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Yuri Myasoedov

Publications and source records attributed to Yuri Myasoedov.

At least 19 recordsLinked to original sources

Thermodynamic evidence for interaction-driven first-order topological quantum phase transitions

Topological quantum phase transitions in non interacting systems occur through continuous gap closing and reopening. In strongly interacting systems, however, competing ordered states have long been predicted to drive first order transitions, although this possibility has remained experimentally unresolved. Recent transport studies of correlated phases in charge neutral rhombohedral graphene were interpreted as evidence for continuous topological transitions. Here, using nanoSQUID on tip magnetometry, we directly image the local orbital magnetization of a spin orbit proximitized rhombohedral graphene quantum anomalous Hall (QAH) state. We provide the first real space visualization of a QAH phase with a record Chern number, reconstruct its local thermodynamic gap, and track the evolution of its magnetization across competing correlated states. Combined with self consistent Hartree Fock calculations, these measurements show that the sequential transitions between the layer antiferromagnetic, QAH, and layer polarized insulating states are first order, accompanied by discontinuous changes in orbital magnetization. Near the phase boundaries, we observe fluctuating magnetic domains, providing direct microscopic evidence of phase coexistence between nearly degenerate competing ordered states. Together, these observations provide the first direct thermodynamic evidence for first order topological quantum phase transitions and establish a microscopic framework for understanding interaction driven topological quantum phase transitions through phase competition and coexistence.

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Reconfigurable chiral superconductivity

Rhombohedral multilayer graphene at high displacement fields hosts superconductivity emerging from a spin valley polarized quarter metal, with transport signatures suggestive of time reversal symmetry (TRS) breaking and chiral superconductivity (CSC). These observations have motivated proposals of topological superconductivity and non-Abelian quasiparticles, yet direct magnetic evidence and microscopic insight into the superconducting state remain lacking, limiting understanding of this unique state. Here we use nanoscale SQUID on tip magnetometry to image isospin-polarized domains in rhombohedral pentalayer graphene and establish CSC via spatially resolved thermodynamic detection of TRS breaking. We find that the density at which domain walls proliferate at elevated temperatures coincides with the onset of CSC, indicating an underlying transition in the parent state that both induces superconductivity and reduces domain wall energy. We further show that the chiral domain structure in the superconducting phase is inherited from the isospin-polarized parent state. Strikingly, the CSC phase exhibits multiple transport regimes governed by configurations of chiral domains separated by highly resistive domain walls. We demonstrate deterministic, ultra low current control of these domains, enabling reversible switching between states of opposite chirality a defining CSC property absent in other superconductors. These results establish rhombohedral graphene as a unique platform for reconfigurable CSC and ultra low power electronic functionality based on controllable isospin textures.

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Electrically controllable valence-conduction band reversals in helical trilayer graphene

In moir\'e graphene systems, electronic interactions lift spin and valley degeneracies, leading to symmetry-broken ground states. In helical trilayer graphene (HTG), we uncover a distinct interaction-driven mechanism in which the roles of sublattice-polarized valence and conduction bands are cyclically reversed. Using scanning nano-SQUID magnetometry, we detect a series of sharp magnetic signatures consistent with seesaw-like transitions, where occupied and unoccupied valence and conduction bands interchange repeatedly with doping, accompanied by a novel form of magnetic hysteresis. These transitions occur entirely within metallic regimes and leave only weak fingerprints in transport measurements. Self-consistent Hartree-Fock calculations reveal that interactions reorganize all eight low-energy flat bands, driving abrupt changes in orbital magnetization. Our results establish HTG as the first system where electronic interactions provide doping-controlled access to all three internal degrees of freedom - spin, valley, and sublattice - introducing a new class of correlated phase transitions.

