Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

International Conference on Ultrafast Phenomena

Picosecond two-color photon echoes in doped molecular solids

Douwe A. Wiersma, D. P. Weitekamp, Koos Duppen

Published Jan 1, 1984• 0 citations
Publisher

Abstract

The three pulse stimulated echo, long known in magnetic resonance (1), has more recently been demonstrated on optical transitions(2). An interesting way of looking at the stimulated-echo-formation relies on the fact that the first two excitation pulses create an "ordered" population as a function of detuning .This ordered population can also be looked upon as a " grating " in frequency space from which a probe pulse can "reflect" an echo. Since a grating in only one of the levels suffices, a corollary is that the echo may be stimulated at some entirely different frequency ω2 than the one ω1, at which the grating was prepared. We report the observation of such a connected two-color stimulated echo(C2CSE) in a solid and use it to confirm the relaxation out of the 747 cm−1 vibrational state of the S1 manifold of pentacene in naphthalene. It has also been realized (3) that after redistribution of the initially excited population grating, that the echo may be stimulated from any state into which the grating has relaxed. We report here the first observation of such a relaxed two-color stimulated echo(R2CSE) and note that this echo can be seen as the optical analogue of the cross-relaxation peak in a two-dimensional nmr spectrum. The rise and fall of this relaxed echo can be used as a probe for the vibrational deactivation pathway(s) subsequent to excitation of various vibrational levels in the S1 manifold. Prior to discussing briefly some of the results we note that from an analysis of this echo effect it is clear that a necessary prerequiste to observation of such two-color photon echoes is that the inhomogeneous broadening on the selected transitions is strongly correlated. Furthermore we note that in these echo effects interference with stimulated emission and super -fluorescence must be avoided by using small-angle excitation pulses. Some of the results are shown in Fig.1. In (A) the decay of the C2CSE is presented with the solid line being a fit to a population decay parameter of the 747 cm-1 level of 33 psec. In (B) the rise of the R2CSE is shown where the probe wavelength is at the pure electronic transition. The dashed line is the expected echo-intensity rise if the initially excited vibration would directly decay into the vibrationless state. The mismatch between the dashed curve and the experimental one shows that intermediate levels in the relaxation pathway must exist. The solid line in (B) is a fit to a model where one intermediate bottleneck level is assumed with a lifetime of 16±2 psec. Other examples will be presented at the meeting.

DOI
10.1364/up.1984.fc4

Related papers

Photon echoes stimulated from an accumulated grating: Theory of generation and detection

Wim H. Hesselink, Douwe A. Wiersma

We present a theoretical description of the generation and detection of photon echoes, stimulated from an accumulated frequency grating in the inhomogeneous distribution. We show that detection of the echoes takes place via interference in the sample between a properly phased and directed probe pulse and the echo polarization. In this description the echo phenomenon emerges as an induced transparency of the sample rather than a burst of coherent radiation. By solving simultaneously the optical Bloch and Maxwell equations, an expression is obtained which correlates quantitatively the echo intensity to the decay parameters, pulse intensity, and the transition moment. As an application of the theory we present results on the intersystem crossing of pentacene in naphthalene at 1.5 K.

The Journal of Chemical Physics•Nov 1, 1981•81 citations

High-Yield Picosecond Photon Echoes by Photochemical Hole-Burning

Rein K. Kaarli, Alexander Rebane, Peeter Saari

The phenomenon of stimulated photon echo [1] has already been investigated in a variety of molecular systems but in all cases the magnitude of echo signals has been limited to a small fraction of the pumping pulses intensity. The main reason for that lies in a rapid relaxation of nonequilibrium population of molecular states, which hinder the formation of spectral population gratings responsible for the stimulation of retarded optical pulses.

