Room-temperature liquid metals, such as eutectic gallium–indium–tin (galinstan), dispersed in a polymer matrix present unique potential as conductors that may have minimal influence on the host polymer mechanical performance while providing enhanced electrical performance. Work described herein systematically evaluates the influence of uncured polydimethylsiloxane (PDMS) viscosity and galinstan loading on final dispersion viscosity and cured modulus. Dispersions of up to 80 vol% galinstan were obtained with relative permittivity values up to 170 that otherwise exhibited similar uncured rheological changes to a solid filler. Cured galinstan-in-PDMS dispersions, however, exhibited a reduced stiffness increase with respect to the host polymer relative to a solid filler. At a critical PDMS viscosity and metal, loading phase inversion to a conductive PDMS-in-metal dispersion was observed. It is anticipated that this work will enable the development of liquid metal polymer composites with independently controlled mechanical and electrical properties for a wide variety of stretchable electronic applications.

Solution-processed metal oxide electronics on flexible substrates can enable applications from military to health care. Due to limited thermal budgets and mismatched coefficients of thermal expansion between oxides and substrates, achieving good performance in solution-processed oxide films remains a challenge. Additionally, the use of traditional photolithographic processes is incompatible with low-cost, high-throughput roll-to-roll processing. Here, we demonstrate solution-deposited oxide thin film transistors (TFTs) on a shape memory polymer substrate, which offers unique control of final device shape and modulus. The key enabling step is the exposure of the precursor film to UV-ozone through a shadow mask to perform patterning and photochemical conversion simultaneously. These TFTs exhibit mobility up to 160 cm2/(V s), subthreshold swing as low as 110 mV/dec, and threshold voltage between −2 and 0 V, while maintaining compatibility with a flexible form factor at processing temperatures below 250 °C.

Seeking a latent-crosslinkable, mechanically flexible, fully thermoplastic shape memory polymer, we have developed a simple but effective macromolecular design that includes pendent crosslinking sites via the chain extender of a polyurethane architecture bearing semicrystalline poly(ε-caprolactone) (PCL) soft segments. This new composition was used to prepare fibrous mats by electrospinning and films by solvent casting, each containing thermal initiators for chemical crosslinking. The one-step synthesis strategy proved successful, and the crosslinking sites within PCL segments resulted in two-way (reversible) shape memory: repeatable elongation (cooling) and contraction (heating) under constant tensile stress. Being fully characterized, the crosslinked fiber mats revealed promising one-way and two-way (reversible) shape memory phenomena, with lower storage moduli though, compared to uncrosslinked films. We observed for both fibrous mats and films that increasing the applied tensile stress led to greater crystallization-induced elongation upon cooling as well as smaller strain hysteresis, particularly for covalently crosslinked samples. Relevant to medical applications, the materials were observed to feature unique, two-stage enzymatic degradation that was sensitive to differences in crystallinity and microstructure among samples.

Metal–resin interpenetrating phase composites (IPCs) have been produced by spontaneously infiltrating unsaturated polyester resin into porous stainless steel fibrous preforms under vacuum conditions. The compressive behaviors of the IPCs were investigated and the fractures were examined. The compressive strength and elastic modulus increase with increasing fiber fraction. The structures, compressive behaviors, and energy absorption capacities of the IPCs exhibit anisotropy. A higher compressive strength, lower elastic modulus, and lower energy absorption efficiency are observed in the through-thickness direction. The energy absorption efficiency slightly decreases with increasing fiber fraction in a certain range rather than monotonically increasing or decreasing. The energy absorption efficiency in the in-plane direction is superior to that in the through-thickness direction. Finer fibers improve the strength and elastic modulus but have little influence on the energy absorption efficiency. Resin collapse, fiber necking, and debonding are the main failure types observed in the composites.

Water-based polyurethane/alumina hollow microsphere (WPU-hAl2O3) composite films were prepared via a facile spin coating method. The pristine WPU, as the matrix of the composite films, was tailor-made by hAl2O3 with the diameter of 2–5 μm to improve the mechanical and physical properties of the films. The hardness, surface morphology, infrared emissivity, wettability, and light transmittance of the WPU-hAl2O3 films with different hAl2O3 contents were investigated. The results indicate that the Vickers hardness, coefficient of friction, infrared emissivity at the wavelength of 2–22 μm, and wetting angle of the WPU-hAl2O3 films (30 wt%) increased by 53.6%, 51.7%, 21.1%, and 19.0%, respectively, compared with the pristine WPU films. Meanwhile, with the rising of hAl2O3 content, the light transmittance decreased by 75.3% at the wavelength of 400–800 nm. This work not only designs a kind of lightweight multifunctional composite film but also provides an effective route for extending further applications of hAl2O3 in the field of composite films.

