Bulk Constituents Research Articles

The Role of Optical Phonon Confinement in the Infrared Dielectric Response of III-V Superlattices.

Polar dielectrics are key materials of interest for infrared (IR) nanophotonic applications due to their ability to host phonon-polaritons that allow for low-loss, subdiffractional control of light. The properties of phonon-polaritons are limited by the characteristics of optical phonons, which are nominally fixed for most "bulk" materials. Superlattices composed of alternating atomically thin materials offer control over crystal anisotropy through changes in composition, optical phonon confinement, and the emergence of new modes. In particular, the modified optical phonons in superlattices offer the potential for so-called crystalline hybrids whose IR properties cannot be described as a simple mixture of the bulk constituents. To date, however, studies have primarily focused on identifying the presence of new or modified optical phonon modes rather than assessing their impact on the IR response. This study focuses on assessing the impact of confined optical phonon modes on the hybrid IR dielectric function in superlattices of GaSb and AlSb. Using a combination of first principles theory, Raman, FTIR, and spectroscopic ellipsometry, the hybrid dielectric function is found to track the confinement of optical phonons, leading to optical phonon spectral shifts of up to 20 cm-1 . These results provide an alternative pathway toward designer IR optical materials.

Multi-functional fluorinated NiTiO3 perovskites for CO2 photocatalytic reduction, electrocatalytic water splitting, and biomedical waste management

Multi-functional F-doped NiTiO3 structures with high stability were prepared by a template-free hydrothermal method. A multi-technique approach including several physicochemical techniques was employed to describe the morphology, electronic properties, and structural characters. The F-doped NiTiO3 catalyst showed a much higher CO2 to CH4 photocatalytic conversion rate (2.6 μmol g−1 h−1) than pristine NiTiO3 (1.6 μmol g−1 h−1), highlighting the key role of F impurities in suppressing the charge carriers recombination. In addition to the higher efficiency and reusability than Pt/C reference electrode toward electrocatalytic water splitting, a lower Tafel slope was recorded for the F-doped structure (81.2 mV dec−1). This implies significant improvement in the reaction kinetics, arising from the synergistic effects between the F sites and bulk constituents to supply more desired active electronic states. The capability of the structures for the biomedical wastewater (containing the Caco-2 cancer cells) treatment was also explored. According to several biochemical assays, the fluorinated material shows a promising performance against the tumor cells at its IC50 concentration, 0.15 μg/mL, in a typical hospital wastewater. Our results pave the way for developing novel multi-functional photoactive titanate perovskites aiming at future clean energy transition.

Review on Developments and Progress in Nickelate‐Based Heterostructure Composites and Superconducting Thin Films

AbstractIn the past decade, the rapid development of modern heterointerface growth and characterization techniques has stimulated great effort to research and design the extraordinary physical properties of transition metal heterostructure composite materials. Here, new physics originates from the rearrangement of orbital, charge, spin, and lattice and the resulting rebalancing of their mutual interactions. In this paper, recent experimental and theoretical progress in the design, preparation, characterization, and physical property measurement of LaNiO3‐based heterostructure composites and the infinite‐layer Ni1 + nickelate superconducting thin films on (001) SrTiO3 substrate is reviewed, mainly by the methods of various X‐ray spectroscopy measurements, scanning transmission electron microscopy, and magneto‐transport measurements. In these materials, the electronic structure and orbital occupation around the Fermi level are modified, enabling nickelate‐based composite materials to exhibit new states of matter and physical phenomena, which are absent in the bulk constituents. Their confined structures, superconductivity, orbital polarization, charge transfer, electronic structures, magnetic properties, and X‐ray spectroscopic analysis, are therefore highlighted, aiming at understanding unconventional superconducting mechanisms and designing new high‐Tc superconducting low‐dimensional materials for device applications.

Coupling Charge and Topological Reconstructions at Polar Oxide Interfaces.

