arXiv subjects

Jiming Bao

Publications and source records attributed to Jiming Bao.

At least 19 recordsLinked to original sources

arXiv2026

Direct Validation of Superconductivity through Contact-Free Detection of Persistent Supercurrents Using Room-Temperature Quantum Magnetometry

The accelerated emergence of new materials is driving the search for high temperature superconductors, but rapid experimental validation remains a critical bottleneck, particularly for microscopic samples under high pressure. Here, we demonstrate one-step direct superconductivity validation through room-temperature, contact-free detection of remnant supercurrents. The technique utilizes a cryogen-free optically pumped atomic magnetometer to detect the temperature-dependent magnetic field produced by supercurrents of a superconductor. The superconducting transition is directly identified by the abrupt disappearance of magnetic field from the remnant supercurrent above the transition temperature and the reversal of the supercurrent direction upon reversing the applied magnetic field. Validated on YBCO microcrystals and REBCO tape, this technique detects pico-Tesla magnetic fields from supercurrents induced by the ambient Earth's magnetic field in a millimeter-sized REBCO square disk, as well as from sub-100 micrometer YBCO microcrystals compatible with high-pressure diamond anvil cells. The use of a ferrite flux guide enables sensitive detection from centimeter-scale distances. Requiring no electrical contacts, magnetic coils, or integrated magnetic sensors, this non-invasive, room-temperature platform offers a scalable approach for high-throughput screening and validation of superconductivity.

cond-mat.supr-con↗

arXiv2026

A Diamagnetic, Light-Driven Tesla Engine Based on a Mechanically Displaced, Magnetically Levitated Graphene Disk

Ferromagnetic materials are widely used in Tesla thermomagnetic engines, whereas diamagnetic counterparts have remained unexplored. Here, we demonstrate the first diamagnetic Tesla engine by exploiting the strong diamagnetism of graphene. A graphene disk, fabricated by stacking graphene sheets, serves as the engine wheel. We first show that the conventional Tesla engine design using a permanent magnet placed near the disk edge to create unbalanced thermomagnetic forces under asymmetric local heating fails to generate rotation. We achieve stable operation by laterally displacing the levitated disk from equilibrium, creating a strong restoring force that drives rotation under light excitation. Calculations and measurements establish the displacement-dependent force, with an optimal offset of 0.8 mm yielding speeds up to 2000 rpm under laser heating and 1000 rpm under direct sunlight. Adding vanes allows the disk to function as a gear, powering a graphene vehicle and transferring energy to another disk. This design utilizes the strong and anisotropic diamagnetism of graphene and paves the way for light-powered sensors, actuators, and micro-vehicles.

physics.app-ph↗

arXiv2025

Thermal Conductivity above 2000 W/m.K in Boron Arsenide by Nanosecond Transducer-less Time-Domain Thermoreflectance

Cubic boron arsenide (c-BAs) has been theoretically predicted to exhibit thermal conductivity \k{appa} comparable to that of diamond, yet experimental measurements have plateaued at ~1300W/mK. We report room-temperature \k{appa} exceeding 2000W/mK in c-BAs, on par with single-crystal diamond. This finding is enabled by high-quality single crystals and a newly developed nanosecond, transducer-less time-domain thermoreflectance technique that allows spatial mapping of \k{appa} without metal transducers. Thermal conductivity correlates with crystal quality, as evidenced by stronger photoluminescence and longer photoluminescence lifetimes. However, the observed nanosecond lifetimes remain shorter than expected for an indirect bandgap semiconductor, suggesting room for further crystal quality improvement and higher \k{appa}. These results challenge current theoretical models and highlight c-BAs as a promising material for next-generation electronics.

physics.app-ph↗

arXiv2025

Optical rotation of ferrofluid on a horizontal substrate by Marangoni and thermomagnetic forces

Light-actuation enables non-contact, precise, and flexible manipulation of liquids in microfluidics and liquid robots. However, it has long been a challenge to achieve optical rotation of liquid on a horizontal substrate because of the weak force of light. Here, we report, for the first time, the laser-induced rotation of macroscopic liquid placed on a horizontal substrate above cylindrical magnets. The investigated ferrofluid exhibits multiple spikes due to the Rosensweig phenomenon on the surface with different strengths of external magnetic field and rotates in a controllable direction by adjusting the laser beam position around ferrofluid spikes. This rotation results from the laser-induced displacement between the ferrofluid gravitational center, magnetic field center, Marangoni force, and non-uniform thermomagnetic force. Movement tracking of the spikes, thermal magnetization, and thermal imaging of ferrofluid were performed to elucidate the mechanism. Additionally, the influence of laser power, laser irradiation position, and magnetic field intensity on laser-induced rotation of ferrofluid are systematically studied. This work demonstrates a novel horizontal rotation of liquid using light and provides a deep understanding of the underlying mechanism and a flexible strategy for manipulating liquid for various optofluidic applications.

physics.optics↗

arXiv2023

Idealizing Tauc Plot for Accurate Bandgap Determination of Semiconductor with UV-Vis: A Case Study for Cubic Boron Arsenide

The Tauc plot method is widely used to determine the bandgap of semiconductors via UV-visible optical spectroscopy due to its simplicity and perceived accuracy. However, the actual Tauc plot often exhibits significant baseline absorption below the expected bandgap, leading to discrepancies in the calculated bandgap depending on whether the linear fit is extrapolated to zero or non-zero baseline. In this study, we show that both extrapolation methods can produce significant errors by simulating Tauc plots with varying levels of baseline absorption. To address this issue, we propose a new method that involves idealizing the absorption spectrum by removing its baseline before constructing the Tauc plot. Experimental verification of this method using a gallium phosphide (GaP) wafer with intentionally introduced baseline absorptions shows promising results. Furthermore, we apply this new method to cubic boron arsenide (c-BAs) and resolve discrepancies in c-BAs bandgap values reported by different groups, obtaining a converging bandgap of 1.835 eV based on both previous and new transmission spectra. The method is applicable to both indirect and direct bandgap semiconductors, regardless of whether the absorption spectrum is measured via transmission or diffuse reflectance, will become essential to obtain accurate values of their bandgaps.

cond-mat.mtrl-sci↗

arXiv2022

Theory and Experiments of Pressure-Tunable Broadband Light Emission from Self-Trapped Excitons in Metal Halide Crystals

Hydrostatic pressure has been commonly applied to tune broadband light emissions from self-trapped excitons (STE) in perovskites for producing white light and study of basic electron-phonon interactions. However, a general theory is still lacking to understand pressure-driven evolution of STE emissions. In this work we first identify a theoretical model that predicts the effect of hydrostatic pressure on STE emission spectrum, we then report the observation of extremely broadband photoluminescence emission and its wide pressure spectral tuning in 2D indirect bandgap CsPb2Br5 crystals. An excellent agreement is found between the theory and experiment on the peculiar experimental observation of STE emission with a nearly constant spectral bandwidth but linearly increasing energy with pressure below 2 GPa. Further analysis by the theory and experiment under higher pressure reveals that two types of STE are involved and respond differently to external pressure. We subsequently survey published STE emissions and discovered that most of them show a spectral blue-shift under pressure, as predicted by the theory. The identification of an appropriate theoretical model and its application to STE emission through the coordinate configuration diagram paves the way for engineering the STE emission and basic understanding of electron-phonon interaction.

cond-mat.mtrl-sci↗

arXiv2022

Generalized Dynamic Junction Theory to Resolve the Mechanism of Direct Current Generation in Liquid-Solid Interfaces

Despite the unsettled mechanism of electricity generation from the continuous flow of liquids on a surface, the charge-discharge theory has been widely accepted for alternating current (AC) generation from a moving droplet. It has been recently extended to rationalize direct current (DC) generation across a droplet moving between two different materials. By designing a reconfigurable contact between a metal wire and a water droplet moving on graphene, we show that the charge-discharge theory cannot explain the reversal of current when water-metal interfaces switch from dynamic to static. All experiments can be described after we distinguish a dynamic from a static interface and generalize the photovoltaic-like effect to all dynamic junctions: excited electrons and holes in a moving interface will be separated and swept under the built-in electrical field, leading to a DC response. This generalized theory will lead to an understanding and the design of efficient electricity generation based on interfacial charge transfer.

cond-mat.mes-hall↗

arXiv2021

Marangoni Convection-Driven Laser Fountains and Waves on Free Surfaces of Liquids

It is well accepted that an outward Marangoni convection from a low surface tension region will make the surface depressed. Here, we report that this established perception is only valid for thin liquid films. Using surface laser heating, we show that in deep liquids a laser beam actually pulls up the fluid above the free surface generating fountains with different shapes. Whereas with decreasing liquid depth a transition from fountain to indentation with fountain in-indentation is observed. Further, high-speed imaging reveals a transient surface process before steady elevation is formed, and this dynamic deformation is subsequently utilized to resonantly excite giant surface waves by a modulated laser beam. Computational fluid dynamics models reveal the underlying flow patterns and quantify the depth-dependent and time-resolved surface deformations. Our discoveries and techniques have upended the century-old perception and opened up a new regime of interdisciplinary research and applications of Marangoni-induced interface phenomena and optocapillary fluidic surfaces-the control of fluids with light.

physics.flu-dyn↗

arXiv2020

Photoacoustic Identification of Laser-induced Microbubbles as Light Scattering Centers for Optical Limiting in Liquid Suspension of Graphene Nanosheets

Liquid suspensions of carbon nanotubes, graphene and transition metal dichalcogenides have exhibited excellent performance in optical limiting. However, the underlying mechanism has remained elusive and is generally ascribed to their superior nonlinear optical properties such as nonlinear absorption or nonlinear scattering. Using graphene as an example, we show that photo-thermal microbubbles are responsible for the optical limiting as strong light scattering centers: graphene sheets absorb incident light and become heated up above the boiling point of water, resulting in vapor and microbubble generation. This conclusion is based on direct observation of bubbles above the laser beam as well as a strong correlation between laser-induced ultrasound and optical limiting. In-situ Raman scattering of graphene further confirms that the temperature of graphene under laser pulses rises above the boiling point of water but still remains too low to vaporize graphene and create graphene plasma bubbles. Photo-thermal bubble scattering is not a nonlinear optical process and requires very low laser intensity. This understanding helps us to design more efficient optical limiting materials and understand the intrinsic nonlinear optical properties of nanomaterials.

physics.optics↗

arXiv2020

Self-formed 2D/3D Heterostructure on the Edge of 2D Ruddlesden-Popper Hybrid Perovskites Responsible for Intriguing Optoelectronic Properties and Higher Cell Efficiency

The observation of low energy edge photoluminescence and its beneficial effect on the solar cell efficiency of Ruddlesden-Popper perovskites has unleashed an intensive research effort to reveal its origin. This effort, however, has been met with more challenges as the underlying material structure has still not been identified; new modellings and observations also do not seem to converge. Using 2D (BA)2(MA)2Pb3Br10 as an example, we show that 3D MAPbBr3 is formed due to the loss of BA on the edge. This self-formed MAPbBr3 can explain the reported edge emission under various conditions, while the reported intriguing optoelectronic properties such as fast exciton trapping from the interior 2D perovskite, rapid exciton dissociation and long carrier lifetime can be understood via the self-formed 2D/3D lateral perovskite heterostructure. The 3D perovskite is identified by submicron infrared spectroscopy, the emergence of XRD signature from freezer-milled nanometer-sized 2D perovskite and its photoluminescence response to external hydrostatic pressure. The revelation of this edge emission mystery and the identification of a self-formed 2D/3D heterostructure provide a new approach to engineering 2D perovskites for high-performance optoelectronic devices.

physics.app-ph↗

arXiv2019

Photoluminescence mapping and time-domain thermo-photoluminescence for rapid imaging and measurement of thermal conductivity of boron arsenide

Cubic boron arsenide (BAs) is attracting greater attention due to the recent experimental demonstration of ultrahigh thermal conductivity \k{appa} above 1000 W/mK. However, its bandgap has not been settled and a simple yet effective method to probe its crystal quality is missing. Furthermore, traditional \k{appa} measurement methods are destructive and time consuming, thus they cannot meet the urgent demand for fast screening of high \k{appa} materials. After we experimentally established 1.82 eV as the indirect bandgap of BAs and observed room-temperature band-edge photoluminescence, we developed two new optical techniques that can provide rapid and non-destructive characterization of \k{appa} with little sample preparation: photoluminescence mapping (PL-mapping) and time-domain thermo-photoluminescence (TDTP). PL-mapping provides nearly real-time image of crystal quality and \k{appa} over mm-sized crystal surfaces; while TDTP allows us to pick up any spot on the sample surface and measure its \k{appa} using nanosecond laser pulses. These new techniques reveal that the apparent single crystals are not only non-uniform in \k{appa}, but also are made of domains of very distinct \k{appa}. Because PL-mapping and TDTP are based on the band-edge PL and its dependence on temperature, they can be applied to other semiconductors, thus paving the way for rapid identification and development of high-\k{appa} semiconducting materials.

cond-mat.mtrl-sci↗

arXiv2019

Graphene Induced Large Shift of Surface Plasmon Resonances of Gold Films: Effective Medium Theory for Atomically Thin Materials

Despite successful modeling of graphene as a 0.34-nm thick optical film synthesized by exfoliation or chemical vapor deposition (CVD), graphene induced shift of surface plasmon resonance (SPR) of gold films has remained controversial. Here we report the resolution of this controversy by developing a clean CVD graphene transfer method and extending Maxwell-Garnet effective medium theory (EMT) to 2D materials. A SPR shift of 0.24 is obtained and it agrees well with 2D EMT in which wrinkled graphene is treated as a 3-nm graphene/air layered composite, in agreement with the average roughness measured by atomic force microscope. Because the anisotropic built-in boundary condition of 2D EMT is compatible with graphene's optical anisotropy, graphene can be modelled as a film thicker than 0.34-nm without changing its optical property; however, its actual roughness, i.e., effective thickness will significantly alter its response to strong out-of-plane fields, leading to a larger SPR shift.

physics.optics↗

arXiv2019

Revealing the Origin of Luminescence Center in 0D Cs4PbBr6 Perovskite

Zero dimensional perovskite Cs4PbBr6 has attracted considerable attention recently not only because of its highly efficient green photoluminescence (PL), but also its two highly debated opposing mechanisms of the luminescence: embedded CsPbBr3 nanocrystals versus intrinsic Br vacancy states. After a brief discussion on the root cause of the controversy, we provide sensitive but non-invasive methods that can not only directly correlate luminescence with the underlying structure, but also distinguish point defects from embedded nanostructures. We first synthesized both emissive and non-emissive Cs4PbBr6 crystals, obtained the complete Raman spectrum of Cs4PbBr6 and assigned all Raman bands based on density functional theory simulations. We then used correlated Raman-PL as a passive structure-property method to identify the difference between emissive and non-emissive Cs4PbBr6 crystals and revealed the existence of CsPbBr3 nanocrystals in emissive Cs4PbBr6. We finally employed a diamond anvil cell to probe the response of luminescence centers to hydrostatic pressure. The observations of fast red-shifting, diminishing and eventual disappearance of both green emission and Raman below Cs4PbBr6 phase transition pressure of ~3 GPa is compatible with CsPbBr3 nanocrystal inclusions as green PL emitters and cannot be explained by Br vacancies. The resolution of this long-lasting controversy paves the way for further device applications of low dimensional perovskites, and our comprehensive optical technique integrating structure-property with dynamic pressure response is generic and can be applied to other emerging optical materials to understand the nature of their luminescent centers.

cond-mat.mtrl-sci↗

arXiv2018

Laser Streaming: Turning a Laser Beam into a Flow of Liquid

Transforming a laser beam into a mass flow has been a challenge both scientifically and technologically. Here we report the discovery of a new optofluidics principle and demonstrate the generation of a steady-state water flow by a pulsed laser beam through a glass window. In order to generate a flow or stream in the same path as the refracted laser beam in pure water from an arbitrary spot on the window, we first fill a glass cuvette with an aqueous solution of Au nanoparticles. A flow will emerge from the focused laser spot on the window after the laser is turned on for a few to tens of minutes, the flow remains after the colloidal solution is completely replaced by pure water. Microscopically, this transformation is made possible by an underlying plasmonic nanoparticle-decorated cavity which is self-fabricated on the glass by nanoparticle-assisted laser etching and exhibits size and shape uniquely tailored to the incident beam profile. Hydrophone signals indicate that the flow is driven via acoustic streaming by a long-lasting ultrasound wave that is resonantly generated by the laser and the cavity through the photoacoustic effect. The principle of this light-driven flow via ultrasound, i.e. photoacoustic streaming by coupling photoacoustics to acoustic streaming, is general and can be applied to any liquids, opening up new research and applications in optofluidics as well as traditional photoacoustics and acoustic streaming.

physics.flu-dyn↗

arXiv2018

Bright Luminescent Surface States on the Edges of Wide-bandgap Two-dimensional Lead Halide Perovskite

Three-dimensional lead halide perovskites have surprised people for their defect-tolerant electronic and optical properties, two-dimensional lead halide layered structures exhibit even more puzzling phenomena: luminescent edge states in Ruddlesden-Popper perovskites and conflicting reports of highly luminescent versus non-emissive CsPb$_{\text{2}}$Br$_{\text{5}}$. In this work, we report the observation of bright luminescent surface states on the edges of CsPb$_{\text{2}}$Br$_{\text{5}}$ microplatelets. We prove that green surface emission makes wide-bandgap single crystal CsPb$_{\text{2}}$Br$_{\text{5}}$ highly luminescent. Using polarized Raman spectroscopy and atomic-resolution transmission electron microscopy, we further prove that polycrystalline CsPb$_{\text{2}}$Br$_{\text{5}}$ is responsible for the bright luminescence. We propose that these bright edge states originate from corner-sharing clusters of PbBr$_{\text{6}}$ in the distorted regions between CsPb$_{\text{2}}$Br$_{\text{5}}$ nanocrystals. Because metal halide octahedrons are building blocks of perovskites, our discoveries settle a long-standing controversy over the basic property of CsPb$_{\text{2}}$Br$_{\text{5}}$ and open new opportunities to understand, design and engineer perovskite solar cells and other optoelectronic devices.

cond-mat.mtrl-sci↗

arXiv2016

Generation and Detection of Surface Plasmon Polaritons by Transition Metal Dichalcogenides for Chip-level Electronic-Photonic Integrated Circuits

The monolithic integration of electronics and photonics has attracted enormous attention due to its potential applications. However, the realization of such hybrid circuits has remained a challenge because it requires optical communication at nanometer scales. A major challenge to this integration is the identification of a suitable material. After discussing the material aspect of the challenge, we identified atomically thin transition metal dichalcogenides (TMDs) as a perfect material platform to implement the circuit. The selection of TMDs is based on their very distinct property: monolayer TMDs are able to emit and absorb light at the same wavelength determined by direct exciton transitions. To prove the concept, we fabricated simple devices consisting of silver nanowires as plasmonic waveguides and monolayer TMDs as active optoelectronic media. Using photoexcitation, direct optical imaging and spectral analysis, we demonstrated generation and detection of surface plasmon polaritons by monolayer TMDs. Regarded as novel materials for electronics and photonics, transition metal dichalcogenides are expected to find new applications in next generation integrated circuits.

cond-mat.mes-hall↗

arXiv2013

Anomalously Strong 2D Band Intensity in Twisted Bilayer Graphene: Raman Evidence for Doubly Degenerate Dirac Band

We report the observation of anomalously strong 2D band in twisted bilayer graphene (tBLG) with large rotation angles under 638-nm and 532-nm visible laser excitation. The 2D band of tBLG can reach four times as opposed to two times as strong as that of single layer graphene. The same tBLG samples also exhibit rotation dependent G-line resonances and folded phonons under 364-nm UV laser excitation. We attribute this 2D band Raman enhancement to the constructive quantum interference between two double-resonance Raman pathways which are enabled by nearly degenerate Dirac band in tBLG Moiré superlattices.

cond-mat.mes-hall↗

arXiv2013

Observation of Low Energy Raman Modes in Twisted Bilayer Graphene

Two new Raman modes below 100 cm^-1 are observed in twisted bilayer graphene grown by chemical vapor deposition. The two modes are observed in a small range of twisting angle at which the intensity of the G Raman peak is strongly enhanced, indicating that these low energy modes and the G Raman mode share the same resonance enhancement mechanism, as a function of twisting angle. The 94 cm^-1 mode (measured with a 532 nm laser excitation) is assigned to the fundamental layer breathing vibration (ZO (prime) mode) mediated by the twisted bilayer graphene lattice, which lacks long-range translational symmetry. The dependence of this modes frequency and linewidth on the rotational angle can be explained by the double resonance Raman process which is different from the previously-identified Raman processes activated by twisted bilayer graphene superlattice. The dependence also reveals the strong impact of electronic-band overlaps of the two graphene layers. Another new mode at 52 cm^-1, not observed previously in the bilayer graphene system, is tentatively attributed to a torsion mode in which the bottom and top graphene layers rotate out-of-phase in the plane.

cond-mat.mes-hall↗