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Scalable fabrication of electrochemically oxidized and moderately reduced graphite paper electrode for flexible energy storage with ultrahigh rate capability.

Authors :
Liu, Fang
Cao, Xueying
Cui, Liang
Yue, Lijun
Jia, Dedong
Liu, Jingquan
Source :
Journal of Power Sources. May2019, Vol. 421, p169-178. 10p.
Publication Year :
2019

Abstract

Abstract The introduction of surface functional groups onto graphite can provide additional pseudocapacitance for supercapacitors. However, the compensation for the loss of electrical conductivity arising from the destruction of the π-π conjugation remains a big challenge. Here, the graphite paper is electrochemically oxidized first, followed by the mild reduction using hydroiodic acid to afford the largely exfoliated and moderately reduced sample (noted as MOGP-4). The as-prepared MOGP-4 not only has the abundant oxygenous groups, but also preserves the highly conductive network (sp2 carbon). Owing to the good conductivity (1.14 × 103 S m−1), MOGP-4 exhibits a high rate capability of 93% (from 18.3 mF cm−2 to 17 mF cm−2) as the current density increases from 0.5 to 10 mA cm−2 and predominant cycling performance. Furthermore, the flexible solid-state supercapacitors (SSCs) based on MOGP-4 with different sizes are assembled and deliver excellent durability, high flexibility and superior rate capability. The high electrochemical performances of the as-fabricated supercapacitors should envision promising applications for energy storage devices. Graphical abstract Image 1 highlights Graphite paper (GP) row material is low-cost, commercial, large-area and flexible. GP is electrochemically oxidized in mixed acids and then mildly reduced by HI. The strategy can introduce oxygenous groups and preserve high conductivity of GP. The fabricated SCs have high rate capability, stability and coulombic efficiency. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03787753
Volume :
421
Database :
Academic Search Index
Journal :
Journal of Power Sources
Publication Type :
Academic Journal
Accession number :
135596782
Full Text :
https://doi.org/10.1016/j.jpowsour.2019.03.011