International Conference on Ultrafast Phenomena•Jan 1, 1984•0 citations

Stimulated nutation echo: application to the driven decoherence study

G. Bimbo, R. Boscaino, M. Cannas +2 more

We study experimentally the dynamical and decay properties of the stimulated nutation echo (SNE) in a two-level spin system, the signal of which allows the observation timescale of the driven coherence relaxation to be extended. This signal appears in the transient response of the system to the second pulse at time τ 1 from its start and coinciding with the duration of the first pulse. The information about the first pulse duration is imprinted into the population difference of the inhomogeneously broadened ensemble of the two-level absorbers. The decay of the SNE signal has two contributions. One originates from the population decay during the time τ between the two pulses. Another is caused by the coherence loss during the excitation by the first pulse and the reading time of the second pulse. Experimental results on the decay properties induced by these mechanisms are presented for the first time. We investigate the dependence of these decay rates on the pulse intensity and we examine its relationship with the anomalous (non-Bloch) decay of other coherent transients in solids.

Journal of Physics Condensed Matter•Jun 6, 2003•3 citations

Superfluorescence-Stimulated Photon Echoes

Alexander I. Lvovsky, Sven R. Hartmann, Fred Moshary

Two closely spaced 778 nm, 4-ps pulses, two-photon resonant with the 5S-5D transition in Rb vapor generate a ground state grating, which later is excited by a similar third pulse, producing conical yoked superfluorescence echo on the 5S-6P, 420-nm transition. The intensity of this emission as a function of the relative delay between the leading excitation pulses is governed by the dynamics of Doppler dephasing and rephasing. This is the first observation of an echo effect induced by a spontaneous relaxation process.

Physical Review Letters•Dec 10, 2002•11 citations

Electronic coupling and coherences in disordered polymers: Femtosecond 2D-photon echo correlation spectroscopy, signatures of an excitonic two-segmental site system: A theoretical study

Vojtech Szőcs, Tibor Pálszegi, Andreas Tortschanoff +1 more

The two-dimensional (2D) temporal shape of the (degenerate) three-pulse photon-echo (3-PPE) polarization P(3)(t′,τ12,τ23=0) has been theoretically analyzed for a weakly interacting two-site system (TSS) in the presence of site inhomogeneous broadening. The TSS has been modeled in terms of two identical, energy-degenerate, excitonically coupled pairs of electronic states in the site-representation (i.e., two S0 and S1 states forming a 4-level system). The 2D time-domain signal S(t′,τ12,τ23=0) has been derived in a closed-form solution which allowed to formulate the analytical Fourier transform analog under sequential δ-pulse excitation. The resulting 2D PE signal in frequency–frequency space S(ωt′,ωτ12) is formed in the region of the resonant, optical carrier frequency by, generally, four peaks, arranged at the edges of a square with distances determined by the excitonic coupling. The two diagonal peaks are of one-exciton origin, while the two off-diagonal (cross) peaks involve two-exciton effects, too. The relative heights of the four peaks are in distinct relation with the mutual orientation of the site-localized transition dipoles, thus these 2D line shapes serving as a structural probe for resonantly interacting molecules. The shapes of the peaks reflect the ratio between homogeneous and inhomogeneous dephasings and can be used for structural studies of statically disordered systems of TSS. The semiclassical two-site model is intended to provide a preparatory platform for mimicking electronically coupled segmental pairs dispersed in energy and space along the strongly disordered main chain contour. The results of the model calculation are taken to discuss the potential and the limitations of 2D line shape echo-spectroscopy in the study of short-range coherences and electronic coupling in π-conjugated polymers.

