Aluminum–silicon alloys are an important class of commercial casting materials having wide applications in automotive and aerospace industries. Etching the Al–Si eutectic leads to selective dissolution of Al, resulting in novel morphology – macroporous Si spheres with a three-dimensional nano network. Up to 5% Al is dissolved in Si, leading to an expansion of the crystal lattice. The resulting porous Si is electrochemically active with lithium and thus can be used as a high capacity anode for lithium-ion batteries. The etching of Al–Si provides a simple and low-cost method of producing nano-structured Si materials.

We develop a simple model to compute the energy-dependent decay factors of metal-induced gap states in metal/insulator interfaces considering the collective behavior of all the bulk complex bands in the gap of the insulator. The agreement between the penetration length obtained from the model (considering only bulk properties) and full first-principles simulations of the interface (including explicitly the interfaces) is good. The influence of the electrodes and the polarization of the insulator are analyzed. The method simplifies the process of screening materials to be used in Schootky barriers or in the design of giant tunneling electroresistance and magnetoresistance devices.

Colloidal quantum dot photovoltaic devices have improved from initial, sub-1% solar power conversion efficiency to current record performance of over 7%. Rapid advances in materials processing and device physics have driven this impressive performance progress. The highest-efficiency approaches rely on a fabrication process that starts with nanocrystals in solution, initially capped with long organic molecules. This solution is deposited and the resultant film is treated using a solution containing a second, shorter capping ligand, leading to a cross-linked, non-redispersible, and dense layer. This procedure is repeated, leading to the widely employed layer-by-layer solid-state ligand exchange. We will review the properties and features of this process, and will also discuss innovative pathways to creating even higher-performing films and photovoltaic devices.

Offering a unique suite of mechanical, physical, and chemical properties, bulk metallic glasses (BMGs) show significant promise as engineering materials. Unfortunately, most BMGs exhibit low tensile ductility at ambient temperature that limits their use as structural (load-bearing) materials. To overcome this problem, BMG composites (BMGCs) containing a second phase are being developed for improving ductility by controlling the mechanics of shear band nucleation and growth in the glassy matrix, which is the primary mode of failure in these materials. This review describes some recent developments in BMGCs and discusses the influence of the type of second phase on mechanical behavior.

We demonstrate that alternating the oxygen partial pressure gradient across a yttria-stabilized zirconia (YSZ) electrolyte membrane prior to solid oxide fuel cell (SOFC) testing with nanoporous Pt electrodes greatly increases (e.g. by >70-fold at 350 °C) peak power density compared with devices without pretreatment. Transiently altering the oxygen activity at the cathode–YSZ interface appears to change the wetting characteristics of the nanoporous Pt, significantly affecting the stability and low-temperature performance of the SOFCs. Image analysis and impedance spectroscopy results suggest that an increase in triple-phase boundary area fraction at the cathode–YSZ interface contributes to the observed effect.

We have prepared stable ultrafine narrow dispersed copper nanoparticles (Cu-NPs) using a facile chemical reduction technique below room temperature (300 K), without any template. X-ray diffraction and high-resolution transmission electron microscopy studies reveal the growth of highly crystalline Cu-NPs with an average diameter of 2.2 nm. Interestingly, these Cu-NPs demonstrate both interband electronic transitions along with usual surface plasmon resonance, a unique phenomenon previously unobserved in any noble metal nanoparticles. These Cu-NPs do not get oxidized easily and could be suitable candidates for different optical devices, heat transfer liquids, and biological applications.

We report a facile way to fabricate three-dimensional (3D) Ni–TiO2 core–shell nanowire arrays through anodic aluminum oxide template-assisted sol–gel TiO2 nanotube shell growth followed by Ni core using room temperature constant current electrodeposition. The 3D Ni–TiO2 nanowire-based dye-sensitized solar cell (DSSC) endows a 67% increase in conversion efficiency as compared with the TiO2 nanotube DSSC and maximum conversion efficiency of 5.07% was obtained by surface treating the photoanode with TiCl4, which provides enhanced light scattering and surface passivation. Indeed, this work paves the way to build reliable 3D Ni–TiO2 nanostructured photoanodes for highly efficient DSSCs.

