Oxide membranes are the foundation of several electrochemical devices and sensors, where functionality is related to selective transport of electrons and ions through a membrane or physical responses from an external perturbation. The ability to engineer power sources and sensors for the rapidly growing field of autonomous systems requires high power density and specific energy. Clamped free-standing nanoscale membranes provide an experimentally tunable platform to explore the limits of dimensionality reduction for such purposes. This review addresses the following: (i) advancing experimental methods to fabricate nanoscale oxide membranes that can sustain a chemical potential gradient, thermomechanically stable under large thermal cycles, and can be electrically interrogated with negligible parasitic loss; (ii) a representative example of high performance energy devices, solid oxide fuel cells, utilizing such membranes; and (iii) a brief discussion on emerging research directions broadly in the areas of condensed matter sciences and energy conversion and storage intersecting low-dimensional complex oxide materials.

Great research efforts to investigate the glass-forming ability (GFA) in alloys have been made, leading to an observation that a pinpoint composition produces the best glass-forming characteristics. The reason for this observation is still unknown, limiting the development of bulk metallic glasses (MGs) with a relatively large size. In this work, systematic experimental measurements coupled with calculations were performed to address this issue using the NiNb binary alloy system. It is found that the atomic-level packing efficiency and the clusters-level regularity parameters strongly contribute to their GFA. In particular, the best glass former found in a pinpoint composition possesses the local maximum of the atomic-packing efficiency and the highest degree of the cluster regularity. This work provides an understanding of GFA from atomic and cluster levels and will shed light on the development of more MGs with relatively large critical casting sizes.

Indentation tests are used to determine the hardness of a material, e.g., Rockwell, Vickers, or Knoop. The indentation process is empirically observed in the laboratory during these tests; the mechanics of indentation is insufficiently understood. We have performed first molecular dynamics computer simulations of indentation resistance of polymers with a chain structure similar to that of high density polyethylene (HDPE). A coarse grain model of HDPE is used to simulate how the interconnected segments respond to an external force imposed by an indenter. Results include the time-dependent measurement of penetration depth, recovery depth, and recovery percentage, with respect to indenter force, indenter size, and indentation time parameters. The simulations provide results that are inaccessible experimentally, including continuous evolution of the pertinent tribological parameters during the entire indentation process.

Interfacial reactions at 100 and 150 °C in the Sn–20.48 at.% In–3.05 at.% Ag (Sn–20.0 wt% In–2.8 wt% Ag)/Ni couples are studied. Three unusual phenomena are observed. First, liquation is found in Sn–20.48 at.% In–3.05 at.% Ag (Sn–In–Ag)/Ni couples that are reacted at 150 °C, which is lower than the melting points of both the solder and the Ni substrate. In addition to the Ni3Sn4 phase, liquid phase is formed in the reaction layer. Second, the liquid phase disappears and isothermal solidification occurs when there is prolonged isothermal heat treatment at 150 °C. The results are similar to those for transient liquid phase bonding. Third, the thickness of the reaction layer in Sn–In–Ag/Ni couples that are reacted for 1440 h at 150 °C is 40 times thicker than that of those reacted at 100 °C. The reaction mechanisms for these three unusual phenomena: liquation, isothermal solidification, and an extraordinary increase in the reaction rate for only 50 °C difference in temperature are elaborated and are related to each other.

A novel combination of low-field magnetic alignment (MA) and templated grain growth (TGG) was used to fabricate highly textured diamagnetic 0.72Pb(Mg1/3Nb2/3)O3–0.28PbTiO3 (0.72PMN–0.28PT) ceramics. Samples were produced by nonaqueous slip casting of PMN–PT slurries, in which diamagnetic plate-like 0.4(Na1/2Bi1/2)TiO3–0.6PbTiO3 (0.4NBT–0.6PT) template particles were aligned by dynamic MA in a 2.2-T permanent magnet array. Template alignment improved as slurry viscosity increased, with a 32-vol% solid loading (a viscosity of ∼0.1 Pa s at 0.1 s−1) giving optimal texture quality (7.85° FWHM, f = 92 vol%) after sintering and TGG. Alignment was stable for more than 3 h during slip casting, allowing fabrication of ∼1-cm thick textured ceramics with high piezoelectric response (d33 = 1222 pC/N). The success of dynamic MA at low magnetic field (2.2 T) is attributed to an increase in driving force for alignment of large (5–10 μm) template particles relative to the randomizing effect of Brownian motion (i.e., thermal energy kBT).

The fabrication methods and the basic properties of the metal-oxide nanostructures referred as nanowires are presented and reviewed in this paper, with particular emphasis to the electrical and optical properties and their useful implementation for chemical and biochemical sensing. The field of chemical sensors has benefited by the wealth of highly crystalline nanostructures produced by physical and chemical methods. Large variation in bulk electrical conductivity, structural stability upon high temperature operation, high degree of crystalline ordering, large impact of point defects and surface states have unveiled the potential for the sensing field and have opened up new perspectives of application and for the realization of novel device architectures. This paper will summarize various techniques for preparation and characterization; then, the growth mechanisms and working principles will be discussed. Finally, the challenges that this field is currently facing are presented to signify the perspectives of expansion.