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Date: | Wed, 17 Mar 2004 11:52:38 +0100 |
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Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
I have another principle question regarding the pulse-streching, it is
mainly for general interest, but we run a directly coupled 2P laser also.
There is also glass in the microscope (at least the lens). Are there
estimates in how far this influences the peaks/pulses? What one has to
roughly expect in the sample, e.g. when the pulse had 50 or 100 fs before
entering the optical system ?
Arthur
At 03:59 17.03.2004, you wrote:
>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
>John Runions wrote:
>
> > Ok, I've got to ask. What is prechirp? I've never heard the term before
> >today and I want to be able to use it in conversation at parties. Over
> >and out, John.
>
>A fibre - like any glass - has dispersion which means that red
>light travels faster than blue. A femtosecond pulse has a spread
>of wavelengths (of a few nm) and since these travel at different
>speeds the pulse becomes longer by the end of the fibre. Prechirping
>means retarding the longer wavelengths so that the shorter ones
>are in front. Then they all come together again at the end of the
>fibre. Obviously the amount of prechirp has to be carefully matched
>to both the length of the fibre and the pulse length. A fiddly
>business and best avoided if possible!
>
> Guy
>
>Assoc. Prof. Guy Cox, ooOOOOOOoo
>E.M. Unit, F09 # oOOOO | | OOOOo #
>University of Sydney ### OOO| | | | | |OOO ###
>NSW 2006, Australia ### OOO | | | | | | OOO ###
>Ph: 02 9351 3176 ### OO | | | | | | | | OO ###
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> ==#####============================#####==
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>http://www.guycox.com ~~#####~~~~~~~~~~~~~~~~~~~~~~~~~~~~#####~~
Dr. Arthur Schuessler
Institute of Botany, FB10, TU Darmstadt
Schnittspahnstrasse 10
D-64287 Darmstadt
GERMANY
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