Loading…

Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions

Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a singl...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of chemical physics 1999-12, Vol.111 (24), p.10934-10956
Main Authors: Albrecht, Allison W., Hybl, John D., Gallagher Faeder, Sarah M., Jonas, David M.
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3
cites cdi_FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3
container_end_page 10956
container_issue 24
container_start_page 10934
container_title The Journal of chemical physics
container_volume 111
creator Albrecht, Allison W.
Hybl, John D.
Gallagher Faeder, Sarah M.
Jonas, David M.
description Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a single pulse are useful in optics. It is demonstrated experimentally that a frequency domain measurement using spectral interferometry can simultaneously measure phase shifts with an accuracy of 0.1 rad (2σ) and time delays with a precision of 40 attoseconds (2σ) for 25 femtosecond optical pulses. Envelope time delays are generated by pathlength differences in an interferometer. Constant spectral phase shifts are demonstrated by diffracting pulses from a variable phase volume diffraction grating. Experimental requirements for phase-resolved spectroscopy are outlined. The theory of phase-locked pulse pair techniques is reexamined, and it is concluded that linear experiments with phase-locked pulse pairs are completely equivalent to Fourier transform absorption spectroscopy and do not measure the refractive index or real part of the susceptibility. It is shown that Fourier sine and cosine transformations of truncated time domain signals which do not match the symmetry of the complete signal can produce a false dispersive susceptibility because they are equivalent to Kramers–Kronig inversion of finite bandwidth absorption data. A procedure for shifting π/2 phase-locked transients by a quarter cycle of delay to generate a transient with a π/2 spectral phase shift is given. Equations used to calculate femtosecond nonlinear optical signals have assumed carrier wave delays. Modifications to these equations are required when envelope delays are generated by interferometer pathlength differences and modified equations are given. The modified equations yield significantly different results for phase-resolved or interferometric experiments. In particular, the modified equations are needed to calculate indirectly (interferometrically) detected frequencies and the real and imaginary parts of two-dimensional Fourier transform spectra. The role of the refractive index and real part of the frequency domain susceptibility in nonlinear experiments with phase-locked pulse pairs is explored. It is concluded that experiments such as the heterodyne detected stimulated photon echo are insensitive to nonlinear refractive index changes under some circumstances. Finally, modifications of some
doi_str_mv 10.1063/1.480457
format article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1063_1_480457</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1063_1_480457</sourcerecordid><originalsourceid>FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3</originalsourceid><addsrcrecordid>eNotUMtKxDAUDaLgOAp-QpZuOiZtHq07GUYdGHCj65LHDa20TUkC2u_wh83MuLoXzuveg9A9JRtKRPVIN6wmjMsLtKKkbgopGnKJVoSUtGgEEdfoJsYvQgiVJVuh393PDKEfYUpqwLaPqZ9M6v2ENaRvgAnPnYqAY9e7FLGaLE6ZjS0MaolPeD_OQ2_UURGx8wE7GJOPYHxmxhlMCj4aPy8nqfEdhByVlykDA_YOmw7G7DDgAOqUHG_RlVNDhLv_uUafL7uP7VtxeH_db58PhSkbmgrODONWlY2lspKaG02dK5WqlWNG5-8aXTnOa221FaqWQmjdcMlUxRlABtfo4exr8o0xgGvn3IQKS0tJeyyzpe25zOoPCNNrzw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions</title><source>American Institute of Physics (AIP) Publications</source><source>American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list)</source><creator>Albrecht, Allison W. ; Hybl, John D. ; Gallagher Faeder, Sarah M. ; Jonas, David M.</creator><creatorcontrib>Albrecht, Allison W. ; Hybl, John D. ; Gallagher Faeder, Sarah M. ; Jonas, David M.</creatorcontrib><description>Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a single pulse are useful in optics. It is demonstrated experimentally that a frequency domain measurement using spectral interferometry can simultaneously measure phase shifts with an accuracy of 0.1 rad (2σ) and time delays with a precision of 40 attoseconds (2σ) for 25 femtosecond optical pulses. Envelope time delays are generated by pathlength differences in an interferometer. Constant spectral phase shifts are demonstrated by diffracting pulses from a variable phase volume diffraction grating. Experimental requirements for phase-resolved spectroscopy are outlined. The theory of phase-locked pulse pair techniques is reexamined, and it is concluded that linear experiments with phase-locked pulse pairs are completely equivalent to Fourier transform absorption spectroscopy and do not measure the refractive index or real part of the susceptibility. It is shown that Fourier