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Physics Condensed Matter

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Tuesday 28 April

Strongly Correlated Electrons

Identifying strong correlation using only the Kohn-Sham density of one-electron states

Strongly correlated systems have long been a central and highly non-trivial topic in condensed matter physics. At the non-interacting level, strong correlation can be associated with powerful (near) degeneracies between occupied and unoccupied states, which leads to a high density of states near the Fermi level in metallic configurations. Such regimes are commonly treated with beyond-density functional theory (DFT) approaches, such as DFT+U or DFT+DMFT while maintaining symmetric configurations. Here, we explore the hypothesis that symmetry breaking in the Kohn-Sham (KS) non-interacting system can qualitatively account for the energetic effects of strong correlation in the corresponding interacting system within standard DFT. By lifting near-degeneracies around the Fermi level, symmetry breaking diminishes the potential correlation effects, reducing the need for an explicit treatment of electron correlation, transforming an otherwise strongly correlated symmetric configuration into a normally correlated one, thus avoiding the need for interacting methods beyond DFT. This naturally connects nonmagnetic to magnetic states. We apply this idea to both strongly and normally correlated metals and observe that spin symmetry breaking leads to a pronounced reduction of the density of states at the Fermi level and a significant lowering of the total energy in strongly correlated cases. To describe the degree of correlation that the interacting system would have relative to the KS state, we introduce a correlation parameter ($\Gamma$), defined as the ratio between the Kohn-Sham density of one-electron states at the Fermi level and that of a corresponding uniform electron gas. This parameter distinguishes strongly correlated systems, which would require explicit treatment, from normally correlated ones, which do not.
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Strongly Correlated Electrons

Tunable thermal conductivity through dual spin-phonon coupling in van der Waals ferromagnetic insulator Cr2Ge2Te6

The active manipulation of phonon transport remains a central challenge in phononics and spin caloritronics due to the charge-neutral nature of heat carriers. Spin-phonon coupling (SPC) offers a promising route for the dynamic control of heat carriers, yet its progress has been limited due to the lack of a unified framework and suitable material platforms. Here, we report on the magnetic field-tunable phonon transport behavior in the ferromagnetic insulator Cr2Ge2Te6. We observed two distinct anomalous regimes at both the high and low fields that were governed by isotropic magnon-phonon hybridization and an anisotropic magnon softening process, respectively. By integrating detailed transport behavior with Brillouin light scattering and ferromagnetic resonance, we uncovered the microscopic origins of these anomalous regimes and demonstrated that both the field magnitude and orientation could act as versatile tuning knobs to manipulate the thermal conductivity. Our findings provide experimental evidence of the SPC effect on phonon transport, demonstrating the dual impact of SPC within a unified system. This work will not only broaden the fundamental understanding of quasiparticle interactions but also establish a viable framework for dynamic phonon engineering. Furthermore, the characteristics of this system highlight the potential for achieving field-tunable phonon transport in similar platforms such as two-dimensional (2D) magnetic materials.
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All authors Zhongbin Wang, Wenlong Tang, Simin Pang, Hongxing Zhu, Renkang Fan, Baohai Jia, Junxue Li, Ben Xu, Jun Zhang, Lin Xie, Jiaqing He

Materials Science

Electric-field control of hydrogen bonding via interfacial charge at atomic resolution

Hydrogen-bond networks govern molecular structure and function across chemistry, biology and materials science, yet their deterministic control at the atomic scale remains a central challenge (1-9).Here, we directly visualize how an external electric field enables reversible control of a hydrogen-bond network in monolayer ice on graphite through interfacial charge redistribution. Low-temperature scanning tunnelling microscopy reveals a field-driven transition from a mobile, physisorbed, non-wetting water phase to an ordered hexagonal monolayer, enabling deterministic nucleation, growth and complete wetting on an otherwise inert surface. Systematic variation of the field induces continuous lattice strain coexisting with discrete conductance states, revealing coupled structural and electronic responses. Reversal of the field polarity drives collective dipolar inversion, enabling switching between symmetry-equivalent configurations without disrupting the lattice. Supported by first-principles theory and bias-dependent imaging, these effects arise from field-induced modification of the interfacial electronic structure rather than purely geometric or orientational effects. These results establish interfacial charge redistribution as a general mechanism for electrically programming hydrogen-bond networks, providing a route to control molecular organization, electronic properties and collective dipolar order at interfaces.
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All authors Nassar Doudin, Jian Jiang, Chun Tang, Xiao Cheng Zeng, Mohammed Th. Hassan

