High-resolution Scanning Transmission Electron Microscopy Research Articles

Structure and redox properties of CeMnO3 thin films

Conformal thin films of a cerium-manganese mixed oxide with a stoichiometry of CeMnOx were deposited on a high-surface-area γ-Al2O3 support by Atomic Layer Deposition (ALD). Upon redox cycling, the CeMnOx film underwent a reversible phase transition between a reduced perovskite CeMnO3 phase and an oxidized fluorite CeMnO3.5 phase, as shown by X-ray diffraction (XRD) and High-Resolution Scanning/Transmission Electron Microscopy (HR-S/TEM). X-ray Photoelectron Spectroscopy (XPS) and Electron Energy Loss Spectroscopy (EELS) revealed that Ce and Mn were in +3-oxidation states in the reduced perovskite phase and +4 and + 3 respectively in the oxidized fluorite phase. The composition of the film as a function of P(O2) at 1073 K was measured by coulometric titration and showed that a transition between Ce3+ and Ce4+ occurred at a P(O2) of 10−9 atm, a value that is much higher than that required for oxidizing either reduced bulk ceria or thin-film ceria on γ-Al2O3. These properties make CeMnOx films an interesting candidate for various catalytic applications.

Time-Resolved Formation and Operation Maps of Pd Catalysts Suggest a Key Role of Single Atom Centers in Cross-Coupling.

An approach to the spatially localized characterization of supported catalysts over a reaction course is proposed. It consists of a combination of scanning, transmission, and high-resolution scanning transmission electron microscopy to determine metal particles from arrays of surface nanoparticles to individual nanoparticles and individual atoms. The study of the evolution of specific metal catalyst particles at different scale levels over time, particularly before and after the cross-coupling catalytic reaction, made it possible to approach the concept of 4D catalysis-tracking the positions of catalytic centers in space (3D) over time (+1D). The dynamic behavior of individual palladium atoms and nanoparticles in cross-coupling reactions was recorded with nanometer accuracy via the precise localization of catalytic centers. Single atoms of palladium leach out into solution from the support under the action of the catalytic system, where they exhibit extremely high catalytic activity compared to surface metal nanoparticles. Monoatomic centers, which make up only approximately 1% of palladium in the Pd/C system, provide more than 99% of the catalytic activity. The remaining palladium nanoparticles changed their shape and could move over the surface of the support, which was recorded by processing images of the array of nanoparticles with a neural network and aligning them using automatically detected keypoints. The study reveals a novel opportunity for single-atom catalysis─easier detachment (capture) from (on) the carbon support surface is the origin of superior catalytic activity, rather than the operation of single atomic catalytic centers on the surface of the support, as is typically assumed.

Cd-Doped Li4–xCdxTi5O12 (x = 0.20) as a High Rate Capable and Stable Anode Material for Lithium-Ion Batteries

Li4Ti5O12 (LTO), an excellent anode for lithium-ion batteries (LIBs), suffers from low electronic conductivity, limiting its high-power rate application. An aliovalent metal ion doping strategy that tunes the electronic/ionic conductivity can mitigate this issue. In this work, we investigated a series of Cd2+ dopings on the Li4–xCdxTi5O12 (x = 0, 0.05, 0.10, and 0.20) anode material by considering its effect on structural and electrochemical performance in Li- and Na-ion batteries. Combined Rietveld refinement and X-ray absorption spectroscopy (XAS) analysis explicitly identified Cd2+ doping into the Li(8a) tetrahedral site of the cubic spinel LTO structure. According to high-resolution powder diffraction (HRPD), scanning electron microscopy (SEM), 4-point probe, and X-ray photoelectron spectroscopy (XPS), an increase in Cd2+ doping from 5 to 20% at the Li (8a) site in the LTO results in a reduction in particle size, an expansion of lattice, an increase in conductivity, and an increase in Ti3+ content to Ti4+ ratio. High-resolution scanning transmission electron microscopy (HR-STEM) confirms that cadmium ions are interstitially doped in the LTO structure. Compared to the pristine LTO electrode in the Li half cell, the Li3.80Cd0.20Ti5O12 (Cd0.20-LTO) electrode showed a significant improvement in capacity at high rates and excellent cycling performance. The improvement in performance for Cd0.20-doped LTO is a consequence of the reduction in the diffusion path and the faster Li-ion kinetics. Therefore, this Cd-doped LTO series of electrodes demonstrates advantageous features for Li-ion battery systems.