sine and cosine transformations of truncated time domain signals which do not match the symmetry of the complete signal can produce a false dispersive susceptibility because they are equivalent to Kramers–Kronig inversion of finite bandwidth absorption data. A procedure for shifting π/2 phase-locked transients by a quarter cycle of delay to generate a transient with a π/2 spectral phase shift is given. Equations used to calculate femtosecond nonlinear optical signals have assumed carrier wave delays. Modifications to these equations are required when envelope delays are generated by interferometer pathlength differences and modified equations are given. The modified equations yield significantly different results for phase-resolved or interferometric experiments. In particular, the modified equations are needed to calculate indirectly (interferometrically) detected frequencies and the real and imaginary parts of two-dimensional Fourier transform spectra. The role of the refractive index and real part of the frequency domain susceptibility in nonlinear experiments with phase-locked pulse pairs is explored. It is concluded that experiments such as the heterodyne detected stimulated photon echo are insensitive to nonlinear refractive index changes under some circumstances. Finally, modifications of some equations used in the theory of coherent control are needed to match theory with experimental practice.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.480457</identifier><language>eng</language><ispartof>The Journal of chemical physics, 1999-12, Vol.111 (24), p.10934-10956</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3</citedby><cites>FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,782,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Albrecht, Allison W.</creatorcontrib><creatorcontrib>Hybl, John D.</creatorcontrib><creatorcontrib>Gallagher Faeder, Sarah M.</creatorcontrib><creatorcontrib>Jonas, David M.</creatorcontrib><title>Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions</title><title>The Journal of chemical physics</title><description>Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a single pulse are useful in optics. It is demonstrated experimentally that a frequency domain measurement using spectral interferometry can simultaneously measure phase shifts with an accuracy of 0.1 rad (2σ) and time delays with a precision of 40 attoseconds (2σ) for 25 femtosecond optical pulses. Envelope time delays are generated by pathlength differences in an interferometer. Constant spectral phase shifts are demonstrated by diffracting pulses from a variable phase volume diffraction grating. Experimental requirements for phase-resolved spectroscopy are outlined. The theory of phase-locked pulse pair techniques is reexamined, and it is concluded that linear experiments with phase-locked pulse pairs are completely equivalent to Fourier transform absorption spectroscopy and do not measure the refractive index or real part of the susceptibility. It is shown that Fourier sine and cosine transformations of truncated time domain signals which do not match the symmetry of the complete signal can produce a false dispersive susceptibility because they are equivalent to Kramers–Kronig inversion of finite bandwidth absorption data. A procedure for shifting π/2 phase-locked transients by a quarter cycle of delay to generate a transient with a π/2 spectral phase shift is given. Equations used to calculate femtosecond nonlinear optical signals have assumed carrier wave delays. Modifications to these equations are required when envelope delays are generated by interferometer pathlength differences and modified equations are given. The modified equations yield significantly different results for phase-resolved or interferometric experiments. In particular, the modified equations are needed to calculate indirectly (interferometrically) detected frequencies and the real and imaginary parts of two-dimensional Fourier transform spectra. The role of the refractive index and real part of the frequency domain susceptibility in nonlinear experiments with phase-locked pulse pairs is explored. It is concluded that experiments such as the heterodyne detected stimulated photon echo are insensitive to nonlinear refractive index changes under some circumstances. Finally, modifications of some equations used in the theory of coherent control are needed to match theory with experimental practice.</description><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNotUMtKxDAUDaLgOAp-QpZuOiZtHq07GUYdGHCj65LHDa20TUkC2u_wh83MuLoXzuveg9A9JRtKRPVIN6wmjMsLtKKkbgopGnKJVoSUtGgEEdfoJsYvQgiVJVuh393PDKEfYUpqwLaPqZ9M6v2ENaRvgAnPnYqAY9e7FLGaLE6ZjS0MaolPeD_OQ2_UURGx8wE7GJOPYHxmxhlMCj4aPy8nqfEdhByVlykDA_YOmw7G7DDgAOqUHG_RlVNDhLv_uUafL7uP7VtxeH_db58PhSkbmgrODONWlY2lspKaG02dK5WqlWNG5-8aXTnOa221FaqWQmjdcMlUxRlABtfo4exr8o0xgGvn3IQKS0tJeyyzpe25zOoPCNNrzw</recordid><startdate>19991222</startdate><enddate>19991222</enddate><creator>Albrecht, Allison W.