TY - JOUR
T1 - A poly(Ethylene oxide)/lithium bis(trifluoromethanesulfonyl)imide-coated polypropylene membrane for a high-loading lithium–sulfur battery
AU - Chiu, Li Ling
AU - Chung, Sheng Heng
N1 - Funding Information:
Acknowledgments: This research was supported in part by the Higher Education Sprout Project, Ministry of Education to the Headquarters of University Advancement at National Cheng Kung University (NCKU).
Funding Information:
Funding: This research was funded by the Ministry of Education (MOE) in Taiwan under the Yushan Young Scholar Program and the Ministry of Science and Technology (MOST) in Taiwan under grant MOST 109-2636-E-006-026 (Young Scholar Fellowship Program).
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/2
Y1 - 2021/2
N2 - In lithium–sulfur cells, the dissolution and relocation of the liquid-state active material (polysulfides) lead to fast capacity fading and low Coulombic efficiency, resulting in poor long-term electrochemical stability. To solve this problem, we synthesize a composite using a gel polymer electrolyte and a separator as a functional membrane, coated with a layer of poly(ethylene oxide) (PEO) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The PEO/LiTFSI-coated polypro-pylene membrane slows the diffusion of polysulfides and stabilizes the liquid-state active material within the cathode region of the cell, while allowing smooth lithium-ion transfer. The lithium-sulfur cells with the developed membrane demonstrate a high charge-storage capacity of 1212 mA∙h g−1, 981 mA∙h g−1, and 637 mA∙h g−1 at high sulfur loadings of 2 mg cm−2, 4 mg cm−2, and 6 mg cm−2, respectively, and maintains a high reversible capacity of 534 mA∙h g−1 after 200 cycles, proving its ability to block the irreversible diffusion of polysulfides and to maintain the stabilized polysulfides as the catholyte for improved electrochemical utilization and stability. As a comparison, reference and control cells fabricated using a PEO-coated polypropylene membrane and a regular separator, respectively, show a poor capacity of 662 mA∙h g−1 and a short cycle life of 50 cycles.
AB - In lithium–sulfur cells, the dissolution and relocation of the liquid-state active material (polysulfides) lead to fast capacity fading and low Coulombic efficiency, resulting in poor long-term electrochemical stability. To solve this problem, we synthesize a composite using a gel polymer electrolyte and a separator as a functional membrane, coated with a layer of poly(ethylene oxide) (PEO) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The PEO/LiTFSI-coated polypro-pylene membrane slows the diffusion of polysulfides and stabilizes the liquid-state active material within the cathode region of the cell, while allowing smooth lithium-ion transfer. The lithium-sulfur cells with the developed membrane demonstrate a high charge-storage capacity of 1212 mA∙h g−1, 981 mA∙h g−1, and 637 mA∙h g−1 at high sulfur loadings of 2 mg cm−2, 4 mg cm−2, and 6 mg cm−2, respectively, and maintains a high reversible capacity of 534 mA∙h g−1 after 200 cycles, proving its ability to block the irreversible diffusion of polysulfides and to maintain the stabilized polysulfides as the catholyte for improved electrochemical utilization and stability. As a comparison, reference and control cells fabricated using a PEO-coated polypropylene membrane and a regular separator, respectively, show a poor capacity of 662 mA∙h g−1 and a short cycle life of 50 cycles.
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U2 - 10.3390/polym13040535
DO - 10.3390/polym13040535
M3 - Article
AN - SCOPUS:85101261913
SN - 2073-4360
VL - 13
SP - 1
EP - 10
JO - Polymers
JF - Polymers
IS - 4
M1 - 535
ER -