Suppression of Thermally Induced Surface Traps in Colloidal Quantum Dot Solids via Ultrafast Pulsed Light.

Thermal annealing (TA) of colloidal quantum dot (CQD) films is considered an important process for recent high-performing CQD solar cells (SCs) due to its beneficial effects on CQD solids, including enhanced electrical conductivity, denser packing of CQD films, and the removal of organic residues and solvents. However, the conventional TA for CQDs, which requires several  minutes, leads to hydroxylation and oxidation on the CQD surface, resulting in the formation of trap states and a subsequent decline in SC performance. To address these challenges, this study introduces a flashlight annealing (FLA) technique that significantly reduces the annealing time to the millisecond scale. Through the FLA approach, it successfully suppressed hydroxylation and oxidation, resulting in decreased trap states within the CQD solids while simultaneously preserving their charge transport properties. As a result, CQD SCs treated with FLA exhibited a notable improvement, achieving an open-circuit voltage of 0.66 V compared to 0.63 V in TA-treated devices, leading to an increase in power conversion efficiency from 12.71% to 13.50%.

Uniform Fabrication of Hollow Titania Using Anionic Modified Acrylated Polymer Template for Phase Composition Effect as Photocatalyst and Infrared Reflective Coating.

Polymer coatings containing thermal blocking and near-infrared (NIR)-reflective pigments have received much attention for their potential applications in energy-saving fields. A drawback of these coatings is sustainability providing similar long-term performance. Surface cleaning is mandatory to remove contaminants that decrease reflectance. In this study, synthesized hollow titania as photocatalyst was used to impart anti-contamination to infrared (IR)-reflective coatings. A TiO2 shell was selectively formed on an anionic polystyrene core, modified by methacrylic acid. According to sintering temperature, the enhancement of light absorption ability and photocatalytic activity as methyl orange decomposition was observed with phase composition change. The methylene blue decomposition reaction, reflectance measurement, and measuring thermal profiling of coated steel confirmed the manifestation of hollow particles to dust degradation characteristics and the enhancement of reflection and thermal shielding.

Deep-Sintered Copper Tracks for Thermal Oxidation Resistance Using Large Pulsed Electron Beam.

Thermal oxidation resistance is an important property in printed electronics for sustaining electrical conductivity for long time and/or under harsh environments such as high temperature. This study reports the fabrication of copper nanoparticles (CuNPs)-based conductive tracks using large pulsed electron beam (LPEB) by irradiation on CuNPs to be sintered. With an acceleration voltage of 11 kV, the LPEB irradiation induced deep-sintering of CuNPs so that the sintered CuNPs exhibited bulk-like electrical conductivity. Consequently, the sintered Cu tracks maintained high electrical conductivity at 220 °C without using any thermal oxidation protection additive, such as silver, carbon nanotube, and graphene. In contrast, the films irradiated with an acceleration voltage of 8 kV and irradiated by intense pulsed light (IPL) showed fast oxidation characteristics and a corresponding reduction of electrical conductivities under high temperatures owing to a thin sintered layer. The performance of highly thermal oxidation-resistant Cu films sintered by LPEB irradiations was demonstrated through the device performance of a Joule heater.

Histopathologic response after hydrophilic polyethylene glycol-coating stent and hydrophobic octadecylthiol-coating stent implantations in porcine coronary restenosis model.

Device-related problems of drug-eluting stents, including stent thrombosis related to antiproliferative drugs and polymers, can cause adverse events such as inflammation and neointimal hyperplasia. Stent surface modification, wherein the drug and polymer are not required, may overcome these problems. We developed hydrophilic polyethylene glycol (PEG)-coating and hydrophobic octadecylthiol (ODT)-coating stents without a drug and polymer and evaluated their histopathologic response in a porcine coronary restenosis model. PEG-coating stents (n = 12), bare-metal stents (BMS) (n = 12), and ODT-coating stents (n = 10) were implanted with oversizing in 34 porcine coronary arteries. Four weeks later, the histopathologic response, arterial injury, inflammation, and fibrin scores were analyzed. A p value < 0.05 was considered statistically significant. There were significant differences in the internal elastic lamina area, lumen area, neointimal area, percent area of stenosis, arterial injury score, inflammation score, and fibrin score among the groups. Compared to the BMS or ODT-coating stent group, the PEG-coating stent group had significantly increased internal elastic lamina and lumen area (all p < 0.001) and decreased neointimal area and percent area of stenosis (BMS: p = 0.03 and p < 0.001, respectively; ODT-coating: p = 0.013 and p < 0.001, respectively). Similarly, the PEG-coating group showed significantly lower inflammation and fibrin scores than the BMS or ODT-coating groups (BMS: p = 0.013 and p = 0.007, respectively; ODT-coating: p = 0.014 and p = 0.008, respectively). In conclusion, hydrophilic PEG-coating stent implantation was associated with lower inflammatory response, decreased fibrin deposition, and reduced neointimal hyperplasia than BMS or hydrophobic ODT-coating stent implantation in the porcine coronary restenosis model.