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hBN alignment orientation controls moir\'e strength in rhombohedral graphene

Rhombohedral multilayer graphene hosts a rich landscape of correlated symmetry-broken phases, driven by strong interactions from its flat band edges. Aligning to hexagonal boron nitride (hBN) creates a moir\'e pattern, leading to recent observations of exotic ground states such as integer and fractional quantum anomalous Hall effects. Here, we show that the moir\'e effects and resulting correlated phase diagrams are critically influenced by a previously underestimated structural choice: the hBN alignment orientation. This binary parameter distinguishes between configurations where the rhombohedral graphene and hBN lattices are aligned near 0{\deg} or 180{\deg}, a distinction that arises only because both materials break inversion symmetry. Although the two orientations produce the same moir\'e wavelength, we find their distinct local stacking configurations result in markedly different moir\'e potential strengths. Using low-temperature transport and scanning SQUID-on-tip magnetometry, we compare nearly identical devices that differ only in alignment orientation and observe sharply contrasting sequences of symmetry-broken states. Theoretical analysis reveals a simple mechanism based on lattice relaxation and the atomic-scale electronic structure of rhombohedral graphene, supported by detailed modeling. These findings establish hBN alignment orientation as a key control parameter in moir\'e-engineered graphene systems and provide a framework for interpreting both prior and future experiments.

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Revealing electron-lattice decoupling by Peltier thermometry and nanoscale thermal imaging in graphene

Electrical currents in low-dimensional quantum materials can drive electrons far from equilibrium, creating stark imbalance between electron and lattice temperatures. Yet, no existing methods enable simultaneous nanoscale mapping of both temperatures at cryogenic conditions. Here, we introduce a scanning probe technique that images the local lattice temperature and extracts electron temperature at gate-defined p-n junctions in graphene. By applying an alternating electrical current and analyzing first- and second-harmonic responses, we disentangle Joule heating from the Peltier effect-the latter encoding the local electron temperature. This enables the first spatially resolved cryogenic imaging of both phenomena in graphene. Even under modest current bias, the electron temperature increases by nearly three orders of magnitude more than the lattice temperature, revealing strong electron-phonon decoupling and indicating a previously unrecognized electron cooling pathway. Our minimally invasive method is broadly applicable to van der Waals heterostructures and opens new avenues for probing energy dissipation and non-equilibrium transport in correlated and hydrodynamic electron systems.

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Visualizing isospin magnetic texture and intervalley exchange interaction in rhombohedral tetralayer graphene

The tunable band structure and nontrivial topology of multilayer rhombohedral graphene lead to a variety of correlated electronic states with isospin orders-meaning ordered states in the combined spin and valley degrees of freedom-dictated by the interplay of spin-orbit coupling and Hunds exchange interactions. However, methods for mapping local isospin textures and determining the exchange energies are currently lacking. Here, we image the magnetization textures in tetralayer rhombohedral graphene using a nanoscale superconducting quantum interference device. We observe sharp magnetic phase transitions that indicate spontaneous time-reversal symmetry breaking. In the quarter-metal phase, the spin and orbital moments align closely, providing a bound on the spin-orbit coupling energy. We also show that the half-metal phase has a very small magnetic anisotropy, which provides an experimental lower bound on the intervalley Hunds exchange interaction energy. This is found to be close to its theoretical upper bound. The ability to resolve the local isospin texture and the different interaction energies will allow a better understanding of the phase transition hierarchy and the numerous correlated electronic states arising from spontaneous and induced isospin symmetry breaking in graphene heterostructures.

