Synthesis of MoS2@MoO3/(Cu+/g-C3N4) ternary composites with double S-scheme heterojunction for peroxymonosulfate activation exposing to visible light.

The construction of semiconductor heterojunction is an effective way for charge separation in photocatalytic degradation of pollutants. In this study, a novel MoS2@MoO3/(Cu+/g-C3N4) ternary composites (MMCCN) was prepared via a simple calcination method. The as-prepared composites exhibited exceptional performance in activating peroxymonosulfate (PMS) for the degradation of rhodamine B (RhB). The activity testing results indicated that 99.41 % of RhB (10 mg·L-1, 10 mL) was effectively removed by the synergistic effect of composites photocatalyst (0.1 g·L-1) and PMS (0.1 g·L-1) under visible light irradiation for 40 min. Its reaction rate constant exceeded that of Cu+/g-C3N4, MoO3 and MoS2 by a factor of 3.56, 17.30 and 11.73 times, respectively. The crystal structure, band gap and density of states (DOS) of the semiconductors were calculated according to the density functional theory (DFT). Free radical trapping tests and electron spin resonance spectroscopy validated that 1O2, O2- and h+ are primary reactive species participating in the decomposition of RhB. The ternary composites demonstrated good stability and maintained excellent degradation efficiency even across four reaction cycles. Furthermore, the activation mechanism and the intermediates produced during the decomposition course of RhB by MMCCN/PMS/vis system were analyzed and elucidated. A double S-scheme heterojunctions was responsible for efficient separation of photo-induced electron-hole pairs. This work presents a novel method in the construction of double S-scheme heterojunctions for PMS activation which is expected to find wide applications in wastewater treatment and environmental remediation.

Development of ternary hybrid composites of transition metal and noble metal-based heterostructures: Ultrasensitive simultaneous electrochemical detection of bisphenol A and bisphenol S in food samples.

Bisphenols threaten human health and sensitive detection is crucial. The present study aims to develop ternary composites of copper metal-organic framework (Cu-MOF) with AuAg microstructures. The composite structure was formed by a galvanic displacement reaction and confirmed using SEM. A binder-free catalyst was used to study the electrochemical redox reaction of bisphenol A (BPA) and bisphenol S (BPS); an irreversible cyclic voltammetric signal at +0.70 V and + 0.91 V (vs. Ag/AgCl), in the dynamic range of 20 nM to 2.0 mM, and 10 nM to 1.0 mM, with limits of detection of 2.9 nM, and 3.2 nM (S/N = 3) was obtained. Practical analysis was applied to frozen tomatoes, tuna fish, milk powder, PET bottles, raw milk, and urine samples with a recovery rate of 94.00-100.80% (n = 3). Voltammetric results were validated using HPLC detection with high precision. The sensor is a promising alternative platform for measuring BPA in food samples.

Ternary composites of poly(vinylidene fluoride-co-hexafluoropropylene) with silver nanowires and titanium dioxide nanoparticles as separator membranes for lithium-ion batteries.

In the realm of polymer composites, there is growing interest in the use of more than one filler for achieving multifunctional properties. In this work, a composite separator membrane has been developed for lithium-ion battery application, by incorporating conductive silver nanowires (AgNWs) and titanium dioxide (TiO2) nanoparticles into a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) polymer matrix. The composite membranes were manufactured by solvent casting and thermally induced phase separation, with total filler content varying up to 10 wt%. The ternary composites composites present improved mechanical characteristics, ionic conductivity and lithium transfer number compared to the neat polymer matrix. On the other hand, the filler type and content within the composite has little bearing on the morphology, polymer phase, or thermal stability. Once applied as a separator in lithium-ion batteries, the highest discharge capacity value was obtained for the 5 wt% AgNWs/5 wt% TiO2/PVDF-HFP membrane at different C-rates, benefiting from the synergetic effect from both fillers. This work demonstrates that higher battery performance can be achieved for next-generation lithium-ion batteries by using separator membranes based on ternary composites.

High Performance Ternary Solid Polymer Electrolytes Based on High Dielectric Poly(vinylidene fluoride) Copolymers for Solid State Lithium-Ion Batteries.

