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Sodium ion batteries (SIBs) have drawn significant attention owing to their low cost and inherent safety. However, the absence of suitable anode materials with high rate capability and long cycling stability is the major challenge for the practical application of SIBs. Herein, an efficient anode material consisting of uniform hollow iron sulfide polyhedrons with cobalt doping and graphene wrapping (named as CoFeS@rGO) is developed for high‐rate and long‐life SIBs. The graphene‐encapsulated hollow composite assures fast and continuous electron transportation, high Na+ ion accessibility, and strong structural integrity, showing an extremely small volume expansion of only 14.9% upon sodiation and negligible volume contraction during the desodiation. The CoFeS@rGO electrode exhibits high specific capacity (661.9 mAh g?1 at 100 mA g?1), excellent rate capability (449.4 mAh g?1 at 5000 mA g?1), and long cycle life (84.8% capacity retention after 1500 cycles at 1000 mA g?1). In situ X‐ray diffraction and selected‐area electron diffraction patterns show that this novel CoFeS@rGO electrode is based on a reversible conversion reaction. More importantly, when coupled with a Na3V2(PO4)3/C cathode, the sodium ion full battery delivers a superexcellent rate capability (496.8 mAh g?1 at 2000 mA g?1) and ≈96.5% capacity retention over 200 cycles at 500 mA g?1 in the 1.0–3.5 V window. This work indicates that the rationally designed anode material is highly applicable for the next generation SIBs with high‐rate capability and long‐term cyclability.  相似文献   

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Antimony (Sb) has emerged as an attractive anode material for both lithium and sodium ion batteries due to its high theoretical capacity of 660 mA h g?1. In this work, a novel peapod‐like N‐doped carbon hollow nanotube encapsulated Sb nanorod composite, the so‐called nanorod‐in‐nanotube structured Sb@N‐C, via a bottom‐up confinement approach is designed and fabricated. The N‐doped‐carbon coating and thermal‐reduction process is monitored by in situ high‐temperature X‐ray diffraction characterization. Due to its advanced structural merits, such as sufficient N‐doping, 1D conductive carbon coating, and substantial inner void space, the Sb@N‐C demonstrates superior lithium/sodium storage performance. For lithium storage, the Sb@N‐C exhibits a high reversible capacity (650.8 mA h g?1 at 0.2 A g?1), excellent long‐term cycling stability (a capacity decay of only 0.022% per cycle for 3000 cycles at 2 A g?1), and ultrahigh rate capability (343.3 mA h g?1 at 20 A g?1). For sodium storage, the Sb@N‐C nanocomposite displays the best long‐term cycle performance among the reported Sb‐based anode materials (a capacity of 345.6 mA h g?1 after 3000 cycles at 2 A g?1) and an impressive rate capability of up to 10 A g?1. The results demonstrate that the Sb@N‐C nanocomposite is a promising anode material for high‐performance lithium/sodium storage.  相似文献   

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