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Observing collisions beyond the secular approximation limit

Junyang Ma, Haisu Zhang, B. Lavorel, Franck Billard, E. Hertz, Jian Wu, C. Boulet, Jean‐Michel Hartmann, O. Faucher

Published Jan 1, 2019• 30 citations
OpenAlex

Abstract

Abstract Quantum coherence plays an essential role in diverse natural phenomena and technological applications. The unavoidable coupling of the quantum system to an uncontrolled environment incurs dissipation that is often described using the secular approximation. Here we probe the limit of this approximation in the rotational relaxation of molecules due to thermal collisions by using the laser-kicked molecular rotor as a model system. Specifically, rotational coherences in N2O gas (diluted in He) are created by two successive nonresonant short and intense laser pulses and probed by studying the change of amplitude of the rotational alignment echo with the gas density. By interrogating the system at the early stage of its collisional relaxation, we observe a significant variation of the dissipative influence of collisions with the time of appearance of the echo, featuring a decoherence process that is well reproduced by the nonsecular quantum master equation for modeling molecular collisions.

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Observing collisions beyond the secular approximation limit

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Abstract Quantum coherence plays an essential role in diverse natural phenomena and technological applications. The unavoidable coupling of the quantum system to an uncontrolled environment incurs dissipation that is often described using the secular approximation. Here we probe the limit of this approximation in the rotational relaxation of molecules due to thermal collisions by using the laser-kicked molecular rotor as a model system. Specifically, rotational coherences in N2O gas (diluted in He) are created by two successive nonresonant short and intense laser pulses and probed by studying the change of amplitude of the rotational alignment echo with the gas density. By interrogating the system at the early stage of its collisional relaxation, we observe a significant variation of the dissipative influence of collisions with the time of appearance of the echo, featuring a decoherence process that is well reproduced by the nonsecular quantum master equation for modeling molecular collisions.

