC; 20% Yb3+) or Er3+ (ErNC; 2% Er3+) and co-doped with Yb3+ and Er3+ (YbErNC; 20% Yb3+ and 2% Er3+) without a surface protection shell and coated with a thin and a thick NaYF4 shell in comparison to single and co-doped bulk materials. Luminescence studies at 375 nm excitation demonstrate backenergy transfer (BET) from the 4G11/2 state of Er3+ to the 2F5/2 state of Yb3+, through which the red Er3+ 4F9/2 state is efficiently populated. Excitation power density (P)-dependent steady state and time-resolved photoluminescence measurements at different excitation and emission wavelengths enable to separate surface-related and volume-related effects for two-photonic and threephotonic processes involved in UCL and indicate a different influence of surface passivation on the green and red Er3+ emission. The intensity and lifetime of the latter respond particularly to an increase in volume of the active UCNC core. We provide a threedimensional random walk model to describe these effects that can be used in the future to predict the UCL behavior of UCNC. KW - Nano KW - Nanomaterial KW - Upconversion KW - Nanoparticle KW - Lanthanide KW - Photoluminescence KW - Quantum yield KW - Pphotophysics KW - Lifetime KW - Sensor KW - Excitation KW - Power density KW - Single particle KW - Brightness KW - NIR KW - Mechanism KW - Modeling KW - Simulation KW - Energy transfer PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-535317 DO - https://doi.org/10.1007/s12274-021-3727-y SN - 1998-0124 VL - 15 IS - 3 SP - 2362 EP - 2373 PB - Springer AN - OPUS4-53531 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Geißler, Daniel A1 - Würth, Christian A1 - Wolter, C. A1 - Weller, H. A1 - Resch-Genger, Ute T1 - Excitation wavelength dependence of the photoluminescence quantum yield and decay behavior of CdSe/CdS quantum dot/quantum rods with different aspect ratios N2 - The excitation wavelength (lexc) dependence of the photoluminescence (PL) quantum yield (FPL) and decay behavior (tPL) of a series of CdSe/CdS quantum dot/Quantum rods (QDQRs), consisting of the same spherical CdSe core and rod-shaped CdS shells, with aspect ratios ranging from 2 to 20 was characterized. lexc between 400–565 nm were chosen to cover the first excitonic absorption band of the CdSe core material, the onset of absorption of the CDs shell, and the region of predominant shell absorption. A strong lexc dependence of relative and absolutely measured FPL and tPL was found particularly for the longer QDQRs with higher aspect ratios. This is attributed to combined contributions from a length-dependent shell-to-core exciton localization efficiency, an increasing number of defect states within the shell for the longest QDQRs, and probably also the presence of absorbing, yet non-emitting shell material. Although the FPL values of the QDQRs decrease at shorter wavelength, the extremely high extinction coefficients introduced by the shell outweigh this effect, leading to significantly higher brightness values at wavelengths below the absorption onset of the CdS Shell compared with direct excitation of the CdSe cores. Moreover, our results present also an interesting example for the comparability of absolutely measured FPL using an integrating sphere setup and FPL values measured relative to common FPL standards, and underline the Need for a correction for particle scattering for QDQRs with high aspect ratios. KW - Quantum dot KW - Quantum rod KW - Quantum yield KW - Integrating sphere KW - Decay time PY - 2017 DO - https://doi.org/10.1039/C7CP02142A SN - 1463-9076 SN - 1463-9084 VL - 19 IS - 19 SP - 12509 EP - 12516 PB - Royal Society of Chemistry (RSC) AN - OPUS4-40814 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meng, M. A1 - Zhang, R. A1 - Fa, X. A1 - Yang, J. A1 - Cheng, Z. A1 - Ansari, A. A. A1 - Ou, Jun A1 - Würth, Christian A1 - Resch-Genger, Ute T1 - Preparation of core–shell structured NaYF4:Yb3+/ Tm3+@NaYF4:Yb3+/Er3+ nanoparticles with high sensitivity, low resolution and good reliability and application of their fluorescence temperature properties N2 - A series of NaYF4:Yb3+/Tm3+@NaYF4:Yb3+/Er3+ nanoparticles doped with Tm3+ and Er3+ were successfully prepared by the solvothermal method. Under 980 nm laser excitation, intense upconversion emission peaks of