Relevant bibliographies by topics / Coherent spectroscopy

Academic literature on the topic 'Coherent spectroscopy'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Coherent spectroscopy"

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Carton, W. R. S. "Coherent atomic spectroscopy." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 31, no. 1-2 (April 1988): 93–101. http://dx.doi.org/10.1016/0168-583x(88)90400-4.

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Kim, Young L., Yang Liu, Vladimir M. Turzhitsky, Hemant K. Roy, Ramesh K. Wali, and Vadim Backman. "Coherent backscattering spectroscopy." Optics Letters 29, no. 16 (August 13, 2004): 1906. http://dx.doi.org/10.1364/ol.29.001906.

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Chen, Peter C. "An Introduction to Coherent Multidimensional Spectroscopy." Applied Spectroscopy 70, no. 12 (December 2016): 1937–51. http://dx.doi.org/10.1177/0003702816669730.

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Coherent multidimensional spectroscopy is a field that has drawn much attention as an optical analogue to multidimensional nuclear magnetic resonance imaging. Coherent multidimensional spectroscopic techniques produce spectra that show the magnitude of an optical signal as a function of two or more pulsed laser frequencies. Spectra can be collected in either the frequency or the time domain. In addition to improving resolution and overcoming spectral congestion, coherent multidimensional spectroscopy provides the ability to investigate and conduct studies based upon the relationship between different peaks. The purpose of this paper is to provide a general introduction to the area of coherent multidimensional spectroscopy, to provide a brief overview of current experimental approaches, and to discuss some emerging developments in this relatively young field.
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Dawlaty, Jahan M., Akihito Ishizaki, Arijit K. De, and Graham R. Fleming. "Microscopic quantum coherence in a photosynthetic-light-harvesting antenna." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 370, no. 1972 (August 13, 2012): 3672–91. http://dx.doi.org/10.1098/rsta.2011.0207.

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We briefly review the coherent quantum beats observed in recent two-dimensional electronic spectroscopy experiments in a photosynthetic-light-harvesting antenna. We emphasize that the decay of the quantum beats in these experiments is limited by ensemble averaging. The in vivo dynamics of energy transport depends upon the local fluctuations of a single photosynthetic complex during the energy transfer time (a few picoseconds). Recent analyses suggest that it remains possible that the quantum-coherent motion may be robust under individual realizations of the environment-induced fluctuations contrary to intuition obtained from condensed phase spectroscopic measurements and reduced density matrices. This result indicates that the decay of the observed quantum coherence can be understood as ensemble dephasing. We propose a fluorescence-detected single-molecule experiment with phase-locked excitation pulses to investigate the coherent dynamics at the level of a single molecule without hindrance by ensemble averaging. We discuss the advantages and limitations of this method. We report our initial results on bulk fluorescence-detected coherent spectroscopy of the Fenna–Mathews–Olson complex.
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Wright, John C. "Multiresonant Coherent Multidimensional Spectroscopy." Annual Review of Physical Chemistry 62, no. 1 (May 5, 2011): 209–30. http://dx.doi.org/10.1146/annurev-physchem-032210-103551.

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Cundiff, Steven T., and Shaul Mukamel. "Optical multidimensional coherent spectroscopy." Physics Today 66, no. 7 (July 2013): 44–49. http://dx.doi.org/10.1063/pt.3.2047.

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Tarasek, Matthew R., David J. Goldfarb, and James G. Kempf. "Coherent NMR Stark spectroscopy." Journal of Magnetic Resonance 214 (January 2012): 346–51. http://dx.doi.org/10.1016/j.jmr.2011.11.018.

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Mukamel, Shaul, Yoshitaka Tanimura, and Peter Hamm. "Coherent Multidimensional Optical Spectroscopy." Accounts of Chemical Research 42, no. 9 (September 15, 2009): 1207–9. http://dx.doi.org/10.1021/ar900227m.

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Zadkov, Viktor N., P. V. Kozlov, S. A. Losev, and V. A. Pavlov. "Coherent shock-wave spectroscopy." Soviet Journal of Quantum Electronics 18, no. 1 (January 31, 1988): 77–81. http://dx.doi.org/10.1070/qe1988v018n01abeh010590.

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Wright, John C. "Coherent multidimensional vibrational spectroscopy." International Reviews in Physical Chemistry 21, no. 2 (April 2002): 185–255. http://dx.doi.org/10.1080/01442350210124506.

