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Proposal of a Quantum Measurement of Boltzmann constant

Ettore Bernardi, Luigi Giannelli, Gabriele Zanelli, Fabrizio Piacentini, Fedor Jelezko, Marco Genovese, Ivo Pietro Degiovanni, Michele Campisi

Published Jan 1, 2025• 0 citations
Publisher

Abstract

The recent redefinition of the International System of Units in 2019 fixes the numerical values of seven defining constants, and links to them the definition of the seven fundamental units. Specifically, the fundamental constant related to the definition of the measurement unit for thermodynamic temperature (the kelvin) is the Boltzmann constant, $k_B$. Measurement of the Boltzmann constant is now done with classical methods. We propose an alternative method based on the measurement of the work done on a quantum system: we will take advantage of the Crooks-Tasaki fluctuation theorem and we will exploit an interferometric method to reduce the uncertainty in the measurement of $k_B$ in specific temperature regimes, i.e. below 100 mK, that are challenging for the realization of the thermometric scale. The work $W$ done on a system of finite size and in contact with a thermal reservoir is a stochastic variable. Every time we repeat the protocol we will measure, in general, a different value for $W$, following a probability distribution $P(W)$. The system considered is a qubit in contact with a thermal reservoir and we perform work on the open system varying a parameter $lambda(t)$ of the system Hamiltonian $H(lambda(t))$. We will use an interferometric technique that takes advantage of an ancilla qubit for measuring the work $W$. We collect the $W$ statistics to obtain $P_{forward}(W)$. The information on $k_B$ is embedded in the magnitude of the inteferometric oscillations at precisely known frequencies. If, starting from the final state, we perform work by applying the inverse protocol $H(lambda(t)), with $lambda’(t)=lambda(-t)$, we will have, in general, a different probability distribution $P_{backward}(W)$. The Crooks-Tasaki theorem connects $P_{forward}(W)$ with $P_{backward}(W)$: $frac{P_{forward}(W)}{P_{backward}(-W})=e^{frac{W-Delta F}{k_BT}}$ where $T$ is the temperature of the reservoir and $W-Delta F$ is the energy dissipated in the forward protocol, being $Delta F$ the difference between the initial and final free energy of the system. Eventually, we evaluate $k_B$ by plotting the logarithm of the left-hand-side of the Crooks-Tasaki theorem equation for different values of $W$ at fixed $T$. By evaluating the slope of the line $y= ln{frac{P_{forward}(W)}{P_{backward}(-W)}$ at fixed $T$, we are able to estimate $k_B$. We note that larger slope values, corresponding to lower temperature, allow better estimation of $k_B$. We propose to use the electronic spin of a Nitrogen-Vacancy centre in diamond as the system qubit, and as an ancillary qubit the nuclear spin of the neighbouring Nitrogen atom. We perform work on the Nitrogen-Vacancy centre varying the intensity and direction of an oscillating magnetic field, taking advantage of the discretization of system energy levels and the not-adiabaticity of the process. This method will establish a quantitative link between the work done and the energy dissipated by a quantum task. Furthermore, this measurement reaches its optimum for very low temperatures (5-80 mK) typical of solid-state quantum computation, thus providing a primary thermometer for such applications.

