聚丙烯腈
碳化
介孔材料
电容
催化作用
钴
电极
材料科学
超级电容器
化学工程
碳纤维
图层(电子)
氧化钴
氮气
无机化学
化学
纳米技术
有机化学
复合材料
聚合物
物理化学
复合数
扫描电子显微镜
工程类
作者
Daiki Tanaka,Natsumi Takemori,Yoshiki Iba,K. Suyama,Shunsuke Shimizu,Takeharu Yoshii,Hirotomo Nishihara,Yoshihiro Kamimura,Yoshihiro Kubota,Satoshi Inagaki
标识
DOI:10.1016/j.micromeso.2024.113294
摘要
Ordered mesoporous carbon CMK-1 was prepared via carbonization at a relatively low temperature (the first step) followed by partial graphitization (the second step of carbonization at higher temperature) inside the ordered mesopores of cobalt-loaded mesoporous silica MCM-48 using polyacrylonitrile (PAN) as a carbon/nitrogen source. This first step of the carbonization is called “infusibilization”, and the resultant material is denoted as PANinf. In an advanced temperature-programmed desorption analysis of the PANinf/MCM-48 composite, the temperature of the observed HCN signal indicated that carbonization was reduced from 550 to 450 °C by a Co catalyst. The amount of typical N2 formation associated with the selective removal of pyridinic N species, resulting in the graphitic surface formation, also increased at a relatively high temperature (approximately 1000 °C) with the aid of the Co catalyst. The CMK-1 prepared through cobalt-catalyzed carbonization exhibited a higher electric double-layer capacitance with an Et4N+BF4–/propylene carbonate electrolyte, and higher electrical conductivity than CMK-1 prepared without a catalyst. This also implied the progress of graphitization within the carbonaceous wall. These results suggest that the edge planes of the graphitic domains in CMK-1 are predominantly exposed on the surfaces of the carbonaceous walls, resulting in an increase in the number of adsorptive sites for the electrolyte during capacitance measurements.
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