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Dissertations / Theses on the topic "Coherent spectroscopy"

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Beaman, R. A. "Two beam coherent spectroscopy." Thesis, Cardiff University, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379609.

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Quilter, John Howard. "Coherent spectroscopy of single quantum dots." Thesis, University of Sheffield, 2014. http://etheses.whiterose.ac.uk/7711/.

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This thesis presents experiments carried out into the coherent properties of charge carriers confined within a single InGaAs/GaAs quantum dot. Specifically the ground state - single exciton qubit system is controlled with ultrafast optical pulses and then the population of the dot is measured by a high-sensitivity photocurrent detection technique. There are two principal results of these experiments, firstly by modulating the bias applied to the quantum dot diode, the detection efficiency of the photocurrent measurement technique is enhanced. The enhancement is possible as the modulated bias allows fast switching of the voltage-dependent carrier tunneling rates. Secondly, when the transition is addressed by an intense, positively detuned laser, the qubit system can be driven to a population inversion. This occurs due to phonon-assisted relaxation of the optical dressed states of the system. Here, the rapid thermalization due to the exciton-phonon interaction actually enables the population inversion, instead of simply being a source of decoherence.
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Viranna, Narendra Balaguru. "Coherent anti-Stokes Raman spectroscopy of diamond." Master's thesis, University of Cape Town, 1997. http://hdl.handle.net/11427/26229.

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Experiments were performed to investigate Coherent Anti-Stokes Raman Scattering (CARS) in diamond. Aspects of this type of non-linear scattering are presented theoretically, and various experimental configurations were attempted in order to study them. These included the dependence of the CARS signal intensity on the intensities of the two exciting frequency-doubled Nd:YAG (pump) and dye (Stokes) lasers, the variation of the CARS signal polarization as a function of the lasers' polarization, and the dependence of the CARS signal intensity on the phase mismatch of the laser beams. The phase mismatch measurement confirmed the predicted sinc² nature of the CARS signal intensity, while· the polarization measurements provided new information on the ratio of the non-vanishing components of the cubic susceptibility x³ of diamond. The CARS signal intensity was found to change linearly with the dye laser intensity and quadratically with the Nd: Y AG laser intensity. The CARS signal was found at the predicted 1332 cm⁻¹ shift from the doubled Nd:YAG emission, and its linewidth of 1.2 cm⁻¹ is in agreement with the spontaneous Raman linewidth.The spectral data were fitted to a modified Voigt profile containing the non-resonant cubic susceptibility contribution, and this allowed us to establish the ratio of the resonant and non-resonant parts of x³. An attempt to generate Stimulated Raman Scattering in diamond was unsuccessful.
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Kirkbride, James M. R. "Coherent transient spectroscopy with quantum cascade lasers." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:c7b897e5-052f-4c15-a3c9-f95ca3b56d70.