Experimental and Theoretical Investigations of Out-of-Plane Ordered Nanolaminate Transition Metal Borides: M4CrSiB2 (M = Mo, W, Nb).

We report the synthesis of three out-of-plane chemically ordered quaternary transition metal borides (o-MAB phases) of the chemical formula M4CrSiB2 (M = Mo, W, Nb). The addition of these phases to the recently discovered o-MAB phase Ti4MoSiB2 shows that this is indeed a new family of chemically ordered atomic laminates. Furthermore, our results expand the attainable chemistry of the traditional M5SiB2 MAB phases to also include Cr. The crystal structure and chemical ordering of the produced materials were investigated using high-resolution scanning transmission electron microscopy and X-ray diffraction by applying Rietveld refinement. Additionally, calculations based on density functional theory were performed to investigate the Cr preference for occupying the minority 4c Wyckoff site, thereby inducing chemical order.

In situ reaction synthesis, microstructure and thermomechanical properties of novel medium-entropy (Ti,V,Nb,Ta)2AlC ceramics

High- and medium-entropy (HE and ME) materials have attracted considerable interest in recent years due to the advantages of designable components and tunable structures with modifiable physicochemical performances. Herein, a dense equiatomic quaternary (Ti,V,Nb,Ta)2AlC solid solution, or denoted as a medium-entropy MAX phase, was fabricated by in-situ reaction in hot-pressing sintering process using easily available elemental powders as raw materials. X-ray diffraction with its Rietveld refinement analysis, scanning electron microscope and high-resolution scanning transmission electron microscope equipped with energy-dispersed spectrometer analysis identify the phase composition and crystal structure of the novel ME-M2AlC (Ti,V,Nb,Ta)2AlC phase. Especially, the atomic-resolution HAADF images directly prove the mutual solution of four metallic elements of the ME (Ti,V,Nb,Ta)2AlC phase. Both the flexural strength and Vickers hardness are enhanced compared with the reported individual components, and the strengthening and hardening results largely benefit from solid-solution effect with lattice distortion in structure. The fracture toughness has not been enhanced due to the lack of effective toughening mechanism. Furthermore, the electrical conductivity of ME (Ti,V,Nb,Ta)2AlC ceramic is distinctly decreased as a result of the increasing carrier lattice scattering and point defect scattering, which is caused by severe lattice distortion. Similarly, the scattering effect of solid solutions is also responsible for the lower thermal conductivity. It is worth noting that size disorder parameter (δsize) is a more effective criterion to evaluate the reduced thermal conductivity than the ideal mixing configurational entropy itself. As a result, applying the medium- and high-entropy design to the MAX phases with chemical and structural diversity can provide a large compositional space with corresponding large range of unexpected performances, which is highly anticipated.

Ultra-Small YPO4 -YAG:Ce Composite Nanophosphors with a Photoluminescence Quantum Yield Exceeding 50.