DOI
10.59161/fvft0921

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The recent redefinition of the International System of Units in 2019 fixes the numerical values of seven defining constants, and links to them the definition of the seven fundamental units. Specifically, the fundamental constant related to the definition of the measurement unit for thermodynamic temperature (the kelvin) is the Boltzmann constant, kBk_BkB​. Measurement of the Boltzmann constant is now done with classical methods. We propose an alternative method based on the measurement of the work done on a quantum system: we will take advantage of the Crooks-Tasaki fluctuation theorem and we will exploit an interferometric method to reduce the uncertainty in the measurement of kBk_BkB​ in specific temperature regimes, i.e. below 100 mK, that are challenging for the realization of the thermometric scale. The work WWW done on a system of finite size and in contact with a thermal reservoir is a stochastic variable. Every time we repeat the protocol we will measure, in general, a different value for WWW, following a probability distribution P(W)P(W)P(W). The system considered is a qubit in contact with a thermal reservoir and we perform work on the open system varying a parameter lambda(t)lambda(t)lambda(t) of the system Hamiltonian H(lambda(t))H(lambda(t))H(lambda(t)). We will use an interferometric technique that takes advantage of an ancilla qubit for measuring the work WWW. We collect the WWW statistics to obtain Pforward(W)P_{forward}(W)Pforward​(W). The information on kBk_BkB​ is embedded in the magnitude of the inteferometric oscillations at precisely known frequencies. If, starting from the final state, we perform work by applying the inverse protocol H(lambda(t)),withH(lambda(t)), with H(lambda(t)),withlambda’(t)=lambda(-t),wewillhave,ingeneral,adifferentprobabilitydistribution, we will have, in general, a different probability distribution ,wewillhave,ingeneral,adifferentprobabilitydistributionP_{backward}(W).TheCrooks−Tasakitheoremconnects. The Crooks-Tasaki theorem connects .TheCrooks−TasakitheoremconnectsP_{forward}(W)withwithwithP_{backward}(W):: :frac{P_{forward}(W)}{P_{backward}(-W})=e^{frac{W-Delta F}{k_BT}}wherewherewhereTisthetemperatureofthereservoirandis the temperature of the reservoir andisthetemperatureofthereservoirandW-Delta Fistheenergydissipatedintheforwardprotocol,beingis the energy dissipated in the forward protocol, beingistheenergydissipatedintheforwardprotocol,beingDelta Fthedifferencebetweentheinitialandfinalfreeenergyofthesystem.Eventually,weevaluatethe difference between the initial and final free energy of the system. Eventually, we evaluatethedifferencebetweentheinitialandfinalfreeenergyofthesystem.Eventually,weevaluatek_Bbyplottingthelogarithmoftheleft−hand−sideoftheCrooks−Tasakitheoremequationfordifferentvaluesofby plotting the logarithm of the left-hand-side of the Crooks-Tasaki theorem equation for different values ofbyplottingthelogarithmoftheleft−hand−sideoftheCrooks−TasakitheoremequationfordifferentvaluesofWatfixedat fixedatfixedT.Byevaluatingtheslopeoftheline. By evaluating the slope of the line .Byevaluatingtheslopeoftheliney= ln{frac{P_{forward}(W)}{P_{backward}(-W)}atfixedat fixedatfixedT,weareabletoestimate, we are able to estimate ,weareabletoestimatek_B.Wenotethatlargerslopevalues,correspondingtolowertemperature,allowbetterestimationof. We note that larger slope values, corresponding to lower temperature, allow better estimation of .Wenotethatlargerslopevalues,correspondingtolowertemperature,allowbetterestimationofk_B$. We propose to use the electronic spin of a Nitrogen-Vacancy centre in diamond as the system qubit, and as an ancillary qubit the nuclear spin of the neighbouring Nitrogen atom. We perform work on the Nitrogen-Vacancy centre varying the intensity and direction of an oscillating magnetic field, taking advantage of the discretization of system energy levels and the not-adiabaticity of the process. This method will establish a quantitative link between the work done and the energy dissipated by a quantum task. Furthermore, this measurement reaches its optimum for very low temperatures (5-80 mK) typical of solid-state quantum computation, thus providing a primary thermometer for such applications.
Abstract Quantum thermodynamics describes dynamic processes by means of the operators of entropy production P and time t . P and t do not commute. It exists the non-vanishing t–P commutator [ t , P ]=ik. Here the Boltzmann constant k has the physical meaning of a quantum of entropy. The t–P commutator immediately leads us to the t–P uncertainty relation ΔtΔP≥k/2. Hence the observables t and P are not sharply defined simultaneously. Similar uncertainty relations can also be expected for other pairs of conjugate variables with products of the physical meaning of an entropy. The free energy F and the reciprocal temperature (1/T) are the respective conjugate variables of an isolated system of many particles, which leads us to the F–(1/T) uncertainty relation ǀΔFǁΔ(1/T)ǀ≥k/2. It can be traced back to the t–P uncertainty relation mentioned above. In this way the Helmholtz free energy F and the temperatur T are introduced into quantum thermodynamics. The uncertainties ǀΔFǀ→0 and ǀΔTǀ→0 are negligible at low temperatures T→0, and quantum thermodynamics turns into the time-independent classical thermodynamics. Against this the uncertainties ǀΔFǀ→∞ and ǀΔTǀ→∞ grow unlimited at high temperatures T→∞, and classical thermodynamics loses its sense. In the limit of one particle the uncertainties cannot be neglected even at low temperatures. However a detailed discussion shows that the free energy f of a single particle vanishes within the whole range of temperatures T. This defines the particle entropy σ=ε/T=ak. The dimensionless entropy number a connects the particle energy ε=akT with the temperature T. The entropy number a of a single (s) independent particle can be calculated with the extended, temperature-dependent Schrödinger equation A s φ=aφ. Here A s=−(Λ 2/4π)∇2 means the dimensionless entropy operator describing the entropy number a and thus the particle entropy σ=ak. Λ is the thermal de Broglie wave length. Finally we calculate by means of quantized particle entropies σ the internal energy E, the Helmholtz free energy F, the entropy S, the chemical potential μ, and the equation of state of an ideal gas of N monatomic free particles in full agreement with classical thermodynamics. We also calculate the partition function q=V/Λ 3 of a single free particle within the volume V. Here Λ 3 is a small volume element taking into account the wave–particle dualism of a single free particle of mass m at temperature T. Extension to a system of N free particles leads us to a simple geometrical model and to the conclusion that an ideal gas of independent particles becomes instable below a critical temperature T C. T C corresponds to the critical temperature T BE of Bose–Einstein condensation.