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This thesis is concerned with coherent effects in high resolution mid-infrared gas phase spectroscopy using quantum cascade lasers (QCLs). An introductory chapter explains the importance of QCLs as radiation sources in the mid-infrared region of the spectrum and goes on to detail their development and structure. A discussion of coherent effects in spectroscopy follows, leading into the second chapter which discusses the theories relevant to the experimental sections of the thesis. In chapter 2 the theory underpinning direct and velocity selective, Doppler-free spectroscopy is discussed and a density matrix formalism is followed to derive the equations of motion that govern coherent excitation effects in two-level systems. In the final part of the chapter this treatment is extended to three-level systems. The equations derived in this chapter form the basis of quantitative interpretations of the phenomena observed in experimental data and presented in the remainder of the thesis. In chapter 3 the characterisation of a high power, narrow linewidth QCL is carried out. This laser is then used to perform direct and sub-Doppler resolution spectroscopy on NO, demonstrating non-linear absorption at high laser intensities and providing a measurement of the laser linewidth in the limit of slow frequency tuning. As the slow tuning rate increases, evidence of coherent transient effects is presented and density matrix theory used to model this behaviour. The data presented include the first observations of asymmetric Lamb dips and the onset of rapid passage oscillations from a Lamb dip. Pump-probe experiments on NO, utilising two cw QCLs are presented in chapter 4. The high level of velocity selection afforded by QCL excitation leads to coherent transient signals at far lower probe scan rates than previously reported. The effect of altering both the scan rate and the gas pressure and the importance of hyperfine structure are presented. A radio frequency noise source applied to one of the lasers is shown to broaden the laser linewidth, leading to rapid dephasing. A two-colour polarisation spectroscopy experiment is also presented which allows the measurement of both the absorption and the Doppler-free dispersion signals and the three-level density matrix formalism presented at the end of chapter 2 used to model the non-linear response of the system. The final chapter details the use of an acousto-optic modulator to create a pulse of mid-IR light using a cw QCL and the application of this to time resolved pump-probe spectroscopy. This capability suggests the prospect of achieving coherent population transfer by stimulated Raman adiabatic passage (STIRAP) using two such pulses. Simulations based on a simple three-level model and including Zeeman coherences are presented, which take the measured properties of the lasers used in this thesis as inputs to predict the potential population transfer achievable in NO as well as providing useful information about the angular momentum polarisation of the excited molecules. An experimental realisation of STIRAP would require the lasers to be stabilised, and so the final part of the chapter details experimental attempts to achieve stabilisation of an external cavity QCL, and suggests future avenues for improved implementation.
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Turner, Daniel Burton. "Investigating exciton correlations using coherent multidimensional optical spectroscopy." Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/62037.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2010.
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Vita. Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (p. 153-166).
The optical measurements described in this thesis reveal interactions among bound electron-hole pairs known as excitons in a semiconductor nanostructure. Excitons are quasiparticles that can form when light is absorbed by a semiconductor. Exciton interactions gained prominence in the 1980s when unexpected signals were observed in studies of carrier dynamics. The presence of exciton interactions in semiconductors motivated an ongoing, focused research effort not only because the materials had valuable commercial applications but also because the interactions could be used to test fundamental theories of many-body physics. Laser light provides a coherent electric field with a well defined phase. In linear spectroscopy, an electric field that is resonant with an exciton transition will induce coherent oscillations of electronic charge density. The charges will oscillate at the transition frequency with a well defined phase, and these oscillations will radiate a signal that has an amplitude proportional to the incident field amplitude and has the same direction as the incident light. If the laser light is intense, its field may induce a high density of excitons, and the field can interact with those excitons to induce transitions to higher-energy states composed of multiple interacting excitons. Many-body interactions among the excitons can predictably modify--or unpredictably scramble--the quantum phase of the exciton. The interactions can produce signals that have amplitudes proportional to high powers of the incident field amplitude, and the signal fields often propagate in directions different than the incident field. The signal fields contain information--often encoded in their phases--that can reveal the nature of the higher-energy states and the many-body interactions that produced them. Thus, many-body interaction studies rely on measurements of exciton phases that are reflected in the optical phases of coherent signals. These measurements require a tool that can detect optical coherence before the exciton phases are scrambled by the environment. Coherent ultrafast optical spectroscopy is that tool. The spectra displayed in this work were measured by an experimental apparatus that separates the electric fields as needed into different laser beams with controllable directions; it controls the optical phase, arrival time, and polarization of the femtosecond light pulse(s) in each of those beams; it then recombines all of the beams at the 5 sample to generate the signal field; and finally it measures the signal field, including its phase. Using this instrument, we isolated--with a high degree of selectivity--signals that arose from different numbers of field interactions and from different microscopic origins using various beam geometries and pulse timing sequences. In this thesis, we present electronic spectra measured at varying orders in the electric field to isolate and measure the properties of excitons and their many-body interactions. As the number of electric fields is increased and the resulting higherorder signals are generated, interactions involving increasing numbers of particles can be measured. The vast majority of previous work focused on the interactions manifest in third-order signals. This thesis not only includes new insights gained from third-order signals, but also includes new phenomena observed in fifth-order and seventh-order signals. We measure signals due to four-particle correlations in the form of bound biexcitons and unbound-but-correlated exciton pairs. We also measure signals due to six-particle correlations in the form of bound triexcitons. Although we searched for them, there were no signals due to eight-particle correlations, indicating that the set of multiexciton states truncates. We thus measured the properties and the extent of many-body interactions in this system. The spectra presented here reveal a large set of excitonic many-body interactions in GaAs quantum wells and answer questions about the many-body interactions posed decades ago. The optical apparatus constructed to perform these measurements will soon be used to measure correlations in a range of systems, including other semiconductors and their nanostructures, molecular aggregates, molecules, and photosynthetic complexes. Because future technologies such as entangled photon sources, advanced photovoltaics, and quantum information processing will rely on these types of materials and their many-body correlations, it is important to develop techniques to measure their microscopic interactions directly.
by Daniel Burton Turner.
Ph.D.
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Somma, Carmine. "Coherent Multidimensional Off-resonant THz Spectroscopy on Semiconductors." Doctoral thesis, Humboldt-Universität zu Berlin, 2017. http://dx.doi.org/10.18452/18512.

