Fabrication of novel electrode materials with ordered proton-migration channels is an effective strategy to enhance the proton conductivity of the electrode for polymer electrolyte membrane fuel cells. Here we report ...Fabrication of novel electrode materials with ordered proton-migration channels is an effective strategy to enhance the proton conductivity of the electrode for polymer electrolyte membrane fuel cells. Here we report the electrochemical fabrication of ordered Nafion?ionomers decorated polypyrrole nanowires to construct the ordered proton-migration channels. Based on the electrostatic interaction between Nafion?ionomers and the polymer intermediate, ordered Nafion?ionomers decorated polypyrrole nanowires could be fabricated via chronoamperometry with varying contents of Nafionionomers. The morphologies, charge-storage performances, electron conductivity and proton conductivity of the composites are investigated by scanning electron microscopy, cyclic-voltammetry, galvanostatic charge–discharge measurement and electrochemical impedance spectroscopy. With the modification effect of Nafionionomers on polypyrrole nanowires, the composite shows greater ordered structure relative to another without Nafion?ionomers and the electrochemical performances change with the content of Nafion?ionomers.The composite could achieve a high specific capacitance of 356 F/g at 1 A/g with a 0.62-fold enhancement compared to polypyrrole nanowires without Nafion?ionomers. It also displays a superior electrical conductivity of 49 S/cm and a quite high proton conductivity of 0.014 S/cm at working conditions of fuel cells, which are associated with the requirements of fuel cells and have the potential to be the electrode material for a large range of electrochemical energy conversion devices.展开更多
High-performance dielectric polymer composites have received increasing attention due to their important applications in the field of energy storage.The rational structural design of hybrid fillers can lead to a balan...High-performance dielectric polymer composites have received increasing attention due to their important applications in the field of energy storage.The rational structural design of hybrid fillers can lead to a balance between high dielectric constant and insulation in composites.In this work,novel hybrid fillers were fabricated by in situ synthesizing one-dimensional polypyrrole nanowires(PPynws)on the twodimensional molybdenum disulfide(MoS_(2)),which integrated the good ion polarization ability of PPynws and the high insulation and adjustable band gap of MoS_(2).Compared with the binary poly(vinylidene fluoride)(PVDF)/MoS_(2) composites,the PVDF/MoS_(2)-PPynws composites exhibited remarkably improved dielectric constant and breakdown strength,while the dielectric loss was still maintained at a low level.An optimal ternary composite with 1 wt%MoS_(2)-PPynws showed a high dielectric constant(15@1kHz),suppressed dielectric loss(0.027@1kHz),and high breakdown strength(422.1 MV/m).PPynws inducing strong interfacial polarization and the highly insulated MoS_(2) nanosheets extending the breakdown path mainly contributed to the synchronously enhanced dielectric constant and breakdown strength.This intriguing synthesis method of PVDF/MoS_(2)-PPynws nanocomposite will open up new opportunities for fabricating nanostructured polymer composites to produce high dielectric materials.展开更多
基金financially supported by the National Natural Science Foundation of China(No.21503228,No.21506209)
文摘Fabrication of novel electrode materials with ordered proton-migration channels is an effective strategy to enhance the proton conductivity of the electrode for polymer electrolyte membrane fuel cells. Here we report the electrochemical fabrication of ordered Nafion?ionomers decorated polypyrrole nanowires to construct the ordered proton-migration channels. Based on the electrostatic interaction between Nafion?ionomers and the polymer intermediate, ordered Nafion?ionomers decorated polypyrrole nanowires could be fabricated via chronoamperometry with varying contents of Nafionionomers. The morphologies, charge-storage performances, electron conductivity and proton conductivity of the composites are investigated by scanning electron microscopy, cyclic-voltammetry, galvanostatic charge–discharge measurement and electrochemical impedance spectroscopy. With the modification effect of Nafionionomers on polypyrrole nanowires, the composite shows greater ordered structure relative to another without Nafion?ionomers and the electrochemical performances change with the content of Nafion?ionomers.The composite could achieve a high specific capacitance of 356 F/g at 1 A/g with a 0.62-fold enhancement compared to polypyrrole nanowires without Nafion?ionomers. It also displays a superior electrical conductivity of 49 S/cm and a quite high proton conductivity of 0.014 S/cm at working conditions of fuel cells, which are associated with the requirements of fuel cells and have the potential to be the electrode material for a large range of electrochemical energy conversion devices.
基金financially supported by the National Natural Science Foundation of China (No. 51673159)the Youth Science and Technology Innovation Team of Sichuan Province of Functional Polymer Composites (No. 2021JDTD0009)supported by the Analytical and Testing Center of Southwest Jiaotong University
文摘High-performance dielectric polymer composites have received increasing attention due to their important applications in the field of energy storage.The rational structural design of hybrid fillers can lead to a balance between high dielectric constant and insulation in composites.In this work,novel hybrid fillers were fabricated by in situ synthesizing one-dimensional polypyrrole nanowires(PPynws)on the twodimensional molybdenum disulfide(MoS_(2)),which integrated the good ion polarization ability of PPynws and the high insulation and adjustable band gap of MoS_(2).Compared with the binary poly(vinylidene fluoride)(PVDF)/MoS_(2) composites,the PVDF/MoS_(2)-PPynws composites exhibited remarkably improved dielectric constant and breakdown strength,while the dielectric loss was still maintained at a low level.An optimal ternary composite with 1 wt%MoS_(2)-PPynws showed a high dielectric constant(15@1kHz),suppressed dielectric loss(0.027@1kHz),and high breakdown strength(422.1 MV/m).PPynws inducing strong interfacial polarization and the highly insulated MoS_(2) nanosheets extending the breakdown path mainly contributed to the synchronously enhanced dielectric constant and breakdown strength.This intriguing synthesis method of PVDF/MoS_(2)-PPynws nanocomposite will open up new opportunities for fabricating nanostructured polymer composites to produce high dielectric materials.