A thorough investigation of nanoindentation response of fiber/matrix composites by using a Berkovich indenter and its equivalent conical counterpart was carried out. Three-dimensional finite element models were developed to study how fiber orientations and the axial distance between the fiber and nanoindenter affect the nanoindentation response of fiber/matrix composites. This demonstrates that the indenter geometry and its orientation have little effect on the nanoindentation response when the fiber is horizontally aligned to the surface. However, when the fiber is vertically embedded in the matrix, the apparent modulus measured by using the Berkovich indenter (depending on the indenter orientation) can be significantly different from its conical counterpart. The results demonstrate that when the ratio of fiber-to-indenter distance over fiber diameter is relatively small, nanoindentation response strongly depends on fiber orientation and distance between fiber and indenter as well as indenter geometry.

Dynamic-mode cantilever sensors are used in many different applications but especially in materials research to study properties of novel (nano)materials. Decreasing sample sizes require an increase in sensitivity of the analysis tools. For cantilever-based methods that is achieved through a reduction in cantilever dimensions. However, the increase in sensitivity has to be balanced with the detectability as also for a small cantilever a reliable detection of its oscillatory state has to be ensured. A recently introduced co-resonant measurement principle for cantilever sensors addresses this challenge by coupling and eigenfrequency matching of a micro- and a nanocantilever. Here, the sensor concept is reviewed with focus on the application in materials research by the instructive example of an iron-filled carbon nanotube, giving insight into the features and benefits of the sensor concept and demonstrating the reliable derivation of magnetic sample properties.

This review aims to consolidate scarce literature on the use of modern nanomechanical testing technique like instrumented nanoindentation in the field of archaeometry materials research. The review showcase on how can the nanoindentation tests provide valuable data about mechanical properties which, in turn, relate to the evolution of ancient biomaterials as well as human history and production methods. This is particularly useful when the testing is limited by confined volumes and small material samples (since the contact size is in the order of few microns). As an emerging novel application, some special considerations are warranted for characterization of archaeometry materials. In this review, potential research areas relating to how nanoindentation is expected to benefit and help improve existing practices in archaeometry are identified. It is expected that these insights will raise awareness for use of nanoindentation at various world heritage sites as well as various museums.

Mechanical properties of Pr (praseodymium)-doped ZnO thin films, deposited on a corning glass substrate and fused quartz at different deposition pressures using DC sputtering were investigated. Crystalline growth in Pr-doped ZnO thin films is more pronounced and improves at 10 mtorr deposition pressure. However, lower sputtering deposition pressure evoked deposition rates to the formation of polycrystalline films emerged in several crystal planes. Pr ions incorporated in the ZnO host lattice was examined by X-ray photoelectron spectroscopy (XPS), AFM, and FESEM. XPS spectroscopy revealed the presence of Pr3+ and Pr4+ at the ZnO surface layer and it was in tandem with EDS mapping. Nanoindentation prior to scratch testing is used for analyzing deformation characteristics. Pr-doped ZnO thin films exhibit better hardness (9.89 ± 0.14 GPa) and Young’s modulus (112.12 ± 3.45 GPa) on the glass substrate. The crack propagation resistance parameter of the films was evaluated using initial critical load, Lc1 ∼ 2250.5 µN for the crack initiation and upper critical load Lc2 ∼ 2754.5 µN for film failure. Better crack propagation resistance was observed for films deposited at 10 mtorr sputtering pressure on both substrates, attributed to better crystalline nature of the films.

Contamination by bacterial biofilms has a strong negative impact, especially on the surface of prostheses, implants, pins, and other medical-surgical devices. To prevent their formation, one of the alternatives is the modification of the metal surface incorporating silver by low-energy ion implantation, thus avoiding initial bacteria adhesion to the modified surface and further development of the biofilm. The bactericidal properties of silver atoms incorporated on commercially pure titanium surfaces by low-energy ion implantation (4 keV) were evaluated. The surface modifications were analyzed by Rutherford backscattering spectrometry, glow discharge-optical emission spectroscopy, contact angle measure, optical profilometry, and X-ray photoelectron spectroscopy. The microbiological assays were conducted by using Escherichia coli (E. coli). The results demonstrated a reduction on bacterial counting. No toxic effect of silver was detected on human MG-63 cells. The choice of parameters to obtain a bactericidal and nontoxic biomaterial for human cells should consider the ideal combination “energy + silver concentration”. Therefore, it can be considered for industrial application.

