arXiv subjects

Jonathan D. Weinstein

Publications and source records attributed to Jonathan D. Weinstein.

14 recordsLinked to original sources

arXiv2025

Long nuclear spin coherence times for molecules trapped in high-purity solid parahydrogen

We measure the ensemble transverse relaxation time (T2*) and spin-echo coherence time (T2) of the proton spin of HD molecules trapped in solid parahydrogen. By using high-purity parahydrogen matrices, we are able to measure significantly longer T2 and T2* times than seen in prior work. We also measure the longitudinal spin relaxation time T1. We examine how these parameters scale with the matrix purity and find limits on the coherence time from the parahydrogen matrix itself.

quant-ph↗

arXiv2025

Quantum sensing in the presence of pulse errors and qubit leakage

Using both simulation and experiment, we investigate the robustness of dynamical decoupling sequences to pulse errors: rotation errors and detuning errors. Whereas prior work examined the effect of errors on coherence times, here we show that quantum sensing can be affected by pulse errors in dramatically different ways than coherence times alone. We also explore the effects of qubit leakage: off-resonant coupling to other quantum levels. We find order-of-magnitude differences between commonly-used dynamical decoupling sequences in both their sensitivity to pulse errors and leakage.

quant-ph↗

arXiv2021

Optical and spin-coherence properties of rubidium atoms trapped in solid neon

In this work, we measure the properties of ensembles of rubidium atoms trapped in solid neon that are relevant for use as quantum sensors of magnetic fields: the spin coherence of the trapped atoms and the ability to optically control and measure their spin state. We use the rubidium atoms as an AC magnetometer (by employing an appropriate dynamical decoupling sequence) and demonstrate NMR detection of Ne-21 atoms co-trapped in the neon matrix.

physics.atom-ph↗

arXiv2021

High-purity solid parahydrogen

Alkali atoms trapped in solid hydrogen matrices have demonstrated ultralong electron spin coherence times, and are promising as quantum sensors. Their spin coherence is limited by magnetic noise from naturally-occurring orthohydrogen molecules in the parahydrogen matrix. In the gas phase, the orthohydrogen component of hydrogen can be converted to parahydrogen by flowing it over a catalyst held at cryogenic temperatures, with lower temperatures giving a lower orthohydrogen fraction. In this work, we use a single cryostat to reduce the orthohydrogen fraction of hydrogen gas and grow a solid matrix from the resulting high-purity parahydrogen. We demonstrate operation of the catalyst down to a temperature of 8 K, and we spectroscopically verify that orthohydrogen impurities in the resulting solid are at a level < 1e-6. We also find that, at sufficiently low temperatures, the cryogenic catalyst provides isotopic purification, reducing the HD fraction.

physics.atom-ph↗

arXiv2021

Radiative properties of rubidium atoms trapped in solid neon and parahydrogen

It is known from ensemble measurements that rubidium atoms trapped in solid parahydrogen have favorable properties for quantum sensing of magnetic fields. To use a single rubidium atom as a quantum sensor requires a technique capable of efficiently measuring the internal state of a single atom, such as laser-induced fluorescence. In this work we search for laser-induced fluorescence from ensembles of rubidium atoms trapped in solid parahydrogen and, separately, in solid neon. In parahydrogen we find no evidence of fluorescence over the range explored, and place upper limits on the radiative branching ratio. In neon, we observe laser induced fluorescence, measure the spectrum of the emitted light, and measure the excited state lifetime in the matrix. Bleaching of atoms from the excitation light is also reported.

physics.atom-ph↗

arXiv2020

Ultralong spin coherence times for rubidium atoms in solid parahydrogen via dynamical decoupling

Coherence time is an essential parameter for quantum sensing, quantum information, and quantum computation. In this work, we demonstrate electron spin coherence times as long as 0.1 s for an ensemble of rubidium atoms trapped in a solid parahydrogen matrix. We explore the underlying physics limiting the coherence time. The properties of these matrix isolated atoms are very promising for future applications, including quantum sensing of nuclear spins. If combined with efficient single-atom readout, this would enable NMR and magnetic resonance imaging of single molecules cotrapped with alkali-metal atom quantum sensors within a parahydrogen matrix.

physics.atom-ph↗

arXiv2020

Electrostatic guiding of the methylidyne radical at cryogenic temperatures

We have produced a cryogenic buffer-gas cooled beam of the diatomic molecular radical CH (methylidyne). This molecule is of interest for studying cold chemical reactions and fundamental physics measurements. Its light mass and ground-state structure make it a promising candidate for electrostatic guiding and Stark deceleration, which allows for control over its kinetic energy. This control can facilitate studies of reactions with tuneable collision energies and trapping for precise spectroscopic studies. Here, we have demonstrated electrostatic guiding of CH with fluxes up to $10^9$ molecules per steradian per pulse

physics.chem-ph↗

arXiv2019

Spin coherence and optical properties of alkali-metal atoms in solid parahydrogen

