TY - JOUR
T1 - Sulfur/polythiophene with a core/shell structure
T2 - Synthesis and electrochemical properties of the cathode for rechargeable lithium batteries
AU - Wu, Feng
AU - Chen, Junzheng
AU - Chen, Renjie
AU - Wu, Shengxian
AU - Li, Li
AU - Chen, Shi
AU - Zhao, Teng
PY - 2011/4/7
Y1 - 2011/4/7
N2 - Novel sulfur/polythiophene composites with core/shell structure composites were synthesized via an in situ chemical oxidative polymerization method with chloroform as a solvent, thiophene as a reagent, and iron chloride as an oxidant at 0 °C. Different ratios of the sulfur/polythiophene composites were characterized by elemental analysis, FTIR, XRD, SEM, TEM, and electrochemical methods. A suitable ratio for the composites was found to be 71.9% sulfur and 18.1% polythiophene as determined by CV and EIS results. Conductive polythiophene acts as a conducting additive and a porous adsorbing agent. It was uniformly coated onto the surface of the sulfur powder to form a core/shell structure, which effectively enhances the electrochemical performance and cycle life of the sulfur cells. The initial discharge capacity of the active material was 1119.3 mA h g-1, sulfur and the remaining capacity was 830.2 mA h g-1 sulfur after 80 cycles. After a rate test from 100 to 1600 mA g-1 sulfur, the cell remained at 811 mA h g-1 sulfur after 60 cycles when the current density returned to 100 mA g-1 sulfur. The sulfur utilization, the cycle life, and the rate performance of the S-PTh core/shell electrode in a lithium-sulfur battery improved significantly compared to that of the pure sulfur electrode. The pore and thickness of the shell affected the battery performance of the lithium ion diffusion channels.
AB - Novel sulfur/polythiophene composites with core/shell structure composites were synthesized via an in situ chemical oxidative polymerization method with chloroform as a solvent, thiophene as a reagent, and iron chloride as an oxidant at 0 °C. Different ratios of the sulfur/polythiophene composites were characterized by elemental analysis, FTIR, XRD, SEM, TEM, and electrochemical methods. A suitable ratio for the composites was found to be 71.9% sulfur and 18.1% polythiophene as determined by CV and EIS results. Conductive polythiophene acts as a conducting additive and a porous adsorbing agent. It was uniformly coated onto the surface of the sulfur powder to form a core/shell structure, which effectively enhances the electrochemical performance and cycle life of the sulfur cells. The initial discharge capacity of the active material was 1119.3 mA h g-1, sulfur and the remaining capacity was 830.2 mA h g-1 sulfur after 80 cycles. After a rate test from 100 to 1600 mA g-1 sulfur, the cell remained at 811 mA h g-1 sulfur after 60 cycles when the current density returned to 100 mA g-1 sulfur. The sulfur utilization, the cycle life, and the rate performance of the S-PTh core/shell electrode in a lithium-sulfur battery improved significantly compared to that of the pure sulfur electrode. The pore and thickness of the shell affected the battery performance of the lithium ion diffusion channels.
UR - http://www.scopus.com/inward/record.url?scp=79953729662&partnerID=8YFLogxK
U2 - 10.1021/jp1114724
DO - 10.1021/jp1114724
M3 - Article
AN - SCOPUS:79953729662
SN - 1932-7447
VL - 115
SP - 6057
EP - 6063
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 13
ER -