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Gangbin Yan

Publications and source records attributed to Gangbin Yan.

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Millimeter-Scale, Atomically Controlled 2D Topological Insulators Revealed by Multimodal Spectroscopy

Quantum spin Hall insulators, or synonymously known as 2D topological insulators, are crucial 2D systems hosting topologically protected edge states. The working temperature of this topological quantum phase is dictated by the inverted bandgap. However, the previously identified large-gap 2D topological insulators are either extremely chemically unstable, or cannot be made with atomistic precision over macroscopic scales. Here, we establish two-quintuple-layer Bi2Te3 and MnBi2Te4/Bi2Te3 heterostructures as atomically controlled, millimeter-scale 2D topological insulators, enabled by precision layer-by-layer growth that yields a carpet-like morphology extending coherently over macroscopic distances. This carpet-like growth mode renders the films amenable to mechanical exfoliation and subsequent wet or dry transfer. Multimodal spectroscopies and microscopies reveal the integer-layer tuned electronic structure of (Bi2Te3)n with excellent agreement to theory. Photon-energy-dependent photoemission and time-resolved photoemission identify band inversion and band dynamics, respectively, while scanning tunneling spectroscopy resolves topological edge states, characteristic of the 2D topological insulator phase. Thickness- and photon-energy-dependent photoemission further validates MnBi2Te4/Bi2Te3 as a robust 2D topological insulator. The large inverted gaps of ~100 meV in (Bi2Te3)2 and ~150 meV in MnBi2Te4/Bi2Te3 suggest operation near ambient temperature. These results define a scalable materials platform for next-generation, low-loss quantum and energy-efficient devices.

cond-mat.mtrl-sci

Crossover Dynamics of Non-Fickian Ionic Diffusion in Solids

Ionic diffusion in solids is central to energy storage, electronics, and catalysis, yet its chemical origins are difficult to resolve because conventional diffusion models struggle with effects of confinement, crystallographic disorder, lattice distortions, and coupling to electronic or phononic carriers. These challenges are especially pronounced in battery materials, where ionic and electronic motion occur together, complicating interpretation of electrochemical measurements. Here we use tracer exchange as a direct, non-electrochemical probe to reveal distinct ion-transport regimes in the one-dimensional conductor olivine Li_xFePO4 (0 <= x <= 1). Lithium isotope exchange validates single-file diffusion governed by strong ion-ion correlations, where 1D confinement suppresses bypassing and preserves spatial order. Kinetic Monte Carlo simulations and chronoamperometry quantify both Faradaic and non-Faradaic surface exchange, identifying electron transport, rather than Li+ mobility, as the rate-limiting step for electrochemical reaction. In addition, Li-Na exchange exhibits apparent superdiffusion, with rates that increase with Na content. Simulations attribute this behavior to surface-exchange limitations and Na-induced lattice strain that enhances cross-channel Li+ hopping and drives a crossover from 1D to quasi-2D transport. Four-dimensional STEM, in situ synchrotron XRD, X-ray absorption spectroscopy, and Mossbauer spectroscopy confirm that lattice softening and concerted polaron motion contribute to the observed dynamics. These results establish tracer exchange as a powerful tool for probing coupled ion-electron transport and provide chemical insight into how lattice mechanics and multicomponent exchange shape ionic diffusion in solids.

cond-mat.mtrl-sci

Spectrally-selective dynamic radiative thermoregulation via phase engineering

Maintaining comfortable temperatures for buildings, humans, and devices consumes a substantial portion of global energy, underscoring the urgent need for energy-efficient thermoregulation technologies. Dynamic radiative thermal emitters that can switch between passive cooling and heating modes offer a promising solution, but most existing devices exhibit broadband optical responses, resulting in unwanted parasitic heat exchange and limited performance. Here, we introduce an elegant strategy that uses a dielectric cap to transform broadband metal-insulator transition (MIT) materials into spectrally selective dynamic emitters. This design creates a highly tunable Fabry-Perot cavity, enabling a tailored thermal emission spectrum by engineering the reflected-wave phase profile. Our Fresnel-formalism-based phasor diagram analysis reveals two key routes for realizing high spectral selectivity: a high-index dielectric cap and a low-loss metallic MIT state, which are further validated by Bayesian optimization. Following this principle, we demonstrated a wide-angle spectrally-selective thermoregulator operating in the atmospheric transparency window (8-13 um), where the thermal emittance can be electrically tuned from about 0.2 to 0.9 through reversible copper electrodeposition on a germanium cavity. Furthermore, this strategy can be extended to multispectral electrochromic windows, enabling switching between solar heating and spectrally-selective radiative cooling. Our work establishes a versatile and generalizable paradigm for spectral engineering of dynamic thermal emitters, opening opportunities in energy-efficient buildings, wearable thermal comfort, spacecraft thermoregulation, and multispectral camouflage.

physics.optics

Defect Engineered Hexagonal-Boron Nitride Enables Ionic Conduction for Lithium Metal Batteries

The practical implementation of lithium-metal anodes has been hindered by uncontrollable dendrite formation and interfacial instability. This study presents a defect-engineering approach of a chemically stable and electrically insulating interfacial layer of hexagonal boron nitride (h-BN) that markedly enhances ionic conductivity through argon ion irradiation. Initially, the electrochemical performance from commercially available, large-area chemical vapor deposition (CVD)-grown h-BN films with industrial-scale argon ion implantation motivated our subsequent detailed investigations using lab-scale exfoliated single-crystal h-BN flakes. Integration of these exfoliated flakes into a hybrid microfluidic-microelectronic chip provided direct evidence that controlled vacancy defects transform h-BN into an efficient lithium-ion conductor while preserving its intrinsic electrical insulation. Experimental validation confirmed improved lithium-metal anode stability, achieving dendrite-free cycling with Li plating/stripping Coulombic efficiencies exceeding 99.5% about 1000 cycles. Further assemble of irradiated h-BN in lithium-sulfur batteries effectively mitigates the polysulfide shuttle effect, sustaining over 97% specific capacity around 300 cycles. These results establish a robust, scalable interface-engineering route for next-generation lithium-metal batteries that combine high ionic transport with excellent electrical insulation.