Synthesis of high quality colloidal Cerium(III) doped yttrium aluminum garnet (Y3 Al5 O12 :Ce3+ , "YAG:Ce") nanoparticles (NPs) meeting simultaneously both ultra-small size and high photoluminescence (PL) performance is challenging, as generally a particle size/PL trade-off has been observed for this type of nanomaterials. The glycothermal route is capable to yield ultra-fine crystalline colloidal YAG:Ce nanoparticles with a particle size as small as 10nm but with quantum yield (QY) no more than 20%. In this paper, the first ultra-small YPO4 -YAG:Ce nanocomposite phosphor particles having an exceptional QY-to-size performance with an QY up to 53% while maintaining the particle size ≈10nm is reported. The NPs are produced via a phosphoric acid- and extra yttrium acetate-assisted glycothermal synthesis route. Localization of phosphate and extra yttrium entities with respect to cerium centers in the YAG host has been determined by fine structural analysis techniques such as X-ray diffration (XRD), solid state nuclear magnetic resonance (NMR), and high resolution scanning transmission electron microscopy (HR-STEM), and shows distinct YPO4 and YAG phases. Finally, a correlation between the additive-induced physico-chemical environment change around cerium centers and the increasing PL performance has been suggested based on electron paramagnetic resonance (EPR), X-ray photoelectronspectrometry (XPS) data, and crystallographic simulation studies.

In-situ and real-time nano/microplastic coatings and dynamics in water using nano-DIHM: A novel capability for the plastic life cycle research

A novel nano-digital inline holographic microscope (nano-DIHM) was used to advance in-situ and real-time nano/microplastic physicochemical research, such as particle coatings and dynamic processes in water. Nano-DIHM data provided evidence of distinct coating patterns on nano/microplastic particles by oleic acid, magnetite, and phytoplankton, representing organic, inorganic, and biological coatings widely present in the natural surroundings. A high-resolution scanning transmission electron microscopy confirmed nano-DIHM data, demonstrating its nano/microplastic research capabilities. The sedimentation of two plastic size categories was examined: (a) ∼10 to 700 µm, and (b) ∼ 1 to 5 mm. Particle size was the primary factor affecting the sedimentation for studied (a) microplastics and (b) pellets. Two types of silicone rubbers exhibited different sedimentation processes. We also demonstrated that inorganic ions in seawater and oleic acid organic coatings altered the sedimentation velocity of studied plastics by 9 – 13% and 5 – 9%, respectively. Semi-empirical probability functions were developed and incorporated into a numerical model (CaMPSim-3D) to simulate the transport of studied microplastics and pellets in the Saint John River estuary. Water dynamics was the driving force of plastic transport, yet the accumulation of plastics was selectively dependant on particle physicochemical properties such as size and density by ∼ 7%. The usage of nano-DIHM for targeted identification of nano/microplastic hotspots and aquatic plastic wastes remediation were discussed.

Size-Controlled Low-Melting-Point-Alloy Particle-Incorporated Transient Liquid-Phase Epoxy Composite Conductive Adhesive with High Performances

With fast developments in the environmental-friendly industry, electrically conductive adhesive (ECA) composites with high electrical conductivity, mechanical strength, and electrochemical migration resistance as well as low cost are highly desirable for emerging power electronics applications. In this study, a category of ECAs, namely, size-controllable sonochemical low-melting-point-alloy (LMPA) particle-incorporated transient liquid-phase ECAs (TLP-ECAs), with excellent electrical conductivity, considerable mechanical strength, and high electrochemical migration resistance has been successfully demonstrated. Experimental results showed that the bulk resistivity of TLP-ECA decreased to a minimum value of 2.37 × 10–4 Ω-cm with the remaining filler content at a low level (the total content of metallic fillers, i.e., 70 wt % in TLP-ECAs), while the mechanical shear strength increased considerably (by 55.4%) compared with pure silver ECA with the same filler content, demonstrating that addition of sonochemical LMPA particles into ECA can simultaneously and considerably improve the electrical and mechanical properties. Moreover, the diffusional reaction mechanism of sonochemical LMPA particle-filled TLP-ECA was systematically investigated via differential scanning calorimetry (DSC), X-ray diffraction (XRD), and high-resolution scanning transmission electron microscopy in high-resolution high-angle annular dark-field mode (STEM-HAADF). The mechanism of the diffusion reaction of TLP-ECA with LMPA particles was rationalized, where Ag9In4 (γ phase, cP52, and P43m) and Ag3Sn (ε phase, oP8, and Pmmm) intermetallic compounds (IMC) and their corresponding nanostructures were responsible for the substantial enhancement in mechanical strength and the antielectrochemical migration property. The sonochemical method is the key to synthesize LMPA particles of desirable compositions and controllable size, thereby enhancing the overall performance of Ag-based TLP-ECAs. Accordingly, the sonochemical LMPA particle-incorporated-TLP-ECAs are the promising interconnection material candidates for power electronics packaging.

