Synergistic adsorption and catalytic effects of Ti3C2Tx/CoO/MoO3 composite on lithium polysulfides for high‐performance lithium–sulfur batteries
The shuttle effect of lithium polysulfides (LiPSs) and their sluggish kinetic processes lead to rapid capacity fading and poor cycling stability in lithium–sulfur (Li–S) batteries, limiting their commercial viability. This study proposes a functionalized separator with adsorption and synergistic cat...
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Veröffentlicht in: | Interdisciplinary materials (Print) 2024-09, Vol.3 (5), p.726-737 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The shuttle effect of lithium polysulfides (LiPSs) and their sluggish kinetic processes lead to rapid capacity fading and poor cycling stability in lithium–sulfur (Li–S) batteries, limiting their commercial viability. This study proposes a functionalized separator with adsorption and synergistic catalysis ability for Li–S batteries. The modified separator comprises Ti3C2Tx sheets, CoO, and MoO3. Experimental and theoretical calculations demonstrate that Ti3C2Tx/CoO/MoO3 composite not only effectively inhibits the shuttle effect of LiPSs, ensuring efficient utilization of active materials, but also enhances reversibility and reaction kinetics among LiPSs. The full exposure of active sites in the Ti3C2Tx/CoO/MoO3 composite and the synergistic action of different catalysts enable efficient capture and conversion of LiPSs molecules at the material surface. Besides, the lithium–sulfur batteries with Ti3C2Tx/CoO/MoO3@PP separator exhibited only a 0.042% capacity decay per cycle at 0.5 C (800 cycles). Moreover, a high areal capacity of 6.85 mAh cm−2 was achieved at high sulfur loading (7.9 mg cm−2) and low electrolyte‐to‐sulfur ratio (10 μL mg−1).
The Ti3C2Tx/CoO/MoO3 composite utilizes multilayer Ti3C2Tx as both a substrate to load catalysts and to serve as a physical barrier. Meanwhile, the bimetallic catalysts CoO and MoO3 anchor lithium polysulfides through synergistic effects, facilitating their rapid conversion. |
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ISSN: | 2767-4401 2767-441X |
DOI: | 10.1002/idm2.12178 |