| DOI | Resolve DOI: https://doi.org/10.1109/CLEOE.2011.5942682 |
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| Author | Search for: Wörner, H.-J.1; Search for: Bertrand, J.B.1; Search for: Kartashov, D.V.1; Search for: Corkum, P.B.1; Search for: Villeneuve, D.M.1 |
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| Affiliation | - National Research Council of Canada
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| Format | Text, Article |
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| Conference | 2011 Conference on Lasers and Electro-Optics Europe and 12th European Quantum Electronics Conference, CLEO EUROPE/EQEC 2011, 22 May 2011 through 26 May 2011, Munich |
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| Subject | Common problems; Excited molecules; Femtochemistry; Femtoseconds; High harmonics; Laser induced; Probe wavelength; Recollision; Spectral selection; Chemical reactions; Diffraction; Molecules; Optics; Quantum electronics; X ray diffraction; Electron optics |
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| Abstract | Using the tools of femtosecond X-ray diffraction [1], electron diffraction [2] and laser-induced recollision [3], scientists are developing new methods to image chemical reactions as they occur. However, all of these methods face a common problem - only a small fraction of the molecules can be excited with an ultrashort pulse. When this problem was confronted in femtochemistry, a careful selection of the probe wavelength provided a way to discriminate excited molecules from unexcited molecules. Spectral selection is not available for any of these new methods. © 2011 IEEE. |
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| Publication date | 2011 |
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| In | |
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| Language | English |
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| Peer reviewed | Yes |
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| NPARC number | 21276258 |
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| Export citation | Export as RIS |
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| Report a correction | Report a correction (opens in a new tab) |
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| Record identifier | 568c92bb-67d8-4c40-a1b1-ef9ecb255598 |
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| Record created | 2015-09-28 |
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| Record modified | 2020-04-21 |
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