arXiv subjects

J. Sous

Publications and source records attributed to J. Sous.

9 recordsLinked to original sources

arXiv2026

Finite-temperature Green's function cluster expansion from thermofield doubles: Breakdown of the polaron picture

We introduce a method, numerically exact in principle, for computing the momentum- and frequency-resolved single-particle Green's function of a polaron at finite temperature. The method, which we refer to as the finite-temperature Green's function cluster expansion, combines two ingredients: the generalized Green's function cluster expansion, a numerically exact extension of the momentum average family of methods that solves the polaron problem at zero temperature through a hierarchy of equations of motion for restricted phonon cloud configurations; and the thermofield double formalism, which maps the thermal trace onto a pure-state expectation value over a doubled Hilbert space. The resulting equations of motion have the same algebraic structure as those of the multi-boson zero-temperature theory, with the temperature entering through a Bogoliubov-type mixing angle that controls the coupling to a set of fictitious bath bosons. We implement the method in our open-source software package and benchmark it on the one-dimensional Holstein polaron, computing spectral functions, dispersions, lifetimes, and effective masses across coupling regimes and temperatures up to $T/\Omega \sim 1$. Where finite-temperature density matrix renormalization group results are available, we find quantitative agreement at affordable computational cost. The method recovers momentum-resolved spectra directly in frequency space, with no time evolution or analytic continuation. We also discuss the practical costs of the approach. In particular, since the doubled phonon Hilbert space has a non-trivial configuration structure in which real and fictitious clouds compete, convergence in the corresponding cloud parameters requires care.

cond-mat.str-el↗

arXiv2022

Bipolaronic superconductivity out of a Coulomb gas

Employing unbiased sign-problem-free quantum Monte Carlo, we investigate the effects of long-range Coulomb forces on BEC of bipolarons using a model of bond phonon-modulated electron hopping. In absence of long-range repulsion, this model was recently shown to give rise to small-size, light-mass bipolarons that undergo a superfluid transition at high values of the critical transition temperature $T_\mathrm{c}$. We find that $T_\mathrm{c}$ in our model even with the long-range Coulomb repulsion remains much larger than that of Holstein bipolarons, and can be on the order of or greater than the typical upper bounds on phonon-mediated $T_\mathrm{c}$ based on the Migdal-Eliashberg and McMillan approximations. Our work points to a physically simple mechanism for superconductivity in the low-density regime that may be relevant to current experiments on dilute superconductors.

cond-mat.supr-con↗

arXiv2022

Bipolaronic high-temperature superconductivity

Electron-lattice interactions play a prominent role in quantum materials, making a deeper understanding of direct routes to phonon-mediated high-transition-temperature ($T_{\mathrm{c}}$) superconductivity desirable. However, it has been known for decades that weak electron-phonon coupling gives rise to low values of $T_{\mathrm{c}}$, while strong electron-phonon coupling leads to lattice instability or formation of bipolarons, generally assumed to be detrimental to superconductivity. Thus, the route to high-$T_{\mathrm{c}}$ materials from phonon-mediated mechanisms has heretofore appeared to be limited to raising the phonon frequency as in the hydrogen sulfides. Here we present a simple model for phonon-mediated high-$T_{\mathrm{c}}$ superconductivity based on superfluidity of light bipolarons. In contrast to the widely studied Holstein model where lattice distortions modulate the electron's potential energy, we investigate the situation where lattice distortions modulate the electron hopping. This physics gives rise to small-size, yet light bipolarons, which we study using an exact sign-problem-free quantum Monte Carlo approach, demonstrating a new route to phonon-mediated high-$T_\mathrm{c}$ superconductivity. We find that $T_\mathrm{c}$ in our model generically and significantly exceeds typical upper bounds based on Migdal-Eliashberg theory or superfluidity of Holstein bipolarons. The key ingredient in this bipolaronic mechanism that gives rise to high $T_\mathrm{c}$ is the combination of light mass and small size of bipolarons. Our work establishes principles towards the design of high-$T_{\mathrm{c}}$ superconductors via functional material engineering.

cond-mat.supr-con↗

arXiv2020

Radio frequency field-induced electron mobility in an ultracold plasma state of arrested relaxation

Penning ionization releases electrons in a state-selected Rydberg gas of nitric oxide entrained in a supersonic molecular beam. Subsequent processes of electron impact avalanche, bifurcation, and quench form a strongly coupled, spatially correlated ultracold plasma of NO$^+$ ions and electrons that exhibits characteristics of self-organized criticality. This plasma contains a residue of nitric oxide Rydberg molecules. A conventional fluid dynamics of ion-electron-Rydberg quasi-equilibrium predicts rapid decay to neutral atoms. Instead, the NO plasma endures for a millisecond or more, suggesting that quenched disorder creates a state of suppressed electron mobility. Supporting this proposition, a 60 MHz radiofrequency field with a peak-to-peak amplitude less than 1 V cm$^{-1}$ acts dramatically to mobilize electrons, causing the plasma to dissipate by dissociative recombination and Rydberg predissociation. An evident density dependence shows that this effect relies on collisions, giving weight to the idea of arrested relaxation as a cooperative property of the ensemble.

physics.atom-ph↗

arXiv2020

mm-wave Rydberg-Rydberg resonances as a witness of intermolecular coupling in the arrested relaxation of a molecular ultracold plasma