Tm3+ and Er3+ were observed for all samples. By doping Tm3+ and Er3+ with core–shell partitioning, not only a significant increase in fluorescence intensity could be achieved, but also simultaneous temperature measurements on multiple thermocouple energy levels could be realised. In addition, the temperature sensing performance of different thermocouple energy levels was also investigated, and it was found that the 3 F3 → 3 H6 and 1 G4 → 3 F4 thermocouple energy level pairs of Tm3+ were the best, with maximum absolute sensitivity and maximum relative sensitivity of up to 0.0250 K−1 and 2.155% K−1 respectively, higher than the sensitivity of other thermocouple energy levels. It has a temperature resolution of less than 0.0139 K, which is lower than that of most materials available today. By using this material as a probe to build a fiber optic temperature sensor platform, it was found to have reliable temperature measurement performance. KW - Flourescence KW - Optical probe KW - Sensor KW - Dye KW - Temperature KW - Nano KW - Particle KW - Upconversion KW - Lanthanide KW - Qantum yield KW - Quality assurance KW - Monitoring KW - Infrastructure PY - 2022 DO - https://doi.org/10.1039/d1ce01729b VL - 24 IS - 9 SP - 1752 EP - 1763 PB - RSC Publishing AN - OPUS4-54416 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ahiboz, D. A1 - Andresen, Elina A1 - Manley, P. A1 - Resch-Genger, Ute A1 - Würth, Christian A1 - Becker, C. T1 - Enhanced photon upconversion using erbium-doped nanoparticles interacting with silicon metasurfaces N2 - Photon upconversion (UC) using trivalent erbium (Er+3) doped crystals is a promising concept to harness near infrared photons of the solar spectrum which cannot be directly absorbed by silicon solar cells. However, their UC efficiency at low-intensity 1 sun illumination is not relevant on device level so far. Exploiting giant near-field enhancement effects on metasurfaces is an appealing approach to enable efficient UC at low irradiance conditions. Here, we report on more than 1000-fold enhanced photon UC of NaYF4:Er+3 nanoparticles interacting with the near-fields supported by a silicon metasurface under 1550 nm excitation. T2 - 48th Photovoltaic Specialists Conference (PVSC) CY - Online meeting DA - 20.06.2021 KW - Nano KW - Nanomaterial KW - Upconversion nanoparticle KW - Lanthanide KW - Photoluminescence KW - Quantum yield KW - Photophysics KW - Lifetime KW - Sensor KW - Excitation power density KW - Brightness KW - NIR KW - Mechanism KW - Modeling KW - Simulation KW - Energy transfer KW - Photonic crystal KW - Enhancement strategy PY - 2021 DO - https://doi.org/10.1109/pvsc43889.2021.9518495 SP - 1 EP - 3 PB - IEEE CY - Berlin AN - OPUS4-53786 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Würth, Christian A1 - Fischer, S. A1 - Grauel, Bettina A1 - Alivisatos, A. P. A1 - Resch-Genger, Ute T1 - Quantum Yields, Surface Quenching, and Passivation Efficiency for Ultrasmall Core/Shell Upconverting Nanoparticles N2 - We synthesized and characterized a set of ultrasmall hexagonal-phase NaGdF4: 20% Yb3+, 2% Er3+ upconversion nanoparticles with core diameters of 3.7 ± 0.5 nm. In order to assess passivation effects and the influence of possible core−shell intermixing and to identify optimum particle structures for combined imaging in the visible and near-infrared (vis−NIR: 410−850 nm) and short-wave infrared (SWIR: 1520 nm), NaYF4 shells of varying thicknesses (monolayer to 10 nm) were introduced and the influence of this parameter on the upconversion and downshifting photoluminescence of these particles was studied at different excitation power densities. This included excitation power-dependent emission spectra, slope factors, quantum yields, and excited state decay kinetics. These measurements revealed enhancement factors of the upconversion quantum yield of >10 000 in the low power region and an excitation power density-independent quantum yield of the downshifted emission at 1520 nm between 0.1 and 14%. The optimized shell thickness for combined vis and SWIR imaging was identified as 5 nm. Moreover, lifetimes and quantum yields can be continuously tuned by shell thickness which can be exploited for lifetime multiplexing and encoding. The fact that we did not observe a saturation of the