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Liisa Hirvonen edited figures/setup3/caption.tex
over 8 years ago
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\label{fig:setup} Schematic diagram of the anisotropy measurements. (a) Simplified diagram of the experimental setup. The sample solution was placed on a confocal microscope stage and excited with a polarised, pulsed laser. The fluorescence from the sample was reflected from a dichroic mirror
(DM), split into parallel and perpendicular polarisation directions with a polarising beam splitter (BS), (DM) and recorded with
two detectors D$_\parallel$ and D$_\perp$. detector (D). The anisotropy (c) was calculated from the fluorescence time decays
in parallel and perpendicular polarisation directions (b) with eq~\ref{eq:anisotropy}, and fitted with an exponential function (eq~\ref{eq:2expfit}).