Continuum modeling approaches are well established in materials science and engineering of metals. They enable the quantitative investigation of diverse questions related to the improved understanding of mechanics and microstructure evolution of various material classes. Applicable to time and length scales relevant in manufacturing and service, continuum modeling approaches are widely used to study engineering-related phenomena such as recrystallization, strain localization, fracture initiation, and phase transformations. However, focusing on individual physical aspects hampers the wider routine use of continuum modeling tools for many engineering applications. With the advent of multi-physics modeling tools developed with the help of and parametrized by (sub-)micrometer-scale simulations and experiments, a huge variety of applications such as hot rolling, bake-hardening, and case-hardening comes within reach for full-field integrated computational materials engineering. Moreover, the integration of experimentally characterized microstructures and the use of user friendly simulation and evaluation tools render powerful modeling approaches feasible for a broad materials science user community. The state of the art and future trends of mechanical, thermodynamic, and kinetic continuum modeling of metallic materials at the grain scale are outlined in this prospective article.

Shape memory ceramics show potential for energy damping and actuation applications. In particular, small-scale structures of zirconia-based ceramics demonstrate significantly enhanced shape memory and superelastic properties compared with their bulk counterparts, mainly because an oligocrystalline or single-crystal microscale structure reduces mismatch stresses amongst grains. In this Prospective article, we review recent experiments that explore the shape memory properties of small-scale zirconia-based ceramics, including the effects of composition, sample and grain size, and cyclic loading. These factors are reviewed with an eye toward rendering shape memory ceramics more useful in future applications.

The demand for high-frequency (HF) and low-cost rectifiers has encouraged many researchers to investigate organic rectifiers. Recently, organic rectifiers with enhanced intrinsic carrier mobility and charge injection efficiency have enabled operating frequencies to reach up to a gigahertz (GHz). The metal/organic and organic/organic interfaces have played a significant role in determining the electrical properties of the organic rectifiers. In this prospective article, we review the structure of organic rectifiers and present the current state-of-the-art to attain their HF performance. We discuss methods for improving their electrical properties using interface engineering and present future prospects for practical use of GHz-operable organic rectifiers.

Rechargeable magnesium (Mg) battery has been considered as a promising candidate for future battery generations because of its potential high-energy density, its safety features and low cost. The challenges lying ahead for the realization of Mg battery in general are to develop proper electrolytes fulfilling a multitude of requirements and to discover cathode materials enabling high-energy Mg batteries. The combination of Mg anode with a sulfur cathode is one of the promising electrochemical couples due to its advantages of safety, low costs, and a high theoretical energy density of over 3200 Wh/L. However, the research on magnesium–sulfur (Mg–S) battery is just at its beginning and the development of suitable electrolytes has been the key challenge for further improvement, and, thus, in the focus of recent research. In this review, we highlight the recent progress achieved in Mg electrolytes and Mg–S batteries and discuss the major technical issues, which must be resolved for the improvement of Mg–S batteries.

This work presents the recent progress in the development of the concurrent atomistic-continuum (CAC) method for coarse-grained space- and time-resolved atomistic simulations of phonon transport. Application examples, including heat pulses propagating across grain boundaries and phase interfaces, as well as the interactions between phonons and moving dislocations, are provided to demonstrate the capabilities of CAC. The simulation results provide visual evidence and reveal the underlying physics of a variety of phenomena, including phonon focusing, wave interference, dislocation drag, interfacial Kapitza resistance caused by quasi-ballistic phonon transport, etc. A new method to quantify fluxes in transient transport processes is also introduced.

Significant developments in micro-electrical-mechanical systems-based devices for use in transmission electron microscopy (TEM) sample holders have recently led to the commercialization of windowed gas cells that now enable the atomic-resolution visualization of phenomena occurring during gas–solid interactions at atmospheric pressure. In situ TEM study under atmospheric pressures provides unique information that is beneficial to correlating the structure–properties relationship of nanomaterials, particularly under real gaseous environments. We here provide a brief introduction of the advanced instrumentation of windowed gas cells and review recent progress of in situ atomic-resolution TEM study under atmospheric pressures, including some application examples of oxidation and reduction processes, dynamic growth of nanomaterials, catalytic reactions, and “operando” TEM.