Corrosion of 1.4016 Ferritic Steel by Urea at High Temperature

The corrosion behavior of a ferritic unstabilized stainless steel 1.4016 during decomposition of aqueous urea solution at high temperature has been investigated. Corrosion was obtained from 100 h of cyclic heating (from room temperature up to 600 °C) and injection of aqueous urea solution on the steel plate in a laboratory-scale test bench. The evaluation procedure covered the metallographic analysis of corroded steel samples by high-resolution scanning electron microscopy (HR-SEM) and transmission electron microscopy (TEM). Uniform corrosion underneath deposits was found as one of the drivers for degradation of the steel. Damage happened by high-temperature depassivation of stainless steel due to the excess of the aggressive medium. Besides uniform corrosion, a nitridation layer underneath surface oxides together with chromium carbonitride particles precipitated through the whole depth of the sample was identified resulting in intergranular attack.

Oriented secondary magnetite micro-inclusions in plagioclase from oceanic gabbro

Abstract Plagioclase-hosted submicrometer to micrometer-sized oriented needle- and lath-shaped magnetite micro-inclusions with their elongation direction aligned parallel to the plagioclase [001] (PL[001]) direction were investigated using correlated optical, scanning electron, and scanning transmission electron microscopy. The PL[001] magnetite micro-inclusions formed from older generations of differently oriented magnetite micro-inclusions by recrystallization during hydrothermal alteration. Six orientation variants of PL[001] magnetite micro-inclusions occur, and they share the same shape orientation but differ in their crystallographic orientation relationships to the plagioclase host. The magnetite-plagioclase interfaces are facetted. High-resolution scanning transmission electron microscopy revealed that interface facets are aligned parallel to low-index lattice planes corresponding to oxygen layers of either magnetite or plagioclase. In addition, the linkage between prominent crystal structure elements of magnetite and plagioclase across the interfaces and accommodation mechanisms minimizing misfit between the two crystal structures were discerned. Combined evidence suggests that the shape and shape orientation, as well as the crystallographic orientation relationships between the magnetite micro-inclusions and the plagioclase host, are crystallographically controlled. The close crystal-structural link between magnetite precipitates and plagioclase host ensures a low-energy configuration driving recrystallization of older generations of differently orientated magnetite micro-inclusions into those that are aligned parallel to PL[001] and facilitates the underlying reaction kinetics. Due to their single to pseudo-single domain characteristics, the plagioclase-hosted magnetite micro-inclusions are particularly robust carriers of natural remanent magnetization. Recrystallization of differently oriented preexisting magnetite micro-inclusions into magnetite micro-inclusions with uniform shape orientation parallel to PL[001] has interesting consequences for the magnetic anisotropy of magnetite-bearing plagioclase grains.

Self-catalyzed GaP nanowire MOVPE growth on Si

Typically, vapour liquid solid (VLS)-grown nanowires via metal–organic vapour phase epitaxy (MOVPE) use gold as a liquid growth catalyst. However, incorporating gold as an impurity during growth is disadvantageous. Therefore, we introduce the self-catalyzed VLS growth of GaP nanowires on Si (111) substrates via MOVPE, utilizing (deposited) Ga droplets as seed particles. To understand and optimize the growth process, the influence of various growth parameters such as Ga precursor preflow, growth temperature, growth time and V/III ratio are studied. As main findings we show that nanowire growth without strong tapering is possible. By varying the V/III gas phase ratio the tapering of nanowires can be manipulated during growth via droplet consumption. In addition, nanowires with lengths up to 10 µm and an aspect ratio of around 20 are demonstrated, showing only slight tapering. High-resolution scanning transmission electron microscopy measurements prove the zincblende crystal structure of the GaP nanowires in horizontal and vertical ultramicrotomy cuts. In vertical cross sections, a high number of microtwin boundaries perpendicular to the growth direction are found.

