From thin film solar cells to metal–oxide–semiconductor (MOS) devices in leading edge integrated circuits, the electronic structure at and near the interfaces between component materials determines the most important fundamental operating characteristics of those devices such as turn-on voltage, power dissipation, and off-state current leakage. Fermi level location at buried interfaces, semiconductor (SC) band bending, charge transfer, oxide defects, and work functions of the constituent materials all contribute to device performance. This paper describes how these important parameters can be determined by employing femtosecond photovoltage spectroscopy, an extension of ultraviolet photoelectron spectroscopy (UPS) using ultrafast lasers. While standard UPS is fundamentally a surface-sensitive spectroscopy, pump/probe techniques add a new dimension to this venerable spectroscopy, permitting the accurate extraction of the underlying band bending in SCs. When combined with the valence band edge location of the SC and oxide, and determination of the system Fermi level, full characterization of the electronic structure of a MOS stack can be obtained providing key insights on device operating properties. This approach can be extended to study key device materials in emerging areas of artificial intelligence and quantum computing. In each case, surprising new details were uncovered that led to performance optimization of these technologically important devices.

A novel ionic liquid/α-ZrP (C16MIM/α-ZrP) lamellar nanocomposite was fabricated via the electrostatic self-assembly deposition technique by using exfoliated α-ZrP nanosheets and guest molecules (1-hexadecyl-3-methylimidazolium bromide) as building blocks under mild conditions. C16MIM/α-ZrP nanocomposite was characterized by various analytical techniques such as X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscope (SEM), Fourier transform infrared spectroscopy, and synchronous thermal analyzer. The net interlayer spacing of α-ZrP determined by XRD confirmed that the C16MIM cations formed a monolayer arrangement between the α-ZrP nanosheets. The morphology and microstructure of C16MIM/α-ZrP composite were observed using SEM and TEM. The C16MIM/α-ZrP modified glass carbon electrode exhibited excellent electrocatalytic activity toward the oxidation of nitrite in weak base media. The results obtained with differential pulse voltammetry demonstrated that the C16MIM/α-ZrP hybrid detected nitrite linearly in the concentration range from 7.3 μM to 1.25 mM with the detection limit of 1.26 μM (S/N = 3). Additionally, the prepared sensor showed outstanding reproducibility, high stability, and anti-interference capability.

Indium tin oxide (ITO) has become a very useful plasmonic and nonlinear optical material because of its highly tunable electrical and optical properties and strong optical nonlinearity. In this work, the authors conducted detailed fabrication process studies by using high-temperature reactive sputtering to finely tune the optical properties of ITO thin films, particularly the epsilon-near-zero (ENZ) wavelength in the near and mid-IR spectrum. Sputtered ITO thin films are characterized by using spectroscopic ellipsometry, surface profilometry, Hall measurements, and 4-point probe testing. Additionally, the effect of post-deposition annealing of ITO films is also investigated.

Metallic thin-film composite membranes are produced by sputtering metal films onto commercial polymer membranes. The separations capability of the membrane substrate is enhanced with the addition of a 10 nm Ta film. The addition of a tantalum layer decreases the molecular weight cutoff of the membrane from 70 kDa dextran (19 nm) to below 5 kDa (6 nm). Water flux drops from 168 LMH/bar (LMH: liters/meters2/hour) (polymer support) to 8.8 LMH/bar (Ta composite). A nanoporous layer is also added to the surface through Mg/Pd film deposition and dealloying. The resulting nanoporous Pd is a promising catalyst with a ligament size of 4.1 ± 0.9 nm. The composite membrane's ability to treat water contaminated with chlorinated organic compounds (COCs) is determined. When pressurized with hydrogen gas, the nanoporous Pd composite removes over 70% of PCB-1, a model COC, with one pass. These nanostructured films can be incorporated onto membrane supports enabling diverse reactions and separations.

Meteorites have one of the most unique and beautiful microstructures, the Widmanstätten structure. This consists of large, elongated bands which form an intricate octahedral lace of crystalline metal. This structure makes meteorites an ideal case to demonstrate the capabilities of mechanical phase mapping using high-speed nanoindentation. In this work, the mechanical properties and composition of the Taza meteorite were mapped using ~100,000 indentations to statistically determine the properties of the individual phases. Five microstructural phases were characterized in this meteorite: Kamacite, Plessite, Tetrataenite, Cloudy Zone, and Schreibersite. Mechanical phase identification was confirmed using EDX measurements, and the first direct, point-to-point correlation of EDX and large-scale indentation maps was achieved. Mechanical phase maps showed superior phase contrast to EDX in two phases. An indentation property map or a mechanical phase map using a 2D histogram was used to visualize and statistically characterize the phases and identify trends in their relationships.

