howto:how_to_measure_the_instrument_response_function_irf
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howto:how_to_measure_the_instrument_response_function_irf [2022/01/24 10:22] – [IRF measurement with KI and Erythrosine B] rezvani | howto:how_to_measure_the_instrument_response_function_irf [2023/02/23 07:05] – lan | ||
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==== Make sure that the detection count rate is much lower than the count rate used for fluorescence decay measurement. ==== | ==== Make sure that the detection count rate is much lower than the count rate used for fluorescence decay measurement. ==== | ||
- | Diluting the scattering solution is better than using grey filters. Ideal is when the decay and the IRF are recorded at the same [[glossary: | + | **Note: |
If the IRF should be measured on a microscope system with SPAD detectors, in the UV range also the Raman-scattering of water can be used. E.g. the Raman scattering can be recorded with a HQ480/40 bandpass filter, if a 405nm diode is used. This method is less suited for long wavelengths, | If the IRF should be measured on a microscope system with SPAD detectors, in the UV range also the Raman-scattering of water can be used. E.g. the Raman scattering can be recorded with a HQ480/40 bandpass filter, if a 405nm diode is used. This method is less suited for long wavelengths, |
howto/how_to_measure_the_instrument_response_function_irf.txt · Last modified: 2023/09/07 22:55 by peter