Publications by authors named "Dingsheng Yuan"

A flexible solid rechargeable Zn-air battery for advanced energy conversion and storage has extensive applications in portable electric sources, wildlife rescue and flexible wearable systems. Herein, the CoSe nanoparticles anchored on cobalt-embedded N-doping carbon nanoplates (CoSe/CoNC) is developed as a highly active bifunctional catalyst via pyrolysis and selenization of bimetallic zeolitic imidazolate frameworks containing Zn and Co. The introduction of inactive Zn generates strong electrochemically active surface areas due to the synergistic effect between CoSe2 nanoparticles and CoNC matrix.

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Background: Berberine (BBR) is always used in combination with florfenicol for treating avian in China.

Objective: This study aims to investigate the effects of BBR on the pharmacokinetics of florfenicol in broilers.

Methods: Male broilers were randomly divided into the control group and the BBR group (BG).

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Borneol is a traditional Chinese medicine. In Chinese veterinary clinics, borneol and its related compounds are often used in combination with florfenicol to treat respiratory infections. This study investigated whether the pharmacokinetics of florfenicol in rats was affected by its concomitant use with borneol.

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We propose a synthetic strategy to synthesize cobalt nanoparticle cores encapsulated in tunable N-doped graphene shells on N-doped reduced graphene oxide as a highly efficient and stable pH-universal electrocatalyst. The superior performance is mainly attributed to the optimization of the electrocatalytic centre and the improvement of the electronic configuration.

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The exploration of low-cost and efficient bifunctional electrocatalysts for oxygen evolution reaction and hydrogen evolution reaction through tuning the chemical composition is strongly required for sustainable resources. Herein, we developed a bimetallic cobalt-manganese sulfide supported on Ni foam (CMS/Ni) via a solvothermal method. It has discovered that after combining with the pure CoS and MnS, the morphologies of CMS/Ni have modulated.

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Earth-abundant and efficient bifunctional electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are highly significant for renewable energy systems. However, the performance of existing electrocatalysts is usually restricted by the low electroic conductivity and the limited amount of exposed active sites. In this work, (FeNi)S tubular spheres supported on Ni foam have been prepared by a sulfuration of FeNi layered double hydroxide spheres grown on Ni foam.

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It is essential to synthesize low-cost, earth-abundant bifunctional electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reactions (OER) for water electrolysis. Herein, we present a one-step sulfurization method to fabricate NiS nanowires directly grown on Ni foam (NiS NWs/Ni) as such an electrocatalyst. This synthetic strategy has several advantages including facile preparation, low cost and can even be expanded to large-scale preparation for practical applications.

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Paeoniflorin is the major constituent in extracts of the paeony root, the purpose of the present study was to assess the effects of paeoniflorin on the activities and mRNA expression of the rat hepatic drug-metabolizing enzymes cytochrome P450 (CYP1A2), CYP2C11 and CYP3A1 .Sprague-Dawley (SD) male rats were treated with paeoniflorin at the dosage of 25, 50 and 100 mg/kg or 0.9% sodium chloride solution by intragastric administration for 7 days, then were given probe drugs phenacetin (CYP1A2), tolbutamide (CYP2C11), or midazolam (CYP3A1) orally on the eighth day.

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Many efforts have been devoted to the exploration of non-noble-metal electrocatalysts for the hydrogen evolution reaction (HER) in recent years. Here, we have developed a 3D-MoO microsphere supported MoSe for HER, via a facile hydrothermal approach followed by selenylation treatment. Loosely stacked MoSe layers are formed on the conductive MoO surface, and act as active sites for HER.

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A flexible asymmetric supercapacitor (ASC) based on a CoAl-layered double hydroxide (CoAl-LDH) electrode and a reduced graphene oxide (rGO) electrode was successfully fabricated. The CoAl-LDH electrode as a positive electrode was synthesized by directly growing CoAl-LDH nanosheet arrays on a carbon cloth (CC) through a facile hydrothermal method, and it delivered a specific capacitance of 616.9 F g at a current density of 1 A g.

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The development of metal-free catalysts to replace the use of Pt has played an important role in relation to its application to fuel cells. We report N-doped carbon nanofibers as the catalyst of an oxygen reduction reaction, which were synthesized via carbonizing bacterial cellulose-polypyrrole composites. The as-prepared material exhibited remarkable catalytic activity toward the oxygen reduction reaction with comparable onset potential and the ability to limit the current density of commercial Pt/C catalysts in both alkaline and acid media due to the unique porous three-dimensional network structure and the doped nitrogen atoms.

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We report a new environmentally-friendly synthetic strategy for large-scale preparation of 16 nm-ultrathin NiCo based layered double hydroxides (LDH). The Ni50Co50-LDH electrode exhibited excellent specific capacitance of 1537 F g(-1) at 0.5 A g(-1) and 1181 F g(-1) even at current density as high as 10 A g(-1), which 50% cobalt doped enhances the electrical conductivity and porous and ultrathin structure is helpful with electrolyte diffusion to improve the material utilization.

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This study reports a simple method for the controlled synthesis of uniformly shaped carbon hollow structures by an ethanol-assisted thermolysis of zinc acetate. The experimental evidence reveals that the generated zinc oxide nanostructures act as in-situ templates to form the carbon hollow structures. The morphologies, including the shell thickness, cavity size, and aspect ratio, can be controlled by the reaction time and the heating procedure, and hollow nanospheres, nanocapsules, nanorods, and microtubes can be obtained.

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An environment-friendly hydrothermal method was used to prepare TiO@C core-shell composite using TiO as core and sucrose as carbon source. TiO@C served as a support for the immobilization of Ag by impregnation in silver nitrate aqueous solution. The chemical structures and morphologies of TiO@C and TiO@C/Ag composite were characterized by x-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, energy dispersive x-ray spectroscopy and Brunauer-Emmett-Teller (BET) analysis.

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