In oxide heterostructures, different materials are integrated into a single artificial crystal, resulting in a breaking of inversion symmetry across the heterointerfaces. A notable example is the interface between polar and nonpolar materials, where valence discontinuities lead to otherwise inaccessible charge and spin states. This approach paved the way for the discovery of numerous unconventional properties absent in the bulk constituents. However, control of the geometric structure of the electronic wave functions in correlated oxides remains an open challenge. Here, we create heterostructures consisting of ultrathin SrRuO_{3}, an itinerant ferromagnet hosting momentum-space sources of Berry curvature, and LaAlO_{3}, a polar wide-band-gap insulator. Transmission electron microscopy reveals an atomically sharp LaO/RuO_{2}/SrO interface configuration, leading to excess charge being pinned near the LaAlO_{3}/SrRuO_{3} interface. We demonstrate through magneto-optical characterization, theoretical calculations and transport measurements that the real-space charge reconstruction drives a reorganization of the topological charges in the band structure, thereby modifying the momentum-space Berry curvature in SrRuO_{3}. Our results illustrate how the topological and magnetic features of oxides can be manipulated by engineering charge discontinuities at oxide interfaces.

Charge‐Transfer‐Induced Multivalent States with Resultant Emergent Magnetism in Transition‐Metal Oxide Heterostructures

AbstractTransition‐metal oxide (TMO) heterostructures provide fertile grounds for creating and manipulating intriguing properties and functionalities. At the interface of TMO heterostructures, electronic reconstructions generally occur via charge transfer and lead to an extraordinary spectrum of emergent phenomena but unattainable in their bulk constituents. However, the basic mechanism of charge transfer at the interface is not fully determined or even understood in heterostructures, which may hide the underlying mechanisms and intriguing physics. Herein, an intrinsic charge transfer and resultant exotic ferromagnetism are unambiguously observed in the heterostructures between the nonmagnetic LaCoO3 (LCO) and SrTiO3 (STO). Combining element‐specific X‐ray absorption spectroscopy and atomic multiplet fitting, direct evidence of charge transfer‐induced multivalence of cobalt ions, interactions of which would contribute to the novel magnetism beyond the intuition, in concert with first‐principles density‐functional‐theory calculations, is demonstrated. Beyond LCO/STO system, a more broadly applicable principle for the heterostructures between 3d TMO and STO where charge transfer and resultant multivalence or conducting interfaces are coexistent is establish. This study represents an advance that the electronic reconstruction and the multiple electron configurations of 3d transition metal ions will constitute a powerful tool for the designs of functional materials and creations of unconventional physical properties.

Electric field control of magnetism at the γ-FeSi2/Si(001) interface

Interfaces often exhibit unique electronic and magnetic properties that are not present in their bulk constituents. Understanding the atomic-level structure and properties of the interface is crucial for their technological applications. In this article, we report a first-principles study of the γ-FeSi2/Si(001) interface to unravel the atomic-level structure property relationship. An external electric field is included in our model to tune the properties of the interface. Based on our calculations, we found a modest application of an electric field (> 0.15 eV/A) could stabilize a sixfold and sevenfold coordinated, spin-active interface over a nonmagnetic (eightfold coordinated) interface-providing direct evidence of electric field control of magnetism at the interface. The sixfold as well as sevenfold coordinated structures are shown to favor antiferromagnetic spin ordering arising from the Fe(d)-Si(p)-Fe(d) super-exchange interaction. The distinct non-linear response of the interface structure to the applied electric field can be attributed to the different electronic and magnetic structures at the interface; the sixfold exhibits the highest polarizability over the other coordinated structures.