Renewable energy sources require efficient energy storage systems. Lithium-ion batteries stand out among those systems, but safety and cycling stability problems still need to be improved. This can be achieved by the implementation of solid polymer electrolytes (SPE) instead of the typically used separator/electrolyte system. Thus, ternary SPEs have been developed based on poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene), P(VDF-TrFE-CFE) as host polymers, clinoptilolite (CPT) zeolite added to stabilize the battery cycling performance, and ionic liquids (ILs) (1-butyl-3-methylimidazolium thiocyanate ([BMIM][SCN])), 1-methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([PMPyr][TFSI]) or lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), incorporated to increase the ionic conductivity. The samples were processed by doctor blade with solvent evaporation at 160 °C. The nature of the polymer matrix and fillers affect the morphology and mechanical properties of the samples and play an important role in electrochemical parameters such as ionic conductivity value, electrochemical window stability, and lithium-transference number. The best ionic conductivity (4.2 × 10-5 S cm-1) and lithium transference number (0.59) were obtained for the PVDF-HFP-CPT-[PMPyr][TFSI] sample. Charge-discharge battery tests at C/10 showed excellent battery performance with values of 150 mAh g-1 after 50 cycles, regardless of the polymer matrix and IL used. In the rate performance tests, the best SPE was the one based on the P(VDF-TrFE-CFE) host polymer, with a discharge value at C-rate of 98.7 mAh g-1, as it promoted ionic dissociation. This study proves for the first time the suitability of P(VDF-TrFE-CFE) as SPE in lithium-ion batteries, showing the relevance of the proper selection of the polymer matrix, IL type, and lithium salt in the formulation of the ternary SPE, in order to optimize solid-state battery performance. In particular, the enhancement of the ionic conductivity provided by the IL and the effect of the high dielectric constant polymer P(VDF-TrFE-CFE) in improving battery cyclability in a wide range of discharge rates must be highlighted.

Pickering emulsions stabilized by zein-proanthocyanidins-pectin ternary composites (ZPAAPs): Construction and delivery studies.

Proanthocyanidins (Pas) are widely used in the preparation of functional foods due to their diverse biological activities. Taking advantage of the effect of Pas on the stability of Pickering emulsions, this study constructed the zein-proanthocyanidins-pectin ternary composites (ZPAAPs) as stabilizer to establish Pickering emulsions with potential delivery capacity. The appearance of the emulsion was pink which could be found in visual observation. The emulsion was stable during long-term storage in the range of 0.1 âˆ¼ 0.7 oil phase. CLSM showed that the oil droplets were coated with covering layer formed by ZPAAPs, which effectively prevented droplets congregating. The rheological results indicated that ZPAAPEs had elastic gel-like structure. In addition, ZPAAPEs still contained 54.4 % curcumin after storage for 15 d. And the bioavailability of curcumin was increased to 39.7 % ± 0.3. These studies may contribute to the controllable fabrication of Pickering emulsions for nutrient delivery in the food and pharmaceutical fields.

Evaluation of the Synergistic Effect of Graphene Oxide Sheets and Co3O4 Wrapped with Vertically Aligned Arrays of Poly (Aniline-Co-Melamine) Nanofibers for Energy Storage Applications.

In the present study, Co3O4 and graphene oxide (GO) are used as reinforcement materials in a copolymer matrix of poly(aniline-co-melamine) to synthesize ternary composites. The nanocomposite was prepared by oxidative in-situ polymerization and used as an electrode material for energy storage. The SEM images revealed the vertically aligned arrays of copolymer nanofibers, which entirely wrapped the GO sheets and Co3O4 nanoparticles. The EDX and mapping analysis confirmed the elemental composition and uniform distribution in the composite. The XRD patterns unveiled composites' phase purity and crystallinity through characteristic peaks appearing at their respective 2θ values in the XRD spectrum. The FTIR spectrums endorse the successful synthesis of composites, whereas TGA analysis revealed the higher thermal stability of composites. The cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy are employed to elucidate the electrochemical features of electrodes. The ternary composite PMCoG-2 displayed the highest specific capacity of 134.36 C/g with 6 phr of GO, whereas PMCoG-1 and PMCoG-3 exhibited the specific capacities of 100.63 and 118.4 C/g having 3 phr and 12 phr GO at a scan rate of 0.003 V/s, respectively. The best electrochemical performance of PMCoG-2 is credited to the synergistic effect of constituents of the composite material.

Material Design and Optimisation of Electrochemical Li-Ion Storage Properties of Ternary Silicon Oxycarbide/Graphite/Tin Nanocomposites.