The long-term stability of mechanically exfoliated MoS2 flakes was compared for storage in the air and storage under vacuum. Significant changes in MoS2 flakes were observed for samples stored in the air, whereas similar flakes on samples stored in vacuum underwent no change. Small speckles were observed to appear on the surface of flakes stored in the air, followed by thinning and eventual decomposition of MoS2 flakes. The speckles are suspected to be formed by oxidation of MoS2 in the presence of atmospheric oxygen and water molecules, resulting in the formation of hydrated MoO3.

Four different vanadium oxide phases [α-vanadium pentoxide (V2O5), β-V2O5, bronze-type vanadium dioxide [VO2(B)], and rutile-type VO2 [VO2(R)])] are investigated from first principles as potential electrode materials for potassium (K) ion batteries. Specifically, insertion energetics and diffusion barriers are computed. These phases are known as promising cathode materials for other types of metal ion batteries. Our results show that the metastable β-V2O5 provides the lowest (strongest) insertion energies for K and the lowest diffusion barriers compared with orthorhombic α-V2O5, VO2(B), and VO2(R). While three of these phases show energetically favorable potassiation and relatively small diffusion barriers, VO2(R) is predicted to be incapable of electrochemical K incorporation.

Chemical vapor deposition is the most proficient method for growing graphene on copper foils due to its scalability, repeatability, and uniformity, etc. Herein, we systematically study the effect of oxygen (O2) exposure on graphene growth. We introduced O2 before and during the growth, and then studied its effects on the morphology, crystallinity, and nucleation density of graphene. We observe that introducing O2 during growth significantly improves the graphene crystallinity while pre-dosing O2 before growth reduces the graphene nucleation density. These studies suggest that intermittent O2 exposure play a significant role in graphene growth, enabling scalable production of high-quality graphene.

We investigate how the local glass-transition temperature (T g) depends on film thickness in monolayer and bilayer thin films with a polystyrene (PS) upper-layer and a poly(methyl methacrylate) (PMMA) lower-layer using coarse-grained simulations. Interactions between overlapping interphases demonstrate a superposition principle for describing their glass-transition behaviors. For supported bilayer films, the free surface effect on a PS film upper-layer is effectively eliminated due to an enhanced local T g near the PS–PMMA interface, which cancels out depressed T g near the free surface. However, at very low PMMA lower-layer thicknesses, the PMMA-substrate effect can penetrate through the polymer–polymer interface, leading to enhanced T g in the PS upper-layer.

Graphene nanopores are utilized in various notable applications such as water desalination, molecular separation, and DNA sequencing. However, the creation of stable nanopores is still challenging due to the self-healing nature of graphene. In this study, using molecular dynamics simulations we explore the drilling of nanopores through graphene by bombardment with Si-nanoparticles. This enables the Si-passivation along the nanopore rim, which is known as an efficient way to stabilize graphene nanopores. The interplay between graphene and projectile causes the anomalous behaviors such as local maxima depending on particle size. The observations are thoroughly analyzed with interaction energy and shape changes.

Cobalt oxide thin films with different thicknesses were synthesized by atomic layer deposition. After a thermal reduction process, under a controlled atmosphere of hydrogen, it was possible to convert cobalt oxide to metallic cobalt. The different thicknesses were obtained considering from 500 to 2000 cycles of CoCp2/O3. The thin films were characterized by x-ray diffraction, scanning electron microscopy, energy-dispersive x-ray microanalysis, and by magneto-optical Kerr effect measurements. The indirect synthesis process allows us to obtain cobalt oxide and cobalt thin films with controlled thicknesses and extraordinary magnetic properties, with coercivities above 500 Oe.

Core–shell silicon–silicon oxide nanowires are synthesized at low temperatures using inorganic and organic compounds of a tin as a catalyst. In situ simultaneous one-dimensional growth of pristine silicon nanowires (SiNWs) using alloy catalyst is reported here. Such a development process generates a high-quality SiNW that is not determined by other atomic species in the plasma. A possible growth model is discussed to understand the synchronized precipitation of a SiNW core and an oxide shell. Nanowires grown here eliminate the additional fabrication steps to deposit anticipated oxide shell that is achieved by precipitation from the same catalyst that precipitates core nanowires.

