Search arXiv⌕ Search
Home/Archive/arXiv

arXiv · hep-lat/0511017

Order, Disorder and Confinement

M. D'Elia·A. Di Giacomo·C. Pica
View original source ↗Read source document ↗Export metadata ↓

Abstract

Studying the order of the chiral transition for $N_f=2$ is of fundamental importance to understand the mechanism of color confinement. We present results of a numerical investigation on the order of the transition by use of a novel strategy in finite size scaling analysis. The specific heat and a number of susceptibilities are compared with the possible critical behaviours. A second order transition in the O(4) and O(2) universality classes are excluded. Substantial evidence emerges for a first order transition. Results are in agreement with those found by studying the scaling properties of a disorder parameter related to the dual superconductivity mechanism of color confinement.

Explore related subjects

hep-lat

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M. D'Elia, A. Di Giacomo, C. Pica. 2005-11-07. Order, Disorder and Confinement. https://doi.org/10.1063/1.2163755

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Efficient Quantum Simulations of Yang-Mills theory with Maximal-tree Gauge

We develop a quantum algorithmic framework for the efficient simulation of Yang--Mills theories, including the $\mathrm{SU}(3)$ gauge theory in Quantum Chromodynamics (QCD). The framework uses maximal-tree gauge in terms of gauge field variables that removes all local gauge redundancies. In the resulting gauge-fixed formulation and digitization in the field-amplitude basis, we show that Hamiltonian time evolution admits an efficient implementation based on quantum singular value transformation (QSVT). We derive upper bounds on the total number of qubits and gate complexity, finding polynomial scaling with the inverse simulation precision $1/\varepsilon_s$, lattice volume $\mathcal{V}$, gauge coupling $g$, and target energy scale $E$. Our results provide a rigorous complexity-theoretic demonstration that non-Abelian Yang--Mills theories can be simulated efficiently on quantum computers, paving the way toward first-principles quantum simulations of non-perturbative QCD dynamics.

hep-lat↗
arXiv2026

Accurate Sampling from Diffusion Models

A new proposal called DM-SMC (Diffusion Model - Sequential Monte Carlo) is investigated, which samples ensembles defined in terms of an action, using diffusion models trained on samples from the ensemble. The SMC setup allows for accurate sampling in spite of an approximate diffusion model and the finite stepsize used in the numerical solution of the stochastic process. Improved update strategies are also investigated. Results are presented for a $Z_2$ symmetric scalar field theory in 2 dimensions near its 2nd order phase transition.

hep-lat↗
arXiv2026

Decomposition of the axial-vector current in a finite box

We consider the matrix element of the axial-vector current between two nucleon states in a finite box. Starting from the chiral Lagrangian density with nucleon and Delta-isobar degrees of freedom, we study the finite-volume effects at the one-loop level. We show that the standard decomposition into the axial-vector and pseudoscalar form factor is incomplete in a finite box. We derive expressions for the complete set of in-box form factors at one loop, and demonstrate how to extract the full set from lattice correlation functions. We verify that the axial Ward identity holds in the chiral limit. We derive the one-loop expressions for the pseudoscalar form factor and verify that the in-box axial Ward identity away from the chiral limit is fulfilled also. Selected numerical results are shown for two flavor-SU(2) lattice ensembles. Sizable finite-volume effects are observed, with an important role for the Delta-isobar. We discuss the implications of our results for lattice studies of the axial-vector current. We conclude that full finite-box results are crucial for a precise determination of the form factors.

hep-lat↗