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Zum ersten Mal konnte die kohärente Erzeugung von ultrakurzen Pulsen mit Feld stärken im MV/cm Bereich mit einem Spektralbereich von 0.1-30 THz im organischen Kristall DSTMS. Kohärente mehrdimensionale Terahertzspektroskopie (CMTS) hat sich zu einer wichtigen Methode zur Untersuchung der niederenergetischen Anregungen von Halbleitern and deren kohärenter Dynamik entwickelt. Eine neuartige CMTS Methode mit drei phasenstarren, zueinander zeitverzögerten Terahertzpulsen wurde entwickelt. Sie beruht auf der kollinearen Wechselwirkung der Pulse mit der Probe, sodass verschiedene Ordnungen des nichtlinearen Signals in gleicher Richtung emittiert werden und deshalb gleichzeitig gemessen werden können. Amplitude und Phase des nichtlinearen Signals können durch elektro-optisches Abtasten vermessen werden, wodurch die zeitliche Entwicklung der kohärenten Wechselwirkungen in Echtzeit untersucht werden kann. CMTS erlaubt zusätzlich die eindeutige Zerlegung des nichtlinearen Signals in die verschiedenen nichtlinearen Ordnungen in der jeweiligen mehrdimensionalen Frequenzdomäne. Die nichtlineare, nicht-resonante Antwort zweier undotierter Halbleiter, des Ferroelektrikums Lithiumniobat (LiNbO3) und Indiumantimonids (InSb) kann mit dieser neuartigen Methode untersucht werden. In LiNbO3 wird das nichtlineare Signal durch einen Femtosekunden nichtlinearen Verschiebestrom (SC) hervorgerufen. SC wird durch die gebrochene Inversionssymmetrie des Kristalls in Verbindung mit einer ultraschnellen Dephasierung der feldinduzierten, kohärenten interband-Polarisation hervorgerufen. Die Dephasierung der interband-Polarisation erlaubt das Tunneln von Elektronen vom Valenzband in das Leitungsband. In InSb wird das kohärente Signal durch sowohl zwei-Phonen als auch zwei-Photonen interband-Anregungen erzeugt. Die impulsive Anregung einer kohärenten zwei-Phononen Polarisation wird durch das große Übergangsdipolmoment von InSb verstärkt, was zu deutlich größeren Amplituden der Polarisation als im linearem Regime führt.
For the first time, the coherent generation of ultrashort MV/cm field pulses with a spectrum covering the frequency range 0.1-30 THz is demonstrated in the organic crystal DSTMS. Coherent multidimensional terahertz spectroscopy (CMTS) has become a prominent technique for, e.g., driving low-energy excitations in semiconductors and monitoring their coherent dynamics. A novel CMTS technique using three phase-locked inter-delayed THz pulses is implemented. It relies on a collinear interaction of the pulses with a sample, so that different contributions to the nonlinear signal are emitted in the same direction, and thus can be measured all at once. Phase-resolved detection by electro-optic sampling allows for measuring amplitude and absolute phase of the nonlinear signal, thereby enabling to investigate the evolution of coherent interactions between quantum excitations in real time. In CMTS, the nonlinear signal is dissected into the distinct nonlinear contributions in the corresponding multidimensional frequency domain. This novel technique is applied to study the nonlinear off-resonant response of two undoped bulk semiconductors, the wide-bandgap ferroelectric lithium niobate (LiNbO3) and the narrow-bandgap indium antimonide (InSb). In LiNbO3, the nonlinear signal is generated by a femtosecond nonlinear shift current (SC), a distinctive characteristic of the bulk photovoltaic effect. The SC stems from the lack of inversion symmetry and the ultrafast dephasing of the field-induced interband coherent polarization due to a sufficiently high decoherence rate, which enables tunneling of electrons from the valence to the conduction band. In InSb, the nonlinear signal is caused by the coherent response on both the two-phonon and two-photon interband excitations. The impulsive generation of the two-phonon coherent polarization is enhanced by the large interband transition dipole of InSb, resulting in much larger polarization amplitudes than in the regime of linear response.
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Branderhorst, Matthijs Pieter Arie. "Coherent control of decoherence." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670035.