Growth of hierarchical gold clusters for use in superomniphobic electrodes.

We developed a method to fabricate a superomniphobic gold electrode by synthesizing hierarchical gold clusters on a gold substrate and treating the surface with low surface energy materials. The reduction of gold ions was repeated several times, causing the gold microparticles to grow in random directions and form hierarchical gold clusters. Treatment of the gold structures with perfluorothiol resulted in a superhydrophobic surface that also exhibited superoleophobicity for oils and liquids with surface tensions as low as 25.6 mN. The resulting electrode was not contaminated by hydrophilic and hydrophobic liquids, and by analyzing the current-voltage characteristics of the electrode with a PEDOT:PSS solution droplet, the electrode was found to be waterproof.

Hybrid Copper-Silver-Graphene Nanoplatelet Conductive Inks on PDMS for Oxidation Resistance Under Intensive Pulsed Light.

A simple, low-cost, and reliable process of production for conductive tracks and their transfer to poly(dimethylsiloxane) (PDMS) substrate has been proposed. Flexible electrodes were fabricated using conductive nanoparticulates under intensive pulsed light, which were then transferred on to a PDMS substrate via a pouring, curing, and peeling process. The combination of copper-silver nitrate-graphene nanoplatelets (GnPs) provided multiple benefits to the conductive tracks, such as oxidation resistance and increased durability on PDMS. The addition of silver nitrate reduced the speed of oxidation during the curing process of PDMS in the presence of heat and air. The addition of GnPs then increased the stability of conductive tracks on PDMS, whereas the films without GnPs were not conductive on PDMS due to mechanical cracks. The copper-silver-GnP electrodes on PDMS were successfully demonstrated as flexible electrodes and reveal the enhancement of oxidation resistance during thermal oxidation for Joule heater application.

Hybrid Copper-Silver Conductive Tracks for Enhanced Oxidation Resistance under Flash Light Sintering.

We developed a simple method to prepare hybrid copper-silver conductive tracks under flash light sintering. The developed metal nanoparticle-based ink is convenient because its preparation process is free of any tedious washing steps. The inks were composed of commercially available copper nanoparticles which were mixed with formic acid, silver nitrate, and diethylene glycol. The role of formic acid is to remove the native copper oxide layer on the surface of the copper nanoparticles. In this way, it facilitates the formation of a silver outer shell on the surface of the copper nanoparticles through a galvanic replacement. In the presence of formic acid, the copper nanoparticles formed copper formate, which was present in the unsintered tracks. However, under illumination by a xenon flash light, the copper formate was then converted to copper. Moreover, the resistance of the copper-only films increased by 6 orders of magnitude when oxidized at high temperatures (∼220 °C). However, addition of silver nitrate to the inks suppressed the oxidation of the hybrid copper-silver films, and the resistance changes in these inks at high temperatures were greatly reduced. In addition, the hybrid inks proved to be advantageous for use in electrical circuits as they demonstrated a stable electrical conductivity after exposure to ambient air at 180 °C.

Magnetorheological Elastomer Films with Tunable Wetting and Adhesion Properties.

We fabricated magnetorheological elastomer (MRE) films consisting of polydimethylsiloxane and various concentrations of fluorinated carbonyl iron particles. The application of a magnetic field to the MRE film induced changes in the surface morphology due to the alignment of the iron particles along the magnetic field lines. At low concentrations of iron particles and low magnetic field intensities, needle-like microstructures predominated. These structures formed more mountain-like microstructures as the concentration of iron particles or the magnetic field intensity increased. The surface roughness increased the water contact angle from 100° to 160° and decreased the sliding angle from 180° to 10°. The wettability and adhesion properties changed substantially within a few seconds simply upon application of a magnetic field. Cyclical measurements revealed that the transition was completely reversible.

CO2-Selective Nanoporous Metal-Organic Framework Microcantilevers.

