摘要
Metal selenides have aroused significant attention in the realm of efficient ion storage attributed to their exceptional chemical and physical properties, whereas their utilization in sodium-ion batteries (SIBs) is hindered by poor rate performance and cycle stability that originated from their substantial volume expansion throughout Na+ insertion/extraction procedures. This work proposes a productive approach to preserve the structure of the FeSe2 anode via in situ coating nitrogen-doped carbon (NC). The powerful interfacial interaction between FeSe2 micro-nanorods and NC facilitates fast Na+/e− transport kinetics and ensures excellent structural stability of FeSe2@NC. Consequently, FeSe2@NC exhibits a capacity of 379.2 mA h g−1 at a high current density of 10 A g−1 and up to 100% reversible capacity over 1000 cycles at 5 A g−1. Furthermore, the invertible Na+ storage mechanism of FeSe2@NC is investigated by ex situ methods. When FeSe2@NC is used as the anode and Na3V2(PO4)2F3@reduced graphene oxide is used as the cathode to assemble a full battery, it also exhibits a capacity of 167.2 mA h g−1 even after 1000 cycles at 1 A g−1. These exemplary results underscore the potential application value of FeSe2@NC in fast-charging SIBs.
危险品化学品经营许可证(带存储)