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quant-pharXiv:2608.25161•Aug 27, 2026•0 citations
Abstract Quantum coherence plays an essential role in diverse natural phenomena and technological applications. The unavoidable coupling of the quantum system to an uncontrolled environment incurs dissipation that is often described using the secular approximation. Here we probe the limit of this approximation in the rotational relaxation of molecules due to thermal collisions by using the laser-kicked molecular rotor as a model system. Specifically, rotational coherences in N2O gas (diluted in He) are created by two successive nonresonant short and intense laser pulses and probed by studying the change of amplitude of the rotational alignment echo with the gas density. By interrogating the system at the early stage of its collisional relaxation, we observe a significant variation of the dissipative influence of collisions with the time of appearance of the echo, featuring a decoherence process that is well reproduced by the nonsecular quantum master equation for modeling molecular collisions.
Abstract Quantum coherence plays an essential role in diverse natural phenomena and technological applications. The unavoidable coupling of the quantum system to an uncontrolled environment incurs dissipation that is often described using the secular approximation. Here we probe the limit of this approximation in the rotational relaxation of molecules due to thermal collisions by using the laser-kicked molecular rotor as a model system. Specifically, rotational coherences in N2O gas (diluted in He) are created by two successive nonresonant short and intense laser pulses and probed by studying the change of amplitude of the rotational alignment echo with the gas density. By interrogating the system at the early stage of its collisional relaxation, we observe a significant variation of the dissipative influence of collisions with the time of appearance of the echo, featuring a decoherence process that is well reproduced by the nonsecular quantum master equation for modeling molecular collisions.
We point out the breakdown of two approximations widely used to describe decoherence in open quantum systems, the secular and Markov approximations. We probe their limits by studying the influence of pressure on the alignment revivals (echoes) created in properly chosen gas mixtures (HCl and CO2, pure and diluted in He) by one (two) intense and short laser pulse(s). Experiments, as well as predictions using molecular dynamics simulations, consistently demonstrate in some of the aforementioned systems the break-down of these approximations at very short times (<15 ps) after the laser kick(s).
Purely quantum phenomena such as dynamical localization (DL) can be observed in a molecular rotor subjected to a periodic train of short and intense laser pulses in the gas phase. Using requantized Classical Molecular Dynamics Simulations, we investigate the impact of collisional effects for O2 molecules. We consider different trains of kicks for which the system exhibits quantum resonance, DL, or Bloch oscillations under collision-free conditions. Within achievable experimental conditions, we demonstrate that, as the gas pressure increases, all the dynamics become progressively similar, leading to a quantum-to-classical transition. We study how decoherence induced by intermolecular collisions reduces the quantum interferences through loss of memory. These findings pave the way for future experimental investigations and further theoretical studies on the influence of dissipation on quantum effects in rotational dynamics.
We experimentally and theoretically investigate the ultrafast collisional dynamics of a symmetric-top molecule (C2H6{\mathrm{C}}_{2}{\mathrm{H}}_{6}C2​H6​) in pure gas and mixtures with He at high density by employing the rotational alignment echo created by a pair of time-delayed intense laser kicks. The decrease of the amplitude of the echo when increasing the delay between the two laser pulses, reflecting the collisional relaxation of the system, is measured by probing the transient birefringence induced in the medium. The theoretical predictions, carried using purely classical molecular dynamics simulations, reproduce well the observed features, as demonstrated previously for a linear molecule. The analysis shows that the dissipation of the ethane alignment, despite the fact that this species has an extra rotational degree of freedom as compared to a linear molecule, barely involves more complex collisional relaxation channels due to characteristics of the ${\mathrm{C}}_{2}{\mathrm{H}}_{6}\ensuremath{-}{\mathrm{C}}_{2}{\mathrm{H}}_{6}$ and ${\mathrm{C}}_{2}{\mathrm{H}}_{6}\ensuremath{-}\mathrm{He}$ interactions. However, our findings reveal that the dissipative dynamics of a symmetric-top molecule can be properly approached using the recently discovered rotational alignment echoes, which, so far, have been only tested for probing rotational decoherence of simpler (linear) molecules.
A quantum system interacting with a dilute gas experiences irreversible dynamics. The corresponding master equation can be derived within two different approaches: The fully quantum description in the low-density limit and the semiclassical collision model, where the motion of gas particles is classical whereas their internal degrees of freedom are quantum. The two approaches have been extensively studied in the literature, but their predictions have not been compared. This is mainly due to the fact that the low-density limit was extensively studied for mathematical physics purposes, whereas the collision models have been essentially developed for quantum information tasks such as a tractable description of the open quantum dynamics. Here we develop and compare both approaches for a spin system interacting with a gas of spin particles. Using some approximations, we explicitly find the corresponding master equations including the Lamb shifts and the dissipators. The low-density limit in the Born approximation for fast particles is shown to be equivalent to the semiclassical collision model in the stroboscopic approximation. We reveal that both approaches give exactly the same master equation if the gas temperature is high enough. This allows to interchangeably use complicated calculations in the low-density limit and rather simple calculations in the collision model.
A macroscopic manifestation of superfluidity is that objects moving through liquid helium experience negligible friction below the Landau critical velocity. How this frictionless motion breaks down at the nanoscale remains an open question. Molecules embedded in helium nanodroplets represent a well-controlled system for studying this breakdown, yet none has reached the regime of strong dissipative coupling, when energy transfer from the molecule to the superfluid dominates the observed dynamics. Molecular rotation, induced by short laser pulses, offer a suitable probe to reach rotational energies in the range of the roton gap, where superfluid helium supports a large number of elementary excitations. However, the solvation shell around a rotating molecule caps the energy reachable by a free rotor after impulsive excitation well below the roton excitation energy. Here we show that continuous driving with an ultraslow optical centrifuge overcomes this limitation: the strong field dresses the molecule into pendular states whose energies fall within the spectrum of the collective excitations of the superfluid, placing the system in the strong-dissipation regime. The resulting rapid thermalization locks the molecule to the rotating field until the rotation-induced level splittings overtake the thermalization rate, beyond which the molecular alignment is progressively lost. Our approach offers a direct measurement of the molecule-bath coupling in a quantum fluid.