Statistical Mechanics · Cross-listed from hep-th

Rethinking Dimensional Regularization in Critical Phenomena

We show that it is possible to use dimensional regularization (DR) beyond the usual $\varepsilon$-expansion in the context of renormalization group (RG) calculations in Critical Phenomena. Based on this fact, we propose a new functional RG scheme - Functional Dimensional Regularization (FDR) - and apply it to a scalar theory in three dimensions. We compute the critical exponents of the Ising universality class directly in $d=3$ under various typical approximations. The method that emerges combines the agility typical of DR with the generality proper of functional RG. Moreover, at a given order of approximation, FDR seems to provide faster convergence and better estimates than other functional RGs.
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Materials Science

Determination of the Fermi Energy of Diamond using Photoluminescence Spectral Analysis

Electronic band structures and the Fermi energy provide essential information for understanding the electronic properties of solids. In semiconductors, the Fermi energy is determined by the donor and acceptor concentrations. For diamond, the relationship between the Fermi energy and the donor-acceptor concentrations is highly nonlinear; therefore, experimental determination of the Fermi energy is important. Here, we report a method to determine the Fermi energy of diamond based on photoluminescence (PL) measurements. The density-functional-theory (DFT) study by Deák et al.~\cite{deak2014formation} showed the relationship between the Fermi energy and the formation energies of nitrogen-vacancy centers in the negatively charged (NV$^-$) and neutrally charged (NV$^0$) charge states. In the present method, we measure the relative populations of the NV$^-$ and NV$^0$ centers from PL spectral analysis and determine the Fermi energy using these populations and the DFT result. Moreover, we show the application of the method by extracting the Fermi energies of several diamond samples and discuss the spin coherence times of their NV centers and their stability against the charge state conversion. The PL-based method is advantageous for determining the Fermi energy with high spatial and fast time resolutions, even in extreme environments, and can be extended to determine various wide bandgap semiconductors.
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All authors Yifan Song, Sina Ilkhani, Leah Webb, Derrick Lin, Gem Nakamura, Helen Highland, Stephen B. Cronin, Susumu Takahashi

Statistical Mechanics

Markovian thermodynamics of non-Markovian Langevin equations

We develop the thermodynamics of non-Markovian generalized Langevin equations by embedding them in a high-dimensional Markovian representation involving auxiliary degrees of freedom. If the memory is linear and satisfies detailed balance with the noise, we provide an explicit construction of the embedding for non-Markovian dynamics with many degrees of freedom and hydrodynamic interactions. Moreover, while the embedding is generally not unique, we show that it results in unique values of thermodynamic quantities of the Markovian system. This allows us to define the Markovian entropy production of a non-Markovian system, which, in contrast to the definition based directly on the non-Markovian dynamics, is guaranteed to increase monotonically with time. Moreover, the Markovian representation allows us to identify the apparent decrease in the non-Markovian entropy with heat and information exchange between the system and the auxiliary degrees of freedom.
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Materials Science

Ultrafast Energy Absorption in Silicon Controlled by Two-Color Double Pulses

We theoretically show that energy absorption in crystalline silicon can be controlled by two-color femtosecond double-pulse irradiation, in which two temporally separated pulses with different wavelengths interact sequentially with the system. Using time-dependent density functional theory, we systematically examine the wavelength and intensity dependence of the absorbed energy over peak intensities of $2\times10^{11}$-$10^{13}$ W/cm$^2$ and wavelengths of 515, 1030, and 2060 nm. We find that the mechanism governing energy absorption and the optimal wavelength combination strongly depend on the intensity regime. In the low-intensity regime, multiphoton interband absorption is dominant, and energy absorption is enhanced for pulse pairs composed of shorter wavelengths. In contrast, in the high-intensity regime, the contributions of tunneling ionization and intraband acceleration become significant, leading to enhanced absorption for longer-wavelength combinations. In the intermediate-intensity regime, a pronounced enhancement is observed when a short-wavelength pulse precedes a long-wavelength pulse. Our analysis reveals that the nonequilibrium electronic state prepared by the first pulse modifies the excitation process induced by the second pulse, thereby enhancing the absorbed energy through an increased energy gain per excited electron. In this regime, the energy absorption is governed not only by the number of excited carriers but also by the energy gain per excited electron, which can be strongly modified by the pulse sequence. These results indicate that ultrafast energy transfer in semiconductors is tunable by appropriately designing the wavelength and intensity combination of the two pulses, and provide microscopic insight into two-color strong-field excitation.
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All authors Eiyu S. Gushiken, Mizuki Tani, Hiroki Katow, Kenichi L. Ishikawa