upconversion quantum yield or the excited state decay kinetics with increasing shell thickness is ascribed to a strong intermixing of the active core with the inert shell during the shelling procedure. This indicates the potential of spectroscopic tools to detect cation intermixing. KW - Nanoparticle KW - Upconversion KW - Quenching PY - 2018 DO - https://doi.org/10.1021/jacs.8b01458 IS - 140 SP - 4922 EP - 4928 PB - American Chemical Society AN - OPUS4-45378 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Meng, M. A1 - Zhang, R. A1 - Cheng, Z. A1 - Fa, X. A1 - Yang, J. A1 - Ansari, A. A. A1 - Ou, Jun A1 - Würth, Christian A1 - Resch-Genger, Ute T1 - Retraction: Effect of Ca2+ doping on the upconversion luminescence properties of NaYF4:Yb3+/Tm3+ nanoparticles and study of its temperature measurement performance N2 - Retraction of "Effect of Ca2+ doping on the upconversion luminescence properties of NaYF4:Yb3+/Tm3+ nanoparticles and study of its temperature measurement performance" by Mingzhou Meng et al., CrystEngComm, 2022, 24, 4887–4898, https://doi.org/10.1039/D2CE00562J. The Royal Society of Chemistry, with the agreement of the authors, hereby wholly retracts this CrystEngComm article due to concerns with the reliability of the data. PY - 2023 DO - https://doi.org/10.1039/d3ce90111d SN - 1466-8033 VL - 25 IS - 33 SP - 4768 PB - Royal Society of Chemistry CY - London AN - OPUS4-58494 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hodenius, M. A1 - Würth, Christian A1 - Jayapaul, J. A1 - Wong, J. E. A1 - Lammers, T. A1 - Gätjens, J. A1 - Arns, S. A1 - Mertens, N. A1 - Slabu, I. A1 - Ivanova, G. A1 - Bornemann, J. A1 - De Cuyper, M. A1 - Resch-Genger, Ute A1 - Kiessling, F. T1 - Fluorescent magnetoliposomes as a platform technology for functional and molecular MR and optical imaging N2 - Here, we present a detailed characterisation of rhodamine B-containing magnetoliposomes (FLU-ML), emphasising the dependence of their fluorescence properties on the presence of iron oxide cores, and the molar fraction of the fluorophore. The magnetoliposome types used exist as colloidally stable, negatively charged clusters with an average hydrodynamic diameter of 95 nm. The molar rhodamine B fractions were 0.67 % and 1.97 %. Rhodamine B normalised fluorescence, quantum yields and fluorescence lifetimes were substantially reduced by inner filter effects as the magnetoliposome concentration is increased, by increasing molar rhodamine B fraction, and by quenching originating from the iron oxide cores. MR relaxometry at 3 T revealed extremely high r2 relaxivities (440 to 554 s-1mM-1) and moderately high r1 values (2.06 to 3.59 s-1mM-1). Upon incubating human prostate carcinoma (PC-3) cells with FLU-ML, a dose-dependent particle internalisation was found by MR relaxometry. In addition, the internalised FLU-ML were clearly visible by fluorescence microscopy. At the FLU-ML concentrations used (up to 3 × 103 M Fe) cell viability was not substantially impaired. These results provide valuable insights on the fluorescence properties of bimodal magnetoliposomes and open promising perspectives for the use of these materials as a platform technology for advanced functional and molecular MR and optical imaging applications. KW - Fluorescent magnetoliposomes KW - Steady state and time resolved fluorometry KW - Quantum yield KW - Fluorescence lifetimes KW - MR relaxivities KW - PC-3 cells KW - Cell viability PY - 2012 DO - https://doi.org/10.1002/cmmi.467 SN - 1555-4309 SN - 1555-4317 VL - 7 IS - 1 SP - 59 EP - 67 PB - Wiley CY - Chichester AN - OPUS4-25577 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zhang, X.