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Ni foam and carbon fiber cloth were tested as three-dimensional (3D) current collectors for a sulfur/polypyrrole composite cathode in lithium batteries. The cell with the carbon fiber current collector has exhibited remarkably enhanced electrochemical performance compared with its Ni foam counterpart, delivering a high initial capacity of 1,278 mAh g?1 and maintaining a discharge capacity at 810 mAh g?1 after 40 cycles at 0.06 C. Furthermore, the carbon fiber-based cell demonstrated a better rate capability and delivered a highly reversible discharge capacity of 397 mAh g?1 after 50 cycles at 0.5 C, representing an increase of 194 mAh g?1 compared to the Ni foam counterpart. The electrochemical property investigations along with scanning electron microscope studies have revealed that the carbon fiber current collector possesses a three-dimensional network structure, provides an effective electron conduction path, and minimizes the loss of electrical contact within the deposited cathode material during cycling. These results indicate that the carbon fiber cloth can be used as a promising, effective, and inexpensive current collector for Li/S batteries.  相似文献   
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Journal of Nanoparticle Research - Graphene and graphene oxide are potential candidates as nanofluids for thermal management applications. Here, we investigate the rheological properties and...  相似文献   
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Sulfur/dehydrogenated polyacrylonitrile composite has been studied as cathode material for lithium–sulfur rechargeable batteries. Nonetheless, capacity fading has been a challenge for the commercialization of batteries. In this study, characterization techniques of scanning electron microscopy, energy dispersive X-ray spectroscopy, elemental analysis, cyclic voltammetry, and electrochemical impedance spectroscopy are used to investigate the change of cathode properties with charge–discharge cycles. Elemental analysis reveals that sulfur accumulates on the surface of the composite at the end of charge, and the sulfur formation decreases with cycle number. Scanning electron microscopy observations indicate that cathode surface morphology changes significantly after several cycles. By modeling the electrochemical impedance spectra of the cell in different discharge states, we suggest that capacity fading arises mainly from the formation and accumulation of irreversible Li2S (and Li2S2) on the cathode surface.  相似文献   
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