Chiolite Na5Ti3F14: A novel sodium titanium fluoride anode for low-cost and high-performance Na-ion batteries

Authors
Kang, JungminAhn, JinhoLee, YongseokPark, HyunyoungKo, WonseokKu, BonyoungChoi, MyungeunJung, Hun-GiRyu, Won-HeeKim, Jongsoon
Issue Date
2023-11
Publisher
Elsevier BV
Citation
Energy Storage Materials, v.63
Abstract
Fluoride-based conversion reaction electrode materials offer exceptional theoretical capacity merit for Na-ion batteries. Nevertheless, it has rarely been considered as potential anode material candidate due to (i) excessive redox potential (> 3 V) and (ii) intrinsically low reaction kinetics related to sluggish structural reorganization process. In this work, we demonstrate that chiolite Na5Ti3F14/carbon nanocomposite can deliver the outstanding electrochemical performances as the promising anode for Na-ion batteries, such as a large specific capacity of ∼425 mAh g?1 at 10 mA g?1 with a low average operating voltage, the capacity retention of ∼78 % compared to the initial capacity after 300 cycle with a high Coulombic efficiency of above 99 %, etc. We demonstrate that the chiolite Na5Ti3F14 phase can store the ∼8.33 mol Na ions through the following conversion reaction; Na5Ti3F14 + 9Na + 9e? 3Ti + 14NaF, which is clearly confirmed by various ex-situ analyses using X-ray diffraction, synchrotron-based X-ray adsorption spectroscopy, etc. We expect that this research can provide guidance toward the development of a new class of low-cost and high-performance anode materials, not only for Na-ion batteries but also for other rechargeable batteries.
Keywords
ELECTROCHEMICAL PERFORMANCE; CATHODE; STORAGE; LITHIUM; CARBON; ELECTRODES; TRANSITION; NANOSHEETS; MECHANISM; GRAPHITE; Na-ion batteries; anode; Conversion reaction; Fluoride; Na5Ti3F14
ISSN
2405-8297
URI
https://pubs.kist.re.kr/handle/201004/79762
DOI
10.1016/j.ensm.2023.103048
Appears in Collections:
KIST Article > 2023
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE