Understanding an exceptionally fast and stable li-ion charging of highly fluorinated graphene with fine-controlled C-F configuration

Authors
Lee, Y.-K.Lee, C.-H.Kang, G.-S.Eom, K.Cho, S.Y.Lee, S.Joh, H.-I.
Issue Date
2021-11-17
Publisher
American Chemical Society
Citation
ACS Applied Materials & Interfaces, v.13, no.45, pp.53767 - 53776
Abstract
Fluorine (F) atoms with the highest electronegativity and low polarizability can easily modify the surface and composition of carbon-based electrode materials. However, this is accompanied by complete irreversibility and uncontrolled reactivity, thus hindering their use in rechargeable electronic devices. Therefore, understanding the electrochemical effects of the C-F configuration might lead to achieving superior electrochemical properties. Here, we demonstrate that the fluorinated and simultaneously reduced graphene oxide (FrGO) was easily synthesized through direct gas fluorination. The as-prepared 11%-FrGO electrode exhibited a high capacity (1365 mAh g-1 at 0.1 A g-1), remarkable rate capability, and good stability (64% retention after 1000 cycles at 5 A g-1). Furthermore, the annealed FrGO (11%-FrGO(A)) electrode in which the C-F bond configurations were controlled by facile thermal treatment shows long-term stability (80% retention after 1000 cycles at 5 A g-1). Above a certain content, F atoms enhance Li-ion adsorption and electron transfer, accelerate Li-ion diffusion, and facilitate the formation of a solid electrolyte interphase layer. In particular, the C-F configuration plays a significant role in retaining the capacity under harsh recharging conditions. The results in this study could provide valuable insights into the field of rechargeable devices. ?
Keywords
DOPED GRAPHENE; ENERGY-STORAGE; ANODE MATERIAL; OXIDE; PERFORMANCE; REDUCTION; ELECTRODES; BATTERY; FUNCTIONALIZATION; MECHANISM; anode; energy storage systems; fluorine; functionalization; graphene
ISSN
1944-8244
URI
https://pubs.kist.re.kr/handle/201004/116120
DOI
10.1021/acsami.1c13811
Appears in Collections:
KIST Article > 2021
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