Statistical Thermodynamics of Polymer Quantum Systems

TL;DR

This paper investigates the statistical thermodynamics of polymer quantum systems, revealing how polymer length influences spectra and thermodynamic properties, including corrections and anomalies like peaks in heat capacity.

Contribution

It introduces a detailed analysis of thermodynamics in polymer quantum systems, highlighting the impact of polymer length and identifying regimes with distinct spectral and thermodynamic behaviors.

Findings

Spectra depend on polymer length, showing vibrational or rotational regimes.

Thermodynamic quantities exhibit corrections due to polymer effects.

Anomalous peak in heat capacity appears for generic polymer lengths.

Abstract

Polymer quantum systems are mechanical models quantized similarly as loop quantum gravity. It is actually in quantizing gravity that the polymer term holds proper as the quantum geometry excitations yield a reminiscent of a polymer material. In such an approach both non-singular cosmological models and a microscopic basis for the entropy of some black holes have arisen. Also important physical questions for these systems involve thermodynamics. With this motivation, in this work, we study the statistical thermodynamics of two one dimensional {\em polymer} quantum systems: an ensemble of oscillators that describe a solid and a bunch of non-interacting particles in a box, which thus form an ideal gas. We first study the spectra of these polymer systems. It turns out useful for the analysis to consider the length scale required by the quantization and which we shall refer to as polymer length. The dynamics of the polymer oscillator can be given the form of that for the standard quantum pendulum. Depending on the dominance of the polymer length we can distinguish two regimes: vibrational and rotational. The first occur for small polymer length and here the standard oscillator in Schr\"odinger quantization is recovered at leading order. The second one, for large polymer length, features dominant polymer effects. In the case of the polymer particles in the box, a bounded and oscillating spectrum that presents a band structure and a Brillouin zone is found. The thermodynamical quantities calculated with these spectra have corrections with respect to standard ones and they depend on the polymer length. For generic polymer length, thermodynamics of both systems present an anomalous peak in their heat capacity $C_V$.