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Xiaoqing He

Publications and source records attributed to Xiaoqing He.

7 recordsLinked to original sources

Using superpixels for interpretable feature reduction in large 2D diffraction datasets

Large 2D diffraction datasets, consisting of hundreds or thousands of measurements, are commonly acquired with 4D-STEM electron diffraction or at synchrotron X-ray beamlines. Machine learning and artificial intelligence offer great promise for analyzing these datasets. However, the sheer volume of data presents a significant data processing bottleneck. Cropping the detector and pixel binning are standard ways to reduce data size. Here we propose grouping and averaging pixels into superpixels of variable area. High-information regions are sampled densely, while low-information areas are collected into larger superpixels. In the process, symmetries in the data are captured and exploited, making this approach suitable for preprocessing 2D diffraction data. We compare two variance-minimizing methods: K-means clustering (top-down) and agglomerative clustering (bottom-up) and demonstrate superior scaling and interpretability for the bottom-up method. As these methods are distance-based, we demonstrate that the construction of superpixels can be accelerated using Gaussian random projection. Finally we show over 100-fold acceleration for phase mapping with Non-negative matrix factorization on a 4D-STEM dataset when superpixels are used as a preprocessing step.

cond-mat.mtrl-sci

Radially symmetric transition-layer solutions in mass-conserving reaction-diffusion systems with bistable nonlinearity

Mass-conserving reaction-diffusion (MCRD) systems are widely used to model phase separation and pattern formation in cell polarity, biomolecular condensates, and ecological systems. Numerical simulations and formal asymptotic analysis suggest that such models can support stationary patterns with sharp internal interfaces. In this work, we establish for a general class of bistable MCRD systems the existence of nonconstant radially symmetric stationary solutions with a single internal transition layer on an $N$-dimensional ball, for general spatial dimension $N$. Our approach incorporates the global mass constraint directly into a refined matched-asymptotic framework complemented by a uniform spectral/linear analysis. Beyond mere existence, our framework yields arbitrarily high-order asymptotic approximations of the constructed solutions together with quantitative uniform error estimates, which provides a quantitative higher-dimensional theory of transition-layer patterns in MCRD systems and a rigorous justification for their use in modeling phase separation and pattern formation in biological and ecological settings.

math.AP

Emergent Spin Fluctuation and Structural Metastability in Self-Intercalated Cr$_{1+x}$Te$_2$ Compounds

Intercalated van der Waals (vdW) magnetic materials host unique magnetic properties due to the interplay of competing interlayer and intralayer exchange couplings, which depend on the intercalant concentration within the van der Waals gaps. Magnetic vdW compound chromium telluride, Cr$_{1+x}$Te$_2$, has demonstrated rich magnetic phases at various Cr concentrations, such as the coexistence of ferromagnetic and antiferromagnetic phases in Cr$_{1.25}$Te$_2$ (equivalently, Cr$_{5}$Te$_8$). The compound is induced by intercalating 0.25 Cr atom per unit cell within the van der Waals gaps of CrTe$_2$. In this work, we report a notably increased Curie Temperature and an emergent in-plane spin fluctuation by slightly reducing the concentration of Cr intercalants in Cr$_{1.25}$Te$_2$. Moreover, the intercalated Cr atoms form a metastable 2$\times$2 supercell structure that can be manipulated by electron beam irradiation. This work offers a promising approach to tuning magnetic and structural properties by adjusting the concentration of intercalated magnetic atoms.

cond-mat.mtrl-sci

Fast 4D-STEM-based phase mapping for amorphous and mixed materials

Interpretation and mapping strategies for 4D-scanning transmission electron microscopy (4D-STEM) are well-developed for crystalline materials, yet in the case of amorphous and mixed materials it is significantly more challenging to separate different phases. Non-negative matrix factorization (NMF) in principle would allow separation of 4D-STEM data into components with interpretable diffraction signatures and intensity maps, independent of the crystalline, amorphous or mixed nature of the material. However, adoption of NMF in this field is hampered by large datasets and conceptual hurdles: NMF tackles a non-convex optimization problem, requiring iterative algorithms. Additionally, the stopping condition has to be chosen carefully. In this work, we show that the factorization of large 4D-STEM datasets can be drastically accelerated using a QB decomposition (i.e. randomized NMF or RNMF), leading to much shorter time per iteration. This allows structure-independent phase mapping on very large 4D-STEM datasets. We validate this approach on a synthetic literature dataset (mixed ZrCuAl), before mapping a thin TiO$_2$ layer on top of SiO$_2$, and an interface between a lithium-ion cathode and solid state electrolyte. We also demonstrate that, before using NMF to transform the data on an interpretable, nonnegative basis, principal component analysis (PCA) can be used for fast exploratory analysis to assess dataset dimensionality and linearity.