-X. A1 - Würth, Christian A1 - Zhao, L. A1 - Resch-Genger, Ute A1 - Ernsting, N.P. T1 - Femtosecond broadband fluorescence upconversion spectroscopy: improved setup and photometric correction N2 - A setup for fluorescence upconversion spectroscopy (FLUPS) is described which has 80 fs temporal response (fwhm) for emission in the spectral range 425–750 nm. Broadband phase matching is achieved with tilted gate pulses at 1340 nm. Background from harmonics of the gate pulse is removed and sensitivity increased compared to previous designs. Photometric calibration of the upconversion process is performed with a set of fluorescent dyes. For Coumarin 153 in methanol the peak position, bandwidth, and asymmetry depending on delay time are reported. KW - Calibration KW - Fluorescence spectroscopy KW - Fluorescence KW - Upconversion KW - Standard KW - Spectral responsivity KW - Time-resolved fluorescence KW - Quality assurance KW - Coumarin 153 KW - Solvation dynamics PY - 2011 DO - https://doi.org/10.1063/1.3597674 SN - 0034-6748 SN - 1089-7623 VL - 82 SP - 063108-1 EP - 063108-8 PB - American Institute of Physics CY - Melville, NY AN - OPUS4-23886 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Resch-Genger, Ute A1 - Würth, Christian A1 - Pauli, Jutta A1 - Weigert, Florian T1 - Quantitative optical-spectroscopic characterization of luminescent nanomaterials - Photoluminescence Quantum Yields N2 - Accurate and quantitative photoluminescence measurements are mandatory for the comparison of different emitter classes and the rational design of the next generation of molecular and nanoscale reporters as well as for most applications relying on their luminescence features in the life and material sciences and nanobiophotonics. In the following, procedures for the determination of the spectroscopic key parameter photoluminescence quantum yield, i.e., the number of emitted per absorbed photons, in the UV/vis/NIR/SWIR are presented including pitfalls and achievable uncertainties and material-specific effects related to certain emitter classes are addressed. Special emphasis is dedicated to luminescent nanocrystals. T2 - International Workshop on "Emerging Nanomaterials for Displays and SSL" CY - Dresden, Germany DA - 11.11.2021 KW - Nano KW - Nanomaterial KW - Nanocrystal KW - Semiconductor quantum dot KW - Lanthanide KW - Photoluminescence KW - Quantum yield KW - Photophysics KW - Lifetime KW - Surface chemistry KW - Brightness KW - NIR KW - SWIR KW - Method KW - Uncertainty KW - Rreference material PY - 2021 AN - OPUS4-53783 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Characterisation of Particle based Fluorescent Biosensor Systems T2 - ANAKON 2009 CY - Berlin, Germany DA - 2009-03-17 PY - 2009 AN - OPUS4-19419 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meng, M. A1 - Zhang, R. A1 - Zhenlong, F. A1 - Yang, J. A1 - Ansari, A. A1 - Ou, Jun A1 - Würth, Christian A1 - Resch-Genger, Ute T1 - Retracted article: Effect of Ca2+ doping on the upconversion luminescence properties of NaYF4:Yb3+/Tm3+ nanoparticles and study of its temperature measurement performance N2 - A solvothermal method was used to prepare a series of Yb3+/Tm3+/Ca2+ co-doped NaYF4 nanoparticles with different Ca2+ contents. Strong upconversion blue fluorescence could be observed under 980 nm laser excitation of the samples. The effect of different Ca2+ contents on the luminescence intensity was investigated, and it was found that the UV-vis upconversion luminescence increased and then decreased with an increasing Ca2+ concentration during the increase of the Ca2+ content from 0 mol% to 25 mol%, reaching the strongest fluorescence at 15 mol%, which was up to about 28 times stronger than that without Ca2+ doping. Furthermore, the mechanism was investigated, and it was found that the doping of Ca2+ disrupted the symmetry of the crystal field, resulting in a significant enhancement of the overall fluorescence. Applied to fluorescence intensity ratio thermometry, the absolute and relative sensitivities are as high as 0.0418 K−1 and 2.31% K−1, respectively, with a minimum temperature resolution of 0.0129 K. KW - Sensor KW - Temperature KW - Lanthanide KW - Luminescence KW - Nanoparticles KW - Upconversion KW - Advanced materials PY - 2022 DO - https://doi.org/10.1039/D2CE00562J SN - 1466-8033 VL - 24 IS - 27 SP - 4887 EP - 4898 PB - Royal Society of Chemistry CY - London AN - OPUS4-56952 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kaiser, M. A1 - Würth, Christian A1 - Kraft, Marco A1 - Hyppänen, I. A1 - Soukka, T. A1 - Resch-Genger, Ute T1 - Power-dependent upconversion quantum yield of NaYF4:Yb3+,Er3+ nano- and micrometer-sized particles – measurements and simulations N2 - Photophysical studies of nonlinear lanthanide-doped photon upconverting nanoparticles (UCNPs) increasingly used in biophotonics and photovoltaics require absolute measurements of the excitation power