Materials Science

Influence of Heterogeneity on the Response of Architected Metamaterials

Architected metamaterials like foams and lattices exhibit complex responses governed by microstructural instabilities, localization, and phase-transition-like phenomena. Their behavior is further affected by heterogeneities inherent in their microstructure often caused through manufacturing processes. In this study we extend a gradient-enhanced, nonlocal continuum formulation to incorporate stochastic material heterogeneity through Gaussian random fields imposed on selected constitutive parameters. The framework enables independent control of both the amplitude and spatial correlation of material fluctuations while preserving thermodynamic consistency and regularization of localization. It also introduces a characteristic lengthscale ratio between the nonlocal and correlation lengthscales, that enables modeling at the limit of random or spatially correlated microstructures. Finite element simulations of confined compression and indentation show that heterogeneity fundamentally alters phase nucleation, localization morphology, and macroscopic response. Overall, the proposed framework provides a unified approach for linking stochastic material variability to instability-driven mechanics in architected metamaterials, enabling improved understanding of imperfection sensitivity, stability and design. It showcases how heterogeneity alone can influence characteristic features of the response, such as stability, slope of the plateau region, and elimination of the initial elastic regime.
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All authors Sarvesh Joshi, Jingye Tan, Craig M. Hamel, Stavros Gaitanaros, Nikolaos Bouklas

Monday 27 April

Materials Science · Cross-listed from cs.LG

Geometry-free prediction of inertial lift forces in microfluidic devices using deep learning

Inertial microfluidic devices (IMDs) offer low-cost, high-throughput alternative techniques for many traditional particle- (or cell-) manipulation tasks, but simulating them requires being able to predict particle migration, and thus particle lift forces, under a variety of possible channel geometries. Recent work has demonstrated that machine learning models can be used to drastically speed up these numerical simulations, but doing so required training individual models for every unique channel cross-section type (e.g., rectangular, triangular) – shifting the burden from the simulation step to the training step. In this paper, we develop a novel approach for predicting particle lift forces that contains no explicit geometric parameters. We train a neural network model using a new parameter set and show that while it performs comparably to existing models on channel geometries in the training set, it is able to generalize to unseen channel geometries far more effectively. We show that the lift force model developed herein can be easily transferred to particle tracing simulation software, where it is capable of predicting particle migration patterns consistent with the literature across a variety of channel designs.
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All authors Jesse Ward-Bond, Ali Mashadian, Timothy C. Y. Chan, Edmond W. K. Young

Strongly Correlated Electrons

Opto-criticality in Drude metals near the plasma frequency

Within a simple unified framework of classical electrodynamics that incorporates background bound charges and currents, we have analytically determined the attenuation constant, phase constant, and reflectivity of Drude metals across the full frequency spectrum ($0 < \omega < \infty$).Our result for reflectivity agrees well with existing experimental data for both plasmas and seawater. Notably, for highly conductive Drude metals ($\omega_p \tau \gg 1$), the attenuation constant simplifies to $k_- \simeq \sqrt{\frac{\mu \epsilon}{2}} \sqrt{\omega_p^2 - \omega^2 + \vert{}\omega_p^2 - \omega^2\vert{}}$ across a broad high-frequency range spanning the plasma frequency $\omega_p$. The branch-point singularity at $\omega=\omega_p$ in this relation reveals opto-critical behavior near $\omega=\omega_p$ in properties such as the attenuation constant, group velocity, and complex dielectric constant, for which we have determined the corresponding opto-critical exponents. Furthermore, we have incorporated quantum corrections into these optical properties via the Drude-Sommerfeld model with Thomas-Fermi screening.
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Statistical Mechanics

Statistical mechanics in continuous space with tensor network methods

Tensor network (TN) methods are well established for computing partition functions in statistical mechanics, though this use has traditionally been limited to lattice models. We extend the scope of TN methodology to interacting particle systems in continuous space. Through a real-space discretization combined with a cell-based coarse-graining scheme, we formulate an effective lattice model that explicitly preserves spatial locality. The partition function of this model is represented as a TN, and the thermodynamic quantities are computed via boundary contraction. We apply this framework to the two-dimensional hard-disk problem and demonstrate the strengths of the TN formulation compared to existing Monte Carlo simulations.
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All authors Gunhee Park, Tomislav Begušić, Si-Jing Du, Johnnie Gray, Garnet Kin-Lic Chan

Disordered Systems and Neural Networks · Cross-listed from physics.chem-ph

Thermal conductivity of aligned polymers with kinks

Thermal conductivity of aligned polymer molecules can be exceptionally high along the alignment direction due to energy transport through strong covalent bonds. At the same time, it is highly sensitive to molecular conformation, varying by orders of magnitude as a result of gauche kinks. Here, we theoretically investigate phonon transport in kinked polymers by numerically evaluating thermal conductivity and interpreting the results in terms of phonon scattering from randomly distributed kinks. For strongly aligned polymers with restricted deviations from a linear backbone, we find that heat transport becomes superdiffusive at long lengths, with thermal conductivity scaling as $\kappa \propto L^{1/3}$. At shorter lengths, thermal conductivity exhibits non-monotonic behavior: it increases at very short scales due to ballistic transport of almost all phonons, then decreases at intermediate lengths due to the Anderson localization of most phonon modes. These results are consistent with experiments and molecular dynamics simulations, and they elucidate the microscopic mechanisms governing heat transport in polymers.
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Mesoscale and Nanoscale Physics