Thermometry in quantum mechanics has traditionally been anchored to the statistics of energy distributions, encapsulated by the Boltzmann factor where the probability of occupying an energy state E is proportional to exp(-E / (k_B T_E)). While effective in near-equilibrium regimes, this energy-centric paradigm falls short in strongly correlated systems, topological phases, and nonequilibrium steady states where energy fluctuations alone fail to capture the complete thermodynamic state. In this paper, we introduce Quantum Phase Thermometry Beyond Energy (QPTE), establishing an independent thermodynamic variable known as phase temperature, denoted as T_phi. Defined through the quantum phase fluctuations and the expectation value of the squared phase velocity operator as T_phi = (hbar * <\dot{\phi}^2>) / k_B, this framework transcends conventional energy measurements. We present a rigorous theoretical foundation showing that quantum phase fluctuations define an effective thermal scale distinct from traditional energy temperature. We explore the profound physical implications of the thermal discrepancy where T_phi not equal to T_E, demonstrating how QPTE expands the conceptual boundaries of statistical mechanics and fundamental thermodynamics.
To understand in detail the relation between unitary quantum theory that describes our world at the microscopic scale and thermodynamics, which was long believed only to apply to macroscopic objects, is one of the most interesting and long-standing problems in physics. Recently, this problem has received renewed attention, in particular from the community of quantum information theory, but also from the field of statistical mechanics, inspired from stochastic thermodynamics. These results suggest that thermodynamics is also relevant for individual quantum systems, provided that they can be brought into contact with thermal baths. In this thesis, I use recently developed tools to provide new results both on fundamental questions, but also on questions which are of practical relevance for potential miniaturized thermal machines. In terms of fundamental questions, the results in this thesis contribute to understanding how the basic laws of thermodynamics and statistical mechanics can be understood directly from unitary quantum mechanics. In particular, I discuss and answer the following questions: i) How can we quantify the third law of thermodynamics using information theoretic methods? ii) How can we quantify the "thermodynamic value" of a state-transition in quantum systems? iii) How can we axiomatically characterize the non-equilibrium free energy and relative entropy? iv) How can we justify statistical ensembles from an operational perspective, without having to introduce either some probability measures or an information theoretic entropy measure? v) How can we understand the equilibration of closed quantum systems, how long does it take and how difficult is it to avoid? In the second part of the thesis I discuss in detail how experimental restrictions, which become important at the quantum scale, influence the ultimate thermodynamic bounds for thermal machines. In particular, the results in this thesis provide thermodynamic bounds on work-extraction and efficiencies of thermal machines in situations where 1.) an experimenter only has limited field strengths available, 2.) an experimenter cannot control the interactions between particles, but external fields arbitrarily well, and 3.) situations in which a small quantum system can only be strongly coupled to heat baths. These bounds are tight and I provide explicit examples illustrating the different behaviours. Finally, I come back to a classic problem in statistical physics: The emergence of spontaneous symmetry breaking. Here, I provide general and rigorous new results that show how symmetry-breaking stationary states emerge from fluctuations in order parameters in dissipative lattice models.
The equipartition theorem is a fundamental law of classical statistical physics, which states that every degree of freedom contributes kBT/2 to the energy, where T is the temperature and kB is the Boltzmann constant. Recent studies have revealed the existence of a quantum version of the equipartition theorem. In the present work, we focus on how to obtain the quantum counterpart of the generalized equipartition theorem for arbitrary quadratic systems in which the multimode Brownian oscillators interact with multiple reservoirs at the same temperature. An alternative method of deriving the energy of the system is also discussed and compared with the result of the quantum version of the equipartition theorem, after which we conclude that the latter is more reasonable. Our results can be viewed as an indispensable generalization of recent works on a quantum version of the equipartition theorem. Published by the American Physical Society 2024
Abstract Controlling and measuring the temperature in different devices and platforms that operate in the quantum regime is, without any doubt, essential for any potential application. In this review, we report the most recent theoretical developments dealing with accurate estimation of very low temperatures in quantum systems. Together with the emerging experimental techniques and developments of measurement protocols, the theory of quantum thermometry will decisively impinge and shape the forthcoming quantum technologies. While current quantum thermometric methods differ greatly depending on the experimental platform, the achievable precision, and the temperature range of interest, the theory of quantum thermometry is built under a unifying framework at the crossroads of quantum metrology, open quantum systems, and quantum many-body physics. At a fundamental level, theoretical quantum thermometry is concerned with finding the ultimate bounds and scaling laws that limit the precision of temperature estimation for systems in and out of thermal equilibrium. At a more practical level, it provides tools to formulate precise, yet feasible, thermometric protocols for relevant experimental architectures. Last but not least, the theory of quantum thermometry examines genuine quantum features, like entanglement and coherence, for their exploitation in enhanced-resolution thermometry.
The probability of a configuration is given in classical theory by the Boltzmann formula $\mathrm{exp}[\ensuremath{-}\frac{V}{\mathrm{hT}}]$ where VVV is the potential energy of this configuration. For high temperatures this of course also holds in quantum theory. For lower temperatures, however, a correction term has to be introduced, which can be developed into a power series of hhh. The formula is developed for this correction by means of a probability function and the result discussed.