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原位活化石墨化制备用于超级电容器的分级多孔石墨碳

In situ activation graphitization to fabricate hierarchical porous graphitic carbon for supercapacitor.

作者信息

Zhao Yanling, Zhang Xiaohua

机构信息

College of Medical Imaging, Shanxi Medical University, Taiyuan, 030001, China.

College of Materials Science and Engineering, Taiyuan University of Science and Technology, Taiyuan, 030024, China.

出版信息

Sci Rep. 2021 Mar 25;11(1):6825. doi: 10.1038/s41598-021-85661-0.

Abstract

In situ activation-graphitization method based on the atomically dispersed K and Fe in organic salts is developed to synthesize hierarchical porous graphitic carbon by directly pyrolysis potassium citrate and iron citrate. Moreover, (NH)CO is also employed as both N dopant and porogen to open up internal structure and regulate pore structure. The inside-out activation leads to the homogeneous reaction and interconnected hierarchical porous structure with few dead pores. Accompanied by high specific surface area, appropriate pore distribution, good conductivity, and N/O functional groups, the sample exhibits high capacitance of 322.6 F g at 0.5 A g, good rate capability, and excellent cycling stability with 101.5% capacitance retention after 15,000 cycles. The supercapacitor shows an energy density of 21.3 W h kg at 456.7 W kg in 1 M NaSO. Easy synthesis, cost-effective, and environmentally benign, the work provides a promising strategy to produce hierarchical porous graphitic carbon applied in energy storage.

摘要

基于有机盐中原子分散的钾和铁的原位活化-石墨化方法被开发出来,通过直接热解柠檬酸钾和柠檬酸铁来合成分级多孔石墨碳。此外,(NH₄)₂CO₃还被用作氮掺杂剂和致孔剂,以打开内部结构并调节孔结构。由内而外的活化导致均匀反应和相互连接的分级多孔结构,几乎没有死孔。伴随着高比表面积、合适的孔径分布、良好的导电性和氮/氧官能团,该样品在0.5 A g时表现出322.6 F g的高电容、良好的倍率性能以及出色的循环稳定性,在15000次循环后电容保持率为101.5%。该超级电容器在1 M Na₂SO₄中,在456.7 W kg时的能量密度为21.3 W h kg。该方法易于合成、成本效益高且环境友好,为生产用于能量存储的分级多孔石墨碳提供了一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b9/7994305/b581f45b93a5/41598_2021_85661_Fig1_HTML.jpg

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