Probing GHz Spin Dynamics Across Magnetic Phase Transitions in CrCl3 Nanoflakes Using Nitrogen-Vacancy Microscopy

CrCl3, a layered van der Waals (vdW) magnet, exhibits in-plane magnetic anisotropy and enhanced interlayer coupling upon stacking, making it an ideal platform to host exotic nanoscale magnetic phenomena such as magnon hydrodynamics and meron-like topological spin defects. When interfaced with other vdW materials, its antiferromagnetic-to-ferromagnetic and ferromagnetic-to-paramagnetic phase transitions and magnetic anisotropy can be tuned by voltage, strain, and layer stacking. Understanding the spin dynamics of CrCl3 at its magnetic phase transitions is crucial to its applications in magnonics. Here, we investigate the spin dynamics of CrCl3 nanoflakes using cryogenic diamond quantum sensing microscopy, based on measuring optically detected magnetic resonance, Rabi oscillations, and spin-lattice relaxation time (T1) of shallow nitrogen vacancy (NV) centers in diamond. In the ferromagnetic regime, we observe a pronounced reduction in the NV spin resonance contrast, a collapse of the Rabi oscillations, and a strong enhancement by two orders of magnitude of the relaxation rate G1 = 1/T1. These observations indicate intensified spin fluctuations in the gigahertz range. Broadband ferromagnetic resonance spectroscopy on CrCl3 crystals reveals resonance frequencies in the 4-15 GHz range together with a linewidth of ~24 mT, further supporting the NV measurements. A phenomenological model of magnetic-noise-induced NV relaxation reproduces the temperature dependence of G1 by combining antiferromagnetic, ferromagnetic, and paramagnetic fluctuation channels, indicating that magnetic noise is strongest in the ferromagnetic regime and evolves markedly across the phase transition. These results are crucial for using CrCl3 in 2D magnonics and hybrid quantum-magnon systems.
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All authors Benjamin Hammons, Jitender Kumar, Sehrish Iqbal, Prem Bahadur Karki, Karishma Prasad, Tianlin Li, Aram Pirali, Ayodimeji E. Aregbesola, Rupak Timalsina, Xia Hong, Jian Wang, Kapildeb Ambal, Ilja Fescenko, Abdelghani Laraoui

Materials Science · Cross-listed from physics.flu-dyn

Effects of temperature-dependent material properties in coldwater Rayleigh-Bénard convection

Water exhibits an anomalous nonlinear density equation of state (EOS) as it approaches freezing, along with an increase in viscosity ($\mu$) and a decrease in thermal conductivity ($k$). Here we ask: how do these temperature-dependent material properties affect thermal convection in coldwater? We examine these effects within the canonical Rayleigh-Bénard convection (RBC) system, performing direct numerical simulations with coldwater between $0^{\circ}$C and the temperature of maximum density $3.98^{\circ}$C. To disentangle the effects of these properties, we consider two main cases: RBC with a quadratic EOS and constant $\mu$ and $k$; and RBC with a quadratic EOS and temperature-dependent $\mu(T)$ and $k(T)$. We show that the most significant consequence is a shift in the mean fluid temperature relative to `standard RBC'. The nonlinear EOS and the temperature-dependent $\mu$ and $k$ drive this shift in opposite directions, with the former dominating and producing a net decrease in the mean temperature. This decrease varies with the Rayleigh number $Ra$, reaching up to $0.08^{\circ}$C at $Ra=10^{8}$. Additionally, the onset of convection is affected, but the influence from the EOS and $\mu(T)$ and $k(T)$ compensate, resulting in a negligible net effect. Despite these changes, the Nusselt and the Reynolds numbers follow classical scalings in all cases. Our results establish how the anomalous material properties of coldwater affect local and global features of convection, evidencing the implications of model selection for studies of cryospheric water bodies.
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Soft Condensed Matter

Entropic Trapping of Hard Spheres in Spherical Confinement

Monodisperse spherical colloidal particles confined within emulsion droplets can crystallize into icosahedral clusters. Experimentally it was observed that a few large colloidal particles added as defects preferentially migrate to the vertices of the icoshedral clusters. To understand this structure formation phenomenon, we simulate the confined self-assembly of hard spheres in the presence of a small number of larger particles. The results demonstrate that large spheres are significantly influenced by concentric shells of small spheres near the crystallization transition. Entropic forces drive the large spheres to the cluster surface, where they settle into free energy minima at the icosahedron vertices. Notably, the addition of twelve large spheres results in the formation of a perfect icosahedral frame. Free energy calculations via umbrella sampling are used to quantify this process and show that both the migration to the cluster surface and the trapping at the vertices with trapping strength of multiple $k_\text{B}T$ results from free energy minimization. Moreover, our study reveals that the crystallization pathway and dynamics of large spheres are consistent across different systems, suggesting robustness of entropic trapping.
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All authors Praveen K. Bommineni, Junwei Wang, Nicolas Vogel, Michael Engel

