RESUMO
Porous, hollow metal carbonate microstructures show many unique properties, and are attractive for various applications. Herein, we report the first demonstration of a general strategy to synthesize hollow metal carbonate structures, including porous MnCO3 hollow cubics, porous CoCO3 hollow rhombuses and porous CaCO3 hollow capsules. For example, the porous, hollow MnCO3 microcubes show larger Brunauer-Emmett-Teller (BET) surface areas of 359.5â m(2) g(-1) , which is much larger than that of solid MnCO3 microcubics (i.e., 12.03â m(2) g(-1) ). As a proof of concept, these porous MnCO3 hollow microcubes were applied to water treatment and exhibited an excellent ability to remove organic pollutants in waste water owing to their hollow structure and large specific surface area.
RESUMO
Ultrathin single-crystalline V2 O5 ·0.76H2 O nanosheets with a thickness of 1.5-2.6 nm are prepared on the basis of molecular-level 'oriented attachment' through special sol-gel chemistry. The initial formation of 3-7 nm nanodiscs by confining the condensation reactions within the ab plane is critical to form nanosheets. As a proof-of-concept, these nanosheets exhibit good properties for hydrogen sensors and supercapacitors.
RESUMO
Double-wall amorphous FePO4 nanotubes are prepared by an oil-phase chemical route. The inward diffusion of vacancies and outward diffusion of ions through passivation layers result in double-wall nanotubes with thin walls. Such a process can be extended to prepare hollow polydedral nanocrystals and hollow ellipsoids. The double-wall FePO4 nanotubes show interesting cathode performance in Li ion batteries.
RESUMO
Electrode materials: Ultrahigh-power insertion-type anodes are developed by simply decorating Pd nanoparticles on commercially available porous carbon.
RESUMO
Graphene quantum dots (GQDs), a novel type of zero-dimensional fluorescent materials, have gained considerable attention owing to their unique optical properties, size and quantum confinement. However, their high cost and low yield remain open challenges for practical applications. In this work, a low cost, green and renewable biomass resource is utilised for the high yield synthesis of GQDs via microwave treatment. The synthesis approach involves oxidative cutting of short range ordered carbon derived from pyrolysis of biomass waste. The GQDs are successfully synthesised with a high yield of over 84%, the highest value reported to date for biomass derived GQDs. As prepared GQDs are highly hydrophilic and exhibit unique excitation independent photoluminescence emission, attributed to their single-emission fluorescence centre. As prepared GQDs are further modified by simple hydrothermal treatment and exhibit pronounced optical properties with a high quantum yield of 0.23. These modified GQDs are used for the highly selective and sensitive sensing of ferric ions (Fe3+). A sensitive sensor is prepared for the selective detection of Fe3+ ions with a detection limit of as low as 2.5 × 10-6 M. The utilisation of renewable resource along with facile microwave treatment paves the way to sustainable, high yield and cost-effective synthesis of GQDs for practical applications.
RESUMO
Vanadium-based materials, such as V2O5, LiV3O8, VO2(B) and Li3V2(PO4)3 are compounds that share the characteristic of intercalation chemistry. Their layered or open frameworks allow facile ion movement through the interspaces, making them promising cathodes for LIB applications. To bypass bottlenecks occurring in the electrochemical performances of vanadium-based cathodes that derive from their intrinsic low electrical conductivity and ion diffusion coefficients, nano-engineering strategies have been implemented to "create" newly emerging properties that are unattainable at the bulk solid level. Integrating this concept into vanadium-based cathodes represents a promising way to circumvent the aforementioned problems as nanostructuring offers potential improvements in electrochemical performances by providing shorter mass transport distances, higher electrode/electrolyte contact interfaces, and better accommodation of strain upon lithium uptake/release. The significance of nanoscopic architectures has been exemplified in the literature, showing that the idea of developing vanadium-based nanostructures is an exciting prospect to be explored. In this review, we will be casting light on the recent advances in the synthesis of nanostructured vanadium-based cathodes. Furthermore, efficient strategies such as hybridization with foreign matrices and elemental doping are introduced as a possible way to boost their electrochemical performances (e.g., rate capability, cycling stability) to a higher level. Finally, some suggestions relating to the perspectives for the future developments of vanadium-based cathodes are made to provide insight into their commercialization.
