Three-phase Sn-based heterostructure nanoparticles anchored on N-doped graphene as a promising anode for lithium/sodium storage

Microstructure modulation by phase engineering induces electrode materials to exhibit excellent energy storage performance due to their adjustable surface/ interface and electronic characteristics. For tin dioxide (SnO2), effective strategies for adjusting their microstructure properties are still l...

全面介绍

书目详细资料
发表在:Journal of Electroanalytical Chemistry
主要作者: 2-s2.0-85185399643
格式: 文件
语言:English
出版: Elsevier B.V. 2024
在线阅读:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85185399643&doi=10.1016%2fj.jelechem.2024.118063&partnerID=40&md5=49728c0b90b4d8db143d8d667f556b48
实物特征
总结:Microstructure modulation by phase engineering induces electrode materials to exhibit excellent energy storage performance due to their adjustable surface/ interface and electronic characteristics. For tin dioxide (SnO2), effective strategies for adjusting their microstructure properties are still lacking. Herein, 2D flexible N-doped graphene (NG) is rationally integrated with SnO2/SnS/Sn heterostructure via hydrothermal and subsequent partial in-situ vulcanization, in which the SnO2/SnS/Sn nanoparticles are tightly anchored on NG network (SnO2/SnS/Sn@NG). The unique SnO2/SnS/Sn heterostructures with modulated electronic properties can induce accelerated charge transfer kinetics and enhanced ions diffusion/adsorption capacities. The hierarchical structure with a large surface area along with nanocomponents can offer better permeability, more available charge storage sites of active material, and a stable electrochemical framework. As expected, the SnO2/SnS/Sn@NG heterostructure as an anode for lithium-ion battery exhibits an excellent charge capacity of 748 mAh g−1 at 0.2 A g−1, long-term cyclic stability of 507 mAh g−1 at 1 A g−1 for 800 cycles, and high-rate capability with of 476 mAh g−1 at 5 A g−1. Moreover, the anode for sodium-ion battery also shows excellent cyclic stability and rate capability. © 2024 Elsevier B.V.
ISSN:15726657
DOI:10.1016/j.jelechem.2024.118063