Abstract

The construction of an anode material with high electrical conductivity and long cycle stability was essential for the practical application of Sodium-ion batteries (SIBs). Hollow Ti3C2@TiSe2 composites were successfully synthesized using in situ selenization methods from MXene-derived materials. The composites obtained in this study exhibited an impressive reversible capacity, attaining a specific capacity of 561 mAh g−1 when tested at a current density of 0.1 A g−1.The specific capacity remained stable at 201 mAh g−1 through 12,000 cycles at a high current density of 10 A g−1. When utilizing Na3V2(PO4)3@C (NVP@C) as the cathode in a full cell, it demonstrated a sustained specific capacity of 138 mAh g−1 over 50 cycles at a current density of 100 mA g−1. Additionally, a capacity of 98 mAh g−1 was maintained over 500 charge-discharge cycles at a higher current density of 1000 mA g−1. The reaction mechanism of Na+ was confirmed through reaction kinetics and ex-situ XRD test. This study demonstrated that the special hollow structure comprised of Ti3C2 and TiSe2 enhanced the material's structural stability as well as the surface activity.

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