Nitinol, being a shape memory and super elastic alloy, is used in medical industry. Surface modification of nitinol helps to reduce the nickel ion leaching in physiological environment. The purpose of this study is to modify the nitinol surface by the silanization technique and to conduct a comparative investigation with the bare nitinol in the aspect of leaching of nickel ion, hemocompatibility, and in vivo animal response. X-ray photoelectron spectroscopy and energy dispersive X-ray spectroscopy studies confirmed the addition of organofunctional alkoxysilane molecules through the silanization process. The histological study showed the presence of adequate number of osteoblasts in silanized nitinol. The fluorochrome labeling study depicted more new bone formation (8 and 21% higher) in silanized nitinol specimens than bare one at one and three months postoperatively. Radiology and SEM study also proved the better performance of silanized samples. The cumulative in vivo results indicate its suitability as the potential bioimplant in various orthopedic surgical uses.

To eliminate the toxic effect of chemotherapy drug of lobaplatin (LBP) on body tissue in liver cancer therapy, this work prepared a nanodrug carrier based on polyethylene glycol-modified carbon nanotubes (PEG–CNTs) and then constructed a targeted drug delivery system (LBP–PEG–CNTs) by loading LBP on PEG–CNTs. Fluorescein isothiocyanate (FITC) was used to label PEG–CNTs to observe the cellular uptake of PEG–CNTs. In addition, the inhibitions of LBP–PEG–CNTs on HepG2 cells were investigated. The results show that the FITC-labeled PEG–CNTs have good cell penetrability; meanwhile, LBP–PEG–CNTs have good stability, pH-controlled release property, and high inhibition rate on HepG2 cells. To be specific, 80% of LBP is released under physiological conditions of liver cancer cells at pH 5.0, and LBP–PEG–CNTs show a high inhibition rate of 77.86% on HepG2 cells, demonstrating that they have targeted, pH-controlled release and inhibition properties on HepG2 cells.

Valvular heart diseases lead to over 300,000 heart valve replacements worldwide each year. Bioprosthetic heart valves (BHVs), derived from glutaraldehyde (GLUT) crosslinked porcine or bovine pericardium, are often used. However, valve failure can occur within 12–15 years due to progressive degradation and/or calcification. Being innovated by previous amino reagent studies used for GLUT detoxification and carbodiimide [1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, EDC] chemistry, in this study, we developed a new fabrication method that utilizes exogenous amino donor arginine or lysine carbodiimide combined treatments to better stabilize the extracellular matrix of porcine pericardium. The carboxyl group density, amine content, differential scanning calorimetry, collagenase and elastase degradation, calcification by rat subdermal implantation, cytotoxicity, and platelet adhesion were characterized. We demonstrated that exogenous amino donor carbodiimide combined treatment for pericardiums had better resistance to elastase degradation (1.63 ± 0.11% and 1.44 ± 0.24% in arginine or lysine versus 3.68 ± 0.16% and 3.04 ± 0.11% in GLUT and GLUT/EDC control) and calcification (0.624 ± 0.193 and 0.637 ± 0.213 Ca µg/mg tissue in arginine or lysine versus 1.610 ± 0.124 and 1.512 ± 0.075 Ca µg/mg tissue in GLUT and GLUT/EDC control). This new strategy combined arginine or lysine and carbodiimide crosslinking would be a promising method to produce more robust BHVs with better structural stability and anticalcification property.

N-(3-Carboxypropyl) triphenylphosphonium bromide chitosan (TPPB-CS) was synthesized and characterized by FTIR, 1H NMR spectrometer, and Zeta potential. TPPB-CS showed a selectivity-toxicity among cancer cell lines (MG-63 and HepG2 cells) and mouse embryonic fibroblast cells (NIH3T3 cells). A significant effect on inhibiting cell migration in HepG2 cells was observed in vitro, and TPPB-CS could effectively inhibit tumor growth in H22-bearing mice in vivo. Furthermore, the distribution of cell cycle, the level of reactive oxygen species (ROS), mitochondrial transmembrane potential (∆ψm), the expression of tumor necrosis factor α (TNF-α), and vascular endothelial growth factor (VEGF) were examined to investigate the antitumor mechanism of TPPB-CS. The results suggested that the antitumor activity of TPPB-CS may be attributed to delay the cell cycle in S phase, alter the ROS and ∆ψm level, as well as regulate the TNF-α and VEGF secretion. TPPB-CS can become a promising anticancer drug for clinical therapy.