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Jerebtsov, Serguei Nikolaevich. "Femtosecond time-resolved spectroscopy of coherent oscillations in nanomaterials." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1358.

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Arlt, Sebastian. "Coherent femtosecond spectroscopy of exciton-continuum interaction in semiconductors /." Zürich, 1999. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=13475.

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Stowe, Matthew C. "Direct frequency comb spectroscopy and high-resolution coherent control." Connect to online resource, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3315768.

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Books on the topic "Coherent spectroscopy"

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Marowsky, Gerd, and Valery V. Smirnov, eds. Coherent Raman Spectroscopy. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-77194-1.

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Cho, Minhaeng, ed. Coherent Multidimensional Spectroscopy. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9753-0.

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Marowsky, Gerd. Coherent Raman Spectroscopy: Recent Advances. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992.

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Shore, Bruce W. The theory of coherent atomic excitation. New York: Wiley, 1990.

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International, Symposium on Coherent Raman Spectroscopy (1990 Samarkand Uzbekistan). Coherent Raman spectroscopy: Recent advances : proceedings of the International Symposium on Coherent Raman Spectroscopy, Samarkand, USSR, September 18-20, 1990. Berlin: Springer-Verlag, 1992.

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Spectroscopy with coherent radiation: Selected papers of Norman F. Ramsey with commentary. Singapore: World Scientific, 1998.

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Cheng, Ji-Xin, and Xiaoliang Sunney Xie. Coherent Raman scattering microscopy. Boca Raton: CRC Press, 2013.

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service), SpringerLink (Online, ed. Studying Atomic Dynamics with Coherent X-rays. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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PECS 2005 (8th 2005 Korolev, Russia). Photon echo and coherent spectroscopy 2005: 18-25 September 2005, Kaliningrad, Russia. Edited by Samart︠s︡ev V. V, Society of Photo-optical Instrumentation Engineers., and Rossiĭskai︠a︡ akademii︠a︡ nauk. Bellingham, Wash., USA: SPIE, 2006.

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Phillips, R. T. Coherent optical interactions in semiconductors. Boston, MA: Springer, 1994.

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Book chapters on the topic "Coherent spectroscopy"

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Demtröder, Wolfgang. "Coherent Spectroscopy." In Laser Spectroscopy, 648–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-08260-7_12.

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Demtröder, Wolfgang. "Coherent Spectroscopy." In Advanced Texts in Physics, 679–724. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05155-9_12.

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Demtröder, Wolfgang. "Coherent Spectroscopy." In Laser Spectroscopy 2, 369–428. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44641-6_7.

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Zinth, Wolfgang, and Wolfgang Kaiser. "Ultrafast Coherent Spectroscopy." In Topics in Applied Physics, 235–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-662-02546-8_6.

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Prokhorov, A. M. "Coherent Laser Spectroscopy." In Laser Spectroscopy VIII, 225–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-540-47973-4_63.

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Zinth, Wolfgang, and Wolfgang Kaiser. "Ultrafast coherent spectroscopy." In Topics in Applied Physics, 235–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/bfb0070983.

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Nelson, Keith A., and Erich P. Ippen. "Femtosecond Coherent Spectroscopy." In Advances in Chemical Physics, 1–35. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470141243.ch1.

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Harel, Elad. "Four-Dimensional Coherent Spectroscopy." In Springer Series in Optical Sciences, 105–24. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9753-0_5.

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Zinth, W., and W. Kaiser. "Ultrafast Coherent Raman Spectroscopy." In Springer Proceedings in Physics, 166–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72758-0_12.

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Shah, Jagdeep. "Coherent Spectroscopy of Semiconductors." In Ultrafast Spectroscopy of Semiconductors and Semiconductor Nanostructures, 27–131. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-03770-6_2.

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Conference papers on the topic "Coherent spectroscopy"

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Ozga, K., I. V. Kityk, A. M. El Naggar, A. Albassam, and J. Jedryka. "Novel optically coherent sensors for nonlinear optical coherent monitoring of pollutions." In Fourier Transform Spectroscopy. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/fts.2019.jw3a.21.

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Ye, Jun. "Advances in Coherent Optical Spectroscopy." In Coherent Optical Technologies and Applications. Washington, D.C.: OSA, 2006. http://dx.doi.org/10.1364/cota.2006.cfa1.