Atomic-Scale Control of Magnetism at the Titanite-Manganite Interfaces

Complex oxide thin-film heterostructures often exhibit magnetic properties different from those known for bulk constituents. This is due to the altered local structural and electronic environment at the interfaces, which affects the exchange coupling and magnetic ordering. The emergent magnetism at oxide interfaces can be controlled by ferroelectric polarization and has a strong effect on spin-dependent transport properties of oxide heterostructures, including magnetic and ferroelectric tunnel junctions. Here, using prototype La2/3Sr1/3MnO3/BaTiO3 heterostructures, we demonstrate that ferroelectric polarization of BaTiO3 controls the orbital hybridization and magnetism at heterointerfaces. We observe changes in the enhanced orbital occupancy and significant charge redistribution across the heterointerfaces, affecting the spin and orbital magnetic moments of the interfacial Mn and Ti atoms. Importantly, we find that the exchange coupling between Mn and Ti atoms across the interface is tuned by ferroelectric polarization from ferromagnetic to antiferromagnetic. Our findings provide a viable route to electrically control complex magnetic configurations at artificial multiferroic interfaces, taking a step toward low-power spintronics.

Tracking small heterogeneity in binary mixtures of aliphatic and aromatic hydrocarbons: NIR spectroscopic, 2DCOS and MCR-ALS studies

To our best knowledge, this is the first spectroscopic study of small heterogeneity at a molecular level in binary mixtures of aliphatic and aromatic hydrocarbons. The composition-dependent spectra of benzene/toluene, benzene/n‑hexane, benzene/cyclohexane, n‑hexane/n‑heptane and n‑hexane/cyclohexane mixtures were recorded by NIR transmission technique in the whole range of mole fractions. A comprehensive exploration of the experimental data was performed by two-dimensional correlation analysis (2DCOS) and chemometric methods. In addition, we calculated excess NIR molar absorption spectra and parameter of ER, which allows for comparison of the degree of deviation from ideality for various mixtures. Our results reveal that all studied mixtures deviate from the ideal mixture. The extent of these deviations is small for the mixtures were both components are aromatic or aliphatic and increases for aromatic/aliphatic mixtures. In addition, molecular shapes have an important effect on the degree of deviation from the ideal mixture. As expected, benzene/n‑hexane is the most non-ideal mixture, while behavior of n‑hexane/n‑heptane and benzene/toluene mixtures is close to the ideal one. Our results suggest that in the mixtures with the largest deviations from ideality are present homoclusters of both components and heteroclusters. The heteroclusters exist in the whole range of compositions, while the homoclusters appears above a certain concentration limit. If both components of the mixture are similar, the molecules with equal probability form the homo- and heteroclusters. In the case of unlike components, the molecules prefer to form the homoclusters. The homoclusters of both components in the mixture are similar as those observed in bulk constituents. This means that deviation from the ideal mixture results from presence of the heteroclusters.

Biomimetic architected materials with improved dynamic performance

In recent decades, material performances improved by the discovery of new bulk materials have slowed down. By contrast, novel and unprecedented material properties have been demonstrated under the concept of “architected materials”, where the material properties are dominated by material microstructure instead of constituents. Knowing that mother nature is “a master of material architecture” through millions of years evolution – nearly all natural materials have elegantly fine and organized structures showing excellent impact resistance and damage tolerance. In this study, we design material architectures mimicking biomaterials and 3D print architected beams with dynamic performance far beyond their bulk constituents. By performing dynamic three-point bending tests and digital image correlation analysis, we characterize five types of bioinspired microstructures and propose the criteria of architecture selection adopting the concept of material indices. The reason why certain microstructures are preferred by certain organisms and how to optimally select material architectures for specific engineering applications are illustrated. Furthermore, microstructure integration approaches that work on multiple length scales (hierarchical designs) and on one specific length scale (hybrid designs) are investigated. Applying these approaches, we have designed architected beams that are flexible and strong, strong and tough, dissipative and stiff, and flexible and responsive, which are typically exclusive in bulk materials. Additionally, material architectures give extra control of fracture patterns, improving the critical impact energy by over 6 times. This work provides insights to the structure–property relationships and will facilitate the development of architected materials with tailored performances of flexibility, strength, toughness, energy dissipation, and fast response.

