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Entropic force and real-time dynamics of holographic quarkonium in a magnetic field
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We continue the study of a recently constructed holographic QCD model supplemented with magnetic field. We consider the holographic dual of a quark, anti-quark pair and investigate its entropy beyond the deconfinement phase transition in terms of interquark distance, temperature and magnetic field. We obtain a clear magnetic field dependence in the strongly decreasing entropy near deconfinement and in the entropy variation for growing interquark separation. We uncover various supporting evidences for inverse magnetic catalysis. The emergent entropic force is found to become stronger with magnetic field, promoting the quarkonium dissociation. We also probe the dynamical dissociation of the quarkonium state, finding a faster dissociation with magnetic field. At least the static predictions should become amenable to a qualitative comparison with future lattice data.
Forward citations
Cited by 4 Pith papers
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Quarkonium spectra with magnetically induced anisotropic confinement
Radially excited charmonium masses fall sharply with magnetic field strength under lattice-inspired anisotropic confinement, while the ground state barely moves.
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A Landau-Zener Hamiltonian fitted to the static charmonium spectrum predicts that fast magnetic-field sweeps drive nonadiabatic transitions between charmonium states, with Stückelberg interference controlling final po...
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Interplay of magnetic field and chemical potential induced anisotropy and frame dependent chaos of a $Q\bar{Q}$ pair in holographic QCD
In a holographic QCD model, chaotic string dynamics appear only for unstable configurations near the horizon, and magnetic field and chemical potential affect chaos oppositely in string and Einstein frames.
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Comparative study of the butterfly velocity in holographic QCD models at finite temperature and chemical potential
Using three independent holographic methods, the authors obtain matching butterfly velocities for four QCD-like models and find a universal increase with temperature and decrease with chemical potential.
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