Electrochemical synthesis and In situ spectroelectrochemistry of conducting NMPy‐TiO2 and ZnO polymer nanocomposites for Li secondary battery applications

Poly(N‐methylpyrrole) (PNMPy), poly(N‐methylpyrrole‐TiO₂) (PNMPy‐TiO₂), and poly (N‐methylpyrrole‐ZnO) (PNMPy‐ZnO) nanocomposites were synthesized by in situ electropolymerization for cathode active material of lithium secondary batteries. The charge–discharging behavior of a Li/LiClO₄/PNMPy battery was studied and compared with Li/LiClO₄/PNMPy‐nanocomposite batteries. The nanocomposites and PNMPy films were characterized by cyclic voltammetry, in situ resistivity measurements, in situ UV–visible, and Fourier transform infra‐red (FTIR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The differences between redox couples (ΔE) were obtained for polymer nanocomposites and PNMPy films. During redox scan, a negative shift of potential was observed for polymer nanocomposite films. Significant differences from in situ resistivity of nanocomposites and PNMPy films were obtained. The in situ UV–visible spectra for PNMPy and polymer nanocomposite films show the intermediate spectroscopic behavior between polymer nanocomposites and PNMPy films. The FTIR peaks of polymer nanocomposite films were found to shift to higher wavelengths in PNMPy films. The SEM and TEM micrographs of nanocomposite films show the presence of nanoparticle in PNMPy backbone clearly. The result suggests that the inorganic semiconductor particles were incorporated in organic conducting PNMPy, which consequently modifies the properties and morphology of the film significantly. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41526.     

Counterion‐Switched Reversibly Hydrophilic and Hydrophobic TiO2‐Incorporated Layer‐By‐Layer Self‐Assembled Membrane for Nanofiltration

The manipulation of surface wettability has been regarded as an efficient strategy to improve the membrane performances. Herein, the counterion‐switched reversibly hydrophilic and hydrophobic surface of TiO₂‐loaded polyelectrolyte membrane are prepared by layer‐by‐layer assembly of poly(sodium 4‐styrene sulfonate) (PSS) and poly(diallydimethyl‐ammoniumchloride (PDDA) containing TiO₂@PDDA nanoparticles (NPs) on the hydrolyzed polyacrylonitrile (PAN) substrate membrane. The obtained polyelectrolyte multilayer (PEM) membranes [PEM‐TiO₂]_4.5⁺X^? (X^? = Cl^?, PFO^? [perfluorooctanoate] etc.) show different hydrophilicity and hydrophobicity with various counterions. The integration of TiO₂ NPs obviously improves the wettability and nanofiltration (NF) performance of PEM membrane for (non)aqueous system of dyes (crystal violet, eriochrome black T) with a high recyclability. The highly hydrophilic [PEM‐TiO₂]_4.5⁺Cl^? (water contact angle [WCA]: 13.2 ± 1.8°) and hydrophobic [PEM‐TiO₂]_4.5⁺PFO^? (WCA: 115.4 ± 2.3°) can be reversibly switched via counterion exchange between Cl^? and PFO^?, verifying the surface with a reversible hydrophilic–hydrophobic transformation. For such membranes, the morphology, wettability, and NF performance rely on the loading of TiO₂@PDDA NPs and surface counterion. Meanwhile, the motion and interaction of water or ethanol in the hydrophilic or hydrophobic membrane are revealed by low‐field nuclear magnetic resonance. This work provides a facile and rapid approach to fabricate smart and tunable wetting surface for potential utilization in (non)aqueous NF separation.     

