Self-assembly, a process in which molecules, polymers, and particles are driven by local interactions to organize into patterns and functional structures, is being exploited in advancing silicon electronics and in emerging, unconventional electronics. Silicon electronics has relied on lithographic patterning of polymer resists at progressively smaller lengths to scale down device dimensions. Yet, this has become increasingly difficult and costly. Assembly of block copolymers and colloidal nanoparticles allows resolution enhancement and the definition of essential shapes to pattern circuits and memory devices. As we look to a future in which electronics are integrated at large numbers and in new forms for the Internet of Things and wearable and implantable technologies, we also explore a broader material set. Semiconductor nanoparticles and biomolecules are prized for their size-, shape-, and composition-dependent properties and for their solution-based assembly and integration into devices that are enabling unconventional manufacturing and new device functions.

The effects of the Mg/Si ratio and aging treatment on the strength and electrical conductivity of Al–Mg–Si 6201 conductor alloys were investigated. Four experimental alloys with different Mg/Si ratios of 2, 1.5, 1, and 0.86 and with a constant Mg level of 0.65 wt% were prepared. It was revealed that excessive Si (a low Mg/Si ratio) increased the peak strength, while the corresponding electrical conductivity decreased. To fulfill the minimum required electrical conductivity (52.5% IACS), the alloys with low Mg/Si ratios required a longer aging time after peak aging to improve electrical conductivity. The alloy with an Mg/Si ratio of ~1 was the best candidate, exhibiting the highest strength up to 54% IACS. On the high end of electrical conductivity (54–56% IACS), the alloy with an Mg/Si ratio of ~1.5 provides a better compromise between strength and electrical conductivity. Furthermore, the strengthening mechanisms and the factors influencing electrical conductivity were discussed for further optimization.

The authors report results of the studies relating to the synthesis of nanodot zirconia that has been utilized for the fabrication of electrochemical biosensing platform for the detection of CYFRA-21-1 biomarker, secreted in saliva samples of oral cancer patients. For the synthesis of nanodot zirconia (ndZrO2), the hydrothermal process was used and further functionalized with 3-aminopropyl triethoxysilane (APTES). Electrophoretic deposition technique was employed for its deposition onto the ITO electrode. The EDC-NHS reaction was used for anti-CYFRA-21-1 immobilization and bovine serum albumin (BSA) was used for blocking of the nonspecific binding sites. The fabricated biosensing platform (BSA/anti-CYFRA-21-1/APTES/ndZrO2/ITO) exhibited a wide linear detection range (0.5–50 ng/mL) with excellent sensitivity (0.53 μA mL/ng cm2).

A new series of ternary perovskite 0.975(0.8Bi1/2Na1/2TiO3–0.2Bi1/2K1/2TiO3)–0.025Bix/3Mgy/3Nbz/3O3 (BNT–BKT–BMN, BMN-xyz) ceramics were designed and synthesized. The effect of the element ratio in the doping component BMN on the strain, ferroelectric, piezoelectric, and dielectric properties of the BNT–BKT matrix were studied. The BMN-430 composition without Nb element exhibits the typical features of non-ergodic relaxor, which is characterized by a higher piezoelectric coefficient d33 and a butterfly-shaped strain curve with negative strain. The introduction of trace Nb can significantly enhance the ergodicity of the system, reflecting in the high positive strain response and strain coefficient $\lpar {d_{33}^\ast \gt 750\;{\rm pm/V}} \rpar$ of BMN-321 composition. In contrast, there is no significant difference in the properties between the presence and absence of Mg element. The temperature-dependent electrical behaviors of BMN-xyz ceramics were analyzed based on impedance spectroscopy. This study may be helpful to the design of the chemical modification strategy for the BNT-based relaxor ferroelectrics.

To reveal the thermal shock resistance of double-layer thermal barrier coatings (TBCs), two types of TBCs were prepared via atmospheric plasma spraying, i.e., Gd2Zr2O7/yttria-stabilized zirconia (GZ/YSZ) TBCs and La2Zr2O7 (LZ)/YSZ TBCs, respectively. Subsequently, thermal cycling tests of the two TBCs were conducted at 1100 °C and their thermal shock resistance and failure mechanism were comparatively investigated through experiments and the finite element method. The results showed that the thermal shock failure of the two TBCs occurred inside the top ceramic coating. However, the GZ/YSZ TBCs had longer thermal cycling life. It was the mechanical properties of the top ceramic coating, and the thermal stresses arising from the thermal mismatch between the top ceramic coating and the substrate that determined the thermal cycling life of the two TBCs together. Compared with the LZ layer in the LZ/YSZ TBCs, the GZ layer in the GZ/YSZ TBCs had smaller elastic modulus, larger fracture toughness, and smaller thermal stresses, which led to the higher crack propagation resistance and less spallation tendency of the GZ/YSZ TBCs. Therefore, the GZ/YSZ TBCs exhibited superior thermal shock resistance to the LZ/YSZ TBCs.

The enhanced reducibility of the surface of ceria relative to the bulk has long been established. Several studies also show that ceria nanoparticles with different facets exhibit different catalytic activities. Despite consensus that the activity is correlated with the surface Ce3+ concentration, experimental measurements of this concentration as a function of termination are lacking. Here, X-ray absorption near-edge spectroscopy (XANES) is used to quantify the Ce3+ concentration in films with (001), (110), and (111) surface terminations under reaction relevant conditions. While an enhanced Ce3+ concentration is found at the surfaces, it is surprisingly insensitive to film orientation.

UV-initiated crosslinking of electrospun poly(ethylene) oxide (PEO)/chitosan (CS) nanofibers doped with zinc oxide nanoparticles (ZnO-NPs) was performed using pentaerythritol triaclyrate (PETA) as the photoinitiator and crosslinker agent. The influence of the addition of PETA to the PEO/CS diameter and crosslinking of nanofibers was evaluated. The effect of irradiation time on the morphology and swelling properties of the crosslinked nanofibers were investigated. For ZnO-NPs, the minimum inhibitory concentrations were found at 1 mg/mL, and the minimum bactericidal concentrations at 2 mg/mL for all the strains tested. The nanofibrous hydrogel antibacterial effect was tested. This material enters the realm of fibrous hydrogels which have potential use in several applications as in the biomedical area.