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Imaging Coulomb interactions and migrating Dirac cones in twisted graphene by local quantum oscillations

Flat band moiré graphene systems have emerged as a quintessential platform to investigate correlated phases of matter. A plethora of interaction-driven ground states have been proposed, and yet despite extensive experimental effort, there has been little direct evidence that distinguishes between the various phases, in particular near charge neutrality point. Here, we use a nanoscale scanning superconducting quantum interference device to image the local thermodynamic quantum oscillations in alternating-twist trilayer graphene at magnetic fields as low as 56 mT, which reveal ultrafine details of the density of states and of the renormalization of the single-particle band structure by Coulomb interactions. We find that the charging self-energy due to occupied electronic states, is critical in explaining the high carrier density physics. At half-filling of the conduction flat band, we observe a Stoner-like symmetry breaking, suggesting that it is the most robust mechanism in the hierarchy of phase transitions. On approaching charge neutrality, where the charging energy is negligible and exchange energy is dominant, we find the ground state to be a nematic semimetal which is favored over gapped states in the presence of heterostrain. In the revealed semimetallic phase, the flat-band Dirac cones migrate towards the mini-Brillouin zone center, spontaneously breaking the C_3 rotational symmetry. Our low-field local quantum oscillations technique presents an alluring avenue to explore the ground states of diverse strongly interacting van der Waals systems.

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Imaging de Haas-van Alphen quantum oscillations and milli-Tesla pseudomagnetic fields

A unique attribute of atomically thin quantum materials is the in-situ tunability of their electronic band structure by externally controllable parameters like electrostatic doping, electric field, strain, electron interactions, and displacement or twisting of atomic layers. This unparalleled control of the electronic bands has led to the discovery of a plethora of exotic emergent phenomena. But despite its key role, there is currently no versatile method for mapping the local band structure in advanced 2D materials devices in which the active layer is commonly embedded in various insulating layers and metallic gates. Utilizing a scanning superconducting quantum interference device, we image the de Haas-van Alphen quantum oscillations in a model system, the Bernal-stacked trilayer graphene with dual gates, which displays multiple highly-tunable bands. By resolving thermodynamic quantum oscillations spanning over 100 Landau levels in low magnetic fields, we reconstruct the band structure and its controllable evolution with the displacement field with unprecedented precision and spatial resolution of 150 nm. Moreover, by developing Landau level interferometry, we reveal shear-strain-induced pseudomagnetic fields and map their spatial dependence. In contrast to artificially-induced large strain, which leads to pseudomagnetic fields of hundreds of Tesla, we detect naturally occurring pseudomagnetic fields as low as 1 mT corresponding to graphene twisting by just 1 millidegree over one μm distance, two orders of magnitude lower than the typical angle disorder in high-quality twisted bilayer graphene devices. This ability to resolve the local band structure and strain on the nanoscale opens the door to the characterization and utilization of tunable band engineering in practical van der Waals devices.

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de Haas-van Alphen spectroscopy and fractional quantization of magnetic-breakdown orbits in moiré graphene

Quantum oscillations originating from the quantization of the electron cyclotron orbits provide ultrasensitive diagnostics of electron bands and interactions in novel materials. We report on the first direct-space nanoscale imaging of the thermodynamic magnetization oscillations due to the de Haas-van Alphen effect in moiré graphene. Scanning by SQUID-on-tip in Bernal bilayer graphene crystal-axis-aligned to hBN reveals abnormally large magnetization oscillations with amplitudes reaching 500 μ_B/electron in weak magnetic fields, unexpectedly low frequencies, and high sensitivity to the superlattice filling fraction. The oscillations allow us to reconstruct the complex band structure in exquisite detail, revealing narrow moiré bands with multiple overlapping Fermi surfaces separated by unusually small momentum gaps. We identify distinct sets of oscillations that violate the textbook Onsager Fermi surface sum rule, signaling formation of exotic broad-band particle-hole superposition states induced by coherent magnetic breakdown.

