Synthesis of high quality 2D carbide MXene flakes using a highly purified MAX precursor for ink applications.

The practical application of 2D MXenes in electronic and energy fields has been hindered by the severe variation in the quality of MXene products depending on the parent MAX phases, manufacturing techniques, and preparation parameters. In particular, their synthesis has been impeded by the lack of studies reporting the synthesis of high-quality parent MAX phases. In addition, controllable and uniform deposition of 2D MXenes on various large-scale substrates is urgently required to use them practically. Herein, a method of pelletizing raw materials could synthesize a stoichiometric Ti3AlC2 MAX phase with high yield and processability, and fewer impurities. The Ti3AlC2 could be exfoliated into 1-2-atom-thick 2D Ti3C2T x flakes, and their applicability was confirmed by the deposition and additional alignment of the 2D flakes with tunable thickness and electrical properties. Moreover, a practical MXene ink was fabricated with rheological characterization. MXene ink exhibited much better thickness uniformity while retaining excellent electrical performances (e.g., sheet resistance, electromagnetic interference shielding ability) as those of a film produced by vacuum filtration. The direct functional integration of MXenes on various substrates is expected to initiate new and unexpected MXene-based applications.

A chemically bonded supercapacitor using a highly stretchable and adhesive gel polymer electrolyte based on an ionic liquid and epoxy-triblock diamine network.

Despite significant advances in the development of flexible gel polymer electrolytes (GPEs), there are still problems to be addressed to apply them to flexible electric double layer capacitors (EDLCs), including interfacial interactions between the electrolyte and electrode under deformation. Previously reported EDLCs using GPEs have laminated structures with weak interfacial interactions between the electrode and electrolyte, leading to fragility upon elongation and low power density due to lower utilization of the surface area of the carbon material in the electrode. To overcome these problems, we present a new strategy for constructing an epoxy-based GPE that can provide strong adhesion between electrode and electrolyte. The GPE is synthesized by polymerization of epoxy and an ionic liquid. This GPE shows high flexibility up to 509% and excellent adhesive properties that enable strong chemical bonding between the electrode and electrolyte. Moreover, the GPE is stable at high voltage and high temperature with high ionic conductivity of ∼10-3 S cm-1. EDLCs based on the developed GPE exhibit good compatibility between the electrode and electrolyte and work properly when deformed. The EDLCs also show a high specific capacitance of 99 F g-1, energy density of 113 W h kg-1, and power density of 4.5 kW g-1. The excellent performance of the GPE gives it tremendous potential for use in next generation electronic devices such as wearable devices.

Controlled Grafting of Colloidal Nanoparticles on Graphene through Tailored Electrostatic Interaction.

Nanoparticle/graphene hybrid composites have been of great interest in various disciplines due to their unique synergistic physicochemical properties. In this study, we report a facile and generalized synthesis method for preparing nanoparticle/exfoliated graphene (EG) composites by tailored electrostatic interactions. EG was synthesized by an electrochemical method, which produced selectively oxidized graphene sheets at the edges and grain boundaries. These EG sheets were further conjugated with polyethyleneimine to provide positive charges at the edges. The primary organic ligands of the colloidal nanoparticles were exchanged with Cl- or MoS42- anions, generating negatively charged colloidal nanoparticles in polar solvents. By simple electrostatic interactions between the EG and nanoparticles in a solution, nanoparticles were controllably assembled at the edges of the EG. Furthermore, the generality of this process was verified for a wide range of nanoparticles, such as semiconductors, metals, and magnets, on the EG. As a model application, designed composites with size-controlled FeCo nanoparticle/EG were utilized as electromagnetic interference countermeasure materials that showed a size-dependent shift of the frequency ranges on the electromagnetic absorption properties. The current generalized process will offer great potential for the large-scale production of well-designed graphene nanocomposites for electronic and energy applications.

Enhancement of Magnetoelectric Conversion Achieved by Optimization of Interfacial Adhesion Layer in Laminate Composites.

