Project description:A series of core@shell SrTiO3@NiFe LDH composites (STONFs) were synthesized and their photocatalytic CO2 reduction performance was studied. The photocatalyst STONF 2 exhibited enhanced CO2 reduction performance with CO yield of 7.9 μmol g-1 h-1. The yield was 25.7 times and 8.8 times higher than that of NiFe LDH and SrTiO3 respectively, and also higher than most LDH based photocatalysts. Compared with two individual components, STONFs exhibited their combined merits of widened absorption spectrum, higher transportation efficiency and alleviated recombination of e-/h+ pairs. In addition, there were fewer oxygen vacancies in STONF 2 than as-prepared SrTiO3. Lower oxygen vacancies concentration would increase the opportunity of direct bonding between interface atoms of two components and successively increase the electron transportation and separation. These factors synergistically contributed to enhanced photocatalytic performance. This work will provide new insight for designing complementary multi-component photocatalysis systems.
Project description:In our previous study, we investigated the synergetic effects of inorganic ions, such as silicate, Mg2+ and Ca2+ ions on the osteoblast-like cell behaviour. Mg2+ ions play an important role in cell adhesion. In the present study, we designed a new composite that releases a high concentration of Mg2+ ions during the early stage of the bone-forming process, and silicate and Ca2+ ions continuously throughout this process. Here, 40SiO2-40MgO-20Na2O glass (G) with high solubility and vaterite-based calcium carbonate (V) were selected as the source of silicate and Mg2+ and Ca2+ ions, respectively. These particles were mixed with poly(lactic-co-glycolic acid) (PLGA) using a kneading method at 110°C to prepare the composite (G-V/PLGA, G/V/PLGA = 4/56/40 (in weight ratio)). Most of the Mg2+ ions were released within 3 days of immersion at an important stage for cell adhesion, and silicate and Ca2+ ions were released continuously at rates of 70-80 and 180 ppm d-1, respectively, throughout the experiment (until day 7). Mouse-derived osteoblast-like MC3T3-E1 proliferated more vigorously on G-V/PLGA in comparison with V-containing PLGA without G particles; it is possible to control the ion-release behaviour by incorporating a small amount of glass particles.
Project description:Black NiO powders were prepared by a hydrothermal method. Moreover, the visible light-driven Ag3PO4/NiO photocatalyst composites were successfully synthesized by in situ precipitation method. These samples were structurally characterized by X-ray diffraction and Rietveld refinement. The strong interaction between the phases and the defects in the samples was affected by the formation of the composites, as identified by Fourier transform infrared spectroscopy and Raman spectroscopy. UV-vis diffuse reflectance spectroscopy exhibited enhanced light absorption for all Ag3PO4/NiO composites, suggesting the effective interaction between the phases. Moreover, field-emission scanning electron microscopy images revealed the presence of NiO microflowers composed of nanoflakes in contact with Ag3PO4 microparticles. The composite with 5% NiO presented enhanced photocatalytic efficiency in comparison with pure Ag3PO4, degrading 96% of rhodamine B (RhB) dye in just 15 min under visible light; however, the recycling experiments confirmed that the composite with 75% NiO showed superior stability. The recombination of the electron-hole pairs was considered for the measurement of the photoluminescence of the samples. These measurements were performed to evaluate the possible causes for the difference in the photocatalytic responses of the composites. From these experimental results, possible photocatalytic mechanisms for RhB degradation over Ag3PO4/NiO composites under visible-light irradiation were proposed.
Project description:Single crystals of strontium tetra-cobalt tris-(orthophosphate) hydroxide, SrCo4(OH)(PO4)3, were grown serendipitously under hydro-thermal conditions at 473 K. The crystal structure consists of undulating chains of edge-sharing [CoO6] octa-hedra that are linked into (010) layers by common vertices between chains. Adjacent layers are linked along [010] into a framework structure by tetra-hedral [CoO4] units and by PO4 tetra-hedra. The framework delimits channels extending along [100] in which the eleven-coordinate strontium cations are situated. Bifurcated O-H⋯O hydrogen bonds of weak strengths consolidate the crystal packing. The title compound was also characterized by infrared spectroscopy.
Project description:Because of the nontoxic solvents contained in CO2-in-water emulsions, porous polymer composites templated from these emulsions are conducive for bio-applications. Herein, bio-active rod-like calcium-organic framworks (Ca-BDC MOFs, BDC= 1,4-benzenedicarboxylate anion) particles co-stabilized CO2-in-water high internal phase emulsion (C/W HIPE) in the presence of polyvinyl alcohol (PVA) is first presented. After curing of the continuous phase, followed by releasing CO2, integral 3D macro-porous Ca-BDC monolith and Ca-BDC/Poly(2-hydroxyethyl methacrylate-co-acrylamide) HIPEs monolithic composites [Ca-BDC/P(AM-co-HEMA)HIPEs] with open-cell macro-porous structures were successfully prepared. The pore structure of these porous composite can be tuned by means of tailoring the Ca-BDC dosage, carbon dioxide pressure, and continuous phase volume fractions in corresponding C/W HIPEs. Results of bio-compatibility tests show that these Ca-BDC/P(AM-co-HEMA)HIPEs monoliths have non-cytotoxicity on HepG2 cells; also, the E. coli can grow either on the surfaces or inside these monoliths. Furthermore, immobilization of ?-amylase on these porous composite presents that ?-amylase can be well-anchored into the porous polymer composites, its catalytic activity can be maintained even after 10 cycles. This work combined bio-active MOFs Ca-BDC, bio-compatible open-cell macroporous polymer PAM-co-HEMA and green C/W HIPEs to present a novel and facile way to prepare interconnected macro-porous MOFs/polymer composites. Compared with the existing other well-known materials such as hydrogels, these porous composites possess well-defined tunable pore structures and superior bio-activity, thereby have promising applications in bio-tissue engineering, food, and pharmaceutical.