The Journal of Chemical Physics•May 8, 2002•12 citations

Coherent Transients by Laser-Acoustical Diffraction Spectroscopy

A. H. Zewail

Recently we have reported[1] on the measurements of electronic dephasing (T_2) and radiationless decay (T_1) in molecules using emission spectroscopy as a probe for the detection of the photon echo. This right-angle photon echo utilizes a single mode of a narrow-band (~MHz) cw dye laser and an intracavity electro-optical (EO) element that modulates the frequency of the laser.[2] Applying voltage pulses into the EO crystal switches the laser frequency from ω_0 (the peak frequency of the transition resonance) into another frequency ω. This switching procedure introduced by Brewer et al. for the observation of transients in the forward direction of the laser allows one to observe coherent transients in gases,[1,2] solids[3-5] and molecular beams.[6] Typically, the dispersion of the nonlinear EO crystal (e.g., AD*P) gives a 60 MHz frequency shift within the inhomogeneous resonance of the optical transition (width ~GHz or larger). Therefore, to switch the laser frequency further, one must use high-voltage signals that are usually hard to obtain especially for multiple-pulse experiments. Secondly, there is a limit on the frequency shift which is conditioned by the mode spacing of the cavity. Thirdly, because the laser is switched into a new group of molecules some complications may arise in interpreting the transient spectra especially in large molecules. This is because in large molecules the density of excited states is high and thus the buildup of transients of w molecules (which could be complex) will be superimposed on the decay of ω_0 molecules. Finally, off-resonance effects (e.g., beats) between the molecules at frequency ω and ω_0 cannot be avoided.