Nanoporous anodic aluminum oxide (AAO) microcantilevers are fabricated and MIL-53 (Al) metal-organic framework (MOF) layers are directly synthesized on each cantilever surface by using the aluminum oxide as the metal ion source. Exposure of the MIL53-AAO cantilevers to various concentrations of CO2, N2, CO, and Ar induces changes in their deflections and resonance frequencies. The results of the resonance frequency measurements for the different adsorbed gas molecules are almost identical when the frequency changes are normalized by the molecular weights of the gases. In contrast, the deflection measurements show that only CO2 adsorption induces substantial bending of the MIL53-AAO cantilevers. This selective deflection of the cantilevers is attributed to the strong interactions between CO2 and the hydroxyl groups in MIL-53, which induce structural changes in the MIL-53 layers. Simultaneous measurements of the resonance frequency and the deflection are performed to show that the diffusion of CO2 into the nanoporous MIL-53 layers occurs very rapidly, whereas the binding of CO2 to hydroxyl groups occurs relatively slowly, which indicates that the adsorption of CO2 onto the MIL-53 layers and the desorption of CO2 from the MIL-53 layers are reaction limited.

Facile detection of Troponin I using dendritic platinum nanoparticles and capillary tube indicators.

A facile method was developed for the detection of Troponin I (TnI) using dendritic platinum nanoparticles and capillary tube indicators. Dendritic platinum nanoparticles were functionalized with TnI antibodies, which were used to capture TnI in human serum. The captured TnI was conjugated to the inner surface of a glass vial, to which a hydrogen peroxide (H2O2) solution was added. After the glass vial was sealed with a screw cap containing a silicon septum, a capillary tube containing a drop of ink was inserted through the septum. The catalytic dissociation of H2O2 to water and oxygen increased the pressure inside the glass vial and raised the ink level in the capillary tube. The ink level increased with the platinum nanoparticle concentration, which is proportional to the TnI concentration. The sensitivity of this assay for TnI in human serum after a 5 min dissociation reaction, detected with the naked eye, was 0.1 ng/mL, which was better than the sensitivity of the conventional colorimetric method using the TMB oxidation reaction under the same experimental conditions. A control experiment using alpha-fetoprotein, interleukin-5, and C-reactive protein revealed that the developed method was highly selective for the detection of TnI.

Adsorption and desorption characteristics of alcohol vapors on a nanoporous ZIF-8 film investigated using silicon microcantilevers.

Zinc oxide nanorods were synthesized directly on a silicon microcantilever and converted into a nanoporous ZIF-8 film via a solvothermal reaction. The simultaneous measurements of the resonance frequency and deflection of the cantilever revealed that the adsorption of alcohol vapors induced a structural change in the ZIF-8 framework.

Communication: anti-icing characteristics of superhydrophobic surfaces investigated by quartz crystal microresonators.

We investigated the anti-icing characteristics of superhydrophobic surfaces with various morphologies by using quartz crystal microresonators. Anodic aluminum oxide (AAO) or ZnO nanorods were synthesized directly on gold-coated quartz crystal substrates and their surfaces were rendered hydrophobic via chemical modifications with octyltrichlorosilane (OTS), octadecyltrichlorosilane (ODS), or octadecanethiol (ODT). Four different hydrophobic nanostructures were prepared on the quartz crystals: ODT-modified hydrophobic plain gold (C18-Au), an OTS-modified AAO nanostructure (C8-AAO), an ODS-modified AAO nanostructure (C18-AAO), and ODT-modified ZnO nanorods (C18-ZnO). The water contact angles on the C18-Au, C8-AAO, C18-AAO, and C18-ZnO surfaces were measured to be 91.4°, 147.2°, 156.3°, and 157.8°, respectively. A sessile water droplet was placed on each quartz crystal and its freezing temperature was determined by monitoring the drastic changes in the resonance frequency and Q-factor upon freezing. The freezing temperature of a water droplet was found to decrease with decreases in the water contact radius due to the decreases in the number of active sites available for ice nucleation.

Characterization of underwater stability of superhydrophobic surfaces using quartz crystal microresonators.

We synthesized porous aluminum oxide nanostructures directly on a quartz crystal microresonator and investigated the properties of superhydrophobic surfaces, including the surface wettability, water permeation, and underwater superhydrophobic stability. After increasing the pore diameter to 80 nm (AAO80), a gold film was deposited onto the AAO80 membrane, and the pore entrance size was reduced to 30 nm (AAO30). The surfaces of the AAO80 and AAO30 were made to be hydrophobic through chemical modification by incubation with octadecanethiol (ODT) or octadecyltrichlorosilane (OTS), which produced three different types of superhydrophobic surfaces on quartz microresonators: OTS-modified AAO80 (OTS-AAO80), ODT-modified AAO30 (ODT-AAO30), and ODT-OTS-modified AAO30 (TS-AAO30). The loading of a water droplet onto a microresonator or the immersion of a resonator into water induced changes in the resonance frequency that corresponded to the water permeation into the nanopores. TS-AAO30 exhibited the best performance, with a low degree of water permeation, and a high stability. These features were attributed to the presence of sealed air pockets and the narrow pore entrance diameter.