Mullite–Nickel Magnetic Nanocomposite Fibers Obtained from Electrospinning Followed by Thermal Reduction

Mullite–nickel nanocomposite fibers with Ni nanoparticles of controllable size, dispersion, and consequent magnetic properties were fabricated using sol–gel/electrospinning method, followed by thermal reduction. The fibers were electrospun from an aqueous solution containing sol–gel mullite precursor and nickel nitrate. These fibers were then heat treated in the reducing atmosphere between 550°C and 750°C to achieve fine‐dis persed metallic Ni nanoparticles (NPs). After the Ni²⁺ was reduced to Ni NPs at 750°C for 10 h, the fibers were then directly transformed to the mullite fibers at 1000°C without the undesirable intermediate spinel phase. In many high‐temperature applications, mullite is the desired phase than spinel. If not fully reduced, the Ni²⁺ cations induce early precipitation of spinel phase before mullite can be formed. This spinel phase was a solid solution between Al₂NiO₄ and Al‐Si spinels, which later reacted with the residual silica and formed a mixture of mullite and spinel at 1400°C. The formation of spinel phase was suppressed or fully eliminated with chemically reducing Ni²⁺ to metal NPs. The average size of nickel NPs within the fibers was ~20 nm, insensitive of the Ni concentration and reducing temperature. However, the Ni NPs on the fiber surface grew as large as ~80 nm due to fast surface diffusion. The magnetic nanocomposites exhibited ferromagnetism with saturation magnetization (M_s) close to pure nickel of the same nominal weight, but coercivity (H_c) much smaller than the bulk nickel, indicating the nature of bimodal magnetic nanoparticle distributions. The majority of small Ni NPs (~20 nm) within the fibers exhibited superparamagnetism, while the minor portion of relatively large NPs (50–80 nm) showed ferromagnetism.     

Poly(L‐Lactide), 8. High‐Temperature Hydrolysis of Poly(L‐Lactide) Films with Different Crystallinities and Crystalline Thicknesses in Phosphate‐Buffered Solution

Poly(L ‐lactide) (PLLA) films having different crystallinities (X_c's) and crystalline thicknesses (L_c's) were prepared by annealing at different temperatures (T_a's) from the melt and their high‐temperature hydrolysis was investigated at 97°C in phosphate‐buffered solution. The changes in remaining weight, molecular weight distribution, and surface morphology of the PLLA films during hydrolysis revealed that their hydrolysis at the high temperature in phosphate‐buffered solution proceeds homogeneously along the film cross‐section mainly via the bulk erosion mechanism and that the hydrolysis takes place predominantly and randomly at the chains in the amorphous region. The remaining weight was higher for the PLLA films having high initial X_c when compared at the same hydrolysis time above 30 h. However, the difference in the hydrolysis rate between the initially amorphous and crystallized PLLA films at 97°C was smaller than that at 37°C, due to rapid crystallization of the initially amorphous PLLA film by exposure to crystallizable high temperature in phosphate‐buffered solution. The hydrolysis constant (k) values of the films at 97°C for the period of 0–8 h, 0.059–0.085 h^–1 (1.4–2.0 d^–1), were three orders of magnitude higher than those at 37°C for the period of 0–12 months, 2.2–3.4×10^–3 d^–1. The melting temperature (T_m) and X_c of the PLLA films decreased and increased, respectively, monotonously with hydrolysis time, excluding the initial increase in T_m for the PLLA films prepared at T_a = 100, 120, and 140°C in the first 8, 16, and 16 h, respectively. A specific peak that appeared at a low molecular weight around 1×10⁴ in the GPC spectra was ascribed to the component of one fold in the crystalline region. The relationship between T_m and L_c was found to be T_m (K) = 467·[1–1.61/L_c (nm)] for the PLLA films hydrolyzed at 97°C for 40 h.     

Polypyrrole‐wrapped Pd nanoparticles hollow capsules as a catalyst for reduction of 4‐nitroaniline

In this study, by in situ reduction of Pd²⁺ ions attached on the surface of the sulfonated polystyrene (PS‐SO₃H) spheres, complete and dense palladium (Pd) nanoparticles (NPs) layer were deposited around PS‐SO₃H spheres. The PS@Pd spheres were wrapped by polypyrrole (PPy) shell, which could avoid escaping of Pd NPs. After selectively etching the PS core, the hollow structures with Pd NPs embedded in PPy capsule shell were obtained. The as‐prepared Pd@PPy hollow capsules showed excellent catalytic activity toward the reduction of 4‐nitroaniline because of the high Pd NPs loading. Furthermore, good reusabilty was demonstrated seven times without any detectible loss in activity. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43933.     

