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Jiade Li

Publications and source records attributed to Jiade Li.

10 recordsLinked to original sources

Direct Measurement of Exciton Dispersion in the Long-Wavelength Limit

Exciton dispersion, which governs the propagation, scattering and radiative decay of electron-hole pairs, is essential to optoelectronics and quantum materials. In two-dimensional systems, weakened dielectric screening and long-range electron-hole exchange are predicted to induce nonanalytic exciton dispersion in the long-wavelength limit. However, direct quantitative characterization of its dimensional evolution remains lacking, especially in the ultralow-q regime (q < 0.02 $\r{A}^{-1}$). Here we employ defocus-engineered momentum-resolved electron energy-loss spectroscopy in scanning transmission electron microscopy, achieving an ultrahigh momentum resolution of 0.0002 $\r{A}^{-1}$. Using freestanding hBN as a prototypical platform, we resolve layer-dependent exciton dispersion and quantify its characteristic crossover momentum and group velocity in the long-wavelength limit. With increasing thickness, the nonanalytic linear-dispersion regime is progressively compressed, manifested by a reduction in characteristic crossover momentum q_c from $1.82 \times 10^{-1} \r{A}^{-1}$ in the monolayer to $3.0 \times 10^{-1} \r{A}^{-1}$ in 25 layers. Meanwhile, the low-q group velocity increases from $2.0 \times 10^{-3} c$ to $2.9 \times 10^{-2} c$, before the dispersion ultimately approaches the bulk-like parabolic limit. We further examine how the exciton band structure of monolayer hBN responds to its surrounding environment, including temperature, adjacent graphene layers, and interlayer twist in BN/graphene heterostructures. These findings uncover the fundamental physics of low-dimensional excitons, deliver valuable guidance for modulating exciton transport, diffusion and quasiparticle coupling in layered quantum materials, and establish a powerful experimental route to explore low-dimensional exciton physics.

cond-mat.mes-hall

Nanoscale Thermal Imaging of Dislocation-Mediated Heat Transport

Dislocations in crystalline materials are widely exploited to tailor the thermal conductivity of semiconductors and thermoelectrics, yet a critical gap persists: direct measurement of local thermal resistance at individual buried dislocations, along with its spatial extent, remains elusive due to the limitations of conventional thermal probes. Here, we use in situ scanning transmission electron microscopy-electron energy-loss spectroscopy to map nanoscale temperature distributions across a low-angle SrTiO3 grain boundary with periodic dislocation arrays. Our results reveal a temperature drop of 47 K across the dislocation array. The associated temperature-field distortions are concentrated near the dislocation cores, consistent with stronger local thermal resistance at these discrete sites rather than a uniformly distributed resistance along the array. We further identify a distinct two-scale heat transport characteristic near the dislocation array: core-dominated effects over approximately 4.8-6.2 nm and extended inter-core influences over approximately 10.3-14.3 nm. Atomic-scale structural and vibrational analyses further reveal core-associated atomic reconstruction and localized optical-phonon perturbations, providing a microscopic basis for the stronger local thermal resistance inferred near dislocation cores. These findings quantitatively resolve spatial heterogeneity of dislocation-mediated heat transport, uncover its atomic-scale mechanism, and provide a quantitative basis for defect engineering, guiding the design of high-performance thermoelectrics, semiconductors, high-temperature structural alloys, and other functional crystalline materials.

cond-mat.mtrl-sci

Dimensionality-Dependent Exciton Dispersion in a Single-Band Mott Insulator

Excitonic band structure is critical for investigating exciton dynamics. Theoretically, quantum effects from exchange scattering between electron-hole pairs significantly modulate exciton dispersion. Here, we report the direct observation of dimensionality-dependent exciton dispersion in a single-band Mott insulator Nb3Cl8 through high-resolution electron energy loss spectroscopy. In the high-temperature phase, the exciton in Nb3Cl8 hosts an exceptionally large binding energy, and exhibits clear quasi-two-dimensional massless linear dispersion. In contrast, in the low-temperature phase, the exciton splits into two bands, both displaying three-dimensional parabolic dispersion. These dramatic changes in the exciton dispersion stem from the dimensional mutation driven by a substantial enhancement of interlayer coupling across the phase transition. This Letter provides a clear and typical example of how exciton behavior evolves with dimensionality.

cond-mat.str-el

From Ferromagnet to Antiferromagnet: Dimensional Crossover in (111) SrRuO3 Ultrathin Films

SrRuO3 is a canonical itinerant ferromagnet, yet its properties in the extreme two-dimensional limit on a (111) crystal plane remain largely unexplored. Here, we demonstrate a complete transformation of its ground state driven by dimensional reduction. As the thickness of (111)-oriented SrRuO3 films is reduced to a few unit cells, the system transitions from a metallic ferromagnet to a semiconducting antiferromagnet. This emergent antiferromagnetism is evidenced by a vanishing magnetic remanence and most strikingly, by the appearance of an unconventional twelve-fold anisotropic magnetoresistance. First-principles calculations confirm that an A-type antiferromagnetic order is the stable ground state in the ultrathin limit. Our findings establish (111) dimensional engineering as a powerful route to manipulate correlated electron states and uncover novel functionalities for antiferromagnetic spintronics.

cond-mat.str-el

Resolving Phonons in Superconductor Bi2Sr2CaCu2O8+{\delta} at Sub-Unit-Cell Resolution

