Construction of hierarchical porous carbon nanosheets from template-assisted assembly of coal-based graphene quantum dots for high performance supercapacitor electrodes

被引:77
作者
Zhang, Su [1 ]
Zhu, Jiayao [1 ]
Qing, Yan [1 ]
Fan, Chengwei [1 ]
Wang, Luxiang [1 ]
Huang, Yudai [1 ]
Sheng, Rui [1 ]
Guo, Yong [1 ]
Wang, Tao [1 ]
Pan, Yanliang [1 ]
Lv, Yan [1 ]
Song, Huaihe [2 ]
Jia, Dianzeng [1 ]
机构
[1] Xinjiang Univ, Inst Appl Chem, Key Lab Adv Funct Mat Autonomous Reg, Key Lab Energy Mat Chem,Minist Educ, Urumqi 830046, Peoples R China
[2] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing Key Lab Electrochem Proc & Technol Mat, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene quantum dot; Coal; Carbon nanosheets; Hierarchical porous structure; Supercapacitor; ENHANCED PHOTOLUMINESCENCE; RAMAN-SPECTROSCOPY; ANTHRACITE COAL; DOPED CARBON; NITROGEN; OXIDE; YIELD; NANOCOMPOSITES; NANOTUBES; NANOCAGES;
D O I
10.1016/j.mtener.2017.08.003
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
Using coal-based graphene quantum dots (GQDs) as the building blocks, we develop a simple template-assisted assembly strategy to prepare hierarchical porous carbon nanosheets (HPCNs) for supercapacitor electrodes. The coal-based GQDs are prepared by a simple liquid phase oxidation of the bituminous coal. Benefiting from their small size, enriched edge structure, abundant functional groups, and good flexibility and chemical reactivity, these GQDs are suitable to construct complex nanoarchitectures for advanced energy storage materials. As a result, the HPCNs show an interconnected loose-stacking graphene-like structure with the specific surface area of 1332 m(2) g(-1), hierarchical pore distribution, excellent conductivity, abundant active sites, and sufficient ion migration channels. An in situ chemical activation is further applied to improve its energy storage performance. Under the optimized conditions, the activated HPCN with a specific surface area of 1450 m(2) g(-1) shows a greatly improved capacitive performance, with a high specific capacitance of 230 F g(-1) (1 A g(-1)) and capacitance retention of 74% at 100 A g(-1) (170 F g(-1)). No obvious capacity fade was found even after cycled at 10 A g(-1) for 10,000 times, demonstrating their excellent endurability. Our work may provide new thought for the effective use of abundant coal resource to design and preparation advanced carbon nanoarchitectures for energy storage. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:36 / 45
页数:10
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