Carbon cycling in the Sargasso Sea water column: Insights from lipid biomarkers in suspended particles

This study compares lipid biomarker and bulk constituents (organic carbon and δ13C, nitrogen and carbonate) in particles (30–4400 m depth) collected at the Oceanic Flux Program site in the northern Sargasso Sea off Bermuda during three periods of contrasting oceanographic conditions: following the spring bloom (April 2015), during the low productivity period (November 2015), and two weeks after the passage of the Category 3 Hurricane Nicole (October 2016). Lipids biomarkers were used to evaluate the contributions of phytoplankton, zooplankton and bacterial sources to the particulate organic carbon (POC), diagenetic transformations of suspended POC throughout the water column and within the nepheloid layer, and seasonal and non-seasonal temporal variability, including the impact of an extreme weather event.Depth profiles of lipid concentration and molecular composition showed seasonal and non-seasonal variability in particle composition throughout the water column. Higher lipid concentrations in April versus November 2015 reflected differences in plankton productivity, while relative abundances in diagnostic phytosterols, C18 polyunsaturated fatty acids and alkenones reflected differences in phytoplankton community structure. A rapid decrease in lipid biomarker concentrations below the euphotic zone was accompanied by a marked transition in lipid composition, e.g. increases in the relative percentages of cholesterol, C16-C18 fatty alcohols, odd- and branched- chain fatty acids. This reveals the intense remineralization of algal-derived carbon and fresh inputs of organic materials from zooplankton and microbial production within the upper mesopelagic zone. Particulate lipids within the bathypelagic zone reveal a close connectivity of deep particulate carbon composition with upper ocean properties, while compositional heterogeneity with depth reflects continuous particle turnover and de novo particle production throughout the deep water column. Additionally, depth trends in the within-class composition of fatty alcohols and bacterial fatty acids were observed, suggesting depth zonation of zooplankton and microbial community structure.Hurricane Nicole (October 2016) strongly impacted upper ocean physics and nutrient supply, resulting in a transient phytoplankton bloom/flux event that increased concentrations of fresh particulate phytodetritus (e.g., C18 polyunsaturated fatty acids) throughout the mesopelagic and upper bathypelagic zones. Concurrent increases in zooplankton and bacterial lipid biomarkers (e.g., 18:1ω9, odd- and branched-chain fatty acids, cholesterol) indicated that this transient pulse of labile carbon stimulated mesopelagic zooplankton and microbial activity, resulting in an enrichment of labile materials in the suspended particle pool throughout the deep ocean. Our study demonstrates that extreme weather events can have a major impact on carbon flux and particle cycling in the deep ocean, with pronounced implications for the ocean carbon pump and deep ocean ecosystems.

Extreme Reconfigurable Nanoelectronics at the CaZrO3 /SrTiO3 Interface.

Complex oxide heterostructures have fascinating emergent properties that originate from the properties of the bulk constituents as well as from dimensional confinement. The conductive behavior of the polar/nonpolar LaAlO3 /SrTiO3 interface can be reversibly switched using conductive atomic force microscopy (c-AFM) lithography, enabling a wide range of devices and physics to be explored. Here, extreme nanoscale control over the CaZrO3 /SrTiO3 (CZO/STO) interface, which is formed from two materials that are both nonpolar, is reported. Nanowires with measured widths as narrow as 1.2 nm are realized at the CZO/STO interface at room temperature by c-AFM lithography. These ultrathin nanostructures have spatial dimensions at room temperature that are comparable to single-walled carbon nanotubes, and hold great promise for alternative oxide-based nanoelectronics, as well as offer new opportunities to investigate the electronic structure of the complex oxide interfaces. The cryogenic properties of devices constructed from quasi-1D channels, tunnel barriers, and planar gates exhibit gate-tunable superconductivity, quantum oscillations, electron pairing outside of the superconducting regime, and quasi-ballistic transport. This newly demonstrated ability to control the metal-insulator transition at nonpolar oxide interface greatly expands the class of materials whose behavior can be patterned and reconfigured at extreme nanoscale dimensions.

