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...
Published in: | JOURNAL OF ELECTROANALYTICAL CHEMISTRY |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Published: |
ELSEVIER SCIENCE SA
2024
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Subjects: | |
Online Access: | https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001173763400001 |
Summary: | 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. |
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ISSN: | 1572-6657 1873-2569 |
DOI: | 10.1016/j.jelechem.2024.118063 |