Search Results (11)

This manuscript describes the synthesis of green long afterglow nanophosphors SrAl₂O₄:Eu²⁺, Nd³⁺ using the combustion process. The study encompassed the photoluminescence behavior, elemental composition, chemical valence, morphology, and phase purity of SrAl₂O₄:Eu²⁺, Nd³⁺ nanoparticles. The results demonstrate that after introducing Eu²⁺ into the matrix lattice, it exhibits an emission band centered at 508 nm when excited by 365 nm ultraviolet light, which is induced by the 4f⁶5d¹→4f⁷ transition of Eu²⁺ ions. The optimal doping concentrations of Eu²⁺ and Nd³⁺ were determined to be 2% and 1%, respectively. Based on X-ray diffraction (XRD) analysis, we have found that the physical phase was not altered by the doping of Eu²⁺ and Nd³⁺. Then, we analyzed and compared the quantum yield, fluorescence lifetime, and afterglow decay time of the samples; the co-doped ion Nd³⁺ itself does not emit light, but it can serve as an electron trap center to collect a portion of the electrons produced by the excitation of Eu²⁺, which gradually returns to the ground state after the excitation stops, generating an afterglow luminescence of about 15 s. The quantum yields of SrAl₂O₄:Eu²⁺ and SrAl₂O₄:Eu²⁺, Nd³⁺ phosphors were 41.59% and 10.10% and the fluorescence lifetimes were 404 ns and 76 ns, respectively. In addition, the E_g value of 4.98 eV was determined based on the diffuse reflectance spectra of the material, which closely matches the calculated bandgap value of SrAl₂O₄. The material can be combined with polyacrylic acid to create optical anti-counterfeiting ink, and the butterfly and ladybug patterns were effectively printed through screen printing; this demonstrates the potential use of phosphor in the realm of anti-counterfeiting printing. Full article

Herein, a series of novel long afterglow nanophosphors BaYAl₃O₇:Eu²⁺, Nd³⁺ was synthesized by the combustion method. The investigation encompassed the characterization of X-ray diffraction, morphology, chemical valence, elemental composition, and photoluminescence behavior of BaYAl₃O₇:Eu²+ and BaYAl₃O₇:Eu²⁺, Nd³⁺ nanoparticles. Under 365 nm excitation, BaYAl₃O₇:Eu²⁺ and BaYAl₃O₇:Eu²⁺, Nd³⁺ show emission bands centered at 497 nm and 492 nm, which are attributed to the 4f⁶5d→4f⁷ transition of Eu²⁺ ions. The optimal samples of BaYAl₃O₇:0.03Eu²⁺ and BaYAl₃O₇:0.03Eu²⁺, 0.02Nd³⁺ have average fluorescence lifetimes of 850 ns and 1149 ns, respectively. The co-doping of Nd³+ ions as the trap centers produced long afterglow luminescence properties, and the afterglow time could reach up to 8 min. Furthermore, the fluorescent powder can be mixed with polyacrylic acid to prepare anti-counterfeiting inks; a clover pattern and snowflake pattern have been successfully printed using screen printing technology, proving its potential application in the field of anti-counterfeiting. Full article

Using a combination of chemical coprecipitation and hydrothermal treatment of the resulting dispersed system, a hierarchically organized NiCo₂O₄ nanopowder was obtained, consisting of slightly elongated initial oxide nanoparticles self-organized into nanosheets about 10 nm thick, which in turn are combined into hierarchical cellular agglomerates of about 2 μm. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HR-TEM) allowed to confirm the formation of NiCo₂O₄ powder with the desired crystal structure via additional heat treatment of the intermediate product. Energy-dispersive X-ray spectroscopy (EDX) was used to confirm the target metal ratio, and the uniform distribution of the elements (Ni, Co and O) was shown by mapping. The resulting nanopowder was employed to prepare functional inks suitable for microplotter printing of the NiCo₂O₄ film. It was found that an oxide film morphology is fully inherited from the hierarchically organized oxide nanopowder used. Atomic force microscopy (AFM) revealed the film thickness (15 μm) and determined the maximum height difference of 500 nm over an area of 25 μm². Kelvin probe force microscopy (KPFM) showed that the surface potential was shifted to the depths of the oxide film, and the work function value of the material surface was 4.54 eV, which is significantly lower compared to those reported in the literature. The electronic state of the elements in the NiCo₂O₄ film under study was analyzed by X-ray photoelectron spectroscopy (XPS). Chemosensor measurements showed that the printed receptor layer exhibited selectivity and high signal reproducibility for ethanol detection. As the relative humidity increases from 0 to 75%, the response value is reduced; however, the sensor response profile and signal-to-noise ratio remain without significant changes. Full article