Ag Nanoparticles‐Enhanced Photoluminescence in LaPO4: Eu Three‐Dimensional Ordered Macroporous Films

The three‐dimensional ordered macroporous (3DOM) LaPO₄:Eu³⁺ films and Ag nanoparticles (NPs) were prepared via a template‐assisted process and sodium citrate reduction method, respectively. Composite systems consisting of 3DOM LaPO₄:Eu³⁺ films and Ag NPs were obtained by adding the Ag NPs into voids of 3DOM LaPO₄:Eu³⁺ films. The influence of Ag NPs on photoluminescence of 3DOM LaPO₄:Eu³⁺ was investigated. The results show that photoluminescence properties of 3DOM LaPO₄:Eu³⁺ films were enhanced after addition of Ag NPs, which was attributed to the local surface plasmons resonance effect of Ag NPs.     

Enhanced mechanical properties and bactericidal activity of polypropylene nanocomposite with dual‐function silica–silver core‐shell nanoparticles

Dual‐function silica–silver core‐shell (SiO₂@Ag) nanoparticles (NPs) with the core diameter of 17 ± 2 nm and the shell thickness of about 1.5 nm were produced using a green chemistry. The SiO₂@Ag NPs were tested in vitro against gram‐positive Staphylococcus aureus (S. aureus) and gram‐negative Escherichia coli (E. coli), both of which are human pathogens. Minimal inhibitory concentrations of the SiO₂@Ag NPs based on Ag content are 4 and 10 μg mL^?1 against S. aureus and E. coli, respectively. These values are similar to those of Ag NPs. SiO₂@Ag NPs were for the first time incorporated to a commodity polypropylene (PP) polymer. This yielded an advanced multifunctional polymer using current compounding technologies i.e., melt blending by twin‐screw extruder and solvent (toluene) blending. The composite containing 5 wt % SiO₂@Ag NPs (0.05 wt % Ag) exhibited efficient bactericidal activity with over 99.99% reduction in bacterial cell viability and significantly improved the flexural modulus of the PP. Anodic stripping voltammetry, used to investigate the antibacterial mechanism of the composite, indicated that a bactericidal Ag⁺ agent was released from the composite in an aqueous environment. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis of amine‐functionalized block copolymers for nanopollutant removal from water

Polyamines are rare in literature owing to increased reactivity, sensitivity to air and moisture, low stability, and processing difficulties. Here, we report the synthesis and characterization of highly processable polyamines and use them for the removal of dissolved metallic nanoparticles from water. Three amphiphilic block polyamines such as poly(N‐aminoethyl acrylamide‐b‐styrene), poly(N‐aminopropyl acrylamide‐b‐styrene), and poly(N‐aminoxylyl acrylamide‐b‐styrene) have been synthesized using atom transfer radical polymerization of ethyl acrylate and styrene followed by aminolysis of the acrylic block. The polymerization and properties of the polymers are studied using different physicochemical techniques. Surface morphology of films prepared from these block copolymers by dissolving in different solvents such as chloroform, tetrahydrofuran and N,N‐dimethylformamide, and drop‐casting polymers on a glass substrate show interesting porous films and spherical nanostructures. In addition, the amine‐functionalized block copolymers have been used for the removal of nanoparticles from water and show high extraction efficiency toward silver (Ag) and gold (Au) nanoparticles. All three amine‐functionalized block copolymers show higher extraction capacities (Q_e) toward Au NPs (50–109 mg g^?1) and Ag NPs (99–117 mg g^?1). Our approach allows us to make amine‐functionalized block copolymers which are stable in air and can be easily processed in nonpolar solvents. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40943.     