We present a joint experimental and theoretical study of spin coherence properties of 39K, 85Rb, 87Rb, and 133Cs atoms trapped in a solid parahydrogen matrix. We use optical pumping to prepare the spin states of the implanted atoms and circular dichroism to measure their spin states. Optical pumping signals show order-of-magnitude differences depending on both matrix growth conditions and atomic species. We measure the ensemble transverse relaxation times (T2*) of the spin states of the alkali-metal atoms. Different alkali species exhibit dramatically different T2* times, ranging from sub-microsecond coherence times for high mF states of 87Rb, to ~100 microseconds for 39K. These are the longest ensemble T2* times reported for an electron spin system at high densities (n > 10^16 cm^-3). To interpret these observations, we develop a theory of inhomogenous broadening of hyperfine transitions of ^2S atoms in weakly-interacting solid matrices. Our calculated ensemble transverse relaxation times agree well with experiment, and suggest ways to longer coherence times in future work.

physics.atom-ph↗

arXiv2018

Enhanced spin coherence of rubidium atoms in solid parahydrogen

We measure the transverse relaxation of the spin state of an ensemble of ground-state rubidium atoms trapped in solid parahydrogen at cryogenic temperatures. We find the spin dephasing time of the ensemble (T$_2^*$) is limited by inhomogeneous broadening. We determine that this broadening is dominated by electrostatic interactions with the host matrix, and can be reduced by preparing nonclassical spin superposition states. Driving these superposition states gives significantly narrower electron paramagnetic resonance lines and the longest reported electron spin $T_2^*$ in any solid-phase system other than solid helium.

physics.atom-ph↗

arXiv2018

Shaped nozzles for cryogenic buffer gas beam sources

Cryogenic buffer gas beams are important sources of cold molecules. In this work we explore the use of a converging-diverging nozzle with a buffer-gas beam. We find that, under appropriate circumstances, the use of a nozzle can produce a beam with improved collimation, lower transverse temperatures, and higher fluxes per solid angle.

physics.atom-ph↗

arXiv2017

Cold, anisotropically-interacting van der Waals molecule: TiHe

We have used laser ablation and helium buffer-gas cooling to produce the titanium-helium van der Waals molecule at cryogenic temperatures. The molecules were detected through laser-induced fluorescence spectroscopy. Ground-state Ti-He binding energies were determined for the ground and first rotationally excited states from studying equilibrium thermodynamic properties, and found to agree well with theoretical calculations based on newly calculated ab initio Ti-He interaction potentials, opening up novel possibilities for studying the formation, dynamics, and non-universal chemistry of van der Waals clusters at low temperatures.

physics.atom-ph↗

arXiv2015

Observation of a classical cheshire cat in an optical interferometer

A recent neutron interferometry experiment claims to demonstrate a paradoxical phenomena dubbed the "quantum Cheshire Cat" \cite{Denkmayr2014}. We have reproduced and extended these results with an equivalent optical interferometer. The results suggest that the photon travels through one arm of the interferometer, while its polarization travels through the other. However, we show that these experimental results belong to the domain where quantum and classical wave theories coincide; there is nothing uniquely quantum about the illusion of this cheshire cat.

quant-ph↗

arXiv2013

Method for traveling-wave deceleration of buffer-gas beams of CH

Cryogenic buffer-gas beams are a promising method for producing bright sources of cold molecular radicals for cold collision and chemical reaction experiments. In order to use these beams in studies of reactions with controlled collision energies, or in trapping experiments, one needs a method of controlling the forward velocity of the beam. A Stark decelerator can be an effective tool for controlling the mean speed of molecules produced by supersonic jets, but efficient deceleration of buffer-gas beams presents new challenges due to longer pulse lengths. Traveling-wave decelerators are uniquely suited to meet these challenges because of their ability to confine molecules in three dimensions during deceleration and the versatility afforded by the analog control of the electrodes. We have created ground state CH($X^2Π$) radicals in a cryogenic buffer-gas cell with the potential to produce a cold molecular beam of $10^{11}$ mol./pulse. We present a general protocol for Stark deceleration of beams with large position and velocity spreads for use with a traveling-wave decelerator. Our method involves confining molecules transversely with a hexapole for an optimized distance before deceleration. This rotates the phase-space distribution of the molecular packet so that the packet is matched to the time varying phase-space acceptance of the decelerator. We demonstrate with simulations that this method can decelerate a significant fraction of the molecules in successive wells of a traveling-wave decelerator to produce energy-tuned beams for cold and controlled molecule experiments.

physics.chem-ph↗

arXiv2009

Entangling the lattice clock: Towards Heisenberg-limited timekeeping

We present a scheme for entangling the atoms of an optical lattice to reduce the quantum projection noise of a clock measurement. The divalent clock atoms are held in a lattice at a ``magic'' wavelength that does not perturb the clock frequency -- to maintain clock accuracy -- while an open-shell J=1/2 ``head'' atom is coherently transported between lattice sites via the lattice polarization. This polarization-dependent ``Archimedes' screw'' transport at magic wavelength takes advantage of the vanishing vector polarizability of the scalar, J=0, clock states of bosonic isotopes of divalent atoms. The on-site interactions between the clock atoms and the head atom are used to engineer entanglement and for clock readout.

quant-ph↗