Tin oxide (SnO2) nanoparticles in gram scale quantity were synthesized from inexpensive Sn feedstock by flame oxidation. Selection of optimal feedstock size based on computational fluid dynamics ensures complete conversion of Sn into SnO2 nanoparticles. The rapid melting and oxidation of feedstock in high-temperature oxidative flame endow the crystalline and phase-pure SnO2 nanoparticles, as evident from x-ray diffraction and transmission electron microscopy analysis. Dye-sensitized solar cells fabricated using flame-SnO2 nanoparticles show higher efficiency (ɳ = 2.72%) than that of commercial SnO2 nanoparticles (ɳ = 1.53%). The increased efficiency is attributed to suppression of electron recombination caused by passivation of sub-band-edge surface states.

Carbon-coated silicon nanowires (C-Si NWs) were prepared as anodes for lithium-ion batteries (LIBs). The C-Si NWs were synthesized using a simple and effective fabrication strategy via magnesiothermic reduction. The synthesis sequence of carbon coating before the chemical etching of the reduced Si NWs/MgO composite was found to be critical for improved battery performance. In addition, carbon coating was found to help to stabilize the solid electrolyte interphase layer during battery cycling, which is important to realize the benefits of Si-based LIBs. This synthesis method provides an efficient route to synthesizing high-performance Si electrodes via magnesiothermic reduction.

Two-step, solar-driven thermochemical fuel production offers the potential of efficient conversion of solar energy into dispatchable chemical fuel. Success relies on the availability of materials that readily undergo redox reactions in response to changes in environmental conditions. Those with a low enthalpy of reduction can typically be reduced at moderate temperatures, important for practical operation. However, easy reducibility has often been accompanied by surprisingly poor fuel production kinetics. Using the La1−x Sr x MnO3 series of perovskites as an example, we show that poor fuel production rates are a direct consequence of the diminished enthalpy. Thus, material development efforts will need to balance the countering thermodynamic influences of reduction enthalpy on fuel production capacity and fuel production rate.

We report that a hexagonal closed-packed (HCP) phase with high cobalt content precipitates in Al0.5CoCrFeNi high entropy alloy (HEA) after 650 °C/8 h heat-treatment. The precipitate with the shape of plate is completely located at the interdendritic region. Results of electron diffraction and high resolution transmission electron microscopy show that the HCP phase was transformed from the body-centered cubic phase through a simple shear and the two phase obey an orientation relationship. The thermodynamic stability of Al0.5CoCrFeNi HEA should be carefully reevaluated, especially at the vulnerable temperature.

The magnetic and magnetocaloric properties of Ni45Mn43CoSn11 have been investigated using heat capacity measurements and magnetization with hydrostatic pressure applications. A shift in the martensitic transition temperature by 40 K to higher temperatures was observed with application of pressure P = 1.06 GPa. The magnetic entropy changes significantly increases from 24 to 42 J/kgK at pressure of 0.73 GPa. A large adiabatic temperature change of 4 K was found from specific heat measurements. Also, the density of states and Debye temperature has been estimated from heat capacity measurements. The mixed effects of pressure and magnetic field on the transition temperature are discussed.

First principles simulations and global optimization predict new mode of binding of Pt clusters with defects on graphene that significantly enhances their stability. Pt clusters were found to firmly bind to monovacancies in configuration transacting the vacancy site, while retaining the integrity of the cluster. Diffusion calculations support tight anchoring of Pt cluster to monovacancy. Pt cluster adsorbed on pristine graphene or other common defects exhibit a different mode of adsorption and only decorate one side of graphene. This study reveals strong influence of defect chemistry on the structure and mobility of Pt nanoclusters adsorbed on graphene and have important implications for catalytic and gas sensing applications.

We present an indentation-scope that interfaces with confocal microscopy, enabling direct observation of the three-dimensional (3D) microstructural response of coatings on substrates. Using this method, we compared microns-thick polymer coatings on glass with and without silica nanoparticle filler. Bulk force data confirmed the >30% modulus difference, while microstructural data further revealed slip at the glass-coating interface. Filled coatings slipped more and about two times faster, as reflected in 3D displacement and von Mises strain fields. Overall, these data indicate that silica-doping of coatings can dramatically alter adhesion. Moreover, this method compliments existing theoretical and modeling approaches for studying indentation in layered systems.