Preparation and Characterization of Copper Gallium Diselenide Thin Films from the Solgel‐Derived Precursors

A simple process for preparing CuGaSe₂ (CGS) absorber layers was developed in this study. The solgel‐derived Cu‐Ga‐O precursor paste with variable Ga³⁺/Cu²⁺ ratios was coated on glass substrates using a doctor‐blade technique. The precursor films were selenided with a selenium vapor at the temperature ranging from 250 to 550°C. The GIXRD patterns showed that single‐phase CuGaSe₂ through the whole films was obtained at a Ga³⁺/Cu²⁺ molar ratio of 1.5 on selenization at 450°C. The Raman measurements also indicated that the grown CuGaSe₂ thin films exhibited the chalcopyrite structure. The SEM images of the films reveal that with an increase in Ga/Cu ratio in the films, the amount of Cu₂Se particles on the surface of the film was reduced. The resistivity of the films was increased with the increase in Ga content in the films. The formation mechanism of CuGaSe₂ thin films was proposed based on the XRD and Raman measurements of the films. The binary copper selenides are formed first, and then these phases lead to the formation of CuGaSe₂.     

Electrochemical Deposition of Highly Dispersed Palladium Nanoparticles on Nafion‐Graphene Film in Presence of Ferrous Ions for Ethanol Electrooxidation

An efficient method was developed to produce highly dispersed Pd nano particles (NPs), supported on Nafion‐graphene film by electrochemical deposition at constant potential in presence of ferrous ions. The Fe²⁺ ions govern the size, shape and morphology of Pd NPs. The as‐prepared catalyst was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X‐ray diffraction (XRD). It was obeserved from TEM that the mean diameter of electrodeposited Pd NPs was 6.4 ± 1.3 nm with narrow diameter range from 4 to 10 nm. The electrocatalytic performance of the Pd NPs deposited on Nafion‐graphene (Nf‐G) catalyst was studied by cyclic voltametry (CV) and chronoamperometric measurements. The highly dispersed Pd NPs on Nf‐G film were obtained in presence of Fe²⁺ ions. This alters electrochemical active surface area and hence catalytic activity of Pd NPs. The prepared Pd/Nf‐G catalyst exhibit highest tolerance to the intermediate poisoning species (ratio I_f/I_b = 2.2). The as‐obtained catalyst shows an efficient electrocatalytic activity and good stability for ethanol oxidation in alkaline medium.     

Galvanic deposition of silver on 80‐μm‐Cu‐fiber for gas‐phase oxidation of alcohols

Microstructured Ag‐based catalysts were developed by galvanically depositing Ag onto 80‐μm‐Cu‐fibers for the gas‐phase oxidation of alcohols. By taking advantages including large voidage, open porous structure and high heat/mass transfer, as‐made catalysts provided a nice combination of high activity/selectivity and enhanced heat transfer. The best catalyst was Ag‐10/80‐Cu‐fiber‐400 (Ag‐loading: 10 wt%; Cu‐fiber pretreated at 400 °C in air), being effective for oxidizing acyclic, benzylic and polynary alcohols. For benzyl alcohol, conversion of 94% was achieved with 99% selectivity to benzaldehyde at 300 °C using a high WHSV of 20 h^?1. Computational fluid dynamics (CFD) calculation and experimental result illustrated significant enhancement of the heat transfer. The temperature difference from reactor wall to central line was about 10–20 °C for the Ag‐10/80‐Cu‐fiber‐400, much lower than that of 100–110 °C for the Ag‐10‐Cu‐2/Al₂O₃ at equivalent conversion and selectivity. Synergistic interaction between Cu₂O and Ag was discussed, being assignable to the activity improvement. © 2014 American Institute of Chemical Engineers AIChE J, 60: 1045–1053, 2014     