This paper presents a strategy to convert hydrophilic cellulose nanofibrils (CNF) into a highly cross-linked hydrophobic network with inorganic nanoparticles to develop a gel ink suitable for gel 3D printing. The CNF were chemically modified initially through a single-electron transfer-living radical polymerization (SET-LRP) of stearyl acrylate (SA) in the presence of the surface-modified cobalt iron oxide (CoFe₂O₄, CFO) nanoparticles. The modified CFO nanoparticles provide their multifunctional properties, such as magnetic and electrochemical, to the CNF hybrid network and, at the same time, act as cross-linking agents between the nanocellulose fibrils, while the grafted poly-stearyl acrylate (PSA) introduces a strong hydrophobicity in the network. A suitable gel ink form of this CNF–PSA–CFO material for gel 3D printing was achieved together with a certain solvent. Some test structure prints were directly obtained with the CNF–PSA–CFO gel and were used to evaluate the consolidation of such 3D objects through solvent exchange and freeze-drying while also keeping the magnetic and electrochemical properties of CFO in the CNF-based composite intact. The pristine CNF and CFO particles and the CNF–PSA–CFO were characterized by FTIR, SEM, XPS, TGA, VSM, and CV measurements. Full article

How to fabricate bone tissue engineering scaffolds with excellent antibacterial and bone regeneration ability has attracted increasing attention. Herein, we produced a hierarchical porous β-tricalcium phosphate (β-TCP)/poly(lactic-co-glycolic acid)-polycaprolactone composite bone tissue engineering scaffold containing tetracycline hydrochloride (TCH) through a micro-extrusion-based cryogenic 3D printing of Pickering emulsion inks, in which the hydrophobic silica (h-SiO₂) nanoparticles were used as emulsifiers to stabilize composite Pickering emulsion inks. Hierarchically porous scaffolds with desirable antibacterial properties and bone-forming ability were obtained. Grid scaffolds with a macroscopic pore size of 250.03 ± 75.88 μm and a large number of secondary micropores with a diameter of 24.70 ± 15.56 μm can be fabricated through cryogenic 3D printing, followed by freeze-drying treatment, whereas the grid structure of scaffolds printed or dried at room temperature was discontinuous, and fewer micropores could be observed on the strut surface. Moreover, the impartment of β-TCP in scaffolds changed the shape and density of the micropores but endowed the scaffold with better osteoconductivity. Scaffolds loaded with TCH had excellent antibacterial properties and could effectively promote the adhesion, expansion, proliferation, and osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells afterward. The scaffolds loaded with TCH could realize the strategy to “kill bacteria first, then induce osteogenesis”. Such hierarchically porous scaffolds with abundant micropores, excellent antibacterial property, and improved bone-forming ability display great prospects in treating bone defects with infection. Full article

