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arXiv:2406.17065 · Physical Review A

Revising the universality hypothesis for room-temperature collisions

James L. Booth, Kirk W. Madison

Published Nov 4, 2024• 3 citations
arXivHTMLPDF

Abstract

Atoms constitute promising quantum sensors for a variety of scenarios including vacuum metrology. Key to this application is knowledge of the collision rate coefficient of the sensor atom with the particles being detected. Prior work demonstrated that, for room-temperature collisions, the total collision rate coefficient and the trap depth dependence of the sensor atom loss rate from shallow traps are both universal, independent of the interaction potential at short range. It was also shown that measurements of the energy transferred to the sensor atom by the collision can be used to estimate the total collision rate coefficient. However, discrepancies found when comparing the results of this and other methods of deducing the rate coefficient call into question its accuracy. Here the universality hypothesis is reexamined and an important correction is presented. We find that measurements of the postcollision recoil energy of sensor atoms held in shallow magnetic traps only provide information about the interaction potential at the very largest interatomic distances (e.g., the value of ${C}_{6}$ for a leading order term of $\ensuremath{-}{C}_{6}/{r}^{6}$). As other non-negligible terms exist at medium and long ranges, the total collision rate coefficient, even if universal, can differ from that computed solely from the value of ${C}_{6}$. By incorporating these other long-range terms into a simple semiclassical (SC) calculation, we find the SC prediction matches that of full, multichannel, quantum mechanical scattering calculations using the complete potential. This work resolves the discrepancies, demonstrates the simplicity of estimating the rate coefficients for universal collision partners, and provides guidance for using atoms as a self-calibrating primary quantum pressure standard.

