| Literature DB >> 26618985 |
Adam P Cohn1, Keith Share1, Rachel Carter1, Landon Oakes1, Cary L Pint1.
Abstract
A maximum sodium capacity of ∼35 mAh/g has hampered the use of crystalline carbon nanostructures for sodium ion battery anodes. We demonstrate that a diglyme solvent shell encapsulating a sodium ion acts as a "nonstick" coating to facilitate rapid ion insertion into crystalline few-layer graphene and bypass slow desolvation kinetics. This yields storage capacities above 150 mAh/g, cycling performance with negligible capacity fade over 8000 cycles, and ∼100 mAh/g capacities maintained at currents of 30 A/g (∼12 s charge). Raman spectroscopy elucidates the ordered, but nondestructive cointercalation mechanism that differs from desolvated ion intercalation processes. In situ Raman measurements identify the Na(+) staging sequence and isolates Fermi energies for the first and second stage ternary intercalation compounds at ∼0.8 eV and ∼1.2 eV.Entities:
Keywords: Graphene; Na+; anode; graphene intercalation compounds; in situ Raman spectroscopy; sodium ion batteries; solvent cointercalation
Year: 2015 PMID: 26618985 DOI: 10.1021/acs.nanolett.5b04187
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189