A Single-Atom-Thick TiO2 Nanomesh on an Insulating Oxide.

The electronic structures and macroscopic functionalities of two-dimensional (2D) materials are often controlled according to their size, atomic structures, and associated defects. This controllability is particularly important in ultrathin 2D nanosheets of transition-metal oxides because these materials exhibit extraordinary multifunctionalities that cannot be realized in their bulk constituents. To expand the variety of materials with exotic properties that can be used in 2D transition-metal-oxide nanosheets, it is essential to investigate fabrication processes for 2D materials. However, it remains challenging to fabricate such 2D nanosheets, as they are often forbidden because of the crystal structure and nature of their host oxides. In this study, we demonstrate the synthesis of a single-atom-thick TiO2 2D nanosheet with a periodic array of holes, that is, a TiO2 nanomesh, by depositing a LaAlO3 thin film on a SrTiO3(001)-(√13×√13)-R33.7° reconstructed substrate. In-depth investigations of the detailed structures, local density of states, and Ti valency of the TiO2 nanomesh using scanning tunneling microscopy/spectroscopy, scanning transmission electron microscopy, and density functional theory calculations reveal an unexpected upward migration of the Ti atoms of the substrate surface onto the LaAlO3 surface. These results indicate that the truncated TiO5 octahedra on the surface of perovskite oxides are very stable, leading to semiconducting TiO2 nanomesh formation. This nanomesh material can be potentially used to control the physical and chemical properties of the surfaces of perovskite oxides. Furthermore, this study provides an avenue for building functional atomic-scale oxide 2D structures and reveals the thin-film growth processes of complex oxides.

Two-dimensional electron gas at the Ti-diffused BiFeO3/SrTiO3 interface

Oxide heterostructures with the broken translational symmetry often trigger a two-dimensional quantum confinement and associated unique electronic properties that cannot be observed in bulk constituents. Particular interest is devoted to the formation of two-dimensional electron gas (2DEG) at heterointerfaces between two insulators, which offers a fertile ground for fabricating advanced electronic devices. Here, we combine atomic force microscopy, transmission electron microscopy, and atomistic first-principles calculations to demonstrate that the (100) BiFeO3/SrTiO3 interface takes on a metallic nature and a 2DEG is generated at this interface. Our findings also reveal that the electronic reconstruction due to the polar discontinuity and the variation in valence state of Ti arising from diffusion of Ti cations in SrTiO3 to Fe sites of BiFeO3 are critical to the formation of 2DEG at the heterointerface.

Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides.

Polar oxide interfaces are an important focus of research due to their novel functionality which is not available in the bulk constituents. So far, research has focused mainly on heterointerfaces derived from the perovskite structure. It is important to extend our understanding of electronic reconstruction phenomena to a broader class of materials and structure types. Here we report from high-resolution transmission electron microscopy and quantitative magnetometry a robust – above room temperature (Curie temperature TC ≫ 300 K) – environmentally stable- ferromagnetically coupled interface layer between the antiferromagnetic rocksalt CoO core and a 2–4 nm thick antiferromagnetic spinel Co3O4 surface layer in octahedron-shaped nanocrystals. Density functional theory calculations with an on-site Coulomb repulsion parameter identify the origin of the experimentally observed ferromagnetic phase as a charge transfer process (partial reduction) of Co3+ to Co2+ at the CoO/Co3O4 interface, with Co2+ being in the low spin state, unlike the high spin state of its counterpart in CoO. This finding may serve as a guideline for designing new functional nanomagnets based on oxidation resistant antiferromagnetic transition metal oxides.

