Capacitive Organic Anode Based on Fluorinated-Contorted Hexabenzocoronene: Applicable to Lithium-Ion and Sodium-Ion Storage Cells

Authors
Park, JaehyunLee, Cheol WooPark, Ju HyunJoo, Se HunKwak, Sang KyuAhn, SeokhoonKang, Seok Ju
Issue Date
2018-12
Publisher
WILEY
Citation
ADVANCED SCIENCE, v.5, no.12
Abstract
Conducting polymer-based organic electrochemical capacitor materials have attracted attention because of their highly conductive nature and highly reversible redox reactions on the surface of electrodes. However, owing to their poor stabilities in aprotic electrolytes, alternative organic electrochemical capacitive electrodes are being actively sought. Here, fluorine atoms are introduced into contorted hexabenzocoronene (cHBC) to achieve the first small-molecule-based organic capacitive energy-storage cells that operate at high current rates with satisfactory specific capacities of approximate to 160 mA h g(-1) and superior cycle capabilities (>400) without changing significantly. This high capacitive behavior in the P2(1)/c crystal phase of fluorinated cHBC (FcHBC) is caused mainly by the fluorine atoms at the end of each peripheral aromatic ring. Combined Monte Carlo simulations and density functional theory (DFT) calculations show that the most electronegative fluorine atoms accelerate ion diffusion on the surface to promote fast Li+ ion uptake and release by an applied current. Moreover, FcHBC has potential applications as the capacitive anode in Na-ion storage cells. The fast dynamics of its capacitive behavior allow it to deliver a specific capacity of 65 mA h g(-1) at a high current of 4000 mA g(-1).
Keywords
ENERGY-STORAGE; PSEUDOCAPACITOR ELECTRODES; SUPERCAPACITOR; INSERTION; NANOMATERIALS; CHALLENGES; CHARGE; FILMS; ENERGY-STORAGE; PSEUDOCAPACITOR ELECTRODES; SUPERCAPACITOR; INSERTION; NANOMATERIALS; CHALLENGES; CHARGE; FILMS; contorted hexabenzocoronene; electrochemical capacitors; fluorination; high current rates; pseudocapacitors
ISSN
2198-3844
URI
https://pubs.kist.re.kr/handle/201004/120624
DOI
10.1002/advs.201801365
Appears in Collections:
KIST Article > 2018
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