The role of phonons in cuprates remains controversial, with their complex lattice structure complicating the investigation. Here, we identify phonon modes originating from charge reservoir and superconducting layers of Bi2Sr2CaCu2O8+{\delta} using sub-unit-cell resolved electron energy loss spectroscopy in a scanning transmission electron microscope. We reveal several phonon modes exhibiting layer-specific localization: ~78 meV in-plane modes localized in the CuO2 planes, ~42 meV hybrid (in-plane and out-of-plane) modes in the CuO2 planes, and ~38 meV hybrid modes in the BiO layers. We also observe a periodic modulation of phonon frequencies induced by the superstructure, spatially correlating with the superconducting gap variation. Our findings offer new insights into the electron-phonon coupling in cuprates, fostering deeper exploration of the microscopic linkage between lattice dynamics and superconductivity.

cond-mat.supr-con

Strongly confined Mid-infrared to Terahertz Phonon Polaritons in Ultra-thin SrTiO3

Phonon polaritons (PhPs) enable subwavelength light control for infrared sensing, imaging, and optoelectronics, but conventional polar materials have narrow Reststrahlen bands, limiting applications. Materials that support PhPs with broad spectral range, strong field confinement, slow group velocity, and high quality factor are therefore needed. Here, using monochromatic electron energy loss spectroscopy in a scanning transmission electron microscope, we demonstrate that ultra-thin SrTiO3 membranes possess the desired properties. Systematic measurements across varying thicknesses reveal two PhP branches with wide spectral dispersion, strong confinement, and anomalously slow group velocities spanning from the mid-infrared to terahertz range. Notably, in 3-nm-thick membranes, these polaritons exhibit unprecedented confinement factors exceeding 500 and group velocities as low as ~ 7 x 10-5c, rivaling the best-performing van der Waals materials. These findings establish perovskite oxide such as SrTiO3 as versatile platforms for tailoring light-matter interactions at the nanoscale, providing critical insights for the design of next-generation photonic devices requiring broadband operation and enhanced optical confinement.

physics.optics

Observation of Topological Nodal-Ring Phonons in Monolayer Hexagonal Boron Nitride

Topological physics has evolved from its initial focus on fermionic systems to the exploration of bosonic systems, particularly phononic excitations in crystalline materials. Two-dimensional (2D) topological phonons emerge as promising candidates for future technological applications. Currently, experimental verification of 2D topological phonons has remained exclusively limited to graphene, a constraint that hinders their applications in phononic devices. Here, we report experimental evidence of topological phonons in monolayer hexagonal boron nitride using advanced high-resolution electron energy loss spectroscopy. Our high-precision measurements explicitly demonstrate two topological nodal rings in monolayer hexagonal boron nitride, protected by mirror symmetry, expanding the paradigm of 2D topological phonons beyond graphene. This research not only deepens fundamental understanding of 2D topological phonons, but also establishes a phononic device platform based on wide-bandgap insulators, crucial for advancements in electronics and photonics applications.

cond-mat.mtrl-sci

Observation of the Breakdown of Optical Phonon Splitting in a Two-dimensional Polar Monolayer

Phonon splitting of the longitudinal optical and transverse optical modes (LO-TO splitting), a ubiquitous phenomenon in three-dimensional (3D) polar materials, is essential for the formation of the 3D phonon polaritons. Theories predict that the LO-TO splitting will break down in two-dimensional (2D) polar systems, but direct experimental verification is still missing. Here, using monolayer hexagonal boron nitride (h-BN) as a prototypical example, we report the direct observation of the breakdown of LO-TO splitting and the finite slope of the LO phonons at the center of the Brillouin zone in 2D polar materials by inelastic electron scattering spectroscopy. Interestingly, the slope of the LO phonon in our measurements is lower than the theoretically predicted value for a freestanding monolayer due to the screening of the Cu foil substrate. This enables the phonon polaritons (PhPs) in monolayer h-BN/Cu foil to exhibit ultra-slow group velocity (~ 5 x 10^-6 c, c is the speed of light) and ultra-high confinement (~ 4000 times smaller wavelength than that of light). Our work reveals the universal law of the LO phonons in 2D polar materials and lays a physical foundation for future research on 2D PhPs.

cond-mat.mtrl-sci

Tunable Interband Transitions in Twisted h-BN/Graphene Heterostructures

In twisted h-BN/graphene heterostructures, the complex electronic properties of the fast-traveling electron gas in graphene are usually considered to be fully revealed. However, the randomly twisted heterostructures may also have unexpected transition behaviors, which may influence the device performance. Here, we study the twist angle-dependent coupling effects of h-BN/graphene heterostructures using monochromatic electron energy loss spectroscopy. We find that the moiré potentials alter the band structure of graphene, resulting in a redshift of the intralayer transition at the M-point, which becomes more pronounced up to 0.25 eV with increasing twist angle. Furthermore, the twisting of the Brillouin zone of h-BN relative to the graphene M-point leads to tunable vertical transition energies in the range of 5.1-5.6 eV. Our findings indicate that twist-coupling effects of van der Waals heterostructures should be carefully considered in device fabrications, and the continuously tunable interband transitions through the twist angle can serve as a new degree of freedom to design optoelectrical devices.

cond-mat.mes-hall

Geometric Effect of High-Resolution Electron Energy Loss Spectroscopy on the Identification of Plasmons: An Example of Graphene

High-resolution electron energy loss spectroscopy (HREELS) is one of the most powerful methods to detect the dispersion of plasmons. However, we find that in the HREELS measurement, the scattering geometric configuration will seriously affect the identification of plasmons. Here, taking graphene as an example, using the HREELS capable of two-dimensional energy-momentum mapping combined with the intensity distribution calculations, we visually display the intensity distribution of the scattering geometric factor. We demonstrate that the energy loss peaks from the scattering geometric effect may be misinterpreted as the features of an acoustic plasmon. In any HREELS measurement, it is necessary to evaluate the effect of the scattering geometry quantitatively to identify the intrinsic surface excitations.

cond-mat.mes-hall