This work describes the performance of the direct carbon fuel cell(DCFC)fuelled by ash-free coal.Employing coal in the DCFC might be problematic,mainly because of the ash deposition after the cell reactions.In the stu...This work describes the performance of the direct carbon fuel cell(DCFC)fuelled by ash-free coal.Employing coal in the DCFC might be problematic,mainly because of the ash deposition after the cell reactions.In the study,the carbonaceous ash-free component of coal is obtained,which is then evaluated as the DCFC fuel and compared with raw coal,active carbon,carbon black,and graphite.The electrolyte-supported SOFC structure is adapted to build the DCFC.The DCFC based on the ash-free coal fuel exhibits good performance with regard to the maximum power density,day-by-day measurements,and durability at continuous run.When the carbon fuels are internally gasified to H2 and CO,the power density is generally much improved,compared to N2 pyrolysis environment.The power generation is most likely related to the concentration of pyrolyzed gases as well as the electrochemical reactivity of the solid carbon.展开更多
Carbon nanotubes （CNTs） supported Pt-Ru and Pt-Ru-Ni catalysts were prepared by chemical reduction of metal precursors with sodium borohydride at room temperature. The crystallographic properties and composition of ...Carbon nanotubes （CNTs） supported Pt-Ru and Pt-Ru-Ni catalysts were prepared by chemical reduction of metal precursors with sodium borohydride at room temperature. The crystallographic properties and composition of the catalysts were characterized by X-ray diffraction （XRD） and energy dispersive X-ray （EDX） analysis, and the catalytic activity and stability for methanol electro-oxidation were measured by electrochemical impedance spectroscopy （EIS）, linear sweep voltammetries （LSV）, and chronoamperometry （CA）. The results show that the catalysts exhibit face-centered cubic （fcc） structure. The particle size of Pt-Ru-Ni/CNTs catalyst is about 4.8 nm. The catalytic activity and stability of the Pt-Ru-Ni/CNTs catalyst are higher than those of Pt-Ru/CNTs catalyst.展开更多
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
In this study, carbon nanotubes （CNTs） were mixed with ABs-type hydrogen storage alloy （HSA）, as catalyst for an anode in a direct borohydride fuel cell （DBFC）. As comparision, a series of traditional carbon mat...In this study, carbon nanotubes （CNTs） were mixed with ABs-type hydrogen storage alloy （HSA）, as catalyst for an anode in a direct borohydride fuel cell （DBFC）. As comparision, a series of traditional carbon materials, such as acetylene black, Vulcan XC-72R, and super activated carbon （SAC） were also employed. Electrochemical measurements showed that the electrocatalytic activity of HSA was improved greatly by CNTs. The current density of the DI3FC employing the HSA/CNTs catalytic anode could reach 1550 mA.cm-2 （at -0.6 V vs the EIg/HgO electrode） and the maximum power density of 65 mW.cm-2 for this cell could be achieved at room temperature. Furthermore, the life time test lasting for 60 h showed that the cell displayed a good stability.展开更多
Ni/Carbon was prepared in two steps： initially cellulose as carbon source and NiCl2·6H2O as catalyst of the carbonization process were submitted to hydrothermal treatment at 200 ℃ and further to thermal treatme...Ni/Carbon was prepared in two steps： initially cellulose as carbon source and NiCl2·6H2O as catalyst of the carbonization process were submitted to hydrothermal treatment at 200 ℃ and further to thermal treatment at 900 ℃ under argon atmosphere. The obtained material contains Ni nanoparticles with face-centered cubic （fcc） structure dispersed on amorphous carbon with graphitic domains. PtRu/C electrocatalysts （carbon- supported PtRu nanoparticles） were prepared by an alcohol-reduction process using Ni/Carbon as support. The materials were characterized by thermogravimetric analysis, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy and tested as anodes in single direct methanol fuel cell （DMFC）. The performances of PtRu/C electrocatalysts using Ni/Carbon as support were superior to those obtained for PtRu/C using commercial carbon black Vulcan XC72 as support.展开更多
Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small...Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 2000 Pt/XC-72R and 5 times better than Hispec 5000 PtRu/XC-72R catalysts.In a full air/hydrogen fuel cell,a membrane-electrode assembly prepared using our Pt/CNT and PtRu/CNT catalysts showed 50% and 100% higher performances than those prepared with commercial Johnson Matthey Pt/XC-72R and PtRu/XC-72R catalysts for the same Pt loading and operating conditions.展开更多
基金supported by the New&Renewable Energy Development Program of the Korea Institute of Energy Technology Evaluation and Planning(KETEP)Grant Funded by the Korean Government’s Ministry of Knowledge Economy(20113020030010)
文摘This work describes the performance of the direct carbon fuel cell(DCFC)fuelled by ash-free coal.Employing coal in the DCFC might be problematic,mainly because of the ash deposition after the cell reactions.In the study,the carbonaceous ash-free component of coal is obtained,which is then evaluated as the DCFC fuel and compared with raw coal,active carbon,carbon black,and graphite.The electrolyte-supported SOFC structure is adapted to build the DCFC.The DCFC based on the ash-free coal fuel exhibits good performance with regard to the maximum power density,day-by-day measurements,and durability at continuous run.When the carbon fuels are internally gasified to H2 and CO,the power density is generally much improved,compared to N2 pyrolysis environment.The power generation is most likely related to the concentration of pyrolyzed gases as well as the electrochemical reactivity of the solid carbon.
