Salt-assisted pyrolysis of covalent organic frameworks to porous heteroatom-doped carbons for supercapacitive energy storage

被引:46
作者
Yan, Dongwan [1 ]
Wu, Yang [1 ,2 ]
Kitaura, Ryo [1 ]
Awaga, Kunio [1 ,2 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Dept Chem, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, IRCCS, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648602, Japan
关键词
NANOPOROUS CARBONS; RECENT PROGRESS; GRAPHENE; CRYSTALLINE; ELECTRODES; BATTERIES; STRATEGY; PLATFORM; FACILE; DESIGN;
D O I
10.1039/c9ta05150c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Supercapacitors have attracted intensive research interest due to their advantages including longer cycling ability and higher power density. Porous heteroatom-doped carbons (PHCs) have been regarded as a class of promising electrode materials for supercapacitors because of their unique porous, electronic and chemical properties. However, synthesis of PHCs with hierarchical mesoporous/microporous structures and ultra-high porosity and electrochemical performance remains a great research challenge. In this research, two oxygen and nitrogen co-doped PHCs (denoted as ONC-T1s) are prepared via a saltassisted pyrolysis method using covalent organic frameworks (COFs) as the precursor. ONC-T1s show a hierarchical porous structure with an ultra-high specific surface area (up to 3451 m(2) g(-1)). The ONC-T1-850-based supercapacitor exhibits a high specific capacitance of 1711 F g(-1) at 1 A g(1), an ultra-fast charge-discharge rate up to 500 A g(-1) with a specific capacitance of 856 F g(-1), and excellent stability. This work establishes a promising strategy for preparation of PHCs using COFs or other porous organic polymers as precursors and demonstrates the great potential of PHC-based supercapacitors.
引用
收藏
页码:26829 / 26837
页数:9
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