Strongly Correlated Electrons

Crystal-Field Symmetry Constraints in Layered Honeycomb ErBr$_3$

Crystal-field symmetry restricts the ground-state Kramers doublet of ErBr$_3$ to one of two classes. We show that the compressed octahedral environment selects the class with $\langle \psi_\pm | J^{\pm} | \psi_\mp \rangle = 0$, suppressing the lowest-order $J^{\pm}$-mediated exchange. Thermodynamic measurements reveal two zero-field anomalies at 0.375 and 0.200 K. Under an in-plane magnetic field, the thermodynamic response separates into a phase boundary and a broader crossover line. Inelastic neutron scattering measurements at 2 K reveal no well-defined low-energy dispersive magnetic modes. These results connect the ground-state symmetry with the field-dependent thermodynamic response of ErBr$_3$, providing a microscopic starting point for understanding its low-energy magnetic behavior.
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All authors Biaoyan Hu, Mingyuan Hu, Franz Demmel, Andrey A. Podlesnyak, Jiaqing He, Liusuo Wu

Statistical Mechanics

On the Mathematics of Information-Thermodynamics

We present a validation of the asdf method, an information-theoretic framework for computing thermodynamic entropy from molecular configurations. The method reformulates entropy estimation as the Shannon entropy of a residual mapping distribution defined between two decorrelated microstates. We demonstrate analytically that for the closed-form Hamiltonians with known solutions, the classical ideal gas and the one-dimensional harmonic oscillator's entropy obtained from the compressibility of the residual mapping object reproduces the exact thermodynamic entropy. In each case, the conditional entropy of the residual mapping object with respect to an uncorrelated microstate is shown to coincide with the ensemble entropy derived from the canonical partition function. These results establish consistency between the asdf formalism and classical statistical mechanics for analytically solvable systems. We further discuss how the framework generalizes to interacting Hamiltonians. The analysis supports the interpretation of thermodynamic entropy as an information measure encoded geometrically in inter-microstate mappings and motivates application of the method to complex condensed phases.
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Materials Science

Visualizing Crystallization Dynamics and Transformation Pathways of Disordered Rocksalt Oxides During Thermally Activated Sol-Gel Synthesis

Sol-gel synthesis is a wet-chemical processing route for the fabrication of functional materials offering control over composition, morphology, and microstructure at relatively low processing temperatures compared to conventional solid-state synthesis methods. While the sol-gel process initiates with intermixed molecular precursors, the transformation pathways at the early nucleation stage are insufficiently understood. Here, the chemical and structural transformation of disordered rocksalt (DRX) Li1.2Mn0.4Ti0.4O2 (LMTO), a promising cathode material for lithium batteries, is studied by multiscale characterization tools. In situ heating transmission electron microscopy (TEM) using a liquid cell visualizes and identifies crystallization pathways at nanoscale. While some regions follow a classical multi-step transition through thermodynamically stable intermediates, others exhibit a kinetic shortcut in which intermediate nanocrystals dissolve into a localized amorphous matrix that directly precipitates the DRX structure. Macroscale FTIR corroborates the findings to be related to chemically distinct microenvironments in the gel precursor, with transition metal ions more strongly incorporated into the acetate-coordinated network than lithium. Although in situ heating TEM captures diverse local transformation pathways, in situ SXRD indicates that the macroscopic transformation proceeds predominantly through spinel LMTO and lithium titanite intermediates toward DRX-LMTO. The findings shed light on the spatiotemporal chemical and structural transformations in sol-gel derived DRX-LMTO materials, and call for fine tuning of such sol-gel chemistries to manipulate the crystallization pathways and achieve target material homogeneity more efficiently.
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All authors Diyi Cheng, Tim Kodalle, Anika T. Promi, Ansuman Halder, Raphael F. Moral, Madeline Grass, Venkata S. Avvaru, Haegyeom Kim, Carolin M. Sutter-Fella, Haimei Zheng

Strongly Correlated Electrons

Dielectric signatures of crystal-field and low-temperature correlated dynamics in NdMgAl11O19

