Self-assembly of multiferroic oxide composites by chemical and biochemical methodology is discussed. The approach involves covalently attaching organic functional groups or oligomeric DNA/RNA to the nanoparticles (NPs). The organic functional groups are only reactive toward functional groups located on different NPs. Using oligomeric DNA/RNA, one could program NPs to only interact with particles possessing complementary DNA/RNA. We have applied both concepts to the assembly of nanostructures with ferrites for the ferromagnetic phase and barium titanate for the ferroelectric phase. The assembled core–shell particles and superstructures obtained in a magnetic field show evidence for strong interactions between the magnetic and ferroelectric subsystems.

The diverse and fascinating properties of transition metal oxides stem from the strongly correlated electronic degrees of freedom; the scientific challenge and range of possible applications of these materials have caused fascination among physicists and materials scientists, thus capturing research efforts for nearly a century. Here, we focus on the binary V x O y and the ternary perovskite AVO3 and review the key aspects from the underlying physical framework and their basic properties, recent strides made in thin-film synthesis, to recent efforts to implement vanadium-based oxides for practical applications that augment existing technologies, which surpass limitations of conventional materials.

Recent advances in synchrotron based x-ray spectroscopy enable materials scientists to emanate fingerprints on important materials properties, e.g., electronic, optical, structural, and magnetic properties, in real-time and under nearly real-world conditions. This characterization in combination with optimized materials synthesis routes and tailored morphological properties could contribute greatly to the advances in solid-state electronics and renewable energy technologies. In connection to this, such perspective reflects the current materials research in the space of emerging energy technologies, namely photocatalysis, with a focus on transition metal oxides, mainly on the Fe2O3- and TiO2-based materials.

The Magnetoelectric (ME) effect has been observed in single phase hexaferrite bulk and thin films of SrCo2Ti2Fe8O19. In this paper we demonstrate that the ME linear coupling depends strongly on the Co ion concentration relative to the Ti ion concentration exhibiting extremum points at a concentration consistent with above formula. The Alternating Target Laser Ablation Deposition technique was utilized to deposit ME hexaferrite films for the first time. This allows for the deposition of transition metal ions at specific sites in the basic unit cell of the hexaferrite.

This work reports the growth of crystalline SrHf x Ti1−x O3 (SHTO) films on Ge (001) substrates by atomic layer deposition. Samples were prepared with different Hf content x to explore if strain, from tensile (x = 0) to compressive (x = 1), affected film crystallization temperature and how composition affected properties. Amorphous films grew at 225 °C and crystallized into epitaxial layers at annealing temperatures that varied monotonically with composition from ~530 °C (x = 0) to ~660 °C (x = 1). Transmission electron microscopy revealed abrupt interfaces. Electrical measurements revealed 0.1 A/cm2 leakage current at 1 MV/cm for x = 0.55.

Epitaxial heterostructures composed of complex oxides have fascinated researchers for over a decade as they offer multiple degrees of freedom to unveil emergent many-body phenomena often unattainable in bulk. Recently, apart from stabilizing such artificial structures along the conventional [001]-direction, tuning the growth direction along unconventional crystallographic axes has been highlighted as a promising route to realize novel quantum many-body phases. Here we illustrate this rapidly developing field of geometrical lattice engineering with the emphasis on a few prototypical examples of the recent experimental efforts to design complex oxide heterostructures along the (111) orientation for quantum phase discovery and potential applications.

Solid oxide fuel cells (SOFCs) efficiently generate electricity, but high operating temperatures (T op > 800 °C) limit their utility. Reducing T op requires mixed ion–electron conducting (MIEC) cathode materials. Density functional theory is used here to investigate the role of potassium substitutions in the MIEC material Sr1−x K x FeO3 (SKFO). We predict that such substitutions are endothermic. SrFeO3 and SKFO have nearly identical metallic electronic structures. Oxygen vacancy formation energies decrease by ~0.2 eV when x K increases from 0 to 0.0625. SKFO is a promising SOFC MIEC cathode material; however, further experimental investigations must assess its long-term stability at the desired operating temperatures.