We have synthesized off-stoichiometric Ni40Cu10Mn35Ti15 all-d-metal Heusler alloy with a B2 cubic crystal structure by an arc melting process and investigated its structural, magnetic, electronic, thermal, and mechanical properties under the influence of a single-step thermal annealing. The compound exhibits an antiferromagnetic ordering accompanied by thermal hysteresis indicating a first-order magneto-structural transition. Curie–Weiss molecular field analysis reveals the presence of ferromagnetic interactions competing with long-range antiferromagnetic ordering. Thermal annealing leads to the appearance of a heat capacity sharp peak around antiferromagnetic transition. Electrical resistivity measurements display abrupt changes close to the magneto-structural transition revealing the strong coupling among spin, lattice, and charge degrees of freedom characteristic of a martensitic transition (MT). We have also evaluated its mechanical properties from microhardness measurements, and the results indicate that this alloy exhibits ductile behavior. The occurrence of MT associated with improved ductility is an essential combination for technological application as shape-memory alloys.

The mitigation of CMAS (calcium–magnesium–aluminum–silicon oxide) infiltration is a major requirement for the stability of thermal barrier coatings. In this study, yttria-stabilized zirconia (YSZ)–Al2O3–SiC, YSZ–Al2O3–Ta2O5, and YSZ–Al2O3–Nb2O5 self-healing composites produced by uniaxially pressing powders were investigated as an alternative to YSZ. CMAS infiltration in these materials was tested at 1250 °C for 10 h. Comparing the depth of CMAS infiltration using scanning electron microscope (SEM) in tandem with electron-dispersive X-ray spectroscopy (EDS), all self-healing materials were found to perform better than the reference materials. While standard YSZ shows massive CMAS infiltration, SEM micrographs and EDS maps revealed a 33-fold improvement in CMAS resistance for the YSZ–Al2O3–Nb2O5 system, which exhibited the best performance among the selected self-repairing materials. X-ray diffraction and high-resolution SEM micrographs taken 10 μm below the surface revealed that CMAS only infiltrated pores in the topmost region of the samples. Both YSZ–Al2O3–Ta2O5 and YSZ–Al2O3–Nb2O5 systems showed no signs of chemical reaction with CMAS.

Graphene and its functionalization are still one of the most prominent two-dimensional crystals. In recent years, the wetting properties of graphene for water (i.e., its hydrophobic, hydrophilic, and also icophobic features) were controversially discussed as well as water intercalation and confined water, that have unusual characteristics. The dispute about wetting properties was originally based on contact angle (/engineering) measurements conducted at ambient pressure. In the meanwhile, detailed ultra-high vacuum (UHV) surface science works and theoretical studies are available. This brief review describes the current knowledge available in the literature about the water/graphene system as well as our own work using experimental UHV surface science techniques. The review starts with a definition of hydrophobicity and briefly touches on a possible correlation with icephobicity as well as discusses briefly confined water. Next, theoretical studies are reviewed, and finally, experimental works are described on which the review focusses. Finally, a brief outlook section discusses water adsorption on functionalized graphene.

Thermochemical interactions between calcium–magnesium–aluminosilicate (CMAS) glass and an environmental barrier coating of ytterbium disilicate (Yb2Si2O7) and ytterbium monosilicate (Yb2SiO5) were investigated. Top coats were deposited by plasma spray-physical vapor deposition onto silicon carbide substrates. CMAS powder was prepared as a glass and cast into a tape to yield a CMAS loading of ~29 mg/cm2. Samples were heat treated with CMAS at 1300 °C for 1–10 h or at 1400 °C for 1 h in air. Polished specimen cross-sections were characterized using scanning electron microscopy, X-ray diffraction, X-ray energy-dispersive spectroscopy, and transmission electron microscopy to evaluate resulting microstructures, phases, and compositions at CMAS/Yb2Si2O7 interfaces. Coatings exposed at 1300 °C—10 h and 1400 °C—1 h were fully infiltrated and compromised by CMAS. Dissolution of ytterbium silicate into molten CMAS followed by precipitation of cyclosilicate, silicocarnotite, and Yb2Si2O7 at 1300 °C and Yb2Si2O7 at 1400 °C enabled CMAS to effectively infiltrate top coats, rendering the predominantly Yb2Si2O7 coating ineffective at arresting molten CMAS degradation.

In this study, a hybrid dual drug-loaded hydroxyapatite-oxidized dextran methacrylate core–shell nanocarrier was formulated and explored for combinatorial delivery of doxorubicin (DOX) and methotrexate (MTX) to bone cancer. The synthesized nanocarrier was well characterized by different techniques. In vitro drug release studies in both acidic (pH 5) and alkaline (pH 7.4) conditions showed sequential release of MTX followed by DOX in a sustained manner for 10 days. Biocompatibility and cytotoxicity studies performed using drug-loaded nanoparticles (NPs) on fibroblast L929 cells and osteosarcoma MG63 cells (OMG63) showed that the NPs were highly biocompatible and showed concentration-dependent toxicity. Gene expression studies in OMG-63 cells exhibited the upregulation of caspase-3 and BAX which confirmed the apoptosis induced by dual drug-loaded NPs. The nanocarrier is expected to be a potential bone void filling material, as well as a platform for sequential delivery of DOX and MTX for the treatment of bone cancer.