In this work, we present the characterization and electrochemical performance of various ternary silicon oxycarbide/graphite/tin (SiOC/C/Sn) nanocomposites as anodes for lithium-ion batteries. In binary SiOC/Sn composites, tin nanoparticles may be produced in situ via carbothermal reduction of SnO2 to metallic Sn, which consumes free carbon from the SiOC ceramic phase, thereby limiting the carbon content in the final ceramic nanocomposite. Therefore, to avoid drawbacks with carbon depletion, we used graphite as a substitute during the synthesis of precursors. The ternary composites were synthesized from liquid precursors and flake graphite using the ultrasound-assisted hydrosilylation method and pyrolysis at 1000 °C in an Ar atmosphere. The role of the graphitic component is to ensure good electric conductivity and the softness of the material, which are crucial for long term stability during alloying-dealloying processes. The presented approach allows us to increase the content of the tin precursor from 40 wt.% to 60 wt.% without losing the electrochemical stability of the final material. The charge/discharge capacity (at 372 mA g-1 current rate) of the tailored SiOC/C/Sn composite is about 100 mAh g-1 higher compared with that of the binary SiOC/Sn composite. The ternary composites, however, are more sensitive to high current rates (above 372 mA g-1) compared to the binary one because of the presence of graphitic carbon.

Constructing Densely Compacted Graphite/Si/SiO2 Ternary Composite Anodes for High-Performance Li-Ion Batteries.

Graphite has dominated the market of anode materials for lithium-ion batteries in applications such as consumer electronic devices and electric vehicles. As commercial graphite anodes are approaching their theoretical capacity, significant efforts have been dedicated towards higher capacity by blending capacity-enhancing additives (e.g., Si) with graphite particles. In spite of the improved gravimetric capacity, the areal capacity of such composite anodes might decrease due to excess void spaces and an incompatible material size distribution. Herein, a rational design of compact graphite/Si/SiO2 ternary composites has been proposed to address the abovementioned issues. Si/SiO2 clusters with an optimal particle size are homogeneously dispersed in the interstitial spaces between graphite particles to promote the packing density, leading to a higher areal capacity than that of pure graphite with equivalent mass loading or electrode thickness. By taking the full intrinsic advantages of graphite, Si, and SiO2, the composite electrodes exhibit 553.6 mAh g-1 after 700 cycles with a capacity retention of 95.2%. Furthermore, the graphite/Si/SiO2 electrodes demonstrate a high coulombic efficiency with an average of 99.68% from 2nd to 200th cycles and areal capacities above 1.75 mAh cm-2 during 200 cycles with an areal mass loading as high as 4.04 mg cm-2. A packing model has been proposed and verified by experimental investigation as a design principle of densely compacted anodes. The effective strategy of introducing Si/SiO2 clusters into the void spaces between graphite particles provides an alternative solution for implementation of graphite-Si composite anodes in next-generation Li-ion cells.

Synthesis and photocatalytic degradation of rhodamine B using ternary zeolite/WO3/Fe3O4composite.

Demand for freshwater increases day by day as impurity increases due to the industrial, domestic and municipal waste in the water. Inappropriate disposal of coal fly ash (CFA) is not eco-friendly, therefore the need is to convert it into some beneficial material like zeolite. Zeolite-based composites with metal oxides show high cation interchange capacity, fast adsorption, and high efficiency for the removal of wastewater pollutants. In this research work, metal oxide along with zeolite (derived for CFA) was prepared. Metal oxide (WO3) and magnetite (Fe3O4) based zeolite composite was used adsorption enhanced photocatalytic degradation of rhodamine B dye. Ternary composite (zeolite/WO3/Fe3O4) was characterized using a scanning electron microscope, x-ray diffraction, Fourier transform infrared spectroscopy. The bandgap energy of composite was estimated using Tauc plot method from the data obtained after UV-visible spectroscopy. The behavior of composite under acidic and basic conditions was analyzed using pHpzcof the composite. Influencing parameters like pH, dye concentration, contact time, and catalyst dosage was optimized under ultraviolet irradiations (254 nm). The results show that maximum degradation was achieved with zeolite/WO3/Fe3O4composite under optimized conditions of pH = 7, catalyst dosage = 10 mg/100 ml, RhB concentration 10 ppm, and time 60 min. The first-order kinetic model was best fitted to the experimental data. RSM was used as a statistical tool to analyze the data.

Facile fabrication of highly catalytic-active Ag2CO3/AgBr/graphene oxide ternary composites towards the photocatalytic wastewater treatment.