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Pazmino-Betancourth, Mauro, Victor Ochoa-Gutierrez, and David Childs. "Organic polymers classification using QCL spectroscopy." In Mid-Infrared Coherent Sources. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/mics.2020.mf1c.6.

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Cundiff, Steven T. "Coherent Spectroscopy of Semiconductors." In Latin America Optics and Photonics Conference. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/laop.2016.ltu3d.2.

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Kiefer, Wolfgang, T. Chen, M. Heid, A. Materny, M. Schmitt, T. Siebert, and A. Vierheilig. "Femtosecond coherent Raman spectroscopy." In XVII International Conference on Coherent and Nonlinear Optics (ICONO 2001), edited by Andrey Y. Chikishev, Valentin A. Orlovich, Anatoly N. Rubinov, and Alexei M. Zheltikov. SPIE, 2002. http://dx.doi.org/10.1117/12.468878.

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Cundiff, Steven T. "Coherent Spectroscopy of Semiconductors." In CLEO: QELS_Fundamental Science. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/cleo_qels.2016.fw4n.1.

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Vieira, Francisco S., Flavio C. Cruz, David F. Plusquellic, and Scott A. Diddams. "Adaptive Resolution Terahertz Dual Frequency Comb Spectroscopy." In Mid-Infrared Coherent Sources. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/mics.2016.mt1c.1.

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Vasiljev, V. A. "Optocapacity spectroscopy method." In PECS'2001: Photon Echo and Coherent Spectroscopy, edited by Vitaly V. Samartsev. SPIE, 2001. http://dx.doi.org/10.1117/12.447942.

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Butcher, R. J. "Hyperfine saturation spectroscopy." In International Conference on Coherent and Nonlinear Optics, edited by Vladimir V. Shuvalov and Alexei M. Zheltikov. SPIE, 1996. http://dx.doi.org/10.1117/12.239791.

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Li, Hebin. "Multi-Quantum Optical Two-dimensional Coherent Spectroscopy of Many-Body Quantum Coherence." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.th3a.6.

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We have implemented multi-quantum (up to eight-quantum) optical two-dimensional coherent spectroscopy in a collinear setup based on acousto-optic phase modulators. The technique has been demonstrated to detect multi-quantum coherence of up to eight atoms.
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Reports on the topic "Coherent spectroscopy"

1

Mukamel, Shaul, Frantisek Sanda, Upendra Harbola, Ravi Venkatramani, and Dmitri Varonine. Coherent Quantum Control of Multidimensional Vibrational Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, May 2006. http://dx.doi.org/10.21236/ada450362.

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Sunney Xie, Wei Min, Chris Freudiger, Sijia Lu. Coherent Anti-Stokes Raman Scattering Spectroscopy of Single Molecules in Solution. Office of Scientific and Technical Information (OSTI), January 2012. http://dx.doi.org/10.2172/1033507.

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3

Siwecki, S., and L. Dosser. Investigation of a simulated tritium plasma using Coherent Anti-Stokes Raman Spectroscopy. Office of Scientific and Technical Information (OSTI), November 1989. http://dx.doi.org/10.2172/5198897.

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Morgen, Michael Mark. Femtosecond Raman induced polarization spectroscopy studies of coherent rotational dynamics in molecular fluids. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/501549.

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Singh, J. P., and Fang-Yu Yueh. Coherent anti-stokes Raman spectroscopy system for point temperature and major species concentration measurement. Office of Scientific and Technical Information (OSTI), October 1993. http://dx.doi.org/10.2172/10189541.

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6

Lucht, Robert. Polarization Spectroscopy And Electronic- Resonance-Enhanced Coherent Anti-stokes Raman Scattering For Quantitative Concentration Measurements. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/1854342.

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Yaney, Perry P., and John W. Parish. Studies of Surface Deactivation of Vibrationally-Excited Homonuclear Molecules in Gaseous Discharge Media Using Coherent Anti-Stokes Raman Spectroscopy (CARS). Fort Belvoir, VA: Defense Technical Information Center, January 1999. http://dx.doi.org/10.21236/ada369109.

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Wolf, Emil. Spatial - Coherence Effects in Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, December 2002. http://dx.doi.org/10.21236/ada408980.

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Wolf, Emil. Coherence Effects in Light Propagation in Scattering and in Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, December 2005. http://dx.doi.org/10.21236/ada442639.

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10

Wolf, Emil. Coherence Effects in Optical Physics with Special Reference to Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, January 1988. http://dx.doi.org/10.21236/ada189520.

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