High–Energy‐Storage Density Capacitors of Bi(Ni1/2Ti1/2)O3–PbTiO3 Thin Films with Good Temperature Stability

High–energy‐storage density capacitors with thin films of 0.5Bi(Ni_1/2Ti_1/2)O₃–0.5PbTiO₃ (BNT–PT) were fabricated by chemical solution deposition technique on Pt/Ti/SiO₂/Si substrates. The dense thin films with pure‐phase perovskite structure could be obtained by annealing at 750°C. High capacitance density (~1925 nF/cm² at 1 kHz) and extremely high‐energy density (~45.1 J/cm³) under an electric field of 2250 kV/cm were achieved at room temperature. The energy‐storage density and efficiency varied little in a wide temperature range from ?190°C to 250°C. The high–energy‐storage density and good temperature stability make BNT–PT films promising candidates for high power electric applications.     

Employment of ultrasonic waves for the preparation of PVA/TiO2‐BSA nanocomposites: Mechanical,thermal, and optical properties

The goal of this project is to obtain poly(vinyl alcohol) (PVA)/TiO₂‐bovine serum albumin (BSA) nanocomposite (NC) films in different weight percentages of modified TiO₂. For this purpose, to prevent the accumulation of nanoparticles (NPs) in the PVA matrix, the surface of the TiO₂ NPs was treated with the BSA molecules. To achieve this aim, ultrasonic waves were used as an environmentally friendly and green process that decrease the time of reactions, help better spreading of TiO₂ NPs and maintain dimensions of TiO₂ NPs in the nanoscale range. In the end, the features of the PVA/TiO₂‐BSA NC films were considered with a variety of techniques. The Fourier transform infrared spectroscopy, energy dispersive X‐ray, and X‐ray diffraction showed that the BSA was well placed on the surface of TiO₂ NPs. The thermal gravimetric analysis and UV‐visible results demonstrated that all the PVA/TiO₂‐BSA NC films have better thermal and optical properties than the pure PVA. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46558.     

Liquid‐phase hydrogenation of cinnamaldehyde over Cu‐Au/SiO2 catalysts

The synthesis, characterization, and application of silica‐supported Cu‐Au bimetallic catalysts in selective hydrogenation of cinnamaldehyde are described. The results showed that Cu‐Au/SiO₂ bimetallic catalysts were superior to monometallic Cu/SiO₂ and Au/SiO₂ catalysts under identical conditions. Adding a small amount of gold (6Cu‐1.4Au/SiO₂ catalyst) afforded eightfold higher catalytic reaction rate compared to Cu/SiO₂ along with the high selectivity (53%, at 55% of conversion) toward cinnamyl alcohol. Characterization techniques such as x‐ray diffraction, H₂ temperature‐programmed reduction, ultraviolet‐visible spectroscopy, transmission electron microscopy, Fourier‐transform infrared spectra of chemisorbed CO, and x‐ray photoelectron spectroscopy were employed to understand the origin of the catalytic activity. A key genesis of the high activity of the Cu‐Au/SiO₂ catalyst was ascribed to the synergistic effect of Cu and Au species: the Au sites were responsible for the dissociative activation of H₂ molecules, and Cu⁰ and Cu⁺ sites contributed to the adsorption‐activation of C?C and C?O bond, respectively. A combined tuning of particle dispersion and its surface electronic structure was shown as a consequence of the formation of Au‐Cu alloy nanoparticles, which led to the significantly enhanced synergy. A plausible reaction pathway was proposed based on our results and the literature. © 2014 American Institute of Chemical Engineers AIChE J, 60: 3300–3311, 2014     

Synthesis and properties of magnetite nanoparticles with peroxide-containing polymer shell and nanocomposites based on them

