TY - JOUR
T1 - Interconnected core-shell pyrolyzed polyacrylonitrile@sulfur/carbon nanocomposites for rechargeable lithium-sulfur batteries
AU - Chang, Zhi
AU - Dou, Hui
AU - Ding, Bing
AU - Wang, Jie
AU - Wang, Ya
AU - Xu, Guiyin
AU - Li, Cheng
N1 - Funding Information:
This work was supported by the National Basic Research Program of China (973 Program) (No. 2014CB239701), the National Natural Science Foundation of China (No. 21173120 and 51372116), the Natural Science Foundation of Jiangsu Province (BK2011030 and BK20151468) and the Fundamental Research Funds for the Central Universities of NUAA (NP2014403). Z. Chang is grateful to the Foundation of Graduate Innovation Center in NUAA (kfjj20150612).
Publisher Copyright:
© The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2016.
PY - 2016
Y1 - 2016
N2 - Elemental sulfur has attracted great interest for rechargeable batteries because of its high theoretical specific capacity and low cost. However, sulfur electrodes still suffer from rapid capacity fading, which is mainly caused by the undesirable dissolution of polysulfide intermediates and the irreversible deposition of discharge products. In this work, we describe an interconnected core-shell pyrolyzed polyacrylonitrile@carbon/sulfur (pPAN@C/S) nanostructure for high-performance lithium-sulfur batteries. Sulfur was firstly confined in a conductive porous carbon host as C/S to enhance the conductivity of sulfur, constrain polysulfide intermediates and alleviate volume expansion during cycling. Then a conductive pPAN shell was formed by annealing of PAN absorbed on the surface of C/S at 300 °C to further prevent polysulfide intermediates from dissolution by an additional physical and chemical barrier. Meanwhile, the conductive pPAN shell could prevent the irreversible deposition of insoluble discharge products, leading to improved cyclic stability. The interconnected core-shell pPAN@C/S electrodes exhibit a very high initial discharge capacity of 1269 mAh g-1 at 0.5 C and show excellent cycling stability and rate performance.
AB - Elemental sulfur has attracted great interest for rechargeable batteries because of its high theoretical specific capacity and low cost. However, sulfur electrodes still suffer from rapid capacity fading, which is mainly caused by the undesirable dissolution of polysulfide intermediates and the irreversible deposition of discharge products. In this work, we describe an interconnected core-shell pyrolyzed polyacrylonitrile@carbon/sulfur (pPAN@C/S) nanostructure for high-performance lithium-sulfur batteries. Sulfur was firstly confined in a conductive porous carbon host as C/S to enhance the conductivity of sulfur, constrain polysulfide intermediates and alleviate volume expansion during cycling. Then a conductive pPAN shell was formed by annealing of PAN absorbed on the surface of C/S at 300 °C to further prevent polysulfide intermediates from dissolution by an additional physical and chemical barrier. Meanwhile, the conductive pPAN shell could prevent the irreversible deposition of insoluble discharge products, leading to improved cyclic stability. The interconnected core-shell pPAN@C/S electrodes exhibit a very high initial discharge capacity of 1269 mAh g-1 at 0.5 C and show excellent cycling stability and rate performance.
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U2 - 10.1039/c6nj00325g
DO - 10.1039/c6nj00325g
M3 - Article
AN - SCOPUS:84985010341
SN - 1144-0546
VL - 40
SP - 7680
EP - 7686
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 9
ER -