Ultrafast Preparation of High-Entropy NASICON Cathode Enables Stabilized Multielectron Redox and Wide-Temperature (-50-60 °C) Workability in Sodium-Ion Batteries
Avoiding severe structural distortion, irreversible phase transition, and realizing the stabilized multielectron redox are vital for promoting the development of high-performance NASICON-type cathode materials for sodium-ion batteries (SIBs). Herein, a high-entropy Na V Fe Ti Mn Cr (PO ) (HE-Na TMP)...
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Veröffentlicht in: | Advanced materials (Weinheim) 2025-01, p.e2418219 |
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Sprache: | eng |
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Zusammenfassung: | Avoiding severe structural distortion, irreversible phase transition, and realizing the stabilized multielectron redox are vital for promoting the development of high-performance NASICON-type cathode materials for sodium-ion batteries (SIBs). Herein, a high-entropy Na
V
Fe
Ti
Mn
Cr
(PO
)
(HE-Na
TMP) cathode material is prepared by ultrafast high-temperature shock, which inhibits the possibility of phase separation and achieves reversible and stable multielectron transfer of 2.4/2.8 e
at voltage range of 2.0-4.45/1.5-4.45 V versus Na
/Na (the capacity of 137.2/162.0 mAh g
). The galvanostatic charge/discharge and in-situ X-ray diffraction tests indicate the sequential redox reactions and approximate solid solution phase transition behavior of HE-Na
TMP. Density functional theory calculations analyze the migration pathways and energy barriers, further confirming the superior reaction kinetics of HE-Na
TMP. Accordingly, the HE-Na
TMP exhibits outstanding wide temperature applicability and can operate stably in the temperature range of -50-60 °C, accompanied by a capacity retention of 92.8% after 400 cycles at -40 °C and a capacity of 73.7 mAh g
even at -50 °C. The assembled hard carbon//HE-Na
TMP full-cell offers an energy density of ≈301 Wh kg
based on total cathode and anode active mass, verifying the application feasibility of HE-Na
TMP. This work provides an innovative and ultrafast pathway to rationally fabricate high-performance cathodes for SIBs. |
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ISSN: | 0935-9648 1521-4095 1521-4095 |
DOI: | 10.1002/adma.202418219 |