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arXiv:2010.11036 · Physical Review Letters

Quantum Thermodynamics of Correlated-Catalytic State Conversion at Small Scale

Naoto Shiraishi, Takahiro Sagawa

Published Apr 12, 2021• 59 citations
arXivHTMLPDF

Abstract

The class of possible thermodynamic conversions can be extended by introducing an auxiliary system called catalyst, which assists in state conversion while its own state remains unchanged. We reveal a complete characterization of catalytic state conversion in quantum and single-shot thermodynamics by allowing an infinitesimal correlation between the system and the catalyst. Specifically, we prove that a single thermodynamic potential, which provides the necessary and sufficient condition for the correlated-catalytic state conversion, is given by the standard nonequilibrium free energy defined with the Kullback-Leibler divergence. This resolves the conjecture raised by Wilming, Gallego, and Eisert [Entropy 19, 241 (2017)ENTRFG1099-430010.3390/e19060241] and by Lostaglio and Müller [Phys. Rev. Lett. 123, 020403 (2019)PRLTAO0031-900710.1103/PhysRevLett.123.020403] in the positive. Moreover, we show that, with the aid of the work storage, any quantum state can be converted into another by paying the work cost equal to the nonequilibrium free energy difference. Our result would serve as a step towards establishing resource theories of catalytic state conversion in the fully quantum regime.

DOI
10.1103/physrevlett.126.150502

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The class of possible thermodynamic conversions can be extended by introducing an auxiliary system called catalyst, which assists in state conversion while its own state remains unchanged. We reveal a complete characterization of catalytic state conversion in quantum and single-shot thermodynamics by allowing an infinitesimal correlation between the system and the catalyst. Specifically, we prove that a single thermodynamic potential, which provides the necessary and sufficient condition for the correlated-catalytic state conversion, is given by the standard nonequilibrium free energy defined with the Kullback-Leibler divergence. This resolves the conjecture raised by Wilming, Gallego, and Eisert [Entropy 19, 241 (2017)ENTRFG1099-430010.3390/e19060241] and by Lostaglio and Müller [Phys. Rev. Lett. 123, 020403 (2019)PRLTAO0031-900710.1103/PhysRevLett.123.020403] in the positive. Moreover, we show that, with the aid of the work storage, any quantum state can be converted into another by paying the work cost equal to the nonequilibrium free energy difference. Our result would serve as a step towards establishing resource theories of catalytic state conversion in the fully quantum regime.
I show that nondecreasing entropy provides a necessary and sufficient condition to convert the state of a physical system into a different state by a reversible transformation that acts on the system of interest and a further "catalyst," whose state has to remain invariant exactly in the transition. This statement is proven both in the case of finite-dimensional quantum mechanics, where von Neumann entropy is the relevant entropy, and in the case of systems whose states are described by probability distributions on finite sample spaces, where Shannon entropy is the relevant entropy. The results give an affirmative resolution to the (approximate) catalytic entropy conjecture introduced by Boes et al. [Phys. Rev. Lett. 122, 210402 (2019)PRLTAO0031-900710.1103/PhysRevLett.122.210402]. They provide a complete single-shot characterization without external randomness of von Neumann entropy and Shannon entropy. I also compare the results to the setting of phenomenological thermodynamics and show how they can be used to obtain a quantitative single-shot characterization of Gibbs states in quantum statistical mechanics.
Quantum catalysis, the ability to enable previously impossible transformations by using auxiliary systems without degrading them, has emerged as a powerful tool in various resource theories. Although catalytically enabled state transformations have been formally characterized by the monotonic behavior of entropic quantifiers (e.g., the von Neumann entropy or nonequilibrium free energy), such characterizations often rely on unphysical assumptions, namely, the ability of using catalysts of infinitely large dimension. This approach offers very limited insights into the practical significance of using catalysis for quantum information processing. Here, we address this problem across a broad class of quantum resource theories. Leveraging quantum information tools beyond the asymptotic regime, we establish sufficient conditions for the existence of catalytic transformations with finite-size catalysts. We further unveil connections between finite-size catalysis and multicopy transformations. Notably, we discover a phenomenon of catalytic resonance: by carefully tailoring the catalysts's state, one can drastically reduce the required dimension of the catalyst, thus enabling efficient catalytic transformations with minimal resources. Finally, we illustrate our findings with examples from the resource theories of entanglement and thermodynamics, as well in the context of catalytic unitary transformations.
Determining whether a given state can be transformed into a target state using free operations is one of the fundamental questions in the study of resource theories. Free operations in resource theories can be enhanced by allowing for a catalyst system that assists the transformation and is returned unchanged, but potentially correlated, with the target state. While this has been an active area of recent research, very little is known about the necessary properties of such catalysts. Here, we prove fundamental limits applicable to a large class of correlated catalytic transformations by showing that a small residual correlation between a catalyst and target state implies that the catalyst needs to be highly resourceful. In fact, the resource required diverge in the limit of vanishing residual correlation. In addition, we establish that in imperfect catalysis a small error generally implies a highly resourceful embezzling catalyst. We develop our results in a general resource theory framework and discuss its implications for the resource theory of athermality, the resource theory of coherence, and entanglement theory.
Quantum thermodynamics investigates how robust the second law of thermodynamics serves as the unique fundamental law in the small quantum world. To tackle this problem, the quantum coherence constitutes a major difficulty of investigations, which provides severe constraints hindering the recovery of a single thermodynamic potential. Here we solve this long-standing problem of quantum information theory by revealing that the state convertibility under thermal operations is fully characterized by the second law of thermodynamics. Specifically, we prove that whether a quantum state with quantum coherence is convertible to another by a thermal operation with a correlated catalyst is completely determined by the free energy ordering. Unlike previous attempts, our setting does not resort to any additional external coherent assist, providing a faithful operational characterization of thermodynamic state transformation.
The generalized second laws of quantum thermodynamics are usually formulated in terms of Rényi divergences and the associated family of generalized free energies. In catalytic thermal transformations, this framework typically certifies the existence of a suitable catalyst but does not make the catalytic contribution explicit in the resulting system-level inequalities. Here we develop a complementary formulation based on non-additive divergences, whose pseudo-additive structure yields a family of generalized free energies with an explicit catalyst-dependent correction term. For uncorrelated catalytic thermal transformations, we show that this leads to non-additive second-law relations providing nontrivial constraints on admissible catalysts when the catalyst is returned only approximately. We also analyze correlated catalytic thermal transformations and show, through explicit finite-dimensional examples, that reduced-state data are generally insufficient to characterize thermodynamic accessibility: the thermo-majorization behavior of the joint transformation can change while the system and catalyst marginals remain fixed, and even states with identical marginals and the same mutual information can exhibit different thermo-majorization accessibility.
The resource theory with covariant Gibbs-preserving operations, also called enhanced thermal operations, is investigated. We prove that with the help of a correlated catalyst, the state convertibility for any coherent state is fully characterized by the free energy defined with the quantum relative entropy. We can extend this result to general resource theories in the form that imposing the covariant condition to a general resource theory does not change the state convertibility, as long as the initial state is coherent and distillable and this resource theory admits the phase estimation and the phase shift. This means that adding a constraint from the law of energy conservation is irrelevant in the correlated-catalytic framework.