Over the past three decades, the combination of inorganic-nanoparticles and organic-polymers has led to a wide variety of advanced materials, including polymer nanocomposites (PNCs). Recently, synthetic innovations for attaching polymers to nanoparticles to create “hairy nanoparticles” (HNPs) has expanded opportunities in this field. In addition to nanoparticle compatibilization for traditional particle–matrix blending, neat-HNPs afford one-component hybrids, both in composition and properties, which avoids issues of mixing that plague traditional PNCs. Continuous improvements in purity, scalability, and theoretical foundations of structure–performance relationships are critical to achieving design control of neat-HNPs necessary for future applications, ranging from optical, energy, and sensor devices to lubricants, green-bodies, and structures.

We study the temperature dependence of thermoelectric transport properties of four FeSb2 nanocomposite samples with different grain sizes. The comparison of the single crystals and nanocomposites of varying grain sizes indicates the presence of substantial phonon drag effects in this system contributing to a large Seebeck coefficient at low temperature. As the grain size decreases, the increased phonon scattering at the grain boundaries leads to a suppression of the phonon-drag effect, resulting in a much smaller peak value of the Seebeck coefficient in the nanostructured bulk materials. As a consequence, the ZT values are not improved significantly even though the thermal conductivity is drastically reduced.

Tetrahedrite-structure compounds, of general composition Cu12−xZnxSb4S13, are an earth-abundant alternative to PbTe for thermoelectric power generation applications in the intermediate high-temperature range (300–400°C). Tetrahedrites can be synthesized in the laboratory using a multi-step process involving long annealing times. However, this compound also exists in natural mineral form, and, in fact, is one of the most abundant copper-bearing minerals in the world. We show here that by simply mixing natural mineral tetrahedrite with pure elements through high-energy ball milling without any further heat treatment, we can successfully obtain material with figure of merit near unity at 723 K.

Two thiophene-based semiconductors, a vapor-deposited small molecule and an amorphous polymer, as well as pentacene for comparison, show potential in enhancing the thermoelectric properties of tellurium (Te) nanowires. For vapor-deposited films, Te nanostructures form directly on glass substrates or organic semiconductor films. The resulting Te power factor (S2σ) was enhanced from 36 to 45 W/mK2 (56 for pentacene) because the bilayer provides an enhancement in Seebeck (S) without compromising conductivity (σ). For solution deposited polymer blends, we obtained power factors from a Te nanowire network that alone would not have sufficient connectivity (up to 0.1 µW/mK2). While the organics are unoptimized, they are prototypical materials for further development.

Textured nickel ferrite (NFO, NiFe2O4) thin films were deposited at room temperature by chemical solution deposition onto c-plane sapphire substrates. A nanoimprint lithography technique using a polydimethylsiloxane stamp was used to transfer a pattern from a master to the thin film, which was subsequently annealed to crystallize the NFO. Atomic force microscopy scans showed good periodicity and feature profile over a large area which was confirmed with cross-sectional transmission electron microscopy. X-ray diffraction revealed textured single-phase inverse spinel NFO. Magnetic measurements of patterned thin films showed a large reduction in coercivity due to demagnetization factors.

Using an effective Hamiltonian of mutiferroic BiFeO3 (BFO) as a toy model, we explore the effect of the coefficient, C, characterizing the strength of the spin–current interaction, on physical properties. We observe that for larger C values and below a critical temperature, the magnetic moments organize themselves in a novel cycloid, which propagates along a low-symmetry direction and is associated with a structural phase transition from polar rhombohedral to a polar triclinic state. We emphasize that both of these magnetic and structural transitions are results of a remarkable self-organization of different solutions of the spin–current model.