Multifunctional, complex oxides capable of exhibiting highly-coupled electrical, mechanical, thermal, and magnetic susceptibilities have been pursued to address a range of salient technological challenges. Today, efforts are focused on addressing the pressing needs of a range of applications and identifying, understanding, and controlling materials with the potential for enhanced or novel responses. In this prospective, we highlight important developments in theoretical and computational techniques, materials synthesis, and characterization techniques. We explore how these new approaches could revolutionize our ability to discover, probe, and engineer these materials and provide a context for new arenas where these materials might make an impact.

Mesocrystal—a new class of crystals compared with conventional single crystals and randomly distributed nanocrystal systems—has captured significant attention in recent decades. Current studies have been focused on the advanced synthesis as well as the intriguing properties of mesocrystal. In order to create new opportunities upon functional mesocrystals, they can be regarded as a new functional entirety when integrated with unique matrix environments. The elegant combination of mesocrystals and matrices has enabled researchers to realize enthralling tunabilities and to derive new functionalities that cannot be found in individual components. Therefore, mesocrystal-embedded system forms a new playground towards multifunctionalities. This review article delivers a general roadmap that portrays the enhancement of intrinsic properties and new functionalities driven by novel mesocrystal-embedded oxide systems. An in-depth understanding and breakthroughs achieved in mesocrystal-embedded oxide systems are highlighted. This article concludes with a brief discussion on potential directions and perspectives along this research field.

We use first-principles calculations based on density functional theory to investigate the interplay between oxygen vacancies, A-site cation size/tolerance factor, epitaxial strain, ferroelectricity, and magnetism in the perovskite manganite series, AMnO3 (A = Ca2+, Sr2+, Ba2+). We find that, as expected, increasing the volume through either chemical pressure or tensile strain generally lowers the formation energy of neutral oxygen vacancies consistent with their established tendency to expand the lattice. Increased volume also favors polar distortions, both because competing rotations of the oxygen octahedra are suppressed and because Coulomb repulsion associated with cation off-centering is reduced. Interestingly, the presence of ferroelectric polarization favors ferromagnetic (FM) over antiferromagnetic (AFM) ordering due to suppressed AFM superexchange as the polar distortion bends the Mn–O–Mn bond angles away from the optimal 180°. Intriguingly, we find that polar distortions compete with the formation of oxygen vacancies, which have a higher formation energy in the polar phases; conversely the presence of oxygen vacancies suppresses the onset of polarization. In contrast, oxygen vacancy formation energies are lower for FM than AFM orderings of the same structure type. Our findings suggest a rich and complex phase diagram, in which defect chemistry, polarization, structure, and magnetism can be modified using chemical potential, stress or pressure, and electric or magnetic fields.

Nanomaterials have been intensively studied over the past decades with many advantages over traditional bulk materials in many applications. Nanomaterials' properties are largely governed by their chemical compositions, sizes, shapes, dimensions, morphologies and structures, which are primarily controlled with the chemical and/or physical fabrication methods and processes. This prospective will highlight recent progress on the modifications of oxide nanomaterials' properties by hydrogenation, namely heat treatment under hydrogen or hydrogen plasma environment, for various applications.

Engineering of a novel heterostructured oxide interface was used to enhance the oxygen surface exchange kinetics of La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF113) thin films. A single-layer decoration of mixed (LaSr)2CoO4±δ (LSC214) and La1−xSrxCoO3−δ (LSC113) and a double-layer decoration of stacked LSC214 and LSC113 grown on the LSCF113 markedly enhanced the surface exchange coefficients of the LSCF113 by up to ~1.5 orders of magnitude relative to the undecorated LSCF113. It is hypothesized that two different types of surface decorations can enable Sr segregation at the interface and surfaces of LSC113 and LSC214, leading to enhancement of the oxygen surface exchange kinetics of decorated LSCF113.

Direct electrical measurement of single grain boundaries is performed for ZnO-based multilayer ceramic varistors with fine grains of 2 µm, using a nano-prober. The effect of ZnO grains on non-linearity is shown to be significant. The microstructure is comprised at least two non-linear types as good- and bad-junctions. The numerical ratio of good to bad is estimated to be about one (non-linearity exponent αmax ≥ 10) to two (<10), which is independent of microstructural development as grain growth. The grain control of twinning as well as crystal orientation and donor concentration is considered effective in the further improvement.