cond-mat.mtrl-sci

Dirac Fermion Cloning, Moir$\bf{é}$ Flat Bands and Magic Lattice Constants in Epitaxial Monolayer Graphene

Tuning interactions between Dirac states in graphene has attracted enormous interest because it can modify the electronic spectrum of the two-dimensional material, enhance electron correlations, and give rise to novel condensed-matter phases such as superconductors, Mott insulators, Wigner crystals and quantum anomalous Hall insulators. Previous works predominantly focus on the flat band dispersion of coupled Dirac states from different graphene layers. In this work, we propose a new route to realizing flat band physics in monolayer graphene under a periodic modulation from substrates. We take gaphene/SiC heterostructure as a role model and demonstrate experimentally the substrate modulation leads to Dirac fermion cloning and consequently, the proximity of the two Dirac cones of monolayer graphene in momentum space. Our theoretical modeling captures the cloning mechanism of Dirac states and indicates that flat bands can emerge at certain magic lattice constants of substrate when the period of modulation becomes nearly commensurate with the $(\sqrt{3}\times\sqrt{3})R30^{\circ}$ supercell of graphene. The results show that the epitaxial monolayer graphene is a promising platform for exploring exotic many-body quantum phases arising from interactions between Dirac electrons.

cond-mat.mes-hall

cryo-ePDF: Overcoming Electron Beam Damage to Study the Local Atomic Structure of Amorphous ALD Aluminum Oxide Thin Films within a TEM

Atomic layer deposition (ALD) provides uniform and conformal thin films that are of interest for a range of applications. To better understand the properties of amorphous ALD films, we need improved understanding of their local atomic structure. Previous work demonstrated measurement of how the local atomic structure of ALD-grown aluminum oxide (AlOx) evolves in operando during growth by employing synchrotron high energy X-ray diffraction (HE-XRD). In this work, we report on efforts to employ electron diffraction pair distribution function (ePDF) measurements using more broadly available transmission electron microscope (TEM) instrumentation to study the atomic structure of amorphous ALD-AlOx. We observe electron beam damage in the ALD-coated samples during ePDF at ambient temperature and successfully mitigate this beam damage using ePDF at cryogenic temperatures (cryo-ePDF). We employ cryo-ePDF and Reverse Monte Carlo (RMC) modeling to obtain structural models of ALD-AlOx coatings formed at a range of deposition temperatures from 150-332°C. From these model structures, we derive structural metrics including stoichiometry, pair distances, and coordination environments in the ALD-AlOx films as a function of deposition temperature. The structural variations we observe with growth temperature are consistent with temperature-dependent changes in the surface hydroxyl density on the growth surface. The sample preparation and cryo-ePDF procedures we report here can be used for routine measurement of ALD-grown amorphous thin films to improve our understanding of the atomic structure of these materials, establish structure-property relationships, and help accelerate the timescale for the application of ALD to address technological needs.

cond-mat.mtrl-sci

180 degree Ferroelectric Stripe Nanodomains in BiFeO3 Thin Films

There is growing evidence that domain walls in ferroics can possess emergent properties that are absent in bulk materials. For example, 180 domain walls in the ferroelectric-antiferromagnetic BiFeO3 are particularly interesting because they have been predicted to possess a range of intriguing behaviors; including electronic conduction and enhanced magnetization. To date, however, ordered arrays of such domain structures have not been reported. Here, we report the observation of 180 stripe nanodomains in (110)-oriented BiFeO3 thin films grown on orthorhombic GdScO3 (010)O substrates, and their impact on exchange coupling to metallic ferromagnets. Nanoscale ferroelectric 180 stripe domains with {112 } domain walls were observed in films < 32 nm thick to compensate for large depolarization fields. With increasing film thickness, we observe a domain structure crossover from the depolarization field-driven 180 stripe nanodomains to 71 domains determined by the elastic energy. Interestingly, these 180 domain walls (which are typically cylindrical or meandering in nature due to a lack of strong anisotropy associated with the energy of such walls) are found to be highly-ordered. Additional studies of Co0.9Fe0.1/BiFeO3 heterostructures reveal exchange bias and exchange enhancement in heterostructures based-on BiFeO3 with 180 domain walls and an absence of exchange bias in heterostructures based-on BiFeO3 with 71 domain walls; suggesting that the 180 domain walls could be the possible source for pinned uncompensated spins that give rise to exchange bias. This is further confirmed by X-ray circular magnetic dichroism studies, which demonstrate that films with predominantly 180 domain walls have larger magnetization than those with primarily 71 domain walls. Our results could be useful to extract the structure of domain walls and to explore domain wall functionalities in BiFeO3.

cond-mat.mtrl-sci