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Scanning SQUID-on-tip microscope in a top-loading cryogen-free dilution refrigerator

The scanning superconducting quantum interference device (SQUID) fabricated on the tip of a sharp quartz pipette (SQUID-on-tip) has emerged as a versatile tool for nanoscale imaging of magnetic, thermal, and transport properties of microscopic devices of quantum materials. We present the design and performance of a scanning SQUID-on-tip microscope in a top-loading probe of a cryogen-free dilution refrigerator. The microscope is enclosed in a custom-made vacuum-tight cell mounted at the bottom of the probe and is suspended by springs to suppress vibrations caused by the pulse tube cryocooler. Two capillaries allow in-situ control of helium exchange gas pressure in the cell that is required for thermal imaging. A nanoscale heater is used to create local temperature gradients in the sample, which enables quantitative characterization of the relative vibrations between the tip and the sample. The spectrum of the vibrations shows distinct resonant peaks with maximal power density of about 27 nm/Hz$^{1/2}$ in the in-plane direction. The performance of the SQUID-on-tip microscope is demonstrated by magnetic imaging of the MnBi$_2$Te$_4$ magnetic topological insulator, magnetization and current distribution imaging in a SrRuO$_3$ ferromagnetic oxide thin film, and by thermal imaging of dissipation in graphene.

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Imaging Chern mosaic and Berry-curvature magnetism in magic-angle graphene

Charge carriers in magic angle graphene come in eight flavors described by a combination of their spin, valley, and sublattice polarizations. When the inversion and time reversal symmetries are broken by the substrate or by strong interactions, the degeneracy of the flavors can be lifted and their corresponding bands can be filled sequentially. Due to their non-trivial band topology and Berry curvature, each of the bands is classified by a topological Chern number, leading to the quantum anomalous Hall and Chern insulator states at integer fillings $ν$ of the bands. It has been recently predicted, however, that depending on the local atomic-scale arrangements of the graphene and the encapsulating hBN lattices, rather than being a global topological invariant, the Chern number C may become position dependent, altering transport and magnetic properties of the itinerant electrons. Using a SQUID-on-tip, we directly image the nanoscale Berry-curvature-induced equilibrium orbital magnetism, the polarity of which is governed by the local Chern number, and detect its two constituent components associated with the drift and the self-rotation of the electronic wave packets. At $ν=1$, we observe local zero-field valley-polarized Chern insulators forming a mosaic of microscopic patches of C=-1, 0, or 1, governed by the local sublattice polarization, consistent with predictions. Upon further filling, we find a first-order phase transition due to recondensation of electrons from valley K to K', which leads to irreversible flips of the local Chern number and the magnetization, and to the formation of valley domain walls giving rise to hysteretic global anomalous Hall resistance. The findings shed new light on the structure and dynamics of topological phases and call for exploration of the controllable formation of flavor domain walls and their utilization in twistronic devices.

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Direct observation of vortices in an electron fluid

Vortices are the hallmarks of hydrodynamic flow. Recent studies indicate that strongly-interacting electrons in ultrapure conductors can display signatures of hydrodynamic behavior including negative nonlocal resistance, Poiseuille flow in narrow channels, and a violation of the Wiedemann-Franz law. Here we provide the first visualization of whirlpools in an electron fluid. By utilizing a nanoscale scanning superconducting quantum interference device on a tip (SQUID-on-tip) we image the current distribution in a circular chamber connected through a small aperture to an adjacent narrow current carrying strip in high-purity type-II Weyl semimetal WTe2. In this geometry, the Gurzhi momentum diffusion length and the size of the aperture determine the vortex stability phase diagram. We find that the vortices are present only for small apertures, whereas the flow is laminar (non-vortical) for larger apertures, consistent with the theoretical analysis of the hydrodynamic regime and in contrast to the expectations of ballistic transport in WTe2 at low temperatures. Moreover, near the vortical-to-laminar transition, we observe a single vortex in the chamber splitting into two vortices, a behavior that can occur only in the hydrodynamic regime and cannot be sustained by ballistic transport. These findings suggest a novel mechanism of hydrodynamic flow: instead of the commonly considered electron-electron scattering at the bulk, which becomes extremely weak at low temperatures, the spatial diffusion of charge carriers' momenta is enabled by small-angle scattering at the planar surfaces of thin pure crystals. This surface-induced para-hydrodynamics opens new avenues for exploring and utilizing electron fluidics in high-mobility electron systems.

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Long-range nontopological edge currents in charge-neutral graphene

Van der Waals heterostructures display a rich variety of unique electronic properties. To identify novel transport mechanisms, nonlocal measurements have been widely used, wherein a voltage is measured at contacts placed far away from the expected classical flow of charge carriers. This approach was employed in search of dissipationless spin and valley transport, topological charge-neutral currents, hydrodynamic flows and helical edge modes. Monolayer, bilayer, and few-layer graphene, transition-metal dichalcogenides, and moire superlattices were found to display pronounced nonlocal effects. However, the origin of these effects is hotly debated. Graphene, in particular, exhibits giant nonlocality at charge neutrality, a prominent behavior that attracted competing explanations. Utilizing superconducting quantum interference device on a tip (SQUID-on-tip) for nanoscale thermal and scanning gate imaging, we demonstrate that the commonly-occurring charge accumulation at graphene edges leads to giant nonlocality, producing narrow conductive channels that support long-range currents. Unexpectedly, while the edge conductance has little impact on the current flow in zero magnetic field, it leads to field-induced decoupling between edge and bulk transport at moderate fields. The resulting giant nonlocality both at charge neutrality and away from it produces exotic flow patterns in which charges can flow against the global electric field. We have visualized surprisingly intricate patterns of nonlocal currents, which are sensitive to edge disorder. The observed one-dimensional edge transport, being generic and nontopological, is expected to support nonlocal transport in many electronic systems, offering insight into numerous controversies in the literature and linking them to long-range guided electronic states at system edges.

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Sputtered MoRe SQUID-on-tip for high-field magnetic and thermal nanoimaging

Scanning nanoscale superconducting quantum interference devices (SQUIDs) are gaining interest as highly sensitive microscopic magnetic and thermal characterization tools of quantum and topological states of matter and devices. Here we introduce a novel technique of collimated differential-pressure magnetron sputtering for versatile self aligned fabrication of SQUID on tip (SOT) nanodevices, which cannot be produced by conventional sputtering methods due to their diffusive, rather than the required directional point-source, deposition. The new technique provides access to a broad range of superconducting materials and alloys beyond the elemental superconductors employed in the existing thermal deposition methods, opening the route to greatly enhanced SOT characteristics and functionalities. Utilizing this method, we have developed MoRe SOT devices with sub-50 nm diameter, magnetic flux sensitivity of 1.2 $μΦ_0/Hz^{1/2}$ up to 3 T at 4.2 K, and thermal sensitivity better than 4 $μK/Hz^{1/2}$ up to 5 T, about five times higher than any previous report, paving the way to nanoscale imaging of magnetic and spintronic phenomena and of dissipation mechanisms in previously inaccessible quantum states of matter.

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Mapping the twist angle and unconventional Landau levels in magic angle graphene

The emergence of flat electronic bands and of the recently discovered strongly correlated and superconducting phases in twisted bilayer graphene crucially depends on the interlayer twist angle upon approaching the magic angle $θ_M \approx 1.1°$. Although advanced fabrication methods allow alignment of graphene layers with global twist angle control of about 0.1$°$, little information is currently available on the distribution of the local twist angles in actual magic angle twisted bilayer graphene (MATBG) transport devices. Here we map the local $θ$ variations in hBN encapsulated devices with relative precision better than 0.002$°$ and spatial resolution of a few moir$é$ periods. Utilizing a scanning nanoSQUID-on-tip, we attain tomographic imaging of the Landau levels in the quantum Hall state in MATBG, which provides a highly sensitive probe of the charge disorder and of the local band structure determined by the local $θ$. We find that even state-of-the-art devices, exhibiting high-quality global MATBG features including superconductivity, display significant variations in the local $θ$ with a span close to 0.1$°$. Devices may even have substantial areas where no local MATBG behavior is detected, yet still display global MATBG characteristics in transport, highlighting the importance of percolation physics. The derived $θ$ maps reveal substantial gradients and a network of jumps. We show that the twist angle gradients generate large unscreened electric fields that drastically change the quantum Hall state by forming edge states in the bulk of the sample, and may also significantly affect the phase diagram of correlated and superconducting states. The findings call for exploration of band structure engineering utilizing twist-angle gradients and gate-tunable built-in planar electric fields for novel correlated phenomena and applications.