We report the effect of epoxy adhesion layers with different mechanical or physical property on a magnetoelectric (ME) composite laminate composed of FeBSi alloy (Metglas)/single-crystal Pb(Mg1/3Nb2/3)O3-Pb(Zr,Ti)O3/Metglas to achieve an improved ME conversion performance. Through theoretical simulation, it was revealed that the Young's modulus and the thickness of interfacial adhesives were major parameters that influence the conversion efficiency in ME composites. In the experimental evaluation, we utilized three epoxy materials with a distinct Young's modulus and adjusted the average thickness of the adhesion layers to optimize the ME conversion. The experimental results show that a thin epoxy layer with a high Young's modulus provided the best performance in the inorganic-based ME conversion process. By tailoring the interfacial adhesion property, the ME laminate generated a high conversion coefficient of 328.8 V/(cm Oe), with a mechanical quality factor of 132.0 at the resonance mode. Moreover, we demonstrated a highly sensitive alternating current magnetic field sensor that had a detection resolution below 10 pT. The optimization of the epoxy layers in the ME laminate composite provided significant enhancement of the ME response in a simple manner.

Multifunctional Epoxy-Based Solid Polymer Electrolytes for Solid-State Supercapacitors.

Solid polymer electrolytes (SPEs) have drawn attention for promising multifunctional electrolytes requiring very good mechanical properties and ionic conductivity. To develop a safe SPE for energy storage applications, mechanically robust cross-linked epoxy matrix is combined with fast ion-diffusing ionic liquid/lithium salt electrolyte (ILE) via a simple one-pot curing process. The epoxy-rich SPEs show higher Young's modulus ( E), with higher glass transition temperature ( Tg) but lower ionic conductivity (σdc) with a higher activation energy, compared to the ILE-rich SPEs. The incorporation of inorganic robust Al2O3 nanowire simultaneously provides excellent mechanical robustness ( E ≈ 1 GPa at 25 °C) and good conductivity (σdc ≈ 2.9 × 10-4 S/cm at 25 °C) to the SPE. This suggests that the SPE has a bicontinuous microphase separation into ILE-rich and epoxy-rich microdomain, where ILE continuous conducting phases are intertwined with a sturdy cross-linked amorphous epoxy framework, supported by the observation of the two Tgs and low tortuosity as well as the microstructural investigation. After assembling the SPE with activated carbon electrodes, we successfully demonstrate the supercapacitor performance, exhibiting high energy and power density (75 W h/kg at 382 W/kg and 9.3 kW/kg at 44 W h/kg). This facile strategy holds tremendous potential to advance multifunctional energy storage technology for next-generation electric vehicles.

Retinol, α-tocopherol, and selected minerals in breast milk of lactating women with full-term infants in South Korea.

BACKGROUND/OBJECTIVES: This study was performed to measure fat-soluble vitamins and minerals in breast milk of Korean lactating mothers who exclusively breastfed their babies. SUBJECTS/METHODS: Breast milk samples were collected from 334 mothers. Concentrations of retinol and α-tocopherol were analyzed by high performance liquid chromatography ultraviolet spectrometry while concentrations of minerals were measured by inductively coupled plasma optical emission spectrometry. RESULTS: Retinol and α-tocopherol contents of breast milk were 39.58 ± 19.64 µg/dL and 0.23 ± 0.13 mg/dL, respectively. Average sodium, potassium, calcium, phosphorus, and magnesium levels in breast milk were 11.11 ± 5.16, 38.56 ± 9.01, 27.87 ± 6.10, 13.56 ± 3.30, and 3.05 ± 0.65 mg/dL, respectively. Contents of trace elements such as iron, zinc, copper, and manganese were 40.26 ± 46.21, 98.40 ± 62.47, 24.09 ± 9.03, and 0.90 ± 1.63 µg/dL, respectively. Fat-soluble vitamin concentration was positively correlated with total fat in milk samples, but no significant differences were observed in levels of retinol, α-tocopherol, or minerals based on whether or not lactating women were taking dietary supplements. CONCLUSIONS: Micronutrient contents of breast milk samples from Korean lactating women were comparable to those of other nations. Retinol and α-tocopherol levels were correlated and also with total fat in breast milk.

Highly Sensitive Wearable Textile-Based Humidity Sensor Made of High-Strength, Single-Walled Carbon Nanotube/Poly(vinyl alcohol) Filaments.