RESUMO
The feasibility of cyanobacteria removal from freshwater by a dielectric barrier discharge (DBD) process is investigated. Seven commercial and environmental cyanobacteria strains, as well as real algae-laden water, were tested. The removal of the cyanobacteria was evaluated by analyzing the changes in chlorophyll a content, total organic carbon (TOC) concentration, and cell morphology. Nearly total removal of chlorophyll a was achieved within 20 min, while the TOC analysis exhibited an increase-decrease-increase trend in 60 min of treatment, likely due to the oxidation of intracellular and intercellular materials. Observation under light microscopy revealed the disruption of intracellular and intercellular structures within 5 min of DBD treatment and thus supported the TOC analysis. Increasing the salinity of the medium from 0 to 5 parts per thousand (ppt) improved treatment efficiency, where similar level of chlorophyll a removal (around 93%) was achieved in only half the treatment time. Application of DBD on real algae-laden water from a fish farm yielded higher treatment efficiency than in synthetic medium, indicating the promising application of DBD as a means to control cyanobacteria bloom in fresh and estuary water bodies.
Assuntos
Cianobactérias/isolamento & purificação , Microbiologia da Água , Purificação da Água/instrumentação , Clorofila/análogos & derivados , Clorofila A , Estudos de Viabilidade , Água Doce , Salinidade , ÁguaRESUMO
Few-layer V(2)O(5) nanosheets with a thickness of 2.1-3.8 nm have been successfully synthesized in this work via a simple and scalable liquid exfoliation technique. The unique nanostructure allows the high-rate transportation of lithium ions and electrons due to very short diffusion paths provided by this ultrathin thickness, resulting in Li-ion cathodes with remarkable energy and power densities.
RESUMO
Ultrathin 2D nanostructures have shown many unique properties and are attractive for various potential applications. Here, we demonstrated a strategy to synthesize ultrathin VOx nanosheets. The as-obtained ultrathin VOx nanosheets showed a large Brunauer-Emmett-Teller (BET) surface area of 136.3 m2 g(-1), which is much larger than that of 1D multilayer VOx nanotubes. As a proof of concept, these hydrophilic ultrathin nanosheets were applied in water treatment and exhibited excellent absorption capability to remove Rhodamine B (RhB) in wastewater owing to their large specific surface area, good hydrophilic property, and more negative zeta potential. In addition, this method could be generalized to prepare other 2D nanostructures with great potential for various attractive applications.
Assuntos
Nanoestruturas/química , Nanotubos/química , Óxidos/química , Compostos de Vanádio/química , Eliminação de Resíduos Líquidos , Águas Residuárias/química , Interações Hidrofóbicas e Hidrofílicas , Rodaminas/química , Propriedades de Superfície , Poluentes da Água/química , Poluentes da Água/isolamento & purificaçãoRESUMO
Olivine-type LiMPO4 (M = Fe, Mn, Co, Ni) has become of great interest as cathodes for next-generation high-power lithium-ion batteries. Nevertheless, this family of compounds suffers from poor electronic conductivities and sluggish lithium diffusion in the [010] direction. Here, we develop a liquid-phase exfoliation approach combined with a solvothermal lithiation process in high-pressure high-temperature (HPHT) supercritical fluids for the fabrication of ultrathin LiMPO4 nanosheets (thickness: 3.7-4.6 nm) with exposed (010) surface facets. Importantly, the HPHT solvothermal lithiation could produce monodisperse nanosheets while the traditional high-temperature calcination, which is necessary for cathode materials based on high-quality crystals, leads the formation of large grains and aggregation of the nanosheets. The as-synthesized nanosheets have features of high contact area with the electrolyte and fast lithium transport (time diffusion constant in at the microsecond level). The estimated diffusion time for Li(+) to diffuse over a [010]-thickness of <5 nm (L) was calculated to be less than 25, 2.5, and 250 µs for LiFePO4, LiMnPO4, and LiCoPO4 nanosheets, respectively, via the equation of t = L(2)/D. These values are about 5 orders of magnitude lower than the corresponding bulk materials. This results in high energy densities and excellent rate capabilities (e.g., 18 kW kg(-1) and 90 Wh kg(-1) at a 80 C rate for LiFePO4 nanosheets).