density (P)-dependent upconversion luminescence (UCL) and luminescence quantum yields (ΦUC) for quantifying the material performance, UCL deactivation pathways, and possible enhancement factors. We present here the P-dependence of the UCL spectra, ΦUC, and slope factors of the different emission bands of representative 25 nm-sized oleate-capped β-NaYF4:17% Yb3+, 3% Er3+ UCNPs dispersed in toluene and as powder as well as ΦUC of 3 μm-sized upconversion particles (UCμP), all measured with a newly designed integrating sphere setup, enabling controlled variation of P over four orders of magnitude. This includes quantifying the influence of the beam shape on the measured ΦUC and comparison of experimental ΦUC with simulations utilizing the balancing power density model of the Andersson-Engels group and the simulated ΦUC of UCμP from the Berry group, underpinned by closely matching decay kinetics of our UC material. We obtained a maximum ΦUC of 10.5% for UCμP and a ΦUC of 0.6% and 2.1% for solid and dispersed UCNPs, respectively. Our results suggest an overestimation of the contribution of the purple and an underestimation of that of the red emission of β-NaYF4:Yb3+,Er3+: microparticles by the simulations of the Berry group. Moreover, our measurements can be used as a guideline to the absolute determination of UCL and ΦUC KW - Upconversion KW - Photophysics KW - Nanoparticles PY - 2017 DO - https://doi.org/10.1039/c7nr02449e VL - 9 IS - 28 SP - 10051 EP - 10058 PB - The Royal Society of Chemistry AN - OPUS4-41550 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Würth, Christian A1 - Grabolle, Markus A1 - Pauli, Jutta A1 - Spieles, Monika A1 - Resch-Genger, Ute T1 - Relative and absolute determination of fluorescence quantum yields of transparent samples N2 - Luminescence techniques are among the most widely used detection methods in the life and material sciences. At the core of these methods is an ever-increasing variety of fluorescent reporters (i.e., simple dyes, fluorescent labels, probes, sensors and switches) from different fluorophore classes ranging from small organic dyes and metal ion complexes, quantum dots and upconversion nanocrystals to differently sized fluorophore-doped or fluorophore-labeled polymeric particles. A key parameter for fluorophore comparison is the fluorescence quantum yield (Φf), which is the direct measure for the efficiency of the conversion of absorbed light into emitted light. In this protocol, we describe procedures for relative and absolute determinations of Φf values of fluorophores in transparent solution using optical methods, and we address typical sources of uncertainty and fluorophore class-specific challenges. For relative determinations of Φf, the sample is analyzed using a conventional fluorescence spectrometer. For absolute determinations of Φf, a calibrated stand-alone integrating sphere setup is used. To reduce standard-related uncertainties for relative measurements, we introduce a series of eight candidate quantum yield standards for the wavelength region of ~350–950 nm, which we have assessed with commercial and custom-designed instrumentation. With these protocols and standards, uncertainties of 5–10% can be achieved within 2 h. PY - 2013 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-294202 DO - https://doi.org/10.1038/nprot.2013.087 SN - 1754-2189 SN - 1750-2799 VL - 8 IS - 8 SP - 1535 EP - 1550 PB - Nature Publishing Group CY - Basingstoke AN - OPUS4-29420 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Koshkina, Olga A1 - Bantz, C. A1 - Würth, Christian A1 - Lang, Thomas A1 - Resch-Genger, Ute A1 - Maskos, Michael T1 - Fluorophore-labeled siloxane-based nanoparticles for biomedical applications N2 - We present the synthesis and characterization of multifunctional fluorophore-labeled poly(organosiloxane) nanoparticles with core-shell architecture, where the fluorescent dye is incorporated into the core. Grafting of heterobifunctional poly(ethylene oxide) (PEO) onto the particle surface leads to water-soluble biocompatible nanoparticles. Two different strategies have been used for the synthesis: The encapsulation of dye-labeled monomers during the polycondensation with additional PEO coating and subsequent dye labeling by covalent attachment of the