Data for: Separating triplet exciton diffusion from triplet-triplet annihilation by the introduction of a mediator
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Solution-based samples used for UV-Vis and emission spectroscopy were prepared in an Mbraun glove box with oxygen and water levels less than 1 ppm. Solvents were degassed with argon prior to use, then prepared and sealed in cuvettes with a cap and PTFE septum. Measurements were performed immediately after preparation. UV-Visible spectra were recorded on a Perkin Elmer LAMBDA 950 instrument, while steady-state emission spectra were measured on an Edinburgh Instruments FLS 1000 spectrofluorometer with a Xenon lamp as the excitation source and a double monochromator to select the wavelength. Solid samples prepared as films on quartz glass were sealed prior to use in photophysical measurements to ensure the absence of oxygen. First exposed to vacuum while being loaded into an Mbraun glove box, samples were sealed under an inert atmosphere by affixing a second quartz plate over the film and sealing the edges using Loctite epoxy glue. Steady-state emission of TTA-UC samples was measured on an Edinburgh Instruments FLS 1000 spectrofluorometer. Either a 450W Xe arc lamp or a Coherent OBIS LX (690 nm) CW laser was used as an excitation source with variable power. Quantum yields were measured using the absolute method, utilizing an integrating sphere purchased from Edinburgh Instruments. Luminescence decays were recorded either by time-correlated single-photon counting (TCSPC) or Multichannel Scaling (MCS) on an Edinburgh FLS 1000 spectrofluorometer, using an MCP or PMT as the detector. An Edinburgh Instruments µF2 or pulsed diode laser (475 nm, 1 MHz) was used as the excitation source. Transient absorption was measured on an Edinburgh Instruments LP 980 spectrometer, with a SpectraPhysics Nd:YAG laser (705 nm, pulse width ~7 ns) coupled to a Spectra-Physics Primoscan optical parametric oscillator (OPO) as excitation. PMT (Hamamatsu R928) or image-intensified CCD camera (ICCD, Andor DH320T-25F-03) detectors were used for recording transient kinetics or spectra, respectively.
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Ansvarig institution/enhet:
Institutionen för kemi och molekylärbiologi
Medverkande:
- Anton M. Berghuis - Eindhoven University of Technology
- Andrew Danos - Durham University - Department of Physics
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