4.7 Article

N-rich reduced graphene oxide film with cross-coupled porous networks as free-standing electrode for high performance supercapacitors

期刊

APPLIED SURFACE SCIENCE
卷 563, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2021.150303

关键词

Porous; Parallel; Vertical; N-rich; Free-standing

资金

  1. National Natural Science Foundation of China [51572078, 51772086, 51872087, 51971089]
  2. Natural Science Foundation of Hunan Province [2018JJ2038]
  3. Major Science and Technology Program of Changsha [kq1804010]

向作者/读者索取更多资源

The freeze-dried N-HRGO films fabricated by a freeze casting method exhibit excellent electrochemical performance due to their cross-coupled porous ion diffusion networks, abundant pore structures for promoting ion diffusion, and nitrogen sites enhancing specific capacitance, resulting in a high specific capacitance of 528 F g(-1) and a high energy density of 14.0 Wh kg(-1) with excellent cycle life (89.3% capacity retention after 5000 cycles at 2 A g(-1)) when assembled into a symmetrical supercapacitor.
Graphene films suffer from poor electrochemical performance due to the undesirable ion diffusion inside its deep area and only electrical double layer absorption mechanism. Here, we proposed a freeze casting method for fabricating the N-rich holey reduced graphene oxide films (Freeze-dried N-HRGO) bearing cross-coupled porous ion diffusion networks. The H2O2 etching and modified vacuum filtration process generate abundant pore structures inside films, which act as ion diffusion path for promoting electrochemical performance. In addition, the N sites serve as pseudocapacitance contributor to react with electrolyte ions, which greatly enhance the specific capacitance. As a result, the freeze-dried N-HRGO films show a high specific capacitance of 528 F g(-1) at a current density of 1 A g(-1). When assembled into symmetrical supercapacitor, it delivers a high energy density of 14.0 Wh kg(-1) and excellent cycle life (89.3% capacity retention after 5000 cycles at 2 A g(-1)).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据