Project description:Composites comprised of Ag3PO4 and bare TiO2 (TiO2@Ag3PO4) or silver doped TiO2 (Ag@TiO2-Ag3PO4) have been synthesized by coupling sol-gel and precipitation methods. For the sake of comparison, also the bare components have been similarly prepared. All the samples have been characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), Fourier transformed infrared spectroscopy (FTIR), photoelectrochemical measurements, and specific surface area (SSA) analysis. The optoelectronic and structural features of the samples have been related to their photocatalytic activity for the degradation of 4-nitrophenol under solar and UV light irradiation. Coupling Ag3PO4 with silver doped TiO2 mitigates photocorrosion of the Ag3PO4 counterpart, and remarkably improves the photocatalytic activity under solar light irradiation with respect to the components, to the TiO2-Ag3PO4 sample, and to the benchmark TiO2 Evonik P25. These features open the route to future applications of this material in the field of environmental remediation.
Project description:Natural structural materials like bone and shell have complex, hierarchical architectures designed to control crack propagation and fracture. In modern composites there is a critical trade-off between strength and toughness. Natural structures provide blueprints to overcome this, however this approach introduces another trade-off between fine structural manipulation and manufacturing complex shapes in practical sizes and times. Here we show that robocasting can be used to build ceramic-based composite parts with a range of geometries, possessing microstructures unattainable by other production technologies. This is achieved by manipulating the rheology of ceramic pastes and the shear forces they experience during printing. To demonstrate the versatility of the approach we have fabricated highly mineralized composites with microscopic Bouligand structures that guide crack propagation and twisting in three dimensions, which we have followed using an original in-situ crack opening technique. In this way we can retain strength while enhancing toughness by using strategies taken from crustacean shells.
Project description:Murals are one of the precious legacies of our ancestors; however, they face severe damage along with archeological discoveries, which need urgent repair. Nowadays, nanotechnology provides new concepts and materials for the consolidation and protection of murals. In this work, an innovative method for the protection of murals was proposed with graphene-based nanomaterials through strategically synthesizing a polyacrylic acid-functionalized graphene/nano-Ca(OH)2 material (PAAG@Ca(OH)2) by a facile and economic aqueous method. As a result, the nanocomposite PAAG@Ca(OH)2 was demonstrated with high porosity, strong adsorption, appropriate hydrophilicity, and better permeability compared to the commercial AC33 sample according to the simulated tests. As expected, the nanocomposite PAAG@Ca(OH)2 displayed a promising application for the reinforcement of murals, which opens up a new avenue for the protection of murals.
Project description:Among the accessible techniques, the production of hydrogen by electrocatalytic water oxidation is the most established process, which comprises oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Here, we synthesized a genomic DNA-guided porous Cu2(OH)PO4/Co3(PO4)2·8H2O rolling pin shape composite structure in one pot. The nucleation and development of the porous rolling pin shape Cu2(OH)PO4/Co3(PO4)2·8H2O composite was controlled and stabilized by the DNA biomolecules. This porous rolling pin shape composite was explored towards electrocatalytic water oxidation for both OER and HER as a bi-functional catalyst. The as-prepared catalyst exhibited a very high OER and HER activity compared to its various counterparts in the absence of an external binder (such as Nafion). The synergistic effects between Cu and Co metals together with the porous structure of the composite greatly helped in enhancing the catalytic activity. These outcomes undoubtedly demonstrated the beneficial utilization of the genomic DNA-stabilised porous electrocatalyst for OER and HER, which has never been observed.
Project description:Architected metals and ceramics with nanoscale cellular designs, e.g., nanolattices, are currently subject of extensive investigation. By harnessing extreme material size effects, nanolattices demonstrated classically inaccessible properties at low density, with exceptional potential for superior lightweight materials. This study expands the concept of nanoarchitecture to dense metal/ceramic composites, presenting co-continuous architectures of three-dimensional printed pyrolytic carbon shell reinforcements and electrodeposited nickel matrices. We demonstrate ductile compressive deformability with elongated ultrahigh strength plateaus, resulting in an extremely high combination of compressive strength and strain energy absorption. Simultaneously, property-to-weight ratios outperform those of lightweight nanolattices. Superior to cellular nanoarchitectures, interpenetrating nanocomposites may combine multiple size-dependent characteristics, whether mechanical or functional, which are radically antagonistic in existing materials. This provides a pathway toward previously unobtainable multifunctionality, extending far beyond lightweight structure applications.