Direct writing of cobalt/cobalt oxide composites has attracted attention for its potential use in catalysts and detectors in microsensors. In this study, cobalt-based composite patterns were selectively formed on glass, polyethylene naphthalate (PEN), and polyethylene terephthalate (PET) substrates via the femtosecond laser reductive sintering of Co₃O₄ nanoparticles in an ambient atmosphere. A Co₃O₄ nanoparticle ink, including the nanoparticles, ethylene glycol as a reductant, and polyvinylpyrrolidone as a dispersant, was spin-coated onto the substrates. Near-infrared femtosecond laser pulses were then focused and scanned across the ink films to form the patterns. The non-sintered nanoparticles were subsequently removed from the substrate. The resulting sintered patterns were found to be made up of Co/CoO composites on the glass substrates, utilizing various pulse energies and scanning speeds, and the Co/CoO/Co₃O₄ composites were fabricated on both the PEN and PET substrates. These results suggest that the polymer substrates with low thermal resistance react with the ink during the reductive sintering process and oxidize the patterns more easily compared with the patterns on the glass substrates. Such a direct writing technique of cobalt/cobalt oxide composites is useful for the spatially selective printing of catalysts and detectors in functional microsensors. Full article

Single-step inkjet printing infiltration with doped ceria Ce_0.9Ye_0.1O_1.95 (YDC) and cobalt oxide (Co_xO_y) precursor inks was performed in order to modify the properties of the doped ceria interlayer in commercial (50 × 50 × 0.5 mm³ size) anode-supported SOFCs. The penetration of the inks throughout the La_0.8Sr_0.2Co_0.5Fe_0.5O_3−δ porous cathode to the Gd_0.1Ce_0.9O₂ (GDC) interlayer was achieved by optimisation of the inks’ rheology jetting parameters. The low-temperature calcination (750 °C) resulted in densification of the Gd-doped ceria porous interlayer as well as decoration of the cathode scaffold with nanoparticles (~20–50 nm in size). The I–V testing in pure hydrogen showed a maximum power density gain of ~20% at 700 °C and ~97% at 800 °C for the infiltrated cells. The latter effect was largely assigned to the improvement in the interfacial Ohmic resistance due to the densification of the interlayer. The EIS study of the polarisation losses of the reference and infiltrated cells revealed a reduction in the activation polarisations losses at 700 °C due to the nano-decoration of the La_0.8Sr_0.2Co_0.5Fe_0.5O_3−δ scaffold surface. Such was not the case at 800 °C, where the drop in Ohmic losses was dominant. This work demonstrated that single-step inkjet printing infiltration, a non-disruptive, low-cost technique, can produce significant and scalable performance enhancements in commercial anode-supported SOFCs. Full article

Ultrasonic spray-coating (USSC)—a wet chemical deposition method to deposit ultrathin (down to 20 nm) coatings—is being applied as a promising alternative deposition method for functional coatings due to an economical, simple, and precise coating process with easy control over its operating parameters. In this research, zinc oxide nanoparticles (ZnO NPs) were ultrasonically spray-coated on commercial-grade polyethylene terephthalate (PET) and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) films. The most suitable parameters for the ink composition, the ultrasonic spray-coating process, and the number of coating passes (up to 50×) were selected on the basis of a series of experiments. The oxygen gas barrier properties in terms of the oxygen transmission rate (OTR) of neat PET, and 3×, 5×, 10×, and 50× ZnO NP-coated PET and PHBHHx substrates were investigated. The OTR values for neat PET, and 3×, 5×, and 10× ZnO NP-coated PET substrates were found to be the same; however, a 5% reduction in OTR for 50× ZnO NP-coated PET substrate was observed compared to the neat PET substrate. No reduction in OTR was found for any above number of coating passes on PHBHHx substrates against the neat PHBHHx substrate. However, the ultraviolet (UV) tests of 3×, 5×, and 10× ZnO NP-coated PET and PHBHH× substrates revealed a significant decrease in percentage transmission for 10× coated PET and PHBHHx substrates as compared to their 3× and 5× ZnO NP-coated substrates, respectively. It was revealed from the study that the 50× ZnO NP coating of the PET substrate created a slight difference in OTR as compared to the reference substrate. However, the ultrasonic spray-coating method created a significant UV barrier effect for 3×, 5×, and 10× ZnO NP-coated PET and PHBHHx substrates, which demonstrates that the optimized coating method cannot be used to create a high oxygen barrier but can certainly be applied for UV barrier applications in food packaging. It is concluded that ultrasonic spray deposition of ZnO NPs on PET and PHBHHx materials has shown promising results for UV barrier properties, demonstrating the advantages of using this method compared to other coating methods with regard to cost-effectiveness, precise coating, and better process control. Full article