Ag2CO3/AgBr/graphene oxide (Ag2CO3/AgBr/GO) ternary composites with different percentages of GO were fabricated by a facile co-precipitation strategy. The composites were characterized in the aspect of phase composition, light absorption performance, and micromorphology etc. The activity of the composites was studied by photocatalytic degradation of colored organic dye (rhodamine B, RhB) and colorless organics (phenol) under the shine of visible light. The optimized Ag2CO3/AgBr/GO-7.5 composites revealed the most excellent photocatalytic activity, which exhibited an apparent reaction rate constant exceeding that of pristine AgBr and Ag2CO3 by a factor of 107 and 5.63, respectively. The outstanding performance can be attributed to the effective separation of electrons and holes as well as the strong light absorption ability resulting from the Ag2CO3/AgBr/GO heterostructure. Moreover, it was verified that h+ and •O2- were two major active substances responsible for the decomposition of organic pollutants according to the free radical-trapping experiments. Besides, a probable reaction mechanism referring to the charge transfer and separation in the composites was proposed and discussed in detail.

Capacitance Enhancement by Incorporation of Functionalised Carbon Nanotubes into Poly(3,4-Ethylenedioxythiophene)/Graphene Oxide Composites.

This paper reports on the role of oxidised carbon nanotubes (oxMWCNTs) present in poly-3,4-ethylenedioxytiophene (PEDOT)/graphene oxide (GOx) composite. The final ternary composites (pEDOT/GOx/oxMWCNTs) are synthesised by an electrodeposition process from the suspension-containing monomer, oxidised carbon nanotubes and graphene oxide. Dissociated functional groups on the surface of graphene oxide play a role of counter-ions for the polymer chains. Detailed physicochemical and electrochemical characterisation of the ternary composites is presented in the paper. The results prove that the presence of oxMWCNTs in the ternary composites doubles the capacitance values compared to the binary ones (450 vs. 270 F cm-3 for PEDOT/GOx/oxMWCNTs and PEDOT/GOx, respectively). The amount of carbon nanotubes in the synthesis solution is crucial for physicochemical properties of the composites, their adhesion to the electrode substrate and the electrochemical performance.

Cellulose nanofibers reinforced biodegradable polyester blends: Ternary biocomposites with balanced mechanical properties.

Blending two biodegradable aliphatic polyesters with complementary bulk properties is an easy way of tuning their final properties. In this work, the ductile poly(butylene succinate) was mixed with polylactide, and as expectable, the blends show improved toughness with sharply reduced strengths. The pristine cellulose nanofibers were then used as the reinforcement for the blends. It is found that most nanofibers are dispersed in the polylactide phase because polylactide has better affinity to nanofibers, and the lower viscosity level of polylactide also favors driving nanofibers into the continuous polylactide phase during melting mixing. In this case, the strength and rigidity losses resulted from the presence of soft poly(butylene succinate) phase are compensated to some extent. To further improve mechanical properties, a two-step approach (reactive processing of blends, followed by the incorporation with nanofibers) was developed. This work provides an interesting way of fabricating fully biodegradable composites with well-balanced mechanical performance.

Nitrogen doped carbon quantum dots and GO modified WO3 nanosheets combination as an effective visible photo catalyst.

Nitrogen doped carbon quantum dots (NCQDs) based highly efficient ternary photocatalyst are fabricated by modifying surface of GO incorporated WO3 nano-sheets. XRD confirmed the formation of monoclinicWO3 nano-sheets. All the characteristic peaks of WO3, GO and NCQDs are obvious in XRD patterns of WO3/GO/NCQDs ternary photocatalysts confirming successful fabrication of the photocatalysts. SEM images showed that WO3 host matrix is distorted after incorporation of GO and NCQDs owing to lower interfacial tension. The surface of WO3 nano-sheets is modified with morphological defects making more active sites available. UV-vis spectra exhibited extended visible light absorption and remarkable reduction of WO3 band gap energy. The photoluminescence spectra confirmed the efficient charge separation in NCQDs modified ternary photocatalyst. The synthesized composites were applied for the photocatalytic degradation of harmful organic dye i.e. methyl orange (MO). The ternary composites represented the excellent photocatalytic activity as compared to binary and pure WO3 photocatalysts. This enhanced photocatalytic activity is attributed to the availability of active sites, extended light absorption in visible region and enhanced charge separation efficiency.

One-Pot Hydrothermal Synthesis of Ternary 1T-MoS2 /Hexa-WO3 /Graphene Composites for High-Performance Supercapacitors.

A new ternary composite of 1T-molybdenum disulfide, hexagonal tungsten trioxide, and reduced graphene oxide (M-W-rGO) is synthesized by using a one-pot hydrothermal process. The synergetic effect of 1T-MoS2 and hexa-WO3 nanoflowers improves the electrochemical performance for supercapacitors by inducing additional active sites and hexagonal tunnels, respectively, which lead to high storage capacity and easy transfer of electrolyte ions. The ternary M-W-rGO composite has a high specific capacitance of 836 F g-1 at 1 A g-1 , which is nearly twice that of binary composites of M-rGO and W-rGO with high capacitance retention of 86.35 % after 3000 cycles at a high current density of 5 A g-1 . This study provides a new ternary composite that can be used as an electrode material for high-performance supercapacitors.

