3-D vertically aligned few layer graphene – partially reduced graphene oxide/sulfur electrodes for high performance lithium–sulfur batteries
D.P. Singh (TU Delft - RST/Fundamental Aspects of Materials and Energy, University of Twente)
N. Soin (University of Bolton, Ulster University)
S. Basak (TU Delft - QN/Zandbergen Lab)
S. Sachdeva (TU Delft - OLD ChemE/Organic Materials and Interfaces)
S.S. Roy (Shiv Nadar University)
H.W. Zandbergen (TU Delft - QN/Zandbergen Lab)
A. McLaughlin (Ulster University)
M Huijben (University of Twente)
M. Wagemaker (TU Delft - RST/Fundamental Aspects of Materials and Energy)
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Abstract
3-D vertically aligned few-layered graphene (FLGs) nanoflakes synthesised using microwave plasma enhanced chemical vapour deposition are melt-impregnated with partially reduced graphene oxide-sulfur (PrGO-S) nanocomposites for use in lithium–sulfur batteries. The aligned structure and the presence of interconnected micro voids/channels in the 3-D FLG/PrGO-S electrodes serves as template not only for the high sulfur loading (up to 80 wt%, areal loading of 1.2 mg cm−2) but also compensates for the volume changes occurring during charge–discharge cycles. The inter-connectivity of the electrode system further facilitates fast electronic and ionic transport pathways. Consequently, the binder-free 3-D FLG/PrGO-S electrodes display a high first-cycle capacity (1320 mA h g−1 at C/20), along with excellent rate capability of ∼830 mA h g−1 and 700 mA h g−1 at 2C and 5C rates, respectively. The residual functional groups of PrGO (–OH, –C–O–C– and –COOH) facilitate fast and reversible capture of Li+ ions while confining the polysulfide shuttles, thus, contributing to excellent cycling capability and retention capacity. The 3D electrodes demonstrate excellent capacity retention of ∼80% (1040 mA h g−1 at C/10) over 350 charge–discharge cycles. Comparatively, the 2-D planar PrGO-S electrodes displayed poor electronic conductivity and can only provide 560 mA h g−1 after 150 cycles, thereby further highlighting the vital role of the electrode morphology in improving the electrochemical performance of Li–S batteries.
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