The preparation of Zn Se/Cd Se core-shell structure nanocomposites by using the re-prepared Zn Se microspheres as the template under the hydrothermal condition was presented. The influence of different mole ratios of ...The preparation of Zn Se/Cd Se core-shell structure nanocomposites by using the re-prepared Zn Se microspheres as the template under the hydrothermal condition was presented. The influence of different mole ratios of ZnS e to Cd（NO3）2 on the morphology and structure of the final product was investigated. And the performances of ZnS e/Cd Se core-shell structure nanocomposites were characterized by the means of X-ray diffraction（XRD） analyses, scanning electron microscopy（SEM）, transmission electron microscopy（TEM） and photoluminescence（PL） spectroscopy. The results indicate that the core-shell structure product can be prepared, when the mole ratio of Zn Se to Cd（NO3）2 is larger than 1：1; and the product will be ball solid structure, when the mole ratio of Zn Se to Cd（NO3）2 is equal to 1：1. The photo luminescence results show that Zn Se/Cd Se core-shell structures have high photo luminescence emission properties, and the product with mole ratio of Zn Se to Cd（NO3）2 being 1：0.5 has the best luminescence properties.展开更多
The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The ef...The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The effects of solution pH,initial concentration of Pb2+ions,contact time,and temperature on the amount of Pb2+adsorbed were investigated.Adsorption isotherms,adsorption kinetics,and thermodynamic analysis were also studied.The results showed that the maximum adsorption capacity of the Fe3O4@SiO2@DMSA composite is 50.5 mg/g at 298 K,which is higher than that of Fe3O4 and Fe3O4@SiO2 magnetic nanoparticles.The adsorption process agreed well with Langmuir adsorption isotherm models and pseudo second-order kinetics.The thermodynamic analysis revealed that the adsorption was spontaneous,endothermic and energetically driven in nature.展开更多
The performance of fuel-cell related electrocatalysis is highly dependent on the morphology,size and composition of a given catalyst.In terms of rational design of Pt-based catalyst,one-dimensional(1 D)ultrafine Pt al...The performance of fuel-cell related electrocatalysis is highly dependent on the morphology,size and composition of a given catalyst.In terms of rational design of Pt-based catalyst,one-dimensional(1 D)ultrafine Pt alloy nanowires(NWs)are considered as a commendable model for enhanced catalysis on account of their favorable mass/charge transfer and structural durability.However,in order to achieve the noble metal catalysts in higher efficiency and lower cost,building high-index facets and shaping hollow interiors should be integrated into 1 D Pt alloy NWs,which has rarely been done so far.Here,we report the first synthesis of a class of spiny Pd/PtFe core/shell nanotubes(SPCNTs)constructed by cultivating PtFe alloy branches with rich high-index facets along the 1 D removable Pd supports,which is driven by the galvanic dissolution of Pd substrates concomitant with Stranski-Krastanov(S-K)growth of Pt and Fe,for achieving highly efficient fuel-cells-related electrocatalysis.This new catalyst can even deliver electrochemical active surface area(ECSA)of 62.7 m^(2)gPt^(-1),comparable to that of commercial carbonsupported Pt nanoparticles.With respect to oxygen reduction catalysis,the SPCNTs showcase the remarkable mass and specific activity of 2.71 A mg^(-1)and 4.32 mA cm^(-2),15.9 and 16.0 times higher than those of commercial Pt/C,respectively.Also,the catalysts exhibit extraordinary resistance to the activity decay and structural degradation during 50,000 potential cycles.Moreover,the SPCNTs serve as a category of efficient and stable catalysts towards anodic alcohol oxidation.展开更多
基金Project(13JJ1005)supported by the Natural Science Foundation for Distinguished Young Scholars of Hunan Province,China
文摘The preparation of Zn Se/Cd Se core-shell structure nanocomposites by using the re-prepared Zn Se microspheres as the template under the hydrothermal condition was presented. The influence of different mole ratios of ZnS e to Cd（NO3）2 on the morphology and structure of the final product was investigated. And the performances of ZnS e/Cd Se core-shell structure nanocomposites were characterized by the means of X-ray diffraction（XRD） analyses, scanning electron microscopy（SEM）, transmission electron microscopy（TEM） and photoluminescence（PL） spectroscopy. The results indicate that the core-shell structure product can be prepared, when the mole ratio of Zn Se to Cd（NO3）2 is larger than 1：1; and the product will be ball solid structure, when the mole ratio of Zn Se to Cd（NO3）2 is equal to 1：1. The photo luminescence results show that Zn Se/Cd Se core-shell structures have high photo luminescence emission properties, and the product with mole ratio of Zn Se to Cd（NO3）2 being 1：0.5 has the best luminescence properties.
基金Project(2013DFA51290)supported by International S&T Cooperation Program of China
文摘The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The effects of solution pH,initial concentration of Pb2+ions,contact time,and temperature on the amount of Pb2+adsorbed were investigated.Adsorption isotherms,adsorption kinetics,and thermodynamic analysis were also studied.The results showed that the maximum adsorption capacity of the Fe3O4@SiO2@DMSA composite is 50.5 mg/g at 298 K,which is higher than that of Fe3O4 and Fe3O4@SiO2 magnetic nanoparticles.The adsorption process agreed well with Langmuir adsorption isotherm models and pseudo second-order kinetics.The thermodynamic analysis revealed that the adsorption was spontaneous,endothermic and energetically driven in nature.
基金the Xplorer Prize,the Beijing Natural Science Foundation(JQ18005,Z190010)the National Natural Science Foundation of China(NSFC)(51671003,and 21771156)+3 种基金National R&D Program of China(2017YFA0206701)the China Postdoctoral Science Foundation(2019M660290)the state Key Laboratory of Solidification Processing in NPU(SKLSP202004)the Start-up supports from Peking University and Young Thousand Talented Program.
文摘The performance of fuel-cell related electrocatalysis is highly dependent on the morphology,size and composition of a given catalyst.In terms of rational design of Pt-based catalyst,one-dimensional(1 D)ultrafine Pt alloy nanowires(NWs)are considered as a commendable model for enhanced catalysis on account of their favorable mass/charge transfer and structural durability.However,in order to achieve the noble metal catalysts in higher efficiency and lower cost,building high-index facets and shaping hollow interiors should be integrated into 1 D Pt alloy NWs,which has rarely been done so far.Here,we report the first synthesis of a class of spiny Pd/PtFe core/shell nanotubes(SPCNTs)constructed by cultivating PtFe alloy branches with rich high-index facets along the 1 D removable Pd supports,which is driven by the galvanic dissolution of Pd substrates concomitant with Stranski-Krastanov(S-K)growth of Pt and Fe,for achieving highly efficient fuel-cells-related electrocatalysis.This new catalyst can even deliver electrochemical active surface area(ECSA)of 62.7 m^(2)gPt^(-1),comparable to that of commercial carbonsupported Pt nanoparticles.With respect to oxygen reduction catalysis,the SPCNTs showcase the remarkable mass and specific activity of 2.71 A mg^(-1)and 4.32 mA cm^(-2),15.9 and 16.0 times higher than those of commercial Pt/C,respectively.Also,the catalysts exhibit extraordinary resistance to the activity decay and structural degradation during 50,000 potential cycles.Moreover,the SPCNTs serve as a category of efficient and stable catalysts towards anodic alcohol oxidation.