High-resolution STEM investigation of the role of dislocations during decomposition of Ti1-xAlxNy

The defect structures forming during high-temperature decomposition of Ti1-xAlxNy films were investigated through high-resolution scanning transmission electron microscopy. After annealing to 950 °C, misfit edge dislocations and a/6〈112〉{111} partial dislocations permeate the interface between TiN-rich and AlN-rich domains to accommodate lattice misfits during spinodal decomposition. The stacking fault energy associated with the partial dislocations decreases with increasing Al content, which facilitates the coherent cubic to wurtzite structure transition of AlN-rich domains. The wurtzite AlN-rich structure is recovered when every third cubic {111} plane is shifted by a/6 along the [211] direction. After annealing to 1100 °C, a temperature where coarsening dominates the microstructure evolution, we observe intersections of stacking faults, which form sessile locks at the interface of the TiN- and AlN-rich domains. These observed defect structures facilitate the formation of semicoherent interfaces and contribute to hardening in Ti1-xAlxNy.

Cascade Reaction of Ethanol to Butadiene over Ag-Promoted, Silica- or Zeolite-Supported Ta, Y, Pr, or La Oxide Catalysts

Ethanol converts to 1,3-butadiene in the presence of suitable multifunctional catalysts. In this work, Lewis acid cations Ta, Y, Pr, and La were dispersed on amorphous silica or β zeolite, and after physically mixing with silica-supported Ag nanoparticles, were tested in the cascade reaction of ethanol to butadiene at 573 K. The Lewis acid catalysts were characterized by X-ray fluorescence, N2 physisorption, scanning transmission electron microscopy (STEM), X-ray diffraction, and diffuse reflectance (DR) UV–vis and X-ray photoelectron spectroscopies. High-resolution STEM images confirmed the small oxide cluster size on the silica support. Results from DR UV–vis spectroscopy showed that zeolite-supported Ta and Pr catalysts had a smaller metal oxide cluster size, relative to their SiO2 counterparts. X-ray photoelectron spectroscopy confirmed that the oxidation state of the cations supported on the zeolite remained the same as that of their SiO2-supported analogues. The selectivity of the C4 coupling products toward butadiene relative to butanol correlated with the acid strength of the Lewis acid cations, as evaluated by the 2-propanol decomposition reaction to propene and acetone, with Ta being the most selective. The rate of C–C coupling over the zeolite-supported cations was enhanced by an order of magnitude compared to those cations supported on amorphous SiO2.

Strain Rate-Dependent Anomalous Work Hardening of a Single-Crystalline CoNi-Base Superalloy

The deformation mechanisms operating in superalloys depend on different parameters such as composition, temperature and deformation rate. So far, the transition from shearing by APB-coupled dislocations to shearing under the formation of stacking faults has been studied exclusively as a function of temperature but not as a function of the strain rate. Therefore, interrupted compression tests with strain rates between 10–3 s−1 and 10–5 s−1 were performed on the single-crystalline CoNi-base superalloy ERBOCo-4 at a temperature of 850 °C. The evolution of the defect structures has been analyzed by conventional transmission electron microscopy. A change of the deformation mechanism from APB-coupled dislocation shearing to stacking fault shearing is found to depend on the strain rate. At lower strain rates, an increased stacking fault density is associated with a higher yield strength and higher work hardening rates at the early stages of plastic deformation due to a very high stacking fault density. After approximately 2.0 pct plastic strain, the stress reaches a plateau and decreases subsequently, which is associated with the formation and thickening of twins as shown by high-resolution scanning transmission electron microscopy. At higher strain rates, the work hardening rate is significantly lower in the early deformation stage. The role of segregation to planar defects and the influence of local phase transformations (LPT) at SESFs is further discussed in reference to the influence of the strain rate. The segregation of W as an η stabilizing element is found to be crucial for the formation of a local phase transformation in ERBOCo-4. At higher strain rates the phase transformation is hindered by insufficient W segregation, resulting in a higher twin density.

