In this study, hydrothermal carbonization(HTC)was applied for surface functionalization of carbon nanotubes(CNTs) in the presence of glucose and urea. The HTC process allowed the deposition of thin nitrogen-doped carb...In this study, hydrothermal carbonization(HTC)was applied for surface functionalization of carbon nanotubes(CNTs) in the presence of glucose and urea. The HTC process allowed the deposition of thin nitrogen-doped carbon layers on the surface of the CNTs. By controlling the ratio of glucose to urea, nitrogen contents of up to 1.7 wt%were achieved. The nitrogen-doped carbon nanotube-supported Pd catalysts exhibited superior electrochemical activity for ethanol oxidation relative to the pristine CNTs.Importantly, a 1.5-fold increase in the specific activity was observed for the Pd/HTC-N1.67%CNTs relative to the catalyst without nitrogen doping(Pd/HTC-CNTs). Furtherexperiments indicated that the introduction of nitrogen species on the surface of the CNTs improved the Pd(0)loading and increased the binding energy.展开更多
Three co-impregnation/chemical reduction methods in acidic solutions of pH 〈 1,including ethylene glycol （EG）,NaBH4,and HCOOH,were compared for Pt-WO3/C catalysts.Pt-WO3/C catalysts containing 10 wt.% and 20 wt.% p...Three co-impregnation/chemical reduction methods in acidic solutions of pH 〈 1,including ethylene glycol （EG）,NaBH4,and HCOOH,were compared for Pt-WO3/C catalysts.Pt-WO3/C catalysts containing 10 wt.% and 20 wt.% platinum per carbon were prepared by the three methods; their morphology and electrocatalytic activities were characterized.The 20 wt.% Pt-WO3/C catalyst prepared by the co-impregnation/EG method presented the optimal dispersion with an average particle size of 4.6 nm and subsequently the best electrocatalytic activity,and so,it was further characterized.Its anodic peak current density for ethanol oxidation from linear sweep voltammetry （LSV） is 7.9 mA·cm^-2,which is 1.4 and 5.2 times as high as those of the catalysts prepared by co-impregnation/NaBH4 and co-impregnation/ HCOOH reduction methods,2.1 times as high as that of the 10 wt.% Pt-WO3/C catalyst prepared by co-impregnation/EG method,respectively.展开更多
Metal oxides have a higher chemical stability in comparison to metals,so they can be utilized as electrocatalysts if the activity could be enhanced.Besides the composition,the morphology of the nanostructures has a co...Metal oxides have a higher chemical stability in comparison to metals,so they can be utilized as electrocatalysts if the activity could be enhanced.Besides the composition,the morphology of the nanostructures has a considerable impact on the electrocatalytic activity.In this work,zinc oxide nano branches-attached titanium dioxide nanofibers were investigated as an economic and stable catalyst for ethanol electrooxidation in the alkaline media.The introduced material has been synthesized by electrospinning process followed by hydrothermal technique.Briefly,electrospinning of colloidal solution consisting of titanium isopropoxide,poly（vinyl acetate） and zinc nanoparticles was performed to produce nanofibers embedding solid nanoparticles.In order to produce TiO2nanofibers containing ZnO nanoparticles,the obtained electrospun nanofiber mats were calcined in air at 600 °C.The formed ZnO nanoparticles were exploited as seeds to outgrow ZnO branches around the TiO2nanofibers using the hydrothermal technique at sub-critical water conditions in the presence of zinc nitrate and bis-hexamethylene triamine.The morphology of the final product,as well as the electrochemical measurements indicated that zinc nanoparticles content in the original electrospun nanofibers has a significant influence on the electrocatalytic activity as the best performance was observed with the nanofibers synthesized from electrospun solution containing 0.1 g Zn,and the corresponding current density was 37 mA/cm2.Overall,this study paves a way to titanium dioxide to be exploited to synthesize effective and stable metal oxide-based electrocatalysts.展开更多
基金financial support of the National Natural Science Foundation of China(Nos.51672045 and 11374053)Key Program of Universityindustry Collaboration from Science and Technology Department of Fujian Province(No.2015H6009)
文摘In this study, hydrothermal carbonization(HTC)was applied for surface functionalization of carbon nanotubes(CNTs) in the presence of glucose and urea. The HTC process allowed the deposition of thin nitrogen-doped carbon layers on the surface of the CNTs. By controlling the ratio of glucose to urea, nitrogen contents of up to 1.7 wt%were achieved. The nitrogen-doped carbon nanotube-supported Pd catalysts exhibited superior electrochemical activity for ethanol oxidation relative to the pristine CNTs.Importantly, a 1.5-fold increase in the specific activity was observed for the Pd/HTC-N1.67%CNTs relative to the catalyst without nitrogen doping(Pd/HTC-CNTs). Furtherexperiments indicated that the introduction of nitrogen species on the surface of the CNTs improved the Pd(0)loading and increased the binding energy.
基金supported by the National Basic Research and Development Program of China (No. 2009CB220100)Beijing Excellent Talent Support Program (No. 20071D1600300396)
文摘Three co-impregnation/chemical reduction methods in acidic solutions of pH 〈 1,including ethylene glycol （EG）,NaBH4,and HCOOH,were compared for Pt-WO3/C catalysts.Pt-WO3/C catalysts containing 10 wt.% and 20 wt.% platinum per carbon were prepared by the three methods; their morphology and electrocatalytic activities were characterized.The 20 wt.% Pt-WO3/C catalyst prepared by the co-impregnation/EG method presented the optimal dispersion with an average particle size of 4.6 nm and subsequently the best electrocatalytic activity,and so,it was further characterized.Its anodic peak current density for ethanol oxidation from linear sweep voltammetry （LSV） is 7.9 mA·cm^-2,which is 1.4 and 5.2 times as high as those of the catalysts prepared by co-impregnation/NaBH4 and co-impregnation/ HCOOH reduction methods,2.1 times as high as that of the 10 wt.% Pt-WO3/C catalyst prepared by co-impregnation/EG method,respectively.
基金the Deanship of Scientific Research at King Saud University for funding the work through the research group project No.RGP-089
文摘Metal oxides have a higher chemical stability in comparison to metals,so they can be utilized as electrocatalysts if the activity could be enhanced.Besides the composition,the morphology of the nanostructures has a considerable impact on the electrocatalytic activity.In this work,zinc oxide nano branches-attached titanium dioxide nanofibers were investigated as an economic and stable catalyst for ethanol electrooxidation in the alkaline media.The introduced material has been synthesized by electrospinning process followed by hydrothermal technique.Briefly,electrospinning of colloidal solution consisting of titanium isopropoxide,poly（vinyl acetate） and zinc nanoparticles was performed to produce nanofibers embedding solid nanoparticles.In order to produce TiO2nanofibers containing ZnO nanoparticles,the obtained electrospun nanofiber mats were calcined in air at 600 °C.The formed ZnO nanoparticles were exploited as seeds to outgrow ZnO branches around the TiO2nanofibers using the hydrothermal technique at sub-critical water conditions in the presence of zinc nitrate and bis-hexamethylene triamine.The morphology of the final product,as well as the electrochemical measurements indicated that zinc nanoparticles content in the original electrospun nanofibers has a significant influence on the electrocatalytic activity as the best performance was observed with the nanofibers synthesized from electrospun solution containing 0.1 g Zn,and the corresponding current density was 37 mA/cm2.Overall,this study paves a way to titanium dioxide to be exploited to synthesize effective and stable metal oxide-based electrocatalysts.
