17 research outputs found

    Studies on Feeding Value for Five Psammophyte Shrubs in Ningxia Region

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    A trial was conducted on five psammophyte shrubs -Caragana intermedia, C. korshinskii, Hedysarum scoparium, H. laeve, Salix psammophylla in the post-fruit period in Ningxia, China. Chemical composition, palatability and in vitro digestibility were studied systematically. The feeding value was evaluated through Fuzzy multifactorial model. According to chemical composition, palatability and in vitro digestibility, C. intermedia, had the highest feeding value and C .korshinskii the lowest

    Uniform yolk-shell iron sulfide-carbon nanospheres for superior sodium-iron sulfide batteries

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    Sodium-metal sulfide battery holds great promise for sustainable and cost-effective applications. Nevertheless, achieving high capacity and cycling stability remains a great challenge. Here, uniform yolk-shell iron sulfide-carbon nanospheres have been synthesized as cathode materials for the emerging sodium sulfide battery to achieve remarkable capacity of ∼545 mA h g-1 over 100 cycles at 0.2 C (100 mA g-1), delivering ultrahigh energy density of ∼438 Wh kg-1. The proven conversion reaction between sodium and iron sulfide results in high capacity but severe volume changes. Nanostructural design, including of nanosized iron sulfide yolks (∼170 nm) with porous carbon shells (∼30 nm) and extra void space (∼20 nm) in between, has been used to achieve excellent cycling performance without sacrificing capacity. This sustainable sodium-iron sulfide battery is a promising candidate for stationary energy storage. Furthermore, this spatially confined sulfuration strategy offers a general method for other yolk-shell metal sulfide-carbon composites

    Yolk-shell silicon-mesoporous carbon anode with compact solid electrolyte interphase film for superior lithium-ion batteries

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    Silicon as an electrode suffers from short cycling life, as well as unsatisfactory rate-capability caused by the large volume expansion (~400%) and the consequent structural degradation during lithiation/delithiation processes. Here, we have engineered unique void-containing mesoporous carbon-encapsulated commercial silicon nanoparticles (NPs) in yolk-shell structures. In this design, the silicon NPs yolk are wrapped into open and accessible mesoporous carbon shells, the void space between yolk and shell provides enough room for Si expansion, meanwhile, the porosity of carbon shell enables fast transport of Li+ ions between electrolyte and silicon. Our ex-situ characterization clearly reveals for the first time that a favorable homogeneous and compact solid electrolyte interphase (SEI) film is formed along the mesoporous carbon shells. As a result, such yolk-shell Si@mesoporous-carbon nanoparticles with a large void exhibits long cycling stability (78.6% capacity retention as long as 400 cycles), and superior rate-capability (62.3% capacity retention at a very high current density of 8.4Ag-1)

    Monodisperse core-shell structured magnetic mesoporous aluminosilicate nanospheres with large dendritic mesochannels

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    The rational design and precise synthesis of multifunctional hybrid nanostructures with a tailored active core and a large, dendritic, modified mesoporous structured shell can promote catalysis, energy storage, and biological applications. Here, an oil-water biphase stratification coating strategy has been developed to prepare monodisperse magnetic dendritic mesoporous silica core-shell structured nanospheres. These sophisticated Fe3O4@SiO2@dendritic-mSiO2 nanospheres feature large dendritic open pores (2.7 and 10.3 nm). Significantly, the silica shells can be converted into dendritic mesoporous aluminosilicate frameworks with unchanged porosity, a Si/Al molar ratio of 14, and remarkably strong acidic sites, through a post-synthesis approach. In addition, the resultant magnetic dendritic mesoporous aluminosilicate nanospheres exhibit outstanding properties and promising application in phosphate removal from wastewater

    TiO2 interpenetrating networks decorated with SnO2 nanocrystals: Enhanced activity of selective catalytic reduction of NO with NH3

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    Highly branched TiO2 interpenetrating network architectures decorated with SnO2 nanocrystals were fabricated through a sacrificial-template approach for selective catalytic reduction of NO with ammonia. Such unique architectures demonstrate outstanding catalytic activity for NO conversion (approx. 90%), high N2 selectivity (approx. 100%), good stability and strong resistance to SO2 and H2O poisoning over a broad temperature range (75-325 °C)
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