We have applied spark ablation technology for producing nanoparticles from platinum ingots (purity of 99.97 wt. %) as a feed material by using air as a carrier gas. A maximum production rate of about 400 mg/h was achieved with an energy per pulse of 0.5 J and a pulse repetition rate of 250 Hz. The synthesized nanomaterial, composed of an amorphous platinum oxide PtO (83 wt. %) and a crystalline metallic platinum (17 wt. %), was used for formulating functional colloidal ink. Annealing of the deposited ink at 750 °C resulted in the formation of a polycrystalline material comprising 99.7 wt. % of platinum. To demonstrate the possibility of application of the formulated ink in printed electronics, we have patterned conductive lines and microheaters on alumina substrates and 20 μm thick low-temperature co-fired ceramic (LTCC) membranes with the use of aerosol jet printing technology. The power consumption of microheaters fabricated on LTCC membranes was found to be about 140 mW at a temperature of the hot part of 500 °C, thus allowing one to consider these structures as promising micro-hotplates for metal oxide semiconductor (MOS) gas sensors. The catalytic activity of the synthesized nanoparticles was demonstrated by measuring the resistance transients of the non-sintered microheaters upon exposure to 2500 ppm of hydrogen. Full article

Carbon monoxide (CO) gas is an odorless toxic combustion product that rapidly accumulates inside ordinary places, causing serious risks to human health. Hence, the quick detection of CO generation is of great interest. To meet this need, high-performance sensing units have been developed and are commercially available, with the vast majority making use of semiconductor transduction media. In this paper, we demonstrate for the first time a fabrication protocol for arrays of printed flexible CO sensors based on a printable semiconductor catalyst-decorated reduced graphene oxide sensor media. These sensors operate at room temperature with a fast response and are deposited using high-throughput printing and coating methods on thin flexible substrates. With the use of a modified solvothermal aerogel process, reduced graphene oxide (rGO) sheets were decorated with tin dioxide (SnO₂) nanoscale deposits. X-ray diffraction data were used to show the composition of the material, and high-resolution X-ray photoelectron spectroscopy (XPS) characterization showed the bonding status of the sensing material. Moreover, a very uniform distribution of particles was observed in scanning (SEM) and transmission electron microscopy (TEM) images. For the fabrication of the sensors, silver (Ag) interdigitated electrodes were inkjet-printed from nanoparticle inks on plastic substrates with 100 µm linewidths and then coated with the SnO₂-rGO nanocomposite by inkjet or slot-die coating, followed by a thermal treatment to further reduce the rGO. The detection of 50 ppm of CO in nitrogen was demonstrated for the devices with a slot-die coated active layer. A response of 15%, response time of 4.5 s, and recovery time of 12 s were recorded for these printed sensors, which is superior to other previously reported sensors operating at room temperature. Full article

The electrochemical reduction of carbon dioxide in methanol was investigated with Cu and Cu₂O-supported carbon black (Vulcan XC-72) nanoparticle electrodes. Herein, Cu or a Cu₂O-deposited carbon black catalyst has been synthesized by the reduction method for a Cu ion, and the drop-casting method was applied for the fabrication of a modified carbon black electrode. A catalyst ink solution was fabricated by dispersing the catalyst particles, and the catalyst ink was added onto the carbon plate. The pH of suspension was effective for controlling the Cu species for the metallic copper and the Cu₂O species deposited on the carbon black. Without the deposition of Cu, only CO and methyl formate were produced in the electrochemical CO₂ reduction, and the production of hydrocarbons could be scarcely observed. In contrast, hydrocarbons were formed by using Cu or Cu₂O-deposited carbon black electrodes. The maximum Faraday efficiency of hydrocarbons was 40.3% (26.9% of methane and 13.4% of ethylene) at −1.9 V on the Cu₂O-deposited carbon black catalyst. On the contrary, hydrogen evolution could be depressed to 34.7% under the condition. Full article