Glass Fiber-Reinforced Phenol Formaldehyde Resin-Based Electrical Insulating Composites Fabricated by Selective Laser Sintering.

In this study, glass fiber (GF)/phenol formaldehyde resin (PF)/epoxy resin (EP) three-phase electrical insulating composites were fabricated by selective laser sintering (SLS) additive manufacturing technology and subsequent infiltration. In the three-phase composites, glass fibers modified by a silane coupling agent (KH-550) were used as reinforcements, phenol formaldehyde resin acted as the binder and matrix, and infiltrated epoxy resin was the filler. Mechanical and electrical properties such as tensile strength, bending strength, dielectric constant, electrical conductivity, and electric breakdown strength of the GF/PF/EP three-phase composite parts were investigated. The results indicated that after being infiltrated with EP, the bending strength and tensile strength of the GF/PF/EP composites increased by 30% and 42.8%, respectively. Moreover, the flexural strength and tensile strength of the GF/PF/EP composite increased with the increase of the glass fiber content. More importantly, the three-phase composites showed high electrical properties. Significant improvement in the dielectric constant, electric breakdown strength, and resistivity with the increase in the content of glass fiber was observed. This enables the prepared GF/PF/EP composites to form complex structural electrical insulation devices by SLS, which expands the materials and applications of additive manufacturing technology.

3D-printed scaffolds of mesoporous bioglass/gliadin/polycaprolactone ternary composite for enhancement of compressive strength, degradability, cell responses and new bone tissue ingrowth.

BACKGROUND: Due to the increasing number of patients with bone defects, bone nonunion and osteo-myelitis, tumor and congenital diseases, bone repair has become an urgent problem to be solved. METHODS: In this study, the 3D-printed scaffolds of ternary composites containing mesoporous bioglass fibers of magnesium calcium silicate (mMCS), gliadin (GA) and polycaprolactone (PCL) were fabricated using a 3D Bioprinter. RESULTS: The compressive strength and in vitro degradability of the mMCS/GA/PCL composites (MGPC) scaffolds were improved with the increase of mMCS content. In addition, the attachment and proliferation of MC3T3-E1 cells on the scaffolds were significantly promoted with the increase of mMCS content. Moreover, the cells with normal phenotype attached and spread well on the scaffolds surfaces, indicating good cytocompatibility. The scaffolds were implanted into the femur defects of rabbits, and the results demonstrated that the scaffold containing mMCS stimulated new bone formation and ingrowth into the scaffolds through scaffolds degradation in vivo. Moreover, the expression of type I collagen into scaffolds was enhanced with the increase of mMCS content. CONCLUSION: The 3D-printed MGPC scaffold with controllable architecture, good biocompatibility, high compressive strength, proper degradability and excellent in vivo osteogenesis has great potential for bone regeneration.

Synthesis and Electrochemical Performance of Molybdenum Disulfide-Reduced Graphene Oxide-Polyaniline Ternary Composites for Supercapacitors.

Molybdenum disulfide/reduced graphene oxide/polyaniline ternary composites (MoS2/rGO/PANI) were designed and synthesized by a facile two-step approach including hydrothermal and in situ polymerization process. The MoS2/rGO/PANI composites presented an interconnected 3D network architecture, in which PANI uniformly coated the outer surface of the MoS2/rGO binary composite. The MoS2/rGO/PANI composites with a weight percent of 80% (MGP-80) exhibits the best specific capacitance (570 F g-1 at 1 A g-1) and cycling stabilities (78.6% retained capacitance after 500 cycles at 1 A g-1). The excellent electrochemical capacitive performance is attributed to its 3D network structure and the synergistic effects among the three components that make the composites obtain both pseudocapacitance and double-layer capacitance.

Sandwich-structured graphene-nickel silicate-nickel ternary composites as superior anode materials for lithium-ion batteries.

We report the synthesis of sandwich-structured graphene-nickel silicate-Ni ternary composites by using the solvothermal method followed by a simple in situ reduction procedure. The composites show an interesting structure with graphene sandwiched between two layers of well-dispersed Ni nanoparticles (NPs) anchored on ultrathin nickel silicate nanosheets. These ternary composites exhibit enhanced performance as anode materials owing to the synergistic effect between the graphene matrix and electrochemically inert Ni nanoparticles, an effect that holds promise for the design and fabrication of other advanced electrode materials.