Aqueous zinc-ion batteries (ZIBs) are considered to be prospective candidates in energy storage devices because of their excellent safety, crustal abundance, low cost and environmental benignity. Whereas, the design of a satisfied cathode material with a large specific capacity, superior rate performance and long-cycle life is still a significant challenge for ZIBs. Herein, a new strategy is proposed to use W doped V2O5 as cathode material for aqueous ZIBs. The W doping can effectively enlarge the lattice spacing and ion migration efficiency of V2O5, and the formation of W—O bond can obviously alleviate the capacity decay problem caused by structural damage and low intrinsic conductivity in the cycling process. As a result, the V2O5-W cathode exhibits an excellent capacity of 195.0 mA·h/g after 100 cycles at 0.1 A/g, and an impressive rate capability of 243.0 mA·h/g at the high current density of 1 A/g after 1000 cycles. This work provides a simple, efficient and feasible strategy for designing high-performance cathode materials in ZIBs.
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Tin-based oxides and their alloys with high specific capacities are considered as promising anode materials for Na-ion batteries. However, the tin-based oxides and their alloys suffer from a large volume variation and particle agglomeration during the charge-discharge process, resulting in electrode pulverization, capacity fading, and poor rate performance. In this paper, Bi/SnOx particles anchored on an ultrathin carbon layer (Bi/SnOx@C) were synthesized by a sodium chloride template method, and a uniform Bi/SnOx@C heterostructure is constructed. The ultrathin carbon layer can effectively inhibit the agglomeration of Bi/SnOx particles and increase the specific surface area of the electrode material, providing more active sites. Bi/SnOx can also contribute the more specific capacity. The synergistic effect of ultrathin carbon layer and Bi/SnOx composite can effectively improve the cycling stability, which is of great significance for the construction of high-performance electrode materials.
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