A dewetting route to grow heterostructured nanoparticles based on thin film heterojunctions.

Heterostructured nanoparticles have received considerable attention for their various applications due to their unique and tunable functionalities with respect to their individual bulk constituents. However, the current wet chemical synthesis of multicomponent heterostructured nanoparticles is rather complicated. Here, we report a simple and quick method to fabricate Co-Au dumbbell arrays by dewetting Co/Au heterojunctions on a Si substrate and demonstrate that the Co-Au dumbbells vary in size from 2 to 28 nm. We further show by chemical mapping that Co bells are covered by a pseudomorphic Au wetting layer of ∼4 Å, preventing the bells from oxidation. By controlling the thickness of metal heterojunctions and the annealing time, the morphology of the Co-Au nanoparticle is found to be transformed from the dumbbell to the core shell. This facile route is demonstrated to be useful for fabricating other metal-metal and metal-oxide heterostructures and hence holds technological promise for functional applications.

Plant extracts in cell-based anti-inflammatory assays—Pitfalls and considerations related to removal of activity masking bulk components

Plants used in traditional medicine represent an important source of new lead compounds. However, cell-based in vitro screening assays with plant material are hampered by the complex nature of plant extracts as mixtures of active and inactive components. Bulk constituents, such as chlorophyll and polyphenols were previously shown to interfere with several biological in vitro assays. Their influence on anti-inflammatory cell-based testing systems has not been thoroughly investigated. Hence, the present study was aimed at comparing different procedures for the removal of bulk constituents from plant extracts and examining the influence of their elimination on selected cell-based anti-inflammatory assays.Malva sp. and Glechoma hederacea L., two plants used in traditional European medicine for the treatment of inflammatory disorders, were subjected to three different methods for the removal of chlorophyll and polyphenols, respectively. Removal of bulk constituents was confirmed by HPLC and mass spectrometry. Extracts were tested before and after the purification procedure, to determine their potential to inhibit the activation of the transcription factor NF-κB in reporter gene assay and to interfere with the secretion of the chemokine IL-8 after stimulation of endothelial cells with tumor necrosis factor (TNF-α) or lipopolysaccharide (LPS). Removal of chlorophyll from tested extracts led to a strong decrease in the anti-inflammatory activities, due to loss of bioactive constituents. In contrast, the effect of the polyphenol-free extracts was either not changed or significantly increased, depending on the purification method used. The study concluded that clearance of bulk compounds represents a valuable strategy for cell-based in vitro anti-inflammatory evaluation of plant extracts. Liquid–liquid partitioning was identified as the optimal method for the elimination of both chlorophyll and polyphenols. It is recommended that removal of chlorophyll from extracts always be accompanied by HPLC profiling to detect a possible loss of active constituents.

Mechanical and durability properties of concretes containing recycled lime powder and recycled aggregates

According to a recent report by the European Commission, within the European Union, the construction and demolition wastes come to at least 450million tons per year. Roughly 75% of the waste is disposed to landfill, despite its major recycling potential. The bulk constituents of demolition debris are concrete (50–55%) and masonry (30–40%) with only small percentages of other materials such as metals, glass and timber. In Cyprus, at present, recycling of waste materials is practically inexistent and almost the entire demolition waste products are disposed in landfill sites, with all possible economic, technical and environmental impacts. This research paper presents the evaluation and the effective reuse of waste construction materials, such as recycled lime powder (RLP) and recycled concrete aggregates (RCA), disposed to landfill sites in Cyprus, due to the lack of a lucid recycling policy and knowledge. Results show that both RLP and RCA have the potential to produce good quality and robust concrete mixtures both in terms of mechanical and durability performance.

