One-pot approach to synthesize PPy@S core–shell nanocomposite cathode for Li/S batteries
Creators
- 1. University of Waterloo, Department of Chemical Engineering (Canada)
Description
A polypyrrole-coated sulfur composite (PPy@S) was synthesized by in situ polymerization of pyrrole monomers on the surface of nano-sulfur particles. High resolution transmission electron microscopy and energy dispersive spectroscopy mapping showed the formation of a highly developed core–shell structure with uniform PPy coating on the surface of sulfur particles. The electrochemical properties of the resulting PPy@S composite cathode have been evaluated by cyclic voltammograms and galvanostatic discharge–charge cycling. The results show that the PPy@S composite exhibits a reversible capacity of 1,200 mAh g−1 at the initial cycle, with 913 mAh g−1 remaining after 50 cycles. Even up to 2.5 C, a reversible capacity of 437 mAh g−1 is obtained. The excellent electrochemical performance can be attributed to the conductive PPy-coating nanolayer, which provides both an effective electron conduction path and a strong physical and chemical confinement setting for elemental sulfur and resident polysulfides, minimizing the loss of active material during cycling
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Nanoparticle Research
- Journal Volume
- 15
- Journal Issue
- 10
- Journal Page Range
- p. 1-7
- ISSN
- 1388-0764
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45028067
- Subject category
- S36: MATERIALS SCIENCE; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- CATHODES; MONOMERS; NANOSTRUCTURES; POLYMERIZATION; PYRROLES; SULFUR; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- AZOLES; CHEMICAL REACTIONS; ELECTRODES; ELECTRON MICROSCOPY; ELEMENTS; HETEROCYCLIC COMPOUNDS; MICROSCOPY; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2013 Springer Science+Business Media Dordrecht