DOI
10.1103/physreva.110.052802

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Atoms constitute promising quantum sensors for a variety of scenarios including vacuum metrology. Key to this application is knowledge of the collision rate coefficient of the sensor atom with the particles being detected. Prior work demonstrated that, for room-temperature collisions, the total collision rate coefficient and the trap depth dependence of the sensor atom loss rate from shallow traps are both universal, independent of the interaction potential at short range. It was also shown that measurements of the energy transferred to the sensor atom by the collision can be used to estimate the total collision rate coefficient. However, discrepancies found when comparing the results of this and other methods of deducing the rate coefficient call into question its accuracy. Here the universality hypothesis is reexamined and an important correction is presented. We find that measurements of the postcollision recoil energy of sensor atoms held in shallow magnetic traps only provide information about the interaction potential at the very largest interatomic distances (e.g., the value of C6{C}_{6}C6​ for a leading order term of \ensuremath−C6/r6\ensuremath{-}{C}_{6}/{r}^{6}\ensuremath−C6​/r6). As other non-negligible terms exist at medium and long ranges, the total collision rate coefficient, even if universal, can differ from that computed solely from the value of C6{C}_{6}C6​. By incorporating these other long-range terms into a simple semiclassical (SC) calculation, we find the SC prediction matches that of full, multichannel, quantum mechanical scattering calculations using the complete potential. This work resolves the discrepancies, demonstrates the simplicity of estimating the rate coefficients for universal collision partners, and provides guidance for using atoms as a self-calibrating primary quantum pressure standard.
Quantum atomic sensors have shown great promise for vacuum metrology. Specifically, the density of gas particles in vacuum can be determined by measuring the collision rate between the particles and an ensemble of sensor atoms. This requires preparing the sensor atoms in a particular quantum state, observing the rate of changes of that state, and using the total collision rate coefficient for state-changing collisions to convert the rate into a corresponding density. The total collision rate coefficient can be known by various methods, including quantum scattering calculations using a computed interaction potential for the collision pair, measurements of the post-collision sensor-atom momentum recoil distribution, or empirical measurements of the collision rate at a known density. Observed discrepancies between the results of these methods call into question their accuracy. To investigate this, we study the ratio of collision rate measurements of co-located sensor atoms, 87Rb and 6Li, exposed to natural abundance versions of H2, He, N2, Ne, Ar, Kr, and Xe gases. This method does not require knowledge of the test gas density and is, therefore, free of the systematic errors inherent in efforts to introduce the test gas at a known density. Our results are systematically different at the level of 3% to 4% from recent theoretical and experiment measurements. This work demonstrates a model-free method for transferring the primacy of one atomic standard to another sensor atom and highlights the utility of sensor-atom cross-calibration experiments to check the validity of direct measurements and theoretical predictions.
This work demonstrates that quantum diffractive collisions, those that result in very small momentum and energy transfer, are universal. Specifically, the cumulative energy distribution transferred to an initially stationary sensor particle by a quantum diffractive collision follows a universal function that depends only on the sensor particle mass and the thermally-averaged, total collision cross section. The characteristic energy scale corresponds to the localization length associated with the collision-induced quantum measurement, and the shape of the universal function is determined {\it only} by the analytic form of the interaction potential at long range. Using cold 87^{87}87Rb sensor atoms confined in a magnetic trap, we observe experimentally the universal function specific to van der Waals collisions, and realize a \emph{self-defining} particle pressure sensor that can be used for any ambient gas. This provides the first primary and quantum definition of the Pascal, applicable to any species and therefore represents a key advance for vacuum and pressure metrology. The quantum pressure standard realized here was compared with a state-of-the-art orifice flow standard transferred by an ionization gauge calibrated for N2_22​. The pressure measurements agreed at the 0.5\% level.
Abstract The room-temperature, velocity-averaged, total cross section for atom–atom and atom–molecule collisions can be approximated using a universal function depending only on the magnitude of the leading order dispersion coefficient, C 6. This feature of the total cross section together with the universal function for the energy distribution transferred by glancing angle collisions ( p QDU6 (Booth et al 2019 New J. Phys. 21 102001)) can be used to empirically determine the total collision cross section and realize a self-calibrating, vacuum pressure standard. This was previously validated for Rb+N2 and Rb+Rb collisions. However, the post-collision energy distribution is expected to deviate from p QDU6 in the limit of small C 6 and small reduced mass. Here we observe this deviation experimentally by performing a direct cross-species loss rate comparison for Rb+H2 and Li+H2 collisions. We measure a velocity averaged total collision cross section ratio of R = ⟨ σ tot v ⟩ Li+H 2 : ⟨ σ tot v ⟩ Rb+H 2 = 0.83 ( 5 ) . Based on an ab initio computation of ⟨ σ tot v ⟩ Li+H 2 = 3.104 × 10 − 15 m3 s−1, we deduce ⟨ σ tot v ⟩ Rb+H 2 = 3.6 ( 2 ) × 10
The authors demonstrate a new method for measuring the C6{}_{6}6​ van der Waals coefficient of the Rb-Rb interaction potential from the loss rate of atoms confined in a shallow atom trap of tunable depth. The technique is based on the universal nature of the room-temperature collisions, which depends only on the long-range potential between the collision partners.
Atomic sensors have shown great promise for density and pressure metrology in the high, ultra-high, and extremely-high vacuum regimes. Specifically, the density of background gas particles in vacuum can be determined by measuring the collision rate between the particles and an ensemble of sensor atoms. This requires preparing the sensor atoms in a particular quantum state, observing the rate of changes of that state, and using the cross section coefficient for state-changing collisions to convert the rate into a corresponding density. The cross section can be known by various methods including by quantum scattering calculations using an ansatz for the interaction potential between the collision pair, by measurements of the post-collision sensor-atom momentum recoil distribution, or by empirical calibration of the sensor atom at a known density. Identifying systematic errors in the results of these methods can be aided by direct comparisons between them. Alternatively, measurements of different sensor atoms exposed to the same background gas offers another point of comparison free of the systematic errors inherent in creating a background gas at a known density. Here, we present such measurements for two sensor atoms, 87^{87}87Rb and 6^66Li, and a variety of atomic and molecular background gases including H2_22​, N2_22​, Ar, Ne, Kr, and Xe. We find results consistent with, yet statistically different at the level of 3.5(5)%, from recent theoretical and experiment measurements. This work demonstrates a model-free method for transferring the primacy of one atomic standard to another sensor atom and highlights the utility of sensor-atom cross-calibration experiments to check the validity of direct measurements and theoretical predictions.
Abstract This work demonstrates that quantum diffractive collisions are governed by a universal law characterized by a single parameter that can be determined experimentally. Specifically, we report a quantitative form of the universal, cumulative energy distribution transferred to initially stationary sensor particles by quantum diffractive collisions. The characteristic energy scale corresponds to the localization length associated with the collision-induced quantum measurement, and the shape of the universal function is determined only by the analytic form of the interaction potential at long range. Using cold 87Rb sensor atoms confined in a magnetic trap, we observe experimentally p QDU 6 , the universal function specific to van der Waals collisions, and use it to realize a self-defining particle pressure sensor that can be used for any ambient gas. This provides the first primary and quantum definition of the Pascal, applicable to any species and therefore represents a fundamental advance for vacuum and pressure metrology. The quantum pressure standard realized here is compared with a state-of-the-art orifice flow standard transferred by an ionization gauge calibrated for N2. The pressure measurements agree at the 0.5% level.