Superparamagnetic Fe Conversion Induces MoS 2 Fast Ion Transport in Wide‐Temperature‐Range Sodium‐Ion Batteries

MoS 2 is widely reported as anode material for sodium‐ion batteries (SIBs). However, its ability to operate effectively across a wide temperature range and at high rates continues to pose fundamental challenges, limiting its further development. Herein, a monolayer Fe‐doped MoS 2 /N,O‐codoped C over...

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Veröffentlicht in:Advanced functional materials 2024-10, Vol.34 (41)
Hauptverfasser: Li, Zhenwei, Han, Meisheng, Wang, Jianlin, Zhang, Leqing, Yu, Peilun, Li, Qiang, Bai, Xuedong, Yu, Jie
Format: Artikel
Sprache:eng
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Zusammenfassung:MoS 2 is widely reported as anode material for sodium‐ion batteries (SIBs). However, its ability to operate effectively across a wide temperature range and at high rates continues to pose fundamental challenges, limiting its further development. Herein, a monolayer Fe‐doped MoS 2 /N,O‐codoped C overlapping structure is designed and employed as an anode for wide‐temperature‐range SIBs. Fe doping imparts MoS 2 electrode with zero bandgap characteristics, an increased interlayer spacing, and low sodium‐ion diffusion energy barriers across wide operation temperatures. Impressively, Fe atoms doped into the MoS 2 lattice can be reduced to superparamagnetic Fe 0 nanocrystals of ≈2 nm during conversion reactions. In situ magnetometry reveals that these Fe 0 nanocrystals can be used as electron acceptor in the formation of space charge zones with Na + , thereby triggering strong spin‐polarized surface capacitance that facilitates fast sodium‐ion storage over a wide temperature range. Consequently, the designed MoS 2 electrode demonstrates exceptional fast‐charging capability in half/full cells operating at −40–60 °C. This study provides novel perspectives on the utilization of heteroatom doping strategies in conversion‐type electrode material design and proves the effectiveness of spin‐polarized surface capacitance effect on enhancing sodium‐ion storage over a wide temperature range.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202404263