| Literature DB >> 26891421 |
Satoshi Kajiyama1, Lucie Szabova2, Keitaro Sodeyama2,3, Hiroki Iinuma1, Ryohei Morita4, Kazuma Gotoh4,3, Yoshitaka Tateyama2,3, Masashi Okubo1,3, Atsuo Yamada1,3.
Abstract
MXene, a family of layered compounds consisting of nanosheets, is emerging as an electrode material for various electrochemical energy storage devices including supercapacitors, lithium-ion batteries, and sodium-ion batteries. However, the mechanism of its electrochemical reaction is not yet fully understood. Herein, using solid-state (23)Na magic angle spinning NMR and density functional theory calculation, we reveal that MXene Ti3C2Tx in a nonaqueous Na(+) electrolyte exhibits reversible Na(+) intercalation/deintercalation into the interlayer space. Detailed analyses demonstrate that Ti3C2Tx undergoes expansion of the interlayer distance during the first sodiation, whereby desolvated Na(+) is intercalated/deintercalated reversibly. The interlayer distance is maintained during the whole sodiation/desodiation process due to the pillaring effect of trapped Na(+) and the swelling effect of penetrated solvent molecules between the Ti3C2Tx sheets. Since Na(+) intercalation/deintercalation during the electrochemical reaction is not accompanied by any substantial structural change, Ti3C2Tx shows good capacity retention over 100 cycles as well as excellent rate capability.Entities:
Keywords: 23Na NMR; MXene; intercalation; negative electrode; sodium-ion battery
Year: 2016 PMID: 26891421 DOI: 10.1021/acsnano.5b06958
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881