We present a quantitative in-situ transmission electron microscope (TEM) study of stress-assisted grain growth in 75 nm thick platinum thin films. We utilized notch-induced stress concentration to observe the microstructural evolution in real time. From quantitative measurements, we find that rapid grain growth occurred above 290 MPa of far field stress and ~0.14% elongation. This value is found to be higher than that required for stable interface motion but lower than the stress required for unstable grain boundary motion. We attribute such grain growth to geometrical incompatibility arising out of crystallographic misorientation in adjoining grains, or in other words, geometrically necessary grain growth.

Two new organic dyes, WS-2.1 and WS-2.2—derivatives of the known dye WS-2—are computationally designed using a recently developed approach with a broad absorption peak at around 775 nm in acetonitrile for WS-2.2 versus 610 nm for WS-2. The red shift includes a significant contribution due to vibrations and is not reproduced by standard computational methods. The oxidation and reduction potentials of the dye render it well suited for use in dye-sensitized solar cells.

We report the synthesis of a direct gap semiconductor, ZnSnN2, by a plasma-assisted vapor–liquid–solid technique. Powder X-ray diffraction measurements of polycrystalline material yielded lattice parameters in good agreement with predicted values. Photoluminescence efficiency at room temperature was observed to be independent of excitation intensity between 103 and 108 W/cm2. The band gap was measured by photoluminescence excitation spectroscopy to be 1.7 ± 0.1 eV. The range of direct band gaps for the Zn(Si,Ge,Sn)N2 alloys is now predicted to extend from 4.5 to 1.7 eV, opening up this little-studied family of materials to a host of important applications.

The S-doped BiOBr composite microspheres were successfully prepared through one-pot solvothermal method. The as-prepared samples exhibit higher photocatalytic activity for the degradation of Rhodamine B and phenol under visible light irradiation, attributed to the improvement of the photo-absorption property and the narrow band gap due to the dopants of S element. The higher efficiency for photodegradation of organic pollutant endows this material with a bright perspective in purification of waste water under visible-light irradiation.

THz-range dielectric spectroscopy and first-principle-based effective-Hamiltonian molecular dynamics simulations were used to elucidate the dielectric response in the paraelectric phase of (Ba, Sr)TiO3 solid solutions. Our analysis suggests a crossover between two regimes: a higher-temperature regime governed by the soft mode only versus a lower-temperature regime exhibiting a coupled soft mode/central mode dynamics. Interestingly, a single model can be used to adjust the THz dielectric response in the entire range of the paraelectric phase. The central peak cannot be discerned anymore in the dielectric spectra when the rate of underlying thermally activated processes exceeds certain characteristic frequency of the system.

Electrical fields can be used to heat selectively dislocations and grain boundaries to a much higher temperature compared with the bulk. This selective joule heating, if uncontrolled by limiting the current flow, can lead to melting of grain boundaries and sintering of poly- and nanocrystalline materials close to the theoretical density in a much shorter time due to fast diffusivities of the order of 10−4 to 10−5 cm2/s in the liquid. I refer to this sintering mode as selective-melt sintering, which can occur at lower overall temperatures with much lower energy consumption compared with conventional sintering involving solid-state diffusion.

We present the study of the synthesis of (001) nickel oxide (NiO) epitaxial nanocrystals grown on (001) strontium titanate (SrTiO3) single crystal substrates. Pulsed laser deposition of the bismuth nickel oxide (BiNiO3, BNO) perovskite precursor followed by post-deposition processing is carried out to form the NiO nanocrystals. A detailed analysis of the dimensions of nanocrystals reveals that the morphology attained differs from the thermodynamically expected equilibrium shape. The deviations from the equilibrium shape are found to follow a systematic trend where the in-plane basal dimensions, that is, the length and width of the nanocrystals grown differ in discretized dimensions. This discretization suggests that for a given interfacial area of nanocrystals there are multiple stable basal rectangular geometries attainable.