fluorescent dye rhodamine B to the (chloromethylphenyl)siloxane groups in the core after polymerization and grafting of PEO onto the surface. Comparison of the fluorescence quantum yields of the nanoparticles before and after PEO coating show a decrease in quantum yield after PEO coating. KW - Biocompatibility KW - Core-shell KW - Fluorescence KW - Fluorescence quantum yield KW - Nanoparticles KW - PEO PY - 2011 DO - https://doi.org/10.1002/masy.201100041 SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 309/310 IS - 1 SP - 141 EP - 146 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-25143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Würth, Christian T1 - Setup for the power-dependent absolute quantum yield measurements of luminescent reporters in the VIS and IR spectral region: example of upconversion nanoparticles N2 - The design of bright of upconversion nanoparticles requires an improved understanding of the radiationless deactivation pathways in UCNP, that are affected by their size1,2, surface chemistry,2 and microenvironment 3,4. In this respect, we discuss experimental requirements of an integrating sphere setup for absolute measurements of the excitation power density dependent quantum yield5,6 (UC(P)) in the VIS to IR spectral region. We report systematic studies of the influence of the UCNP size, surface ligands, and solvent on the UC(P), the up- and downconversion luminescence decay behavior, the power dependent intensities of the individual emission bands, and their slope factors. T2 - SPIE Photonics West CY - San Francisco, USA DA - 11.02.2016 KW - Upconversion KW - Quantum Yield PY - 2016 AN - OPUS4-38406 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Amouroux, B. A1 - Würth, Christian A1 - Roux, C. A1 - Eftekhari, A. A1 - Sliwa, M. A1 - Bouchet, A. A1 - Micheau, J.-C. A1 - Resch-Genger, Ute A1 - Coudret, C. T1 - Time-Resolved Rate Equation Analysis Disclose Kinetics Controlling Luminescence of Nanometer Tm-Upconverting Nanoparticles N2 - Upconversion luminescence of lanthanide-based upconversion nanoparticles (UCNPs) is a nonlinear step-wise process in which the consecutive absorption of multiple, low-energy photons results in the subsequent emission of a high-energy photon. The primary upconversion mechanism is energy transfer upconversion (ETU) from a sensitizer (Yb3+) to an activator (Tm3+). It requires the absorption of several excitation lowenergy photons by Yb3+, followed by the sequential energy transfer to Tm3+ions. Excited states relax to their ground states either radiatively by emitting a high-energy photon or non-radiatively by multiphonon relaxation through the crystalline host matrix. The time-resolved rise and decay luminescence curves of a set of five ultrasmall have been recorded under varying power near-infrared μs pulses. Six wavelengths have been used to monitor the evolution of the main Yb and Tm excited states. We use an average rate equations model to decipher the relationships between the compositional constraints and size of these ultrasmall UCNPs and the luminescence kinetic parameters. Several rate constants of ETU and other depopulation processes involving the multiple states of the Tm3+ energy scaffold have been retrieved from the simultaneous fit of the recorded curves. Their values have been interpreted by considering bulk and surface quenching, radiative and multi-phonon relaxations, and ion-to-ion hopping. Energy transfer between Yb3+ and Tm3+ is mainly occurring within neighbor atoms. The importance of mismatches on multiphonon relaxations, ETUs, and back-transfers has also been highlighted. For these numerical modeling, it appears that changing the composition and synthesis conditions with the aim to improve a single-specific parameter could remain a major challenge as this modification would automatically impact other properties with immediate consequences on UCNP dynamics. KW - Nano KW - Particle KW - Synthesis KW - Shell KW - Fluorescence KW - Lifetime KW - Decay kinetics KW - Method KW - Modelling KW - Quality assurance KW - Energy transfer KW - Upconversation PY - 2024 DO - https://doi.org/10.1021/acs.jpcc.4c04969 VL - 128 IS - 44 SP - 18836 EP - 18848 PB - ACS Publications AN - OPUS4-61645 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -