arXiv subjects

Xuedong Bai

Publications and source records attributed to Xuedong Bai.

27 records · Page 2Linked to original sources

arXiv2018

Towards the growth of single-crystal boron nitride monolayer on Cu

Atom-layered hexagonal boron nitride (hBN), with excellent stability, flat surface and large bandgap, has been reported to be the best 2D insulator to open up the great possibilities for exciting potential applications in electronics, optoelectronics and photovoltaics. The ability to grow high-quality large single crystals of hBN is at the heart for those applications, but the size of single-crystal 2D BN is less than a millimetre till now. Here, we report the first epitaxial growth of a 10*10 cm2 single-crystal hBN monolayer on a low symmetry Cu(110) "vicinal surface". The growth kinetics, unidirectional alignment and seamless stitching of hBN domains are unambiguously illustrated using centimetre- to the atomic-scale characterization techniques. The findings in this work are expected to significantly boost the massive applications of 2D materials-based devices, and also pave the way for the epitaxial growth of broad non-centrosymmetric 2D materials.

cond-mat.mtrl-sci↗

arXiv2018

Diffusion-controlled Alloying of Single-phase Multi-principal Covalent Transition Metal Carbides with Enhanced Damage tolerance and Exceptional Thermal Properties

Multicomponent alloying has displayed extraordinary potential for producing exceptional structural and functional materials. However, the synthesis of single-phase, multi-principal covalent compounds remains a challenge. Here we present a diffusion-controlled alloying strategy for the successful realization of covalent multi-principal transition metal carbides (MPTMCs) with a single face-centered cubic (FCC) phase. The increased interfacial diffusion promoted by the addition of a nonstoichiometric compound leads to rapid formation of the new single phase at much lower sintering temperature. Direct atomic-level observations via scanning transmission electron microscopy demonstrate that MPTMCs are composed of a single phase with a random distribution of all cations, which holds the key to the unique combinations of improved fracture toughness, superior Vickers hardness, and extremely lower thermal diffusivity achieved in MPTMCs. The present discovery provides a promising approach toward the design and synthesis of next-generation high-performance materials.

cond-mat.mtrl-sci↗

arXiv2018

Atomic Origin of Ti Deficient Dislocation in SrTiO3 Bicrystal and Their Electronic Structures

Dislocations in perovskite oxides have important impacts on their physical and chemical properties, which are determined by their unique atomic environments. In the present study, the structure of dislocations in a 10° low-angle grain boundary of SrTiO3 (STO) is characterized by spherical aberration corrected scanning transmission electron microscopy (Cs-STEM) and spectroscopy. In contrast to previous studies, the deficiency instead of enrichment of titanium (Ti) is observed at the dislocation cores mainly due to the Sr substitution and under occupancy of Ti. The presence of oxygen vacancies and partially reduced Ti are also detected at the Ti deficient dislocations cores. These findings indicate the atomic structure of dislocations can be very different even they have the same Burges vectors. Controllable elemental segregation in the dislocations and grain boundaries via bicrystal engineering should be very useful for design of devices with novel functions.

cond-mat.mtrl-sci↗

arXiv2018

Electrochemical solid-state amorphization in the immiscible Cu-Li system: Size matters

As a typical immiscible binary system, copper (Cu) and lithium (Li) show no alloying and chemical intermixing under normal circumstances. A notable example that takes advantages of the immiscibility between Cu and Li is the widespread utilization of Cu foils as the anodic current collector in Li-ion batteries. Here we show that the nanoscale size effect can play a subtle yet critical role in mediating the chemical activity of Cu and therefore its miscibility with Li, such that the electrochemical alloying and solid-state amorphization will occur in such an immiscible system when decreasing Cu nanoparticle sizes into ultrasmall range. This unusual observation was accomplished by performing in-situ studies of the electrochemical lithiation processes of individual CuO nanowires inside a transmission electron microscopy (TEM). Upon lithiation, CuO nanowires are first electrochemically reduced to form discrete ultrasmall Cu nanocrystals that, unexpectedly, can in turn undergo further electrochemical lithiation to form amorphous CuLix nanoalloys. Real-time dynamic observations by in-situ TEM unveil that there is a critical grain size (ca. 6 nm), below which the crystalline Cu nanoparticles can be continuously lithiated and amorphized. Electron energy loss spectra indicate that there is a net charge transfer from Li to Cu in the amorphous CuLix nanoalloys. Another intriguing finding is that the amorphous alloying phenomena in Cu-Li system is reversible, as manifested by the in-situ observation of electron-beam-induced delithiation of the as-formed amorphous CuLix nanoalloys.

cond-mat.mtrl-sci↗

arXiv2013

Systematic Determination of Absolute Absorption Cross-section of Individual Carbon Nanotubes

Determination of optical absorption cross-section is always among the central importance of understanding a material. However its realization on individual nanostructures, such as carbon nanotubes, is experimentally challenging due to the small extinction signal using conventional transmission measurements. Here we develop a technique based on polarization manipulation to enhance the sensitivity of single-nanotube absorption spectroscopy by two-orders of magnitude. We systematically determine absorption cross-section over broad spectral range at single-tube level for more than 50 chirality-defined single-walled nanotubes. Our data reveals chirality-dependent one-dimensional photo-physics through the behaviours of exciton oscillator strength and lifetime. We also establish an empirical formula to predict absorption spectrum of any nanotube, which provides the foundation to determine quantum efficiencies in important photoluminescence and photovoltaic processes.

cond-mat.mes-hall↗

arXiv2011

In situ TEM investigation of oxygen migration as a key mechanism for resistive switching in Pr0.7Ca0.3MnO3

Low temperature growth Pr0.7Ca0.3MnO3 (PCMO) thin film showed high performance in electric field induced resistance switching (RS). To understand the micro-mechanism of RS in Metal/PCMO/Metal devices, structure evolution of PCMO under external electric field monitored inside transmission electron microscope (TEM) were performed. Evolution of the modulation stripe in as-grown PCMO sample was investigated when applying electric field. The new-generated modulation stripe gradually disappeared. These results indicate that oxygen ion migration plays a key role in RS.

cond-mat.mes-hall↗

arXiv2008

Highly Conducting Graphene Sheets and Langmuir-Blodgett Films

Graphene is an intriguing material with properties that are distinct from those of other graphitic systems. The first samples of pristine graphene were obtained by peeling off and epitaxial growth. Recently, the chemical reduction of graphite oxide was used to produce covalently functionalized single-layer graphene oxide. However, chemical approaches for the large-scale production of highly conducting graphene sheets remain elusive. Here, we report that the exfoliation-reintercalation-expansion of graphite can produce high-quality single-layer graphene sheets stably suspended in organic solvents. The graphene sheets exhibit high electrical conductance at room and cryogenic temperatures. Large amounts of graphene sheets in organic solvents are made into large transparent conducting films by Langmuir-Blodgett assembly in a layer-by-layer manner. The chemically derived high quality graphene sheets could lead to future scalable graphene devices.

cond-mat.mtrl-sci↗

arXiv2007

Strongly enhanced critical current density in Fe-sheathed MgB2 tapes by stearic acid and stearate doping

Fe-sheathed MgB2 tapes with cheap stearic acid, Mg stearate and Zn stearate doping were prepared through the in situ powder-in-tube method. It is found that Jc, Hirr, and Hc2 were significantly enhanced by doping. Compared to the pure tapes, Jc for all the doped samples was improved by more than an order of magnitude in a high-field regime. At 4.2 K, the transport Jc reached 2.02x10^4 A/cm^2 at 10 T for the Zn stearate doped tapes and 3.72x10^3 A/cm^2 at 14 T for the stearic acid doped samples, respectively, equivalent to that of tapes achieved by nanoscale SiC or carbon doping. The improvement of Jc-H properties in doped samples can be attributed to the increase of Hc2 resulting from the incorporation of C atoms into the MgB2 crystal lattice as well as a high density of flux-pinning centers.

cond-mat.supr-con↗

arXiv2006

Significantly enhanced critical current densities in MgB2 tapes made by a scaleable, nano-carbon addition route

Nanocarbon-doped Fe-sheathed MgB2 tapes with different doping levels were prepared by the in situ powder-in-tube method. Compared to the undoped tapes, Jc for all the C-doped samples was enhanced by more than an order of magnitude in magnetic fields above 9 T. At 4.2 K, the transport Jc for the 5 at% doped tapes reached 1.85x104 A/cm2 at 10 T and 2.8x103 A/cm2 at 14 T, respectively. Moreover, the critical temperature for the doped tapes decreased slightly. Transmission electron microscopy showed a number of intra-granular dislocations and the dispersed nanoparticles embedded within MgB2 grains induced by the C doping. The mechanism for the enhancement of flux pinning is also discussed. These results indicate that powder-in-tube-processed MgB2 tape is very promising for high-field applications.

cond-mat.supr-con↗