Photocatalytic reduction of carbon dioxide (CO2) into renewable hydrocarbon fuels using solar energy has gained much attention in the effort to conserve energy and enhance carbon cycling. This paper begins with a brief description of the basic concepts of the photocatalytic reduction of CO2, introduces some experimental challenges in the gas photoreaction system and provides a review of perovskite oxide semiconductor catalysts, including tantalates, niobates, titanates, zirconates and cerates, for use in the gas phase photoreduction of CO2. The prospects for the future research of CO2 photoreduction are also presented.

Tin oxide (SnO2) hollow spheres modified with titanium dioxide (TiO2) nanowires (NWs) synthesized by sequential hydrothermal reactions were investigated as photoanodes for dye-sensitized solar cells. Not only does the hydrothermal treatment form numerous short TiO2 NWs on the surface of SnO2 spheres, but also passivates the surface of SnO2. Consequently, the specific surface area of the photoanode and dye loading are almost doubled, at the same time the surface defects and charge recombination are both appreciably reduced. As a result, the short-circuit photocurrent density and open-circuit photovoltage both greatly increased. The power conversion efficiency of the solar cells increases from 0.4% to 2.9%.

Nickel–molybdenum (Ni–Mo) materials are widely used functional oxide catalysts for the hydrogen evolution reaction. In this work, we investigate the high activity of Ni–Mo by depositing size-controlled Ni nanocrystals (NCs) onto Mo substrates. We observe a synergistic increase in catalytic activity that does not scale with the Ni–Mo interface length. This evidence points to a bulk electronic interaction of the two metals that is separate from the mechanism of enhancement seen in conventionally co-deposited Ni–Mo electrocatalysts. In addition to elucidating the catalytic behavior of the Ni–Mo system, this work offers a general NC-based paradigm for investigating fundamental interactions and synergistic effects in electrocatalytic materials.

Nanostructured cerium oxide (CeO2) with outstanding physical and chemical properties has attracted extensive interests over the past few decades in environment and energy-related applications. With controllable synthesis of nanostructured CeO2, much more features were technologically brought out from defect chemistry to structure-derived effects. This review highlights recent progress on the synthesis and characterization of nanostructured ceria-based materials as well as the traditional and new applications. Specifically, several typical applications based on the desired ceria nanostructures are focused to showcase the importance of nanostructure-derived effects. Moreover, some challenges and perspectives on the nanostructured ceria are presented, such as defects controlling and retainment, scale-up fabrication, and monolithic devices. Hopefully, this review can provide an improved understanding of nanostructured CeO2 and offer new opportunities to promote the further research and applications in the future.

Multiferroic nanostructures have been attracting tremendous attention not only for novel phenomena associated with fundamental physics, but also due to exciting application potentials in future nanoelectronic devices. In this mini-review, we first introduce several fabrication techniques recently developed for single phase and composite multiferroic nanostructures. Then, the topologic vortex domain structures in various ferroic nanostructures, which may bring about additional fundamental discoveries and applications in ultrahigh density recording, are discussed. Particular attention is paid to magnetoelectric effects in multiferroic nanodots, including room temperature electric field induced magnetic domain switching. Finally, existing challenges and new directions, e.g., cross-couplings among multiple functionalities, are prospected. We genuinely hope that this mini-review will arouse the readers' interest in this fascinating field.

Silver nanowire-based contacts represent one of the major new directions in transparent contacts for opto-electronic devices with the added advantage that they can have Indium-Tin-Oxide-like properties at substantially reduced processing temperatures and without the use of vacuum-based processing. However, nanowires alone often do not adhere well to the substrate or other film interfaces; even after a relatively high-temperature anneal and unencapsulated nanowires show environmental degradation at high temperature and humidity. Here we report on the development of ZnO/Ag-nanowire composites that have sheet resistance below 10 Ω/sq and >90% transmittance from a solution-based process with process temperatures below 200 °C. These films have significant applications potential in photovoltaics and displays.