Ethnopharmacological in vitro studies on Austria's folk medicine—An unexplored lore in vitro anti-inflammatory activities of 71 Austrian traditional herbal drugs

Ethnopharmacological relevanceIn Austria, like in most Western countries, knowledge about traditional medicinal plants is becoming scarce. Searching the literature concerning Austria's ethnomedicine reveals its scant scientific exploration.Aiming to substantiate the potential of medicinal plants traditionally used in Austria, 63 plant species or genera with claimed anti-inflammatory properties listed in the VOLKSMED database were assessed for their in vitro anti-inflammatory activity. Material and methods71 herbal drugs from 63 plant species or genera were extracted using solvents of varying polarities and subsequently depleted from the bulk constituents, chlorophylls and tannins to avoid possible interferences with the assays. The obtained 257 extracts were assessed for their in vitro anti-inflammatory activity. The expression of the inflammatory mediators E-selectin and interleukin-8 (IL-8), induced by the inflammatory stimuli tumor necrosis factor alpha (TNF-α) and the bacterial product lipopolysaccharide (LPS) was measured in endothelial cells. The potential of the extracts to activate the nuclear factors PPARα and PPARγ and to inhibit TNF-α-induced activation of the nuclear factor-kappa B (NF-κB) in HEK293 cells was determined by luciferase reporter gene assays. ResultsIn total, extracts from 67 of the 71 assessed herbal drugs revealed anti-inflammatory activity in the applied in vitro test systems. Thereby, 30 could downregulate E-selectin or IL-8 gene expression, 28 were strong activators of PPARα or PPARγ (inducing activation of more than 2-fold at a concentration of 10µg/mL) and 21 evoked a strong inhibition of NF-κB (inhibition of more than 80% at 10µg/mL). ConclusionOur research supports the efficacy of herbal drugs reported in Austrian folk medicine used for ailments associated with inflammatory processes. Hence, an ethnopharmacological screening approach is a useful tool for the discovery of new drug leads.

Atomistic geometry and bonding characteristics at the Sr2FeTaO6/SrTiO3 interface

Oxide heterointerfaces with broken translational symmetry offer a fertile ground for exploring fascinating physical properties that are absent in bulk constituents. Here, we apply advanced transmission electron microscopy to the Sr2FeTaO6/SrTiO3 interface and elucidate that the deposited Sr2FeTaO6 thin film bonds directly to the SrTiO3 substrate in an epitaxial, coherent, and atomically abrupt way. Combined with density-functional-theory calculations, we determine the explicit interface atomistic structure, the exact valence state of transition metals, the covalent interfacial bonding nature, and identify the antiferromagnetic superexchange magnetic coupling path between Fe ions as Fe-O-Ta-O-Fe.

Cross‐Sectional Scanning Tunneling Microscopy Applied to Complex Oxide Interfaces

AbstractUnderstanding interfacial science is critical to many modern technologies. It is very common in solid‐state physics for electronic properties to show novel phenomena when combining various dissimilar materials at atomically abrupt interfaces. For example, semiconductor interfaces have provided the foundation of modern electronic devices for several decades. Now with advances in growth and synthesis, controllable high quality complex oxide heterojunctions can be routinely fabricated. Since complex oxide materials exhibit a wide variety of functionalities owing to their strong coupling to the electron, lattice, orbital and spin degrees of freedom, these materials display a wide spectrum of interesting functionalities. Combining dissimilar complex oxides at interfaces allows one to explore and create intriguing phenomena that are not attainable in the lone bulk constituents. However, the key challenge has been the direct characterization of these interfaces at the nanoscale in order to understand the physical properties found at complex oxide interfaces. This requires the development of new experimental approaches. In this paper, we review the utilization of cross‐sectional scanning tunneling microscopy/spectroscopy as a direct probe of these oxide interfaces at the nanoscale. This technique provides valuable insight to both structural and electronic properties of these unique systems and enables understanding of the detailed electronic structure (e.g., local electronic density of states (LDOS), charge transfer, band bending, etc.) at oxide interfaces, which is of key interest to both fundamental and applied science.