Emergent Quantum Geometric Phases in Holey Graphene
Pablo Canteli, Yuriko Baba, Juan Salvador-Sánchez, Jorge Estrada-Álvarez, Ana Pérez-Rodríguez, Carlos Sánchez-Sánchez, Vito Clericò, Takashi Taniguchi, Kenji Watanabe, Francisco Domínguez-Adame, Rafael A Molina, Enrique Diez, Elena Díaz, Mario Amado
cond-mat.mes-hallquant-phSubmitted Sep 30, 2026• Announced Oct 1, 2026• Revised Oct 7, 2026 (v2)
In graphene and other two-dimensional materials, periodic modulations of the electron density can significantly alter the energy spectrum and transport properties. Here, we report magnetotransport measurements in encapsulated monolayer graphene with ultra-high-quality patterned periodic antidot lattices that preserve the intrinsic electronic properties of the material. This lithographically defined platform enables controlled access to commensurability and superlattice phenomena at length scales otherwise difficult to achieve. By systematically tuning the lattice dimensions, we reveal a hierarchy of classical commensurability features arising from cyclotron orbits with comparable radii that follow multiple classical trajectories, resulting in broadened resistance peaks beyond the conventional single-orbit picture. Superimposed on these features, we observe pronounced Brown-Zak oscillations arising from the quantum commensurability between the magnetic flux quantum and the unit cell of the engineered Bravais lattices. We demonstrate that the intrinsic geometric phase of our system is directly measurable and show a precise matching of the magnetic field periodicity to the lithographic periodic patterning, where moiré-like electronic spectra can be geometrically generated in single-layer graphene without the need for twist, lattice mismatch, or multilayer stacking. Our results establish nanopatterned graphene as a clean, tunable, and scalable platform for realizing and exploring moiré physics through on-demand real-space design
In graphene and other two-dimensional materials, periodic modulations of the electron density can significantly alter the energy spectrum and transport properties. Here, we report magnetotransport measurements in encapsulated monolayer graphene with ultra-high-quality patterned periodic antidot lattices that preserve the intrinsic electronic properties of the material. This lithographically defined platform enables controlled access to commensurability and superlattice phenomena at length scales otherwise difficult to achieve. By systematically tuning the lattice dimensions, we reveal a hierarchy of classical commensurability features arising from cyclotron orbits with comparable radii that follow multiple classical trajectories, resulting in broadened resistance peaks beyond the conventional single-orbit picture. Superimposed on these features, we observe pronounced Brown-Zak oscillations arising from the quantum commensurability between the magnetic flux quantum and the unit cell of the engineered Bravais lattices. We demonstrate that the intrinsic geometric phase of our system is directly measurable and show a precise matching of the magnetic field periodicity to the lithographic periodic patterning, where moiré-like electronic spectra can be geometrically generated in single-layer graphene without the need for twist, lattice mismatch, or multilayer stacking. Our results establish nanopatterned graphene as a clean, tunable, and scalable platform for realizing and exploring moiré physics through on-demand real-space design
Moiré lattices formed by superimposing rotated two-dimensional (2D) periodic sublattices, such as twisted bilayer graphene, can exhibit fascinating properties not observed in their individual constituent layers. Despite extensive research on 2D moiré lattices, the physics of three-dimensional (3D) moiré lattices—formed by superimposing rotated 3D periodic sub-lattices with crystallographic symmetries, which exhibit unique 3D potentials determined by twisting angles—remains largely unexplored. In this work, we demonstrate that depending on the choice of rotation angles, moiré potentials composed of two cubic sub-lattices can exhibit three different phases: they can be fully 3D incommensurate, incommensurate in only one spatial direction (while remaining periodic in the orthogonal plane), or fully periodic. These incommensurate potentials, which can be created for condensates of non-interacting atoms using judiciously combined laser beams, are shown to support compact states of three distinct types: fully localized in space, confined to a line, or confined to a specific plane. Our findings establish a foundation for controlling wave localization in incommensurate 3D moiré systems, with potential applications in cold atom systems, optics, and beyond. 3D moiré lattices can exhibit distinct incommensurate phases depending on twist angles. Here, authors demonstrate phase-controlled emergence of fully localized, line-localized, and plane-localized states, enabling tunable 3D transport in cold atom and optical systems.
Inspired by the rich physics of twisted 2D bilayer moiré systems, we study Coulomb interacting systems subjected to two overlapping finite 1D lattice potentials of unequal periods through exact numerical diagonalization. Unmatching underlying lattice periods lead to a 1D bichromatic "moiré" superlattice with a large unit cell and consequently a strongly flattened band, exponentially enhancing the effective dimensionless electron-electron interaction strength and manifesting clear signatures of enhanced Mott gaps at discrete fillings. An important nonperturbative finding is a remarkable fine-tuning effect of the precise lattice commensuration, where slight variations in the relative lattice periods may lead to a suppression of the correlated insulating phase, in qualitative agreement with the observed fragility of the correlated insulating phase in twisted bilayer graphene. Our predictions, which should be directly verifiable in bichromatic optical lattices, establish that the competition between interaction and incommensuration is a key element of the physics of moiré superlattices.
