Application of Y-MOF-CNT-Derived Y 2 O 3 -C@CNT Composites in Lithium-Sulfur Battery Separators
In order to mitigate the shuttle effect of lithium polysulfides in lithium-sulfur batteries, we propose a yttrium-metal-organic framework-carbon nanotube (Y-MOF-CNT)-derived Y O -C@CNT composite for modifying the separator in this study. The Y-MOFs, comprising yttrium (Y) rare earth metal and tereph...
Gespeichert in:
Veröffentlicht in: | Langmuir 2024-11, Vol.40 (44), p.23529-23537 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | In order to mitigate the shuttle effect of lithium polysulfides in lithium-sulfur batteries, we propose a yttrium-metal-organic framework-carbon nanotube (Y-MOF-CNT)-derived Y
O
-C@CNT composite for modifying the separator in this study. The Y-MOFs, comprising yttrium (Y) rare earth metal and terephthalic acid, exemplify a prototypical category of metal-organic framework (MOF) materials. They manifest the advantageous attributes associated with MOFs while concurrently possessing distinctive catalytic traits ascribed to rare earth elements. In this study, Y-MOF nanoparticles were synthesized on carbon nanotube (CNT) substrates via a facile aqueous solution method, succeeded by high-temperature carbonization to yield Y
O
-C@CNT composite materials. These composites were subsequently employed as coatings on one side of polyethylene (PE) separators. The resultant Y
O
-C@CNT composite inherits the particle-like morphology and porosity from its precursor Y-MOF, alongside the inherent conductivity in carbon-based materials. This amalgamation is conducive to polysulfide capture and catalytic conversion processes within lithium-sulfur batteries. The application of the Y
O
-C@CNT-coated PE separator effectively mitigated polysulfide shuttle effects and significantly enhanced the battery electrochemical performance. At a sulfur loading level of 3 mg cm
under a 0.5 C rate, an initial discharge specific capacity of 900 mAh g
was achieved. After 400 cycles, the discharge specific capacity remained at 483.85 mAh g
with a capacity retention rate of 53.7%. Upon increasing sulfur loading to 5 mg cm
, the discharge specific capacity at a lower rate (0.1 C) reached 817.8 mAh g
; even after 100 cycles, it maintained a value of 700 mAh g
with a capacity retention rate of 85.6%. Notably, our modified Y
O
-C@CNT separator demonstrated exceptional cycling stability, even under conditions involving high sulfur loading. |
---|---|
ISSN: | 0743-7463 1520-5827 |
DOI: | 10.1021/acs.langmuir.4c03408 |