Coherent twin-oriented Al3Sc-based precipitates in Al matrix

Al3(Sc,Zr,Ti) nanoparticles with an ideal twin-type orientation relationship to Al host matrix were found in cold-rolled and subsequently annealed Al-based alloy. Atomic-scale investigations using high-resolution scanning transmission electron microscopy identified particles that form prominent coherent (111) twin-type interfaces along their longer facets and semi-coherent twin interfaces on their shorter facets. Ab-initio calculations showed that a coherent Al/Al3Sc twin-like phase boundary corresponds to a local energy minimum. A model is proposed explaining the formation of the twin orientation relationship of an Al3Sc nanoparticle with the Al host matrix.

Identification of the Bravais lattice and cell parameters through quantitative model-based transmission electron microscopy and Niggli cell reduction theory: the case of intermetallic Ni5Pb2Te3

This article demonstrates a simple and effective way to accurately determine the Bravais lattice type and cell parameters of an unknown phase by combining quantitative model-based high-resolution (scanning) transmission electron microscopy and Niggli cell reduction theory. This method was applied to the Ni5Pb2Te3 phase in the Ni–Pb–Te ternary system, which exists at high temperatures and forms from the interaction of Ni contacts with PbTe thermoelectric materials. The structure was identified to be triclinic with the space group P1 and cell parameters a = 5.43 ± 0.09 Å, b = 3.93 ± 0.03 Å, c = 3.75 ± 0.01 Å, α = 115.4 ± 0.2°, β = 93.4 ± 0.6° and γ = 91.1 ± 0.1°. The methodology is particularly beneficial for the class of problems where the phase under study coexists in a multiphase environment.

Predicting chemoevasion potential of cancer cells from statistical chromatin packing behavior.

In malignancy, genetic, metabolic, or environmental insults may remodel chromatin structure, potentially increasing the plasticity of aberrant cell state transitions. Observed alterations to the epigenetic landscape of chromatin include gain-of-function mutations of Polycomb repressor EZH2 that block differentiation. Nucleosome remodeling and higher-order chromatin organization may also increase malignancy, with abnormalities ranging from prevalent mutations of ATP-dependent chromatin remodelers to mixing between transcriptionally active and inactive compartments. However, a universal relationship between chromatin structure and the disease state does not yet exist. Here, using the first principles of physics, we demonstrate that chromatin packing, or the statistical distribution of chromatin density in 4D, is a genome-wide regulator of phenotypic plasticity. The nucleus is a highly crowded, heterogeneous environment where DNA, RNA, proteins, and other macromolecules exert excluded volume effects, altering the kinetics and efficiency of transcription reactions. As chromatin is the major crowder in the nucleus, characterizing the chromatin mass density distribution facilitates a more complete understanding of transcription processes in a realistic nuclear environment. Combining high-resolution chromatin scanning transmission electron microscopy (ChromSTEM) and live-cell, label-free Partial Wave Spectroscopy (PWS) along with polymer physics-based analysis, we identified the existence of spatially separable packing domains, around 80 nm in radius. We then employed our understanding of fundamental chromatin packing to build a chromatin-mediated model of transcription that incorporates two pertinent aspects of phenotypic plasticity: transcriptional malleability, the ability of a cell to upregulate certain genes within a critical time frame, and transcriptional heterogeneity, a cell population's range of functional states. Finally, we extended our transcription model to predict how the average chromatin packing behavior of a cell population contributes directly to cancer cell survival upon chemotherapy treatment. Experimental observations confirmed model predictions, underlying the importance of chromatin packing in chemoevasion processes.

