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arXiv:2306.01955 · Physical Review Letters

Controlled Excitation of Rotons in Superfluid Helium with an Optical Centrifuge

A. Milner, Valery Milner

Published Oct 18, 2023• 3 citations
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Abstract

We experimentally demonstrate a controlled transfer of angular momentum to roton pairs in superfluid helium. The control is executed with an optical centrifuge and detected with coherent time- and frequency-resolved Raman scattering. We show that the sign of the Raman shift, and hence the orientation of the angular momentum transferred from the laser field to the rotons, is dictated by the centrifuge. The magnitude of the shift reflects the two-roton energy and indicates that the centrifuge-induced roton pairs are far from the equilibrium with the quantum bath. The observed decay of the coherent Raman signal suggests that the decoherence is governed by the scattering on thermal rotons and phonons. The demonstrated method offers ways of examining microscopic origins of superfluidity by controlling collective excitations in superfluids.

DOI
10.1103/physrevlett.131.166001

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We experimentally demonstrate a controlled transfer of angular momentum to roton pairs in superfluid helium. The control is executed with an optical centrifuge and detected with coherent time- and frequency-resolved Raman scattering. We show that the sign of the Raman shift, and hence the orientation of the angular momentum transferred from the laser field to the rotons, is dictated by the centrifuge. The magnitude of the shift reflects the two-roton energy and indicates that the centrifuge-induced roton pairs are far from the equilibrium with the quantum bath. The observed decay of the coherent Raman signal suggests that the decoherence is governed by the scattering on thermal rotons and phonons. The demonstrated method offers ways of examining microscopic origins of superfluidity by controlling collective excitations in superfluids.
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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.
We experimentally demonstrate that the rotation of molecules embedded in helium nanodroplets can be controlled with an optical centrifuge, allowing for the study of molecular dynamics inside the strongly interacting many-body environment of superfluid helium at variable levels of rotational excitation. By doping the droplets with dimers of nitric oxide, (NO)_{2}, and measuring the degree of their centrifuge-induced alignment as a function of time, we show both the forced in-field rotation of molecules in a continuous range of frequencies, as well as the field-free resonant rotation with a long nanosecond-scale decay. The ability to control and monitor the rotational dynamics of molecular rotors inside the superfluid medium may shed new light on superfluidity and the interaction of superfluids with defects at the atomic level.
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Molecules immersed in liquid helium are excellent probes of superfluidity. Their electronic, vibrational, and rotational dynamics provide valuable clues about the superfluid at the nanoscale. Here we report on the experimental study of the laser-induced rotation of helium dimers inside the superfluid 4 He bath at variable temperature. The coherent rotational dynamics of He 2 ∗ is initiated in a controlled way by ultrashort laser pulses and tracked by means of time-resolved laser-induced fluorescence. We detect the decay of rotational coherence on the nanosecond time scale and investigate the effects of temperature on the decoherence rate. The observed temperature dependence suggests a nonequilibrium evolution of the quantum bath, accompanied by the emission of the wave of second sound. The method offers ways of studying superfluidity with molecular nanoprobes under variable thermodynamic conditions.