基金The project is supported by the National Natural Science Foundation of China (20576023)the Science and Technology Project of Guangzhou City (2005 J1-C0361)the Key Project of Education Bureau of Guangzhou City (2052).
文摘Carbon nanotubes （CNTs） supported Pt-Ru and Pt-Ru-Ni catalysts were prepared by chemical reduction of metal precursors with sodium borohydride at room temperature. The crystallographic properties and composition of the catalysts were characterized by X-ray diffraction （XRD） and energy dispersive X-ray （EDX） analysis, and the catalytic activity and stability for methanol electro-oxidation were measured by electrochemical impedance spectroscopy （EIS）, linear sweep voltammetries （LSV）, and chronoamperometry （CA）. The results show that the catalysts exhibit face-centered cubic （fcc） structure. The particle size of Pt-Ru-Ni/CNTs catalyst is about 4.8 nm. The catalytic activity and stability of the Pt-Ru-Ni/CNTs catalyst are higher than those of Pt-Ru/CNTs catalyst.
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.
文摘In this study, carbon nanotubes （CNTs） were mixed with ABs-type hydrogen storage alloy （HSA）, as catalyst for an anode in a direct borohydride fuel cell （DBFC）. As comparision, a series of traditional carbon materials, such as acetylene black, Vulcan XC-72R, and super activated carbon （SAC） were also employed. Electrochemical measurements showed that the electrocatalytic activity of HSA was improved greatly by CNTs. The current density of the DI3FC employing the HSA/CNTs catalytic anode could reach 1550 mA.cm-2 （at -0.6 V vs the EIg/HgO electrode） and the maximum power density of 65 mW.cm-2 for this cell could be achieved at room temperature. Furthermore, the life time test lasting for 60 h showed that the cell displayed a good stability.
基金support for this work was provided by the National Natural Science Foundation of China （No. 20976044）, the Fundamental Research Funds for the Central Universities （No. WK1013001）, Shanghai Leading Academic Discipline Project （No. B502）.
基金CNP_q,FAPESPFINEP-MCT-ProH_2 for financial support
文摘Ni/Carbon was prepared in two steps： initially cellulose as carbon source and NiCl2·6H2O as catalyst of the carbonization process were submitted to hydrothermal treatment at 200 ℃ and further to thermal treatment at 900 ℃ under argon atmosphere. The obtained material contains Ni nanoparticles with face-centered cubic （fcc） structure dispersed on amorphous carbon with graphitic domains. PtRu/C electrocatalysts （carbon- supported PtRu nanoparticles） were prepared by an alcohol-reduction process using Ni/Carbon as support. The materials were characterized by thermogravimetric analysis, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy and tested as anodes in single direct methanol fuel cell （DMFC）. The performances of PtRu/C electrocatalysts using Ni/Carbon as support were superior to those obtained for PtRu/C using commercial carbon black Vulcan XC72 as support.
基金supported by the National Natural Science Foundation of China (Grant Nos. 20676032,20876062)
文摘Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 2000 Pt/XC-72R and 5 times better than Hispec 5000 PtRu/XC-72R catalysts.In a full air/hydrogen fuel cell,a membrane-electrode assembly prepared using our Pt/CNT and PtRu/CNT catalysts showed 50% and 100% higher performances than those prepared with commercial Johnson Matthey Pt/XC-72R and PtRu/XC-72R catalysts for the same Pt loading and operating conditions.