cond-mat.mtrl-sci

Epitaxial Electrodeposition of Fe with Controlled In-Plane Variants for Reversible Metal Anode in Aqueous Electrolyte

The development of reversible metal anodes is a key challenge for advancing aqueous battery technologies, particularly for scalable and safe stationary energy storage applications. Here we demonstrate a strategy to realize epitaxial electrodeposition of iron (Fe) on single-crystal copper (Cu) substrates in aqueous electrolytes. We compare the electrodeposition behavior of Fe on polycrystalline and single-crystalline Cu substrates, revealing that the latter enables highly uniform, dense, and crystallographically aligned Fe growth. Comprehensive electron backscatter diffraction (EBSD) and X-ray diffraction (XRD) analysis confirms the formation of Fe with specific out-of-plane and in-plane orientations, including well-defined rotational variants. Our findings highlight that epitaxial electrodeposition of Fe can suppress dendritic growth and significantly enhance Coulombic efficiency during plating/stripping cycles. This approach bridges fundamental crystallography with practical electrochemical performance, providing a pathway toward high-efficiency aqueous batteries utilizing Earth-abundant materials.

cond-mat.mtrl-sci

High-efficiency broadband active metasurfaces via reversible metal electrodeposition

Realizing active metasurfaces with substantial tunability is important for many applications but remains challenging due to difficulties in dynamically tuning light-matter interactions at subwavelength scales. Here, we introduce reversible metal electrodeposition as a versatile approach for enabling active metasurfaces with exceptional tunability across a broad bandwidth. As a proof of concept, we demonstrate a dynamic beam-steering device by performing reversible copper (Cu) electrodeposition on a reflective gradient metasurface composed of metal-insulator-metal resonators. By applying different voltages, the Cu atoms can be uniformly and reversibly electrodeposited and stripped around the resonators, effectively controlling the gap-surface plasmon resonances and steering the reflected light. This process experimentally achieved >90% diffraction efficiencies and >60% reflection efficiencies in both specular and anomalous modes, even after thousands of cycles. Moreover, these high efficiencies can be extended from the visible to the near- and mid-infrared regimes, demonstrating the broad versatility of this approach in enabling various active optical and thermal devices with different working wavelengths and bandwidths.

physics.optics

A Topological Superconductor Tuned by Electronic Correlations

A topological superconductor, characterized by either a chiral order parameter or a chiral topological surface state in proximity to bulk superconductivity, is foundational to topological quantum computing. As in other topological phases of matter, electronic correlations can tune topological superconductivity via modifications of the low-energy Fermiology. Such tuning has not been realized so far. Here we uncover a unique topological superconducting phase in competition with electronic correlations in 10-unit-cell thick FeTe$_{x}$Se$_{1-x}$ films grown on SrTiO$_{3}$ substrates. When the Te content $x$ exceeds $0.7$, we observe a rapid increase of the effective mass for the Fe $d_{xy}$ band, with the emergence of a superconducting topological surface state confirmed by high-resolution angle-resolved photoemission spectroscopy; however, near the FeTe limit, the system enters an incoherent regime where the topological surface state becomes unidentifiable and superconductivity is suppressed. Theory suggests that the electron-electron interactions in the odd-parity $xy^-$ band with a strong $d_{xy}$ character lead to an orbital-selective correlated phase. Our work establishes FeTe$_{x}$Se$_{1-x}$ thin films as a unique platform where electronic correlations sensitively modulate topological superconductivity, suggesting opportunities to use tunable electron-electron interactions to engineer new topological phases in a broad class of materials.

cond-mat.supr-con

Cooperative and Inhibitory Ion Transport in Functionalized Angstrom-Scale Two-Dimensional Channels

Significant success has been achieved in fabricating angstrom-scale artificial solid ionic channels aiming to replicate the biological ion channels (BICs).Besides high selectivity, BICs also exhibit sophisticated ion gating and interplay. However, such behavior and functionality are seldomly recreated in the artificial counterparts due to the insufficient understanding of the molecular origin. Here we report cooperative and inhibitory ion transport in angstrom-scale acetate functionalized MoS2 two dimensional channels.

physics.bio-ph

Preservation of Topological Surface States in Millimeter-Scale Transferred Membranes

Ultrathin topological insulator membranes are building blocks of exotic quantum matter. However, traditional epitaxy of these materials does not facilitate stacking in arbitrary orders, while mechanical exfoliation from bulk crystals is also challenging due to the non-negligible interlayer coupling therein. Here we liberate millimeter-scale films of topological insulator Bi$_2$Se$_3$, grown by molecular beam epitaxy, down to 3 quintuple layers. We characterize the preservation of the topological surface states and quantum well states in transferred Bi$_{2}$Se$_{3}$ films using angle-resolved photoemission spectroscopy. Leveraging the photon-energy-dependent surface sensitivity, the photoemission spectra taken with $6$ eV and $21.2$ eV photons reveal a transfer-induced migration of the topological surface states from the top to the inner layers. By establishing clear electronic structures of the transferred films and unveiling the wavefunction relocation of the topological surface states, our work paves the physics foundation crucial for the future fabrication of artificially stacked topological materials with single-layer precision.

cond-mat.mtrl-sci