We report dielectric spectroscopy of single-crystalline \ce{NdMgAl11O19}, a magnetoplumbite hexaaluminate in which localized \ce{Nd^{3+}} moments coexist with a polarizable \ce{AlO5} bipyramidal network. The real part of the permittivity, $\varepsilon'_{c}(T)$, measured along the crystallographic $c$ axis, increases as the temperature is lowered from 275~K to 30~K and is frequency-independent between 4~Hz and 50~kHz. At lower temperatures, a frequency-dependent decrease in permittivity is observed, followed by a further upturn below 2~K. The high-frequency $\varepsilon'_{c}(T)$ is described by a Barrett formula supplemented by an effective two-level contribution, yielding a robust gap of $\Delta = 25.85 \pm 0.32$~K consistent with the lowest \ce{Nd^{3+}} crystal-electric-field (CEF) splitting. Below $\sim 30$~K, the dielectric response becomes strongly frequency and magnetic-field dependent. Isothermal $\varepsilon_c'(H)$ measurements reveal a reproducible low-field crossover near $\mu_0H_c \simeq 0.85$~T, which we attribute to the competition between antiferromagnetic correlations and Zeeman splitting of the ground-state Kramers doublet. \ce{NdMgAl11O19} thus provides a Kramers reference system in which dielectric signatures of the excited-state CEF manifold can be distinguished from those of the field-tuned, correlation-dominated ground-state doublet sector in a centrosymmetric frustrated magnetoplumbite host
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All authors Sonu Kumar, Gaël Bastien, Maxim Savinov, Małgorzata Śliwińska-Bartkowiak, Ross H. Colman, Stanislav Kamba

Disordered Systems and Neural Networks

Theory of Anderson localization on the hyperbolic plane

The two-dimensional hyperbolic plane, $\mathbb{H}^2$, is an unusual system in that dimensionality changes with scale: locally two-dimensional and planar at short distances, but effectively infinite-dimensional at large scales, it provides an interesting paradigm for the study of (quantum) phase transitions, notably the disorder-driven Anderson transition. Generalizing previous work, which treated short and large distance scales separately, we develop a unified framework interpolating between the principles of low- and high-dimensional Anderson localization. As a main result, we derive a two-parameter flow in a plane spanned by scale-dependent curvature (setting the system's effective dimensionality) and conductivity, with an extended critical line separating metallic and insulating phases.
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All authors Alexander Altland, Tobias Micklitz, Devasheesh Sharma, Maksimilian Usoltcev, Carolin Wille

Quantum Gases

Phase diagram of a dual-species Rydberg atom ladder

Dual-species Rydberg atom arrays extend single-species platforms by introducing competing interaction scales and enhanced quantum fluctuations, enabling phenomena beyond homogeneous settings. In this work, we study the ground-state phase diagram of a one-dimensional dual-species Rydberg atom ladder using large-scale density-matrix renormalization group calculations. We identify disordered phases, multiple ordered phases with $\mathbb{Z}_2$, $\mathbb{Z}_3$, and $\mathbb{Z}_4$ symmetry, as well as floating phases characterized by incommensurate wave vectors and algebraically decaying correlations. Importantly, we observe a smooth crossover between distinct $\mathbb{Z}_2$-ordered regimes, reflecting a reorganization of low-energy degrees of freedom rather than a true phase transition, which is absent in single-species Rydberg arrays. We further uncover a multi-critical point at the boundary between the $\mathbb{Z}_2 \otimes \mathbb{Z}_2$ and $\mathbb{Z}_3 \otimes \mathbb{Z}_3$ ordered phases, where Ising, chiral, and first-order transition lines intersect. Our results demonstrate that dual-species Rydberg atom arrays provide a unique platform for realizing crossover physics and multi-critical behavior inaccessible in single-species architectures.
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All authors Lei-Yi-Nan Liu, Shi-Rong Peng, Ze-Yuan Huang, Xing-Man Wei, Yun-Han Zou, Su Yi, Jian Cui

Strongly Correlated Electrons

Symmetry-Protected Topological Phases in the Triangular Majorana-Hubbard Ladder

We uncover a family of symmetry-protected topological phases in a model of interacting Majorana fermions on triangular-lattice ladders. Included among these phases is one in which symmetry-protected topological order coexists with spontaneous symmetry breaking associated with an adiabatically evolving set of symmetries. Our results indicate a mechanism through which interactions among Majorana modes generate nontrivial symmetry-fractionalized orders. These phases may be realized in arrays of vortex-bound Majorana zero modes on the surface of topological superconductors.
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All authors Will Holdhusen, Alberto Nocera, Jian-Xin Zhu, Armin Rahmani

Quantum Gases

Uncovering Exotic Paired States in the 2D Spin-Imbalanced Fermi Gas with Neural Wave Functions

We study the zero-temperature phase diagram of the 2D spin-imbalanced Fermi gas with short-ranged attractive interactions using the recently developed neural network variational Monte Carlo method with the AGPs FermiNet Ansatz. The Fulde-Ferrell-Larkin-Ovchinnikov phase is observed in the weakly interacting BCS limit and a polarised superfluid is seen in the strongly interacting BEC limit. When the interactions are strong, the minority-spin momentum density is reduced almost to zero in the momentum-space region occupied by the unpaired majority-spin electrons. When the interactions are very strong, phase separation occurs, with regions containing bosonic pairs and unpaired regions occupied by the remaining majority-spin particles. In addition, we observe translational symmetry breaking at intermediate interaction strengths, where the system forms an exotic crystal of Cooper pairs in a Fermi fluid of unpaired majority-spin particles. We provide a possible explanation for the formation of the crystalline phase, explain the origins of the k-space momentum-density hole when the pairs are tightly bound, and discuss how our approach opens new directions for future work.
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All authors Wan Tong Lou, Gino Cassella, Andres Perez Fadon, Halvard Sutterud, David Pfau, James S. Spencer, Johannes Knolle, W.M.C. Foulkes