Journal of the Optical Society of America A•May 1, 1978•1 citation
The three pulse stimulated echo, long known in magnetic resonance (1), has more recently been demonstrated on optical transitions(2). An interesting way of looking at the stimulated-echo-formation relies on the fact that the first two excitation pulses create an "ordered" population as a function of detuning .This ordered population can also be looked upon as a " grating " in frequency space from which a probe pulse can "reflect" an echo. Since a grating in only one of the levels suffices, a corollary is that the echo may be stimulated at some entirely different frequency ω2 than the one ω1, at which the grating was prepared. We report the observation of such a connected two-color stimulated echo(C2CSE) in a solid and use it to confirm the relaxation out of the 747 cm−1 vibrational state of the S1 manifold of pentacene in naphthalene. It has also been realized (3) that after redistribution of the initially excited population grating, that the echo may be stimulated from any state into which the grating has relaxed. We report here the first observation of such a relaxed two-color stimulated echo(R2CSE) and note that this echo can be seen as the optical analogue of the cross-relaxation peak in a two-dimensional nmr spectrum. The rise and fall of this relaxed echo can be used as a probe for the vibrational deactivation pathway(s) subsequent to excitation of various vibrational levels in the S1 manifold. Prior to discussing briefly some of the results we note that from an analysis of this echo effect it is clear that a necessary prerequiste to observation of such two-color photon echoes is that the inhomogeneous broadening on the selected transitions is strongly correlated. Furthermore we note that in these echo effects interference with stimulated emission and super -fluorescence must be avoided by using small-angle excitation pulses. Some of the results are shown in Fig.1. In (A) the decay of the C2CSE is presented with the solid line being a fit to a population decay parameter of the 747 cm-1 level of 33 psec. In (B) the rise of the R2CSE is shown where the probe wavelength is at the pure electronic transition. The dashed line is the expected echo-intensity rise if the initially excited vibration would directly decay into the vibrationless state. The mismatch between the dashed curve and the experimental one shows that intermediate levels in the relaxation pathway must exist. The solid line in (B) is a fit to a model where one intermediate bottleneck level is assumed with a lifetime of 16±2 psec. Other examples will be presented at the meeting.
We present a theoretical description of the generation and detection of photon echoes, stimulated from an accumulated frequency grating in the inhomogeneous distribution. We show that detection of the echoes takes place via interference in the sample between a properly phased and directed probe pulse and the echo polarization. In this description the echo phenomenon emerges as an induced transparency of the sample rather than a burst of coherent radiation. By solving simultaneously the optical Bloch and Maxwell equations, an expression is obtained which correlates quantitatively the echo intensity to the decay parameters, pulse intensity, and the transition moment. As an application of the theory we present results on the intersystem crossing of pentacene in naphthalene at 1.5 K.
We study experimentally the dynamical and decay properties of the stimulated nutation echo (SNE) in a two-level spin system, the signal of which allows the observation timescale of the driven coherence relaxation to be extended. This signal appears in the transient response of the system to the second pulse at time τ 1 from its start and coinciding with the duration of the first pulse. The information about the first pulse duration is imprinted into the population difference of the inhomogeneously broadened ensemble of the two-level absorbers. The decay of the SNE signal has two contributions. One originates from the population decay during the time τ between the two pulses. Another is caused by the coherence loss during the excitation by the first pulse and the reading time of the second pulse. Experimental results on the decay properties induced by these mechanisms are presented for the first time. We investigate the dependence of these decay rates on the pulse intensity and we examine its relationship with the anomalous (non-Bloch) decay of other coherent transients in solids.
Two closely spaced 778 nm, 4-ps pulses, two-photon resonant with the 5S-5D transition in Rb vapor generate a ground state grating, which later is excited by a similar third pulse, producing conical yoked superfluorescence echo on the 5S-6P, 420-nm transition. The intensity of this emission as a function of the relative delay between the leading excitation pulses is governed by the dynamics of Doppler dephasing and rephasing. This is the first observation of an echo effect induced by a spontaneous relaxation process.
The two-dimensional (2D) temporal shape of the (degenerate) three-pulse photon-echo (3-PPE) polarization P(3)(t′,τ12,τ23=0) has been theoretically analyzed for a weakly interacting two-site system (TSS) in the presence of site inhomogeneous broadening. The TSS has been modeled in terms of two identical, energy-degenerate, excitonically coupled pairs of electronic states in the site-representation (i.e., two S0 and S1 states forming a 4-level system). The 2D time-domain signal S(t′,τ12,τ23=0) has been derived in a closed-form solution which allowed to formulate the analytical Fourier transform analog under sequential δ-pulse excitation. The resulting 2D PE signal in frequency–frequency space S(ωt′,ωτ12) is formed in the region of the resonant, optical carrier frequency by, generally, four peaks, arranged at the edges of a square with distances determined by the excitonic coupling. The two diagonal peaks are of one-exciton origin, while the two off-diagonal (cross) peaks involve two-exciton effects, too. The relative heights of the four peaks are in distinct relation with the mutual orientation of the site-localized transition dipoles, thus these 2D line shapes serving as a structural probe for resonantly interacting molecules. The shapes of the peaks reflect the ratio between homogeneous and inhomogeneous dephasings and can be used for structural studies of statically disordered systems of TSS. The semiclassical two-site model is intended to provide a preparatory platform for mimicking electronically coupled segmental pairs dispersed in energy and space along the strongly disordered main chain contour. The results of the model calculation are taken to discuss the potential and the limitations of 2D line shape echo-spectroscopy in the study of short-range coherences and electronic coupling in π-conjugated polymers.
Recently we have reported[1] on the measurements of electronic dephasing (T_2) and radiationless decay (T_1) in molecules using emission spectroscopy as a probe for the detection of the photon echo. This right-angle photon echo utilizes a single mode of a narrow-band (~MHz) cw dye laser and an intracavity electro-optical (EO) element that modulates the frequency of the laser.[2] Applying voltage pulses into the EO crystal switches the laser frequency from ω_0 (the peak frequency of the transition resonance) into another frequency ω. This switching procedure introduced by Brewer et al. for the observation of transients in the forward direction of the laser allows one to observe coherent transients in gases,[1,2] solids[3-5] and molecular beams.[6] Typically, the dispersion of the nonlinear EO crystal (e.g., AD*P) gives a 60 MHz frequency shift within the inhomogeneous resonance of the optical transition (width ~GHz or larger). Therefore, to switch the laser frequency further, one must use high-voltage signals that are usually hard to obtain especially for multiple-pulse experiments. Secondly, there is a limit on the frequency shift which is conditioned by the mode spacing of the cavity. Thirdly, because the laser is switched into a new group of molecules some complications may arise in interpreting the transient spectra especially in large molecules. This is because in large molecules the density of excited states is high and thus the buildup of transients of w molecules (which could be complex) will be superimposed on the decay of ω_0 molecules. Finally, off-resonance effects (e.g., beats) between the molecules at frequency ω and ω_0 cannot be avoided.