Out-of-equilibrium, strong correlation in a many-body system triggers emergent properties that can act in important ways to constrain the natural dissipation of energy and matter. Networks of atoms, intricately engineered to arrange positions and tune interaction energies, exhibit striking dynamics. But, strong correlation itself can also act to restrict available phase space. Relaxation confined by strong correlation gives rise to scale invariance and density distributions characteristic of self-organized criticality. For some time, we have observed signs of self-organization in the avalanche, bifurcation and quench of a state-selected Rydberg gas of nitric oxide to form an ultracold, strongly correlated ultracold plasma. The robust arrested relaxation of this system forms a disordered state with quantum-mechanical properties that appear to support a coherent destruction of transport. Work reported here focuses on initial stages of avalanche and quench, using the mm-wave spectroscopy of an embedded quantum probe to characterize the intermolecular interaction dynamics associated with the evolution to plasma. Double-resonance excitation prepares a Rydberg gas of nitric oxide composed of a single selected state, $n_0f(2)$. Penning ionization, followed by an avalanche of electron-Rydberg collisions, forms a plasma of NO$^+$ ions and weakly bound electrons, in which a residual population of $n_0$ Rydberg molecules evolves to high-$\ell$. At long times, $n_0\ell(2) \rightarrow (n_0 \pm 1)d(2)$ depletion resonances signal collision-free energy redistribution in the basis of central-field Rydberg states. The widths and asymmetries of Fano lineshapes witness the degree to which coupling to the arrested bath broadens the bright state as well as how bright-state predissociation mixes the network of levels in the localized ensemble.

cond-mat.quant-gas↗

arXiv2019

Dissipative dynamics of atomic and molecular Rydberg gases: Avalanche to ultracold plasma states of strong coupling

Not long after metastable xenon was photoionized in a magneto-optical trap, groups in Europe and North America found that similar states of ionized gas evolved spontaneously from state-selected, high principal quantum number Rydberg gases. Studies of atomic xenon and molecular nitric oxide entrained in a supersonically cooled molecular beam subsequently showed much the same final state evolved from a sequence of prompt Penning ionization and electron-impact avalanche to plasma, well-described by coupled rate-equation simulations. But, measured over longer times, the molecular ultracold plasma was found to exhibit an anomalous combination of very long lifetime and very low apparent electron temperature. This review summarizes early developments in the study of ultracold plasmas formed by atomic and molecular Rydberg gases, and then details observations as they combine to characterize properties of the nitric oxide molecular ultracold plasma that appear to call for an explanation beyond the realm of conventional plasma physics.

physics.plasm-ph↗

arXiv2018

Similarity transformed equation of motion coupled cluster theory revisited: a benchmark study of valence excited states

The similarity transformed equation of motion coupled cluster (STEOM-CC) method is benchmarked against CC3 and EOM-CCSDT-3 for a large test set of valence excited states of organic molecules studied by Schreiber et al. [M. Schreiber, M.R. Silva-Junior, S.P. Sauer, and W. Thiel, J. Chem. Phys. $\textbf{128}$, 134110 (2008)]. STEOM-CC is found to behave quite satisfactorily and provides significant improvement over EOM-CCSD, CASPT2 and NEVPT2 for singlet excited states, lowering standard deviations of these methods by almost a factor of 2. Triplet excited states are found to be described less accurately, however. Besides the parent version of STEOM-CC, additional variations are considered. STEOM-D includes a perturbative correction from doubly excited determinants. The novel STEOM-H ($ω$) approach presents a sophisticated technique to render the STEOM-CC transformed Hamiltonian hermitian. In STEOM-PT, the expensive CCSD step is replaced by many-body second-order perturbation theory (MBPT(2)), while extended STEOM (EXT-STEOM) provides access to doubly excited states. To study orbital invariance in STEOM, we investigate orbital rotation in the STEOM-ORB approach. Comparison of theses variations of STEOM for the large test set provides a comprehensive statistical basis to gauge the usefulness of these approaches.

physics.chem-ph↗

arXiv2018

Phonon-mediated repulsion, sharp transitions and (quasi)self-trapping in the extended Peierls-Hubbard model

We study two identical fermions, or two hard-core bosons, in an infinite chain and coupled to phonons by interactions that modulate their hopping as described by the Peierls/Su-Schrieffer-Heeger (SSH) model. We show that exchange of phonons generates effective nearest-neighbor repulsion between particles and also gives rise to interactions that move the pair as a whole. The two-polaron phase diagram exhibits two sharp transitions, leading to light dimers at strong coupling and the flattening of the dimer dispersion at some critical values of the parameters. This dimer (quasi)self-trapping occurs at coupling strengths where single polarons are mobile. This illustrates that, depending on the strength of the phonon-mediated interactions, the coupling to phonons may completely suppress or strongly enhance quantum transport of correlated particles.

cond-mat.str-el↗

arXiv2017

Arrested relaxation in an isolated molecular ultracold plasma

Spontaneous avalanche to plasma splits the core of an ellipsoidal Rydberg gas of nitric oxide. Ambipolar expansion first quenches the electron temperature of this core plasma. Then, long-range, resonant charge transfer from ballistic ions to frozen Rydberg molecules in the wings of the ellipsoid quenches the centre-of-mass ion/Rydberg molecule velocity distribution. This sequence of steps gives rise to a remarkable mechanics of self-assembly, in which the kinetic energy of initially formed hot electrons and ions drives an observed separation of plasma volumes. These dynamics adiabatically sequester energy in a reservoir of mass transport, starting a process that anneals separating volumes to form an apparent glass of strongly coupled ions and electrons. Short-time electron spectroscopy provides experimental evidence for complete ionization. The long lifetime of this system, particularly its stability with respect to recombination and neutral dissociation, suggests that this transformation affords a robust state of arrested relaxation, far from thermal equilibrium.

physics.plasm-ph↗