假电容
超级电容器
材料科学
碳纤维
电容
化学工程
热解
电化学
氮气
纳米结构
氧化还原
法拉第效率
水溶液
兴奋剂
纳米技术
电极
化学
有机化学
复合数
复合材料
光电子学
工程类
物理化学
冶金
作者
Congcong Su,Chengjie Pei,Bingxia Wu,Junfeng Qian,Yiwei Tan
出处
期刊:Small
[Wiley]
日期:2017-06-08
卷期号:13 (29)
被引量:47
标识
DOI:10.1002/smll.201700834
摘要
Nitrogen‐doped and nitrogen and oxygen codoped carbon nanobelts (CNBs) (denoted as N–CNBs and N–O–CNBs, respectively) are respectively obtained by pyrolyzing the self‐aligned polypyrrole (PPy) NBs and Se@poly(2‐methoxy‐5‐nitroaniline) core@shell nanowires. Particularly, the uniform size, unique nanostructure, and well‐defined edges of the PPy NBs result in the uniform size of the doped CNBs with an extraordinarily high N doping level (≈16 at%), especially the very large concentrations of the redox active pyridinic (9 at%) and pyrrolic N (3.5 at%) species. Furthermore, the precursors in highly self‐aligned, dense arrays give rise to a very high packing density for the N–CNBs and N–O–CNBs. These incomparable features provide not only appropriate pathways for the introduction of pseudocapacitance via rapid Faradaic reactions and enhancement of volumetric capacitance but also structural design and synthesis approach to new types of nanostructured carbon. Notably, the N–CNBs obtained at the pyrolysis temperature of 800 °C (N–CNB8) in symmetric electrochemical cells deliver a specific capacitance of 458 F g −1 and ultrahigh volumetric capacitance of 645 F cm −3 in aqueous solution, which are among the best performance ever reported for carbon‐based supercapacitive materials.
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