Strongly Correlated Electrons

Anomaly and symmetry-charge flow in mixed states

The $(1+1)$-dimensional chiral anomaly is a paradigmatic exact result in quantum field theory, traditionally formulated for zero-temperature pure states where it arises from spectral flow induced by external gauge fields and captures universal ground-state properties. In mixed states, however, the participation of many states and charge exchange with the environment invalidate this mechanism. Naive extensions yield model-dependent anomaly coefficients, calling its universality into question. Here, we resolve this problem for Abelian symmetries by deriving the anomaly from an algebraic relation between the symmetry and its flux-insertion operator. We obtain symmetry-charge flow, a mixed-state generalization of spectral flow, in which an applied field redistributes statistical weight across symmetry-resolved charge sectors. Fixed solely by symmetry, the anomaly restores universality and applies to both pure and mixed states in fermionic and bosonic systems. We substantiate these results in tight-binding fermionic models with continuous symmetry and in spin models with discrete symmetries.
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Strongly Correlated Electrons

Dynamical dimer structure factor of the triangular $S=1/2$ Heisenberg antiferromagnet

The dynamical dimer structure factor is an observable probing spin-singlet excitations of quantum magnets distinct from those commonly studied by the spin structure factor. We report the dimer response for the extended spin-$1/2$ antiferromagnetic Heisenberg model on the triangular lattice using large-scale GPU-accelerated matrix-product-state simulations. We investigate the ordered phases with $120^\circ$ coplanar, collinear stripe, and tetrahedral spin order, as well as candidate quantum spin-liquid (QSL) regimes, comprising an expected gapless $U(1)$ Dirac QSL and a chiral QSL at finite spin-scalar-chirality coupling. In the ordered phases, we find low-energy modes below the onset of the two-magnon continuum illustrating avoided quasiparticle decay. Within the candidate gapless QSL, we observe absolute dispersion minima at momenta of half the Brillouin zone corners, $X\equiv K/2$, in agreement with field-theory predictions that singlet monopole excitations of the $U(1)$ Dirac spin liquid become gapless at these points. Thus, the high-resolution dynamical dimer response provides support for a $U(1)$ Dirac QSL with singlet monopole excitations.
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All authors Markus Drescher, Laurens Vanderstraeten, Roderich Moessner, Frank Pollmann, Johannes Knolle

Mesoscale and Nanoscale Physics

Dispersion of Anyon Bloch Bands

Fractional Chern insulators (FCIs) are zero magnetic field analogs of fractional quantum Hall states. While the electrons forming an FCI are not subject to an external magnetic field, their anyonic excitations experience a magnetic field with finite-flux due to a many-body Berry phase, whose lattice periodicity generically induces some dispersion. From Laughlin wavefunctions at filling 1/m, we analytically construct single-anyon Bloch states in an ideal band, providing a basis to efficiently compute the dispersion. The anyon spectrum exhibits an $m$-fold degeneracy in the reduced magnetic Brillouin zone (BZ), which originates from the topological degeneracy of the FCI. From our wavefunctions, we derive the m^2-fold degeneracy seen in previous works, showing it to be a splicing of anyon momenta into the electronic BZ. Finally, we find that the anyon dispersion bandwidth is controlled by quantum geometry non-uniformity, growing linearly at weak modulation and saturating at strong modulation. Remarkably, higher harmonics of the quantum geometry alone strongly suppress the dispersion, which we attribute to emergent magnetic translation symmetries. When combined with the first harmonic, a positive (negative) second harmonic drives the system toward a second- (first-) harmonic-dominated regime, thereby reducing (enhancing) the bandwidth. Our results offer an analytically controlled method for evaluating anyon spectra in ideal band FCI, shedding light on how non-uniform quantum geometry and emergent symmetries shape the dispersion of anyons.
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All authors Kishore Iyer, Andreas Feuerpfeil, Valentin Crépel, Nicolas Regnault, Christophe Mora