Textile-based humidity sensors can be an important component of smart wearable electronic-textiles and have potential applications in the management of wounds, bed-wetting, and skin pathologies or for microclimate control in clothing. Here, we report a wearable textile-based humidity sensor for the first time using high strength (∼750 MPa) and ultratough (energy-to-break, 4300 J g-1) SWCNT/PVA filaments via a wet-spinning process. The conductive SWCNT networks in the filaments can be modulated by adjusting the intertube distance by swelling the PVA molecular chains via the absorption of water molecules. The diameter of a SWCNT/PVA filament under wet conditions can be as much as 2 times that under dry conditions. The electrical resistance of a fiber sensor stitched onto a hydrophobic textile increases significantly (by more than 220 times) after water sprayed. Textile-based humidity sensors using a 1:5 weight ratio of SWCNT/PVA filaments showed high sensitivity in high relative humidity. The electrical resistance increases by more than 24 times in a short response time of 40 s. We also demonstrated that our sensor can be used to monitor water leakage on a high hydrophobic textile (contact angle of 115.5°). These smart textiles will pave a new way for the design of novel wearable sensors for monitoring blood leakage, sweat, and underwear wetting.

High-Strength Single-Walled Carbon Nanotube/Permalloy Nanoparticle/Poly(vinyl alcohol) Multifunctional Nanocomposite Fiber.

Magnetic nanocomposite fibers are a topic of intense research due to their potential breakthrough applications such as smart magnetic-field-response devices and electromagnetic interference (EMI) shielding. However, clustering of nanoparticles in a polymer matrix is a recognized challenge for obtaining a property-controllable nanocomposite fiber. Another challenge is that the strength and ductility of the nanocomposite fiber decrease significantly with increased weight loading of magnetic nanoparticles in the fiber. Here, we report high-strength single-walled carbon nanotube (SWNT)/permalloy nanoparticle (PNP)/poly(vinyl alcohol) multifunctional nanocomposite fibers fabricated by wet spinning. The weight loadings of SWNTs and PNPs in the fiber were as high as 12.0 and 38.0%, respectively. The tensile strength of the fiber was as high as 700 MPa, and electrical conductivity reached 96.7 S m(-1). The saturation magnetization (Ms) was as high as 24.8 emu g(-1). The EMI attenuation of a fabric woven from the prepared fiber approached 100% when tested with electromagnetic waves with a frequency higher than 6 GHz. The present study demonstrates that a magnetic-field-response device can be designed using the fabricated multifunctional nanocomposite fiber.

Dispersion of single walled carbon nanotubes in organogels by incorporation into organogel fibers.

We prepared hybrid organogels, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. The SWNTs were covalently functionalized with organic branches that had a similar structure to the organogelator. The effect of relative interactions between the carbon nanotubes (CNTs), organogelator, and solvent molecules on the hybrid organogel structure was investigated. Compounds 1 and 2 were synthesized from 3,4,5-tris(decyloxy)benzoic acid and 1,8-diaminooctane, as an organogelator and a functional group for SWNTs, respectively. Organogelator 1 showed excellent ability to gelate alkanes and alcohols. The pristine SWNTs were oxidized by acids to create carboxylic acid groups and functionalized covalently with compound 2 using thionyl chloride. Hybrid organogels of compound 1 with functionalized SWNTs (f-SWNTs) were prepared in decane and N,N-dimethylformamide (DMF). Transmission electron microscopy (TEM) images showed that the f-SWNTs in the hybrid organogel formed in decane were mainly located inside or on the surface of the organogel fibers, while the f-SWNTs in the hybrid organogel formed in DMF were distributed evenly over the sample. When an organogelator had a different chemical structure to that of an organic functional group on the SWNT surface, SWNTs existed as large aggregates, or long bundles, which were not incorporated inside of the organogel fibers.

Molecularly imprinted mesoporous silica particles showing a rapid kinetic binding.

We used periodic mesoporous silica particles for molecular imprinting. The imprinted silica particles showed fast kinetic binding for the template due to their nanosized wall thickness and high surface area.