Polyurethane/cellulose composites were synthesized from castor-oil-derived polyols and isophorone diisocyanate using dibutyltin dilaurate (DBTDL) as the catalyst. Materials were obtained by adding 2% cellulose in the form of either microcrystals (20 μm) or nanocrystals obtained by acid hydrolysis. The aim was to assess the effects of filler particle size and the use of a catalyst on the physicochemical properties and biological response of these composites. The addition of the catalyst was found to be essential to prevent filler aggregations and to enhance the tensile strength and elongation at break. The cellulose particle size influenced the composite properties, as its nanocrystals heighten hydrogen bond interactions between the filler surface and polyurethane domains, improving resistance to hydrolytic degradation. All hybrids retained cell viability, and the addition of DBTDL did not impair their biocompatibility. The samples were prone to calcification, which suggests that they could find application in the development of bioactive materials.

Three photosensitizers containing zinc(II) porphyrin, ruthenium(II) dipyridine, and their combined porphyrin–polypyridyl metal complexes were used to modify TiO2 nanotubes that were obtained through the hydrothermal method to get inorganic–organic nanocomposite photocatalysts. The photosensitizer with distinctive structure can expand the photoresponse range of TiO2 toward the range of visible light, and the complexes with large conjugated π-electron systems are beneficial for improving the separation of photoelectrons from vacancies, effectively extending the life of excited electrons and thus enhancing the photocatalytic efficiency, thus establishing a favorable foundation for an efficient photocatalysis reaction. The photocatalytic reduction of CO2 aqueous solution into methanol was used to evaluate the photocatalytic effect of sensitized samples. All the photosensitized catalysts exhibited superior selectivity in liquid products during this process and methanol was the only liquid product in the system. The ZnPyP–RuBiPy sensitized TiO2 nanotubes showed the best photocatalytic effect. A possible mechanism for the photoreduction was also proposed in this paper.

Efficiency potential of crystalline Si solar cells is analyzed by considering external radiative efficiency (ERE), voltage, and fill factor losses. Crystalline Si solar cells have an efficiency potential of more than 28.5% by realizing ERE of 20% from about 5% and normalized resistance of less than 0.05 from around 0.1. Nonradiative recombination losses in single-crystalline and multicrystalline Si solar cells are also discussed. Especially, nonrecombination and resistance losses in multicrystalline Si solar cells are shown to be higher than those of single-crystalline cells. Importance of further improvement of minority-carrier lifetime in crystalline Si solar cells is suggested for further improvement of crystalline Si solar cells. High efficiency of more than 28.5% will be realized by realizing high minority-carrier lifetime of more than 30 ms. Key issues for those ends are reduction in carbon concentration of less than 1 × 1014 cm−3, oxygen precipitated and dislocations even in single-crystalline Si solar cells, and reduction in dislocation density of less than 3 × 103 cm−2 in multicrystalline Si solar cells.

Aluminum gallium nitride (AlGaN) metal–semiconductor–metal photodetectors were successfully fabricated with different contact materials and structures and were tested with ultrafast lasers. The experimental results were compared with the finite element simulations based on APSYS and showed consistent trend with respect to the device I–V properties and response behaviors. Persistent photoconductivity (PPC) was observed for devices with both gold and aluminum contacts and various structures, and the decay time can be longer than 10 ms. The response time and responsivity were found to be affected by the bias voltage, operating temperature, and incident power. The mechanism behind the long decay time is analyzed from the perspective of the materials properties and factors influencing the decay time are examined. The nature of the metal–semiconductor contact is studied to help understand the PPC effect, and the contact showed ohmic-like behavior.

Temperature-dependent (173–373 K) hyperpolarized 129Xe nuclear magnetic resonance (129Xe NMR) analyses along with transmission electron microscopy and N2 adsorption measurements have been applied to understand pore structure and interconnectivity of bare and grafted mesoporous silicon sponge (MSS) materials. The Xe NMR chemical shift data indicate the existence of micropores inside the larger mesopore channels and the effects of grafting on the pore surfaces. The grafted layer estimated at 2 nm in thickness blocks the micropores on the surfaces of mesoporous channels. Partitioning of Xe between the micropores and the mesopores in the MSS materials is temperature-dependent, with Xe principally occupying the micropores at lower temperatures. In addition, the temperature-dependent Xe peak shift of MSS materials verifies the increased uniformity and interconnectivity of mesopores after surface grafting. The results from this study provide useful information for design and development of novel materials.