Mesoscale and Nanoscale Physics

Absence of Quasi-Majorana False Positives in Full-Shell Hybrid Nanowires

Tunneling spectroscopy cannot be used as an unambiguous detection tool for Majorana zero modes (MZMs) in conventional partial-shell nanowires. The presence of smooth confinement at the end of the hybrid wire (among other sources of disorder) can create exponentially pinned zero-energy states, called quasi-MZMs, that mimic all local signatures of MZMs but lack topological protection. We find that this ambiguity in MZM detection does not occur in full-shell hybrid nanowires, an alternative nanowire design where a superconducting shell fully surrounds the semiconductor core. Acting as a synthetic vortex, a full-shell hybrid nanowire hosts Caroli-de Gennes-Matricon state analogs. In the presence of smooth confinement, these states create a topologically trivial skin at the wire's end that prevents the local probe from detecting quasi-MZMs. In this way, the same mechanism that creates MZM impostors makes them invisible in tunneling spectroscopy, avoiding false positives produced by smooth disorder.
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All authors Carlos Payá, César Robles, Pablo San-Jose, Elsa Prada

Statistical Mechanics · Cross-listed from quant-ph

Randomised measurements of a disorder-induced entanglement transition in a neutral atom quantum processor

The development and spread of entanglement in complex quantum systems is central to exploring many-body phenomena out of equilibrium. Measuring entanglement dynamics can shed light on information scrambling and thermalisation, namely on transitions from many-body quantum chaos to localisation in disordered, interacting systems. In quantum computing systems, entanglement entropy and other nonlinear functions of the density matrix have been recently measured, in particular by using the randomised measurement toolbox. However, it is difficult to implement the required arbitrary unitary rotations on specific subsystems without universal local control. Here we devise and demonstrate the measurement of entanglement entropy in a programmable analogue quantum simulator using a randomised measurement protocol that leverages local energy tuning together with a global field to bypass the need for local gate control. We implement this on a commercially available neutral-atom quantum simulator, QuEra's Aquila, and use it to show how programmable disorder in the local Hamiltonian parameters leads to a transition from chaotic to localised entanglement dynamics. Given current decoherence times, we clearly resolve disorder-specific, time-dependent entanglement spreading in small systems. Our work extends the utility of programmable analogue quantum simulators, and opens further opportunities for wider randomised measurement toolboxes in a range of other analogue systems.
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All authors Apollonas S. Matsoukas-Roubeas, Oscar Scholin, Lucas Sá, Arinjoy De, Majd Hamdan, Alexei Bylinskii, Andrew J. Daley, Dorian A. Gangloff

Strongly Correlated Electrons

Universal Topological Power Transfer with Arbitrarily Large Chern Number in Driven Quantum Spin Chains

Topological frequency converters exploit a quantized transfer of power between two driving fields in a quantum system, a phenomenon topologically protected by the Chern number of the associated fiber bundle. While realizations with few-spin systems have theoretically demonstrated this effect, the conversion factors have typically been restricted to small integer values. Here, we investigate an interacting $XXZ$ Heisenberg spin-$1/2$ chain driven adiabatically by two magnetic drives with incommensurate frequencies. The Chern number, determined by the degeneracy points enclosed by the adiabatic trajectory, increases systematically with the chain length and can be tuned through the exchange anisotropy, providing direct control of the topological pumping strength. We reveal a universal dependency of the anisotropy and magnetic field strength for odd and even chain lengths of the quantum critical points. This provides a mechanism for a topological frequency converter with an arbitrarily large, quantized conversion ratio in interacting quantum spin chains. The mechanism remains the same for arbitrary coupling regions of the drives.
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Strongly Correlated Electrons

Magnetic phases of the anisotropic triangular Hubbard model from the ghost-Gutzwiller approximation in the rotating spin-frame

We investigate the magnetic phase diagram of the half-filled Hubbard model on the anisotropic triangular lattice using the Gutzwiller approximation (GA) and its ghost generalization (ghost-GA). By combining a rotating spin-frame formulation with high-resolution momentum grids, we determine magnetic ground states through direct total-energy minimization over the ordering wavevector. We benchmark standard GA and ghost-GA against dynamical mean-field theory (DMFT) and dual-fermion results. We show that GA already captures the qualitative structure of the phase diagram, but systematically overestimates the stability of magnetic order due to the absence of dynamical fluctuations. We find that introducing a small number of auxiliary ”ghost” orbitals is sufficient to recover most dynamical effects and significantly improves quantitative agreement with DMFT. Exploring the full Brillouin zone, we obtain a phase diagram comprising paramagnetic and various magnetic phases. In contrast to ladder dual-fermion susceptibility-based predictions, we find that the one-dimensional antiferromagnetic phase is never stabilized, despite being the leading instability in certain regimes. Our results establish ghost-GA as an efficient and systematically improvable framework for studying magnetism in frustrated systems, capable of achieving near-DMFT accuracy at a fraction of the computational cost. They also highlight that standard GA performs qualitatively well for capturing the general phase diagram, enabling the investigation of incommensurate magnetic orders in more complex systems.
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All authors Azin Kazemi-Moridani, Samuele Giuli, Tsung-Han Lee, A.-M. S. Tremblay, Michel Côté, Nicola Lanatà, Olivier Gingras