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TECHNIQUES & INSTRUMENTATION
                                             TCSPC                                        PUMP-PROBE                                 TCSPC-CSM
              Observing the local environment                      Observing energy transfer using                Observing molecular scale organization
                   of a molecular probe                            pump-probe spectroscopy                          and interactions

                       [Learn more]                                 [Learn more]                                     [Learn more]


                                             FRAP                                  LANGMUIR-BLODGETT TROUGH
                                 Observing translation diffusion and                    Forming monomolecular films and monitoring
                                mobility of probe molecules and films                         film formation and deposition

                                          [Learn more]                                               [Learn more]




TIME CORRELATED SINGLE PHOTON COUNTING INSTRUMENT


Schematic of the time-correlated single photon counting (TCSPC) instrument, showing source beam (green), sample (yellow), and detection components.




TIME-RESOLVED FLUORESCENCE MEASUREMENTS

Fluorescence lifetime and anisotropy decay data are acquired using a time-correlated single photon counting (TCSPC) instrument. The light source for this instrument is a synchronously pumped cavity dumped dye laser excited by the output of a passively mode locked Nd:YVO4 laser. The source laser produces 13 ps pulses at 80 MHz repetition rate. The dye laser is cavity dumped to control the repetition rate. The dye laser output can be turned from 430 to 850 nm depending on the dye and optics used and the excitation wavelength.

The fundamental excitation pulse from the dye laser is divided, with one portion of the pulse directed to a reference photodiode and the other portion directed to the sample.

Emission is collected using a 40x reflecting microscope objective. The colected emission is separated into polarization components parallel and perpendicular to the vertically polarized excitation pulse using a polarizing cube beam splitter. The parallel and perpendicular polarized signal components are detected simultaneously using microchannel plate photomultiplier tubes (PMT), each equipped with a subtractive double monochromator for wavelength selection.

The detection electronics resolve the parallel and perpendicular transients separately. The detection electronics include a time-to-amplitude converter (TAC) and a constant fraction discriminator (CFD) that temporally resolves the fluorescence signal for each polarization component. Data are collected using multichannel analyzers (MCAs), which are integral components of the detection electronics.








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