Quartz resonator for simultaneously measuring changes in the mass and electrical resistance of a polyaniline film.

A novel quartz resonator was developed to measure, simultaneously, changes in the mass and electrical resistance of a polyaniline film during the absorption of water vapor. Interdigitated gold electrodes were vacuum-deposited on the sensing surfaces of the quartz crystals, and polyaniline films were drop-cast on the electrodes used to measure the changes in the electrical resistance. Two symmetric semicircular gold electrodes were deposited on the bottom surface of the quartz crystal. These electrodes were used to measure the changes in the mass of absorbed water based on the changes in the resonance frequency. The simultaneous measurements of mass and electrical resistance shed light on the interactions between the water vapor and the polyaniline film. The resonator was exposed to various organic gases, including ethanol, acetone, or chloroform, and each gas was found to produce characteristic changes in the normalized electrical resistance.

A facile and sensitive detection of pathogenic bacteria using magnetic nanoparticles and optical nanocrystal probes.

We report a facile and sensitive analytical method for the detection of pathogenic bacteria. Salmonella bacteria in milk were captured by antibody-conjugated magnetic nanoparticles (MNPs) and separated from analyte samples by applying an external magnetic field. The MNP-Salmonella complexes were re-dispersed in a buffer solution then exposed to antibody-immobilized TiO(2) nanocrystals (TNs), which absorb UV light. After magnetically separating the MNP-Salmonella-TN complexes from solution, the UV-Vis absorption spectrum of the unbound TN solution was obtained. Because the light absorption intensity was reversely proportional to the Salmonella concentration, the assay exhibited high sensitivity toward low concentrations of Salmonella bacteria. The detection limit of Salmonella in milk was found to be more than 100 cfu mL(-1).

Highly sensitive diagnostic assay for the detection of protein biomarkers using microresonators and multifunctional nanoparticles.

We developed a novel gravimetric immunoassay for sensitive detection of multiple protein biomarkers using silicon microcantilever arrays and multifunctional hybrid nanoparticles. Magnetic-photocatalytic hybrid nanoparticles with a highly crystalline TiO(2) shell were synthesized using a solvothermal reaction without a calcination process. After functionalizing the hybrid nanoparticles and silicon cantilevers with antibodies, the nanoparticles were used to magnetically separate target biomarkers from human serum. Frequency changes of the microcantilevers due to the binding of the nanoparticles were measured using a dip-and-dry method. Frequency changes were further amplified using a photocatalytic silver reduction reaction. Several biomarkers, including interleukin-6, interferon-γ, and alpha-fetoprotein, were selectively detected using arrays of eight silicon microcantilevers. The detection limit of this assay was ∼0.1 pg/mL, which is superior to the clinical threshold of the biomarkers.

A visible light-induced photocatalytic silver enhancement reaction for gravimetric biosensors.

We have developed a novel microgravimetric immunosensor using a WO(3) nanoparticle-modified immunoassay and a silver enhancement reaction. When the nanoparticles in silver ion solution (i.e.  AgNO(3)) are exposed to visible light, the silver ions are photocatalytically reduced and form a metallic silver coating on the nanoparticles. This silver coating consequently induces changes in the mass and light absorption spectrum. Although photocatalytic reduction reactions can be achieved using ultraviolet (UV) light and TiO(2) nanoparticles as described in our previous publication (Seo et al 2010 Nanotechnology 21 505502), the use of UV light in biosensing applications has drawbacks in that UV light can damage proteins. In addition, conventional quartz crystal substrates must be passivated to prevent undesirable silver ion reduction on their gold-coated sensing surfaces. We addressed these problems by adopting a visible light-induced photocatalytic silver enhancement method using WO(3) nanoparticles and lateral field excited (LFE) quartz crystals. As a proof-of-concept demonstration of the technique, streptavidin was adsorbed onto an LFE quartz crystal, and its mass was enhanced with biotinylated WO(3) nanoparticles, this being followed by a photocatalytic silver enhancement reaction. The mass change due to the enhancement was found to be > 30 times greater than the mass change obtained with the streptavidin alone.