In the present study,the electrophoretic deposition method was successfully applied as a binder-free and scalable approach to deposit carbonaceous nanomaterials on carbon fiber paper(CFP)for cathode applications in Li...In the present study,the electrophoretic deposition method was successfully applied as a binder-free and scalable approach to deposit carbonaceous nanomaterials on carbon fiber paper(CFP)for cathode applications in Li-S batteries.The microstructural studies of the EPD-CNT film using scanning electron microscopy(SEM)revealed the formation of a crack-free and porous layer of CNTs being uniformly distributed on the CFP surface.The EPD:CFP/CNT/S cathode delivered a capacity around 2.2 times higher than that obtained in the absence of the EPD-CNT film(CFP/S cell)after 50 cycles and a capacity of935 mAh g^-1 after 100 cycles at 0.1 C.The EPD method was then employed to fabricate layer-by-layer structures where the EPD-CNT film was decorated with carbon black particles.The initial capacity as well as the reversible capacity after 100 cycles was further increased by the EPD:CFP/CNT/KB/S layer-by-layer structure to 1473 and 1033 mAh g^-1,respectively,indicating effective suppression of the shuttle effect.In addition,the rate performance of CFP/S was improved by depositing the EPD-CNT and EPD-CNT/carbon black architectures on CFP surface,and even further enhanced through the co-deposition of CNT and Pt nanoparticles by EPD,delivering a specific capacity of around 730 mAh g^-1 at 1 C.Finally,the cathodes fabricated by EPD were observed to outperform those made by the conventional casting method in terms of cycling performance,internal resistance,and polarization.This difference was ascribed to the non-uniform microstructure of the Cast-CNT film,which resulted in poor interfacial connection between the CNT agglomerates,hindering uniform sulfide/sulfur deposition during cycling.The obtained results suggested that the binder-free C/S nanocomposite cathode made by EPD is key to further enhance the specific capacity and energy density of Li-S batteries.展开更多
基金financially supported by the City University of Hong Kong through the SRG projects#7004545support from the Research G rants Council(RGC)of Hong Kongthe Hong Kong Ph D Fellowship Scheme(HKPFS)。
文摘In the present study,the electrophoretic deposition method was successfully applied as a binder-free and scalable approach to deposit carbonaceous nanomaterials on carbon fiber paper(CFP)for cathode applications in Li-S batteries.The microstructural studies of the EPD-CNT film using scanning electron microscopy(SEM)revealed the formation of a crack-free and porous layer of CNTs being uniformly distributed on the CFP surface.The EPD:CFP/CNT/S cathode delivered a capacity around 2.2 times higher than that obtained in the absence of the EPD-CNT film(CFP/S cell)after 50 cycles and a capacity of935 mAh g^-1 after 100 cycles at 0.1 C.The EPD method was then employed to fabricate layer-by-layer structures where the EPD-CNT film was decorated with carbon black particles.The initial capacity as well as the reversible capacity after 100 cycles was further increased by the EPD:CFP/CNT/KB/S layer-by-layer structure to 1473 and 1033 mAh g^-1,respectively,indicating effective suppression of the shuttle effect.In addition,the rate performance of CFP/S was improved by depositing the EPD-CNT and EPD-CNT/carbon black architectures on CFP surface,and even further enhanced through the co-deposition of CNT and Pt nanoparticles by EPD,delivering a specific capacity of around 730 mAh g^-1 at 1 C.Finally,the cathodes fabricated by EPD were observed to outperform those made by the conventional casting method in terms of cycling performance,internal resistance,and polarization.This difference was ascribed to the non-uniform microstructure of the Cast-CNT film,which resulted in poor interfacial connection between the CNT agglomerates,hindering uniform sulfide/sulfur deposition during cycling.The obtained results suggested that the binder-free C/S nanocomposite cathode made by EPD is key to further enhance the specific capacity and energy density of Li-S batteries.