</creator><creator>Hybl, John D.</creator><creator>Gallagher Faeder, Sarah M.</creator><creator>Jonas, David M.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19991222</creationdate><title>Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions</title><author>Albrecht, Allison W. ; Hybl, John D. ; Gallagher Faeder, Sarah M. ; Jonas, David M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Albrecht, Allison W.</creatorcontrib><creatorcontrib>Hybl, John D.</creatorcontrib><creatorcontrib>Gallagher Faeder, Sarah M.</creatorcontrib><creatorcontrib>Jonas, David M.</creatorcontrib><collection>CrossRef</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Albrecht, Allison W.</au><au>Hybl, John D.</au><au>Gallagher Faeder, Sarah M.</au><au>Jonas, David M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions</atitle><jtitle>The Journal of chemical physics</jtitle><date>1999-12-22</date><risdate>1999</risdate><volume>111</volume><issue>24</issue><spage>10934</spage><epage>10956</epage><pages>10934-10956</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>Two different definitions of phase shifts and time delays are contrasted and shown to match different experimental methods of generating delayed pulses. Phase shifts and time delays are usually defined in terms of a carrier wave in magnetic resonance, but definitions based on the envelope of a single pulse are useful in optics. It is demonstrated experimentally that a frequency domain measurement using spectral interferometry can simultaneously measure phase shifts with an accuracy of 0.1 rad (2σ) and time delays with a precision of 40 attoseconds (2σ) for 25 femtosecond optical pulses. Envelope time delays are generated by pathlength differences in an interferometer. Constant spectral phase shifts are demonstrated by diffracting pulses from a variable phase volume diffraction grating. Experimental requirements for phase-resolved spectroscopy are outlined. The theory of phase-locked pulse pair techniques is reexamined, and it is concluded that linear experiments with phase-locked pulse pairs are completely equivalent to Fourier transform absorption spectroscopy and do not measure the refractive index or real part of the susceptibility. It is shown that Fourier sine and cosine transformations of truncated time domain signals which do not match the symmetry of the complete signal can produce a false dispersive susceptibility because they are equivalent to Kramers–Kronig inversion of finite bandwidth absorption data. A procedure for shifting π/2 phase-locked transients by a quarter cycle of delay to generate a transient with a π/2 spectral phase shift is given. Equations used to calculate femtosecond nonlinear optical signals have assumed carrier wave delays. Modifications to these equations are required when envelope delays are generated by interferometer pathlength differences and modified equations are given. The modified equations yield significantly different results for phase-resolved or interferometric experiments. In particular, the modified equations are needed to calculate indirectly (interferometrically) detected frequencies and the real and imaginary parts of two-dimensional Fourier transform spectra. The role of the refractive index and real part of the frequency domain susceptibility in nonlinear experiments with phase-locked pulse pairs is explored. It is concluded that experiments such as the heterodyne detected stimulated photon echo are insensitive to nonlinear refractive index changes under some circumstances. Finally, modifications of some equations used in the theory of coherent control are needed to match theory with experimental practice.</abstract><doi>10.1063/1.480457</doi><tpages>23</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9606
ispartof The Journal of chemical physics, 1999-12, Vol.111 (24), p.10934-10956
issn 0021-9606
1089-7690
language eng
recordid cdi_crossref_primary_10_1063_1_480457
source American Institute of Physics (AIP) Publications; American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list)
title Experimental distinction between phase shifts and time delays: Implications for femtosecond spectroscopy and coherent control of chemical reactions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T18%3A08%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Experimental%20distinction%20between%20phase%20shifts%20and%20time%20delays:%20Implications%20for%20femtosecond%20spectroscopy%20and%20coherent%20control%20of%20chemical%20reactions&rft.jtitle=The%20Journal%20of%20chemical%20physics&rft.au=Albrecht,%20Allison%20W.&rft.date=1999-12-22&rft.volume=111&rft.issue=24&rft.spage=10934&rft.epage=10956&rft.pages=10934-10956&rft.issn=0021-9606&rft.eissn=1089-7690&rft_id=info:doi/10.1063/1.480457&rft_dat=%3Ccrossref%3E10_1063_1_480457%3C/crossref%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c291t-54c45da29d1737b5cb1ff2aa8af4cb7249b3f558bdbd6a8766bb9574a354ee9b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true