Electrostatic Self-Assembly Enabling Integrated Bulk and Interfacial Sodium Storage in 3D Titania-Graphene Hybrid.
basic_science · Level V
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- Record sourced from PubMed, PMID 29240435.
- Also identified by DOI 10.1021/acs.nanolett.7b04193.
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Abstract
Room-temperature sodium-ion batteries have attracted increased attention for energy storage due to the natural abundance of sodium. However, it remains a huge challenge to develop versatile electrode materials with favorable properties, which requires smart structure design and good mechanistic understanding. Herein, we reported a general and scalable approach to synthesize three-dimensional (3D) titania-graphene hybrid via electrostatic-interaction-induced self-assembly. Synchrotron X-ray probe, transmission electron microscopy, and computational modeling revealed that the strong interaction between titania and graphene through comparably strong van der Waals forces not only facilitates bulk Na<sup>+</sup> intercalation but also enhances the interfacial sodium storage. As a result, the titania-graphene hybrid exhibits exceptional long-term cycle stability up to 5000 cycles, and ultrahigh rate capability up to 20 C for sodium storage. Furthermore, density function theory calculation indicated that the interfacial Li<sup>+</sup>, K<sup>+</sup>, Mg<sup>2+,</sup> and Al<sup>3+</sup> storage can be enhanced as well. The proposed general strategy opens up new avenues to create versatile materials for advanced battery systems.