Boosting Sodium Storage of Double-Shell Sodium Titanate Microspheres Constructed from 2D Ultrathin Nanosheets via Sulfur Doping

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 30(2018), 49 vom: 30. Dez., Seite e1804157
Auteur principal: Wang, Nana (Auteur)
Autres auteurs: Xu, Xun, Liao, Ting, Du, Yi, Bai, Zhongchao, Dou, Shixue
Format: Article en ligne
Langue:English
Publié: 2018
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article 2D ultrathin nanosheets double-shell sodium storage sulphur doping
Description
Résumé:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Sodium-ion batteries (SIBs) have drawn remarkable attention due to their low cost and the practically inexhaustible sodium sources. The major obstacle for the practical application of SIBs is the absence of suitable negative electrode materials with long cycling stability and high rate performance. Here, sulfur-doped double-shell sodium titanate (Na2 Ti3 O7 ) microspheres constructed from 2D ultrathin nanosheets are synthesized via a templating route combined with a low-temperature sulfurization process. The resulting double-shell microspheres deliver a high specific capacity (≈222 mAh g-1 at 1 C), excellent cycling stability (162 mAh g-1 after 15 000 cycles at 20 C), and superior rate capability (122 mAh g-1 at 50 C) as anode for SIBs. The improved electrochemical properties originate from synergistic effects between the unique double-shell nanostructures built from 2D nanosheets architecture and sulfur doping. This synergistic effect not only stabilize Na2 Ti3 O7 -based electrode during the cycling, but also improve the sluggish Na insertion/extraction kinetics by narrowing the bandgap of Na2 Ti3 O7 . The synthesis strategy proposed here can be developed into a technical rationale for generating high-performance sodium-storage devices
Description:Date Completed 17.12.2018
Date Revised 01.10.2020
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.201804157