Collective Magnetic Behavior in Vanadium Telluride Induced by Self-Intercalation

Self-intercalation of native magnetic atoms within the van der Waals (vdW) gap of layered two-dimensional (2D) materials provides a degree of freedom to manipulate magnetism in low-dimensional systems. Among various vdW magnets, the vanadium telluride is an interesting system to explore the interlayer order-disorder transition of magnetic impurities due to its flexibility in taking nonstoichiometric compositions. In this work, we combine high-resolution scanning transmission electron microscopy (STEM) analysis with density functional theory (DFT) calculations and magnetometry measurements, to unveil the local atomic structure and magnetic behavior of V-rich V1+xTe2 nanoplates with embedded V3Te4 nanoclusters grown by chemical vapor deposition (CVD). The segregation of V intercalations locally stabilizes the self-intercalated V3Te4 magnetic phase, which possesses a distorted 1T'-like monoclinic structure. This phase transition is controlled by the electron doping from the intercalant V ions. The magnetic hysteresis loops show that the nanoplates exhibit superparamagnetism, while the temperature-dependent magnetization curves evidence a collective superspin-glass magnetic behavior of the nanoclusters at low temperature. Using four-dimensional (4D) STEM diffraction imaging, we reveal the formation of collective diffuse magnetic domain structures within the sample under the high magnetic fields inside the electron microscope. Our results shed light on the studies of dilute magnetism at the 2D limit and on strategies for the manipulation of magnetism for spintronic applications.

Epitaxial growth of a β-Ga2O3 (−201)-oriented thin film on a threefold symmetrical SrTiO3 (111) substrate for heterogeneous integration

Epitaxial growth of a wide bandgap semiconductor β-Ga2O3 thin film with high crystal quality plays a decisive role in constructing optical and electronic devices. However, except for the native substrate, the scarcity of appropriate non-native substrates or the poor crystallization of the deposit in thin film growth severely limits the fabrication and applicability of the final heterostructures and devices. Here, by taking the consistent symmetry and closely matched atomic spacing between β-Ga2O3 (−201) and the cubic perovskite (111)-oriented plane of SrTiO3, we realize the epitaxial growth of single crystal β-Ga2O3 (−201) thin films on the SrTiO3 (111) substrate by the pulsed laser deposition method, as confirmed by wide-range reciprocal-space mapping and high-resolution scanning transmission electron microscopy. The fabricated β-Ga2O3 (−201) photodetector device on the SrTiO3 (111) substrate exhibits excellent ultraviolet optical detection performance with large on/off switching ratios and a fast response speed. Moreover, the β-Ga2O3/SrTiO3 (111) heterojunction shows type-II heterostructure characteristics for energy band alignment, which displays superior ability for electron–hole pairs separation with large conduction and small valance band offsets of 1.68 and 0.09 eV, respectively. The results offer us a new way to obtain high-quality β-Ga2O3 (−201) thin film heterostructures on cubic SrTiO3 (111) substrates and fabricate β-Ga2O3-based optical and electronic devices.

Non-Centrosymmetric Sr2IrO4 Obtained Under High Pressure.

Sr2IrO4 with strong spin-orbit coupling and Hubbard repulsion (U) hosts Mott insulating states. The similar crystal structure and magnetic and electronic properties, particularly the d-wave gap observed in Sr2IrO4 enhanced the analogies to the cuprate high-Tc superconductor, La2CuO4. The incomplete analogy was due to the lack of broken inversion symmetry phases observed in Sr2IrO4. Here, under high-pressure and high-temperature conditions, we report a noncentrosymmetric Sr2IrO4. The crystal structure and its noncentrosymmetric character were determined by single-crystal X-ray diffraction and high-resolution scanning transmission electron microscopy. The magnetic characterization confirms the Ir4+ with S = 1/2 at low temperature in Sr2IrO4 with magnetic ordering occurring at around 86 K, where a larger moment is observed than the ambient pressure Sr2IrO4. Moreover, the resistivity measurement shows three-dimensional Mott variable-range hopping (VRH) existed in the system. This noncentrosymmetric Sr2IrO4 phase appears to be a unique material that offers a further understanding of high-Tc superconductivity.