Magnetite nanoparticles (Fe₃O₄ NPs) with peroxide-containing polymer shell have been synthesized using the method of coprecipitation from the mixture solutions of Fe (II) and Fe (III) salts in the presence of peroxide-containing copolymer (PCC). Polymer shell presence has been proved by elemental and complex thermal analysis. Synthesized Fe₃O₄ NPs possess superparamagnetic properties. Their specific saturation magnetization decreases gradually from 65 to 54 A·m²·kg⁻¹ with increasing PCC concentration owing to the surface spin pinning effect caused by a polymer shell. The average sizes of Fe₃O₄ NPs estimated from the data of XRD analysis and magnetic measurements are in the range of 9–12 nm. The NP sizes determined by the DLS method lie in the range of 150–270 nm; this result is significantly larger than the sizes estimated by the two aforementioned methods evidencing a tendency for Fe₃O₄ NPs toward self-association. Cross-linked composite films based on polyvinyl alcohol have been obtained via radical curing initiated by the PCC shell of nanoparticles. The resulting composite films are magnetically sensitive films with rather high physico-mechanical properties (tensile strength reaches 48–67 MPa and relative elongation – 4%–21% depending on cross-linking degree), a priori non-toxic and biocompatible, which makes them promising materials for various applications.     

Thermal and morphology characterization study of bio‐active poly(amide‐imide)‐based nanocomposites reinforced with modified SiO2 nanoparticle with poly(vinyl alcohol)

Among the nanoparticles (NPs), the amorphous SiO₂ NPs are very useable, because of their important characteristics for different applications, such as mechanical performance, thermal properties, and biodegradability effects. For this manifest features SiO₂ NPs were used as filler in this study. Firstly, these NPs were modified with poly(vinyl alcohol) (PVA). Then, the poly(amide‐imide) (PAI) was synthesized from reaction between N‐trimellitylimido‐l ‐methionine and 4,4′‐diaminodiphenylether in the presence of ionic liquid and triphenyl phosphite. Next, the modified SiO₂ NPs with PVA (SiO₂‐PVA) were incorporated into the PAI matrix for the preparation of PAI‐SiO₂‐PVA nanocomposites (PSiPNs). Finally, the resulting SiO₂‐PVA and PSiPNs were characterized by different analyses like field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscopy, and thermogravimetric analysis (TGA). TGA showed high thermal stability of the obtained PSiPNs compared to the pure PAI. POLYM. COMPOS. 37:1231–1237, 2016. © 2014 Society of Plastics Engineers     

Study of Carbon Deposition Behavior on Cu–Co/CeO2–YSZ Anodes for Direct Butane Solid Oxide Fuel Cells

Electro‐catalytic activity of Cu–Co/CeO₂–YSZ anodes towards oxidation of H₂ and n‐C₄H₁₀ fuels and carbon depositions are investigated using different Cu–Co loadings. Cu–Co/CeO₂–YSZ anode based SOFCs with YSZ as electrolyte and LSM/YSZ as cathode were prepared by tape casting and wet impregnation methods and performance was analyzed using I–V characteristics and impedance spectroscopy. The Cu–Co/CeO₂–YSZ anodes with Cu–Co loading of 10, 15, and 25 wt.% produced power density of 60, 197, and 400 mW cm^–2 in H₂ and 190, 225, and 275 mW cm^–2 in n‐C₄H₁₀ at 800 °C. The power density is increased with the increase in Cu–Co loading in Cu–Co/CeO₂–YSZ anodes. The electrochemical impedance spectra shows less ohmic and polarization resistance for 25 wt.% Cu–Co loading in comparison to 10 and 15 wt.% Cu–Co. Scanning electron microscopy and high resolution transmission electron microscopy shows that the carbon fibers formed are hollow in nature with 70 nm size, whereas, thermal gravimetric analysis and X‐ray diffraction points out that they are amorphous in nature. The performance degradation of Cu–Co/CeO₂–YSZ anodes in n‐C₄H₁₀ in 16 h is attributed to increasing amount of carbon deposition with time, which is contrary to our earlier observation in Cu‐Fe/CeO₂–YSZ anode.     