Recent experiments in moiré quantum materials exhibit quantized Hall states without an external magnetic field, motivating continuum mechanisms based on smooth moiré-periodic pseudospin textures. We present a controlled theory of skyrmion Chern bands generated by such textures. An exact local SU(2) transformation reveals an emergent non-Abelian gauge field; for large branch splitting we perform an operator-level Schrieffer-Wolff expansion, yielding a single-branch Hamiltonian together with systematically dressed physical operators that define the projected interacting theory beyond strict adiabaticity. The leading dynamics is governed by a U(1) Berry connection whose flux is set by the skyrmion density, while controlled non-adiabatic corrections are fixed by the texture's real-space quantum geometric tensor. In a Landau-level representation built from the averaged emergent field, moiré-periodic modulations induce Umklapp-resolved deformations of Girvin-MacDonald-Platzman kinematics and microscopic sources of excess optical quantum weight above the topological lower bound. Assuming a gapped Hall phase, we further derive a skyrmion-crystal effective field theory with a universal Berry-phase term and a noncommutative magnetophonon. Our results provide experimentally accessible signatures for twisted transition-metal dichalcogenide homobilayers and rhombohedral graphene aligned with hexagonal boron nitride.
Tailoring pure valley-Zeeman spin-orbit coupling in WSe2-encapsulated monolayer graphene
Engineering proximity effects in twisted van der Waals heterostructures offers a powerful platform for designing electronic properties. While theoretical predictions of quantum interference in transition metal dichalcogenide-encapsulated graphene can selectively control the spin-orbit coupling component, experimental realizations have remained elusive. Here, we report pure valley-Zeeman spin-orbit coupling in monolayer graphene, achieved by encapsulation between two parallel twisted WSe2 monolayers. We observed a symmetry-enforced reordering of Landau levels, which is driven by the competition between the fixed valley-Zeeman energy and the magnetic-field-dependent cyclotron energy. This reordering is characterized by a transition from symmetry-broken states in the quantum Hall effect to a restored fourfold degeneracy with integer or half-integer quantum Hall sequences. We also demonstrate the ability to completely quench the proximity spin-orbit coupling by tuning the encapsulated geometry.
Magnetotransport underlines many important phenomena in condensed matter physics, such as the Hall effect and magnetoresistance (MR) effect. Thus far, most magnetotransport studies are based on bulk resistance measurements without direct access to microscopic details of the spatial transport pattern. Here, we report nanoscale imaging of magnetotransport using a scanning single-spin quantum magnetometer, which is demonstrated in a graphene-metal hybrid device at room temperature. By visualizing the current flow at elevated magnetic fields (~0.5 T), we directly observe the Lorentz deflection of current near the graphene-metal interface, which is a hallmark of magnetotransport. Combining the local current distribution with global resistance measurements, we reveal that transport properties of the hybrid are governed by a complex interplay of intrinsic MR around the Dirac cone, carrier hydrodynamics, interface resistance, and the nanoscale device geometry. Furthermore, accessing the local transport pattern across the interface enables quantitative mapping of spatial variations in contact resistance, which is commonly present in electronic devices made from two-dimensional materials yet non-trivial to characterize. Our work demonstrates the potential of nanoscale current imaging techniques for studying complex electronic transport phenomena that are difficult to probe by resistance-based measurements.
Two-dimensional van der Waals materials offer a highly tunable platform for engineering electronic band structures and interactions. By employing techniques such as twisting, gating, or applying pressure, these systems enable precise control over the electronic excitation spectrum. In moir\'e bilayer graphene, the tunability facilitates the transition from a symmetric Dirac semimetal phase through a quantum critical point into an interaction-induced long-range ordered phase with a finite band gap. At charge neutrality, the ordered state proposed to emerge from twist-angle tuning is the Kramers intervalley-coherent insulator. In this case, the transition falls into the quantum universality class of the relativistic Gross-Neveu-XY model in 2+1 dimensions. Here, we refine estimates for the critical exponents characterizing this universality class using an expansion around the lower critical space-time dimension of two. We compute the order-parameter anomalous dimension ${\ensuremath{\eta}}_{\ensuremath{\varphi}}$ and the correlation-length exponent $\ensuremath{\nu}$ at one-loop order, and the fermion anomalous dimension ${\ensuremath{\eta}}_{\ensuremath{\psi}}$ at two-loop order. Combining these results with previous findings from the expansion around the upper critical dimension, we obtain improved estimates for the universal exponents in 2+1 dimensions via Pad\'e interpolation. For Nf=4 four-component Dirac fermions, relevant to moir\'e bilayer graphene, we estimate $1/\ensuremath{\nu}=0.916(5), {\ensuremath{\eta}}_{\ensuremath{\varphi}}=0.926(13)$, and ${\ensuremath{\eta}}_{\ensuremath{\psi}}=0.0404(13)$. For Nf=2, potentially relevant to recent tetralayer WSe2 experiments, the Gross-Neveu-XY fixed point may be unstable owing to a fixed-point collision at Nf,c, with ${N}_{\text{f,c}}=1+\sqrt{2}+\mathcal{O}(\ensuremath{\epsilon})$ in the expansion around the lower critical dimension.