Improvement of Na Ion Electrode Activity of Metal Oxide via Composite Formation with Metal Sulfide
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- 作者：Seung Mi Oh ; In Young Kim ; Sharad B. Patil ; Boyeon Park ; Jang Mee Lee ; Kanyaporn Adpakpang ; Seen Ae Chae ; Oc Hee Han ; Seong-Ju Hwang
- 刊名：ACS Applied Materials & Interfaces
- 出版年：2017
- 出版时间：January 25, 2017
- 年：2017
- 卷：9
- 期：3
- 页码：2249-2260
- 全文大小：777K
- ISSN：1944-8252
文摘
The composite formation with a conductive metal sulfide domain can provide an effective methodology to improve the Na-ion electrode functionality of metal oxide. The heat treatment of TiO<sub>2sub>(B) under CS<sub>2sub> flow yields an intimately coupled TiO<sub>2sub>(B)–TiS<sub>2sub> nanocomposite with intervened TiS<sub>2sub> domain, since the reaction between metal oxide and CS<sub>2sub> leads to the formation of metal sulfide and CO<sub>2sub>. The negligible change in lattice parameters and significant enhancement of visible light absorption upon the reaction with CS<sub>2sub> underscore the formation of conductive metal sulfide domains. The resulting TiO<sub>2sub>(B)–TiS<sub>2sub> nanocomposites deliver greater discharge capacities with better rate characteristics for electrochemical sodiation–desodiation process than does the pristine TiO<sub>2sub>(B). The <sup>23sup>Na magic angle spinning nuclear magnetic resonance analysis clearly demonstrates that the electrode activities of the present nanocomposites rely on the capacitive storage of Na<sup>+sup> ions, and the TiS<sub>2sub> domains in TiO<sub>2sub>(B)–TiS<sub>2sub> nanocomposites play a role as mediators for Na<sup>+sup> ions to and from TiO<sub>2sub>(B) domains. According to the electrochemical impedance spectroscopy, the reaction with CS<sub>2sub> leads to the significant enhancement of charge transfer kinetics, which is responsible for the accompanying improvement in electrode performance. The present study provides clear evidence for the usefulness in composite formation between the semiconducting metal oxide and metal sulfide in exploring new efficient NIB electrode materials.