UV–VIS absorption and NIR‐stimulated emission of Nd3+: PVA films

Neodymium‐doped polyvinyl alcohol films were prepared and the optical properties of the films were investigated. By applying Judd–Ofelt theory, the Ω parameters were obtained from the absorption spectrum. Various radiative parameters like transition probability for each level (A_J), total transition probability (A_T), branching ratio (β_R), radiative lifetime (τ_rad), and absorption cross‐section (σ_A) were calculated. The theoretically obtained branching ratio and integrated absorption cross‐section are found to be greater for the transition ⁴F_3/2 → ⁴I_11/2. From the emission spectrum peaked at 1064‐nm stimulated emission cross‐section (σ_E), the line width (Δλ_eff) is calculated to be 6.21 × 10^?21 cm² and 41 nm, respectively. Further the variation of the optical gain with the length of the film was studied and the slope efficiency (η = 8.5%) was determined from laser measurements. These results clearly support the potentiality of the Nd³⁺: polyvinyl alcohol films in realizing optical amplification and stimulated emission. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Synthesis and Electrochemical Properties of BaFe1−xCuxO3−δ Perovskite Oxide for IT‐SOFC Cathode

A series of iron‐based perovskite oxides BaFe_1−xCu_xO_3−δ (x = 0.10, 0.15, 0.20 and 0.25, abbreviated as BFC‐10, BFC‐15, BFC‐20 and BFC‐25, respectively) as cathode materials have been prepared via a combined EDTA‐citrate complexing sol‐gel method. The effects of Cu contents on the crystal structure, chemical stability, electrical conductivity, thermal expansion coefficient (TEC) and electrochemical properties of BFC‐x materials have been studied. All the BFC‐x samples exhibit the cubic phase with a space group Pm3m (221). The electrical conductivity decreases with increasing Cu content. The maximum electrical conductivity is 60.9 ± 0.9 S cm⁻¹ for BFC‐20 at 600 °C. Substitution of Fe by Cu increases the thermal expansion coefficient. The average TEC increases from 20.6 × 10⁻⁶ K⁻¹ for BFC‐10 to 23.7 × 10⁻⁶ K⁻¹ for BFC‐25 at the temperature range of 30–850 °C. Among the samples, BFC‐20 shows the best electrochemical performance. The area specific resistance (ASR) of BFC‐20 on SDC electrolyte is 0.014 Ω cm² at 800 °C. The single fuel cell with the configguration of BFC‐20/SDC/NiO‐SDC delivers the highest power density of 0.57 W cm⁻² at 800 °C. The favorable electrochemical activities can be attributed to the cubic lattice structure and the high oxygen vacancy concentration caused by Cu doping.     

High strength nanocomposite hydrogels with outstanding UV‐shielding property

A novel series of nanocomposite hydrogels (TAD gels) with high mechanical strength and excellent UV‐shielding property were prepared by in situ free‐radical copolymerization of acrylamide (AM) and N,N‐dimethylacrylamide (DMAA) in aqueous solutions of TiO₂ nanoparticles (TiO₂ NPs). It was found that the TiO₂ NPs were uniformly dispersed in the copolymer matrix and acted as inorganic crosslinking agents in TAD gels owing to their hydrogen bonding interactions with polymer chains. The TAD gels exhibited excellent mechanical properties such as large elongations at break, high elastic moduli, and ultimate stresses, all of these properties as well as swelling ratios of TAD gels could be easily controlled by changing the AM ratios and TiO₂ contents in the initial solutions. In addition, the TAD gels with low AM ratios could be prepared into thin films in a customized Teflon model and these films showed high transparency in visible light but could completely block the UV light with wavelength below 366 nm and prevent the methylene blue from degradation under UV irradiation. POLYM. COMPOS., 37:810–817, 2016. © 2014 Society of Plastics Engineers