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Nanoscale imaging of equilibrium quantum Hall edge currents and of the magnetic monopole response in graphene

The recently predicted topological magnetoelectric effect and the response to an electric charge that mimics an induced mirror magnetic monopole are fundamental attributes of topological states of matter with broken time reversal symmetry. Using a SQUID-on-tip, acting simultaneously as a tunable scanning electric charge and as ultrasensitive nanoscale magnetometer, we induce and directly image the microscopic currents generating the magnetic monopole response in a graphene quantum Hall electron system. We find a rich and complex nonlinear behavior governed by coexistence of topological and nontopological equilibrium currents that is not captured by the monopole models. Furthermore, by utilizing a tuning fork that induces nanoscale vibrations of the SQUID-on-tip, we directly image the equilibrium currents of individual quantum Hall edge states for the first time. We reveal that the edge states that are commonly assumed to carry only a chiral downstream current, in fact carry a pair of counterpropagating currents, in which the topological downstream current in the incompressible region is always counterbalanced by heretofore unobserved nontopological upstream current flowing in the adjacent compressible region. The intricate patterns of the counterpropagating equilibrium-state orbital currents provide new insights into the microscopic origins of the topological and nontopological charge and energy flow in quantum Hall systems.

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Imaging work and dissipation in the quantum Hall state in graphene

Topology is a powerful recent concept asserting that quantum states could be globally protected against local perturbations. Dissipationless topologically protected states are thus of major fundamental interest as well as of practical importance in metrology and quantum information technology. Although topological protection can be robust theoretically, in realistic devices it is often fragile against various dissipative mechanisms, which are difficult to probe directly because of their microscopic origins. By utilizing scanning nanothermometry, we visualize and investigate microscopic mechanisms undermining the apparent topological protection in the quantum Hall state in graphene. Our simultaneous nanoscale thermal and scanning gate microscopy shows that the dissipation is governed by crosstalk between counterpropagating pairs of downstream and upstream channels that appear at graphene boundaries because of edge reconstruction. Instead of local Joule heating, however, the dissipation mechanism comprises two distinct and spatially separated processes. The work generating process that we image directly and which involves elastic tunneling of charge carriers between the quantum channels, determines the transport properties but does not generate local heat. The independently visualized heat and entropy generation process, in contrast, occurs nonlocally upon inelastic resonant scattering off single atomic defects at graphene edges, while not affecting the transport. Our findings offer a crucial insight into the mechanisms concealing the true topological protection and suggest venues for engineering more robust quantum states for device applications.

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Imaging resonant dissipation from individual atomic defects in graphene

Conversion of electric current into heat involves microscopic processes that operate on nanometer length-scales and release minute amounts of power. While central to our understanding of the electrical properties of materials, individual mediators of energy dissipation have so far eluded direct observation. Using scanning nano-thermometry with sub-micro K sensitivity we visualize and control phonon emission from individual atomic defects in graphene. The inferred electron-phonon 'cooling power spectrum' exhibits sharp peaks when the Fermi level comes into resonance with electronic quasi-bound states at such defects, a hitherto uncharted process. Rare in the bulk but abundant at graphene's edges, switchable atomic-scale phonon emitters define the dominant dissipation mechanism. Our work offers new insights for addressing key materials challenges in modern electronics and engineering dissipation at the nanoscale.

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