RESUMO
The need for large scale energy storage has become a priority to integrate renewable energy sources into the electricity grid. Redox flow batteries are considered the best option to store electricity from medium to large scale applications. However, the current high cost of redox flow batteries impedes the wide spread adoption of this technology. The membrane is a critical component of redox flow batteries as it determines the performance as well as the economic viability of the batteries. The membrane acts as a separator to prevent cross-mixing of the positive and negative electrolytes, while still allowing the transport of ions to complete the circuit during the passage of current. An ideal membrane should have high ionic conductivity, low water intake and excellent chemical and thermal stability as well as good ionic exchange capacity. Developing a low cost, chemically stable membrane for redox flow cell batteries has been a major focus for many groups around the world in recent years. This paper reviews the research work on membranes for redox flow batteries, in particular for the all-vanadium redox flow battery which has received the most attention.
RESUMO
A simple, non-template, non-surfactant and environmentally friendly hydrothermal method is presented based on the controlled release of the reactants into the reaction solvents to induce slow nucleation and growth of three-dimensional hierarchical nanostructures of transition metal oxides. This method is a general approach, which can be used to prepare Co(3)O(4), CuO, and Ni(OH)(2)/NiO. These metal oxides with hierarchical nanostructures can be used as anode materials for lithium-ion batteries with good Li storage performance, e.g. high specific capacities and stable cyclability.
RESUMO
An organic-free sol-gel method was developed to synthesize crack-free, high surface roughness and visible-light-active C-N-codoped TiO(2) films. These films were subsequently evaluated for its photodegradation efficient using stearic acid as the model pollutant compound. The current approach avoids the use of hazardous organic solvents and employs carbon black as the carbon source as well as a template to increase the surface roughness. The presence of carbon and nitrogen species in TiO(2) was studied and discussed. The concentrations of carbon and nitrogen dopants in the TiO(2) films were affected by calcination temperature and the concentration of carbon black. Optimal visible light photocatalytic activity was observed for C-N-codoped TiO(2) film at 10.0 wt.% C, which was more than double that of the N-doped TiO(2) film. The enhancement in visible light photocatalytic activities of the C-N-codoped TiO(2) films was attributed to the synergistic effects of carbon and nitrogen dopants, and high surface roughness of the prepared films.
Assuntos
Poluentes Ambientais/química , Recuperação e Remediação Ambiental/métodos , Fotólise , Titânio/química , Carbono , Catálise , Nitrogênio , Fotoquímica , Ácidos EsteáricosRESUMO
Reduced graphene oxide (rGO) supported highly porous polycrystalline V(2)O(5) spheres (V(2)O(5)/rGO) were prepared by using a solvothermal approach followed by an annealing process. Initially, reduced vanadium oxide (rVO) nanoparticles with sizes in the range of 10-50 nm were formed through heterogeneous nucleation on rGO sheets during the solvothermal process. These rVO nanoparticles were oxidized to V(2)O(5) after the annealing process in air at 350 °C and assembled into polycrystalline porous spheres with sizes of 200-800 nm. The weight ratio between the rGO and V(2)O(5) is tunable by changing the weight ratio of the precursors, which in turn affects the morphology of V(2)O(5)/rGO composites. The V(2)O(5)/rGO composites display superior cathode performances with highly reversible specific capacities, good cycling stabilities and excellent rate capabilities (e.g. 102 mA h g(-1) at 19 C).