Zhao Yunbo, Yuan Ye, Xu Yanmei, Zheng Guiyue, Zhang Qian, Jiang Yuqian, Wang Zeyu, Bu Naishun, Xia Lixin, Yan Zhuojun
College of Chemistry, Liaoning University, Shenyang 110036, China.
Nanoscale. 2021 Jan 28;13(3):1961-1969. doi: 10.1039/d0nr07480b.
Ultramicropores (size < 0.7 nm) are critically demanded to provide an efficient path for the penetration and transportation of electrolytes to achieve high-performance supercapacitors. Here, a self-sacrificial template approach is adopted, which introduces C8 alkyl chains with a kinetic diameter of 0.8-1 nm to occupy the cavity of a porous aromatic framework (PAF). During the heating process, the alkyl chains decompose from the dense architecture as the temperature increased from 500 to 600 °C, forming ∼1 nm micropores. The newly-obtained cavities provide sites for thermal-driven skeleton engineering (700-900 °C) to obtain ultramicropores. Based on the well-defined pore structure, the carbonized PAF solid revealed outstanding electrochemical performances, including high rate and long-term stability in a 6 M KOH electrolyte. Notably, the specific capacitance (294 F g-1) derived from the self-sacrificial template method exceeds the capability of all the other methods for the construction of ultramicropores including self-template strategy, carbonization of nanoparticles, and template-assisted strategy. The synthesis of ultramicroporous carbons via the self-sacrificial template route opens up a promising gate to adjust the porous structure for high-performance applications in supercapacitors.
为了实现高性能超级电容器,迫切需要超微孔(尺寸<0.7纳米)为电解质的渗透和传输提供有效路径。在此,采用了一种自牺牲模板法,该方法引入动力学直径为0.8-1纳米的C8烷基链来占据多孔芳香框架(PAF)的空腔。在加热过程中,随着温度从500℃升高到600℃,烷基链从致密结构中分解,形成约1纳米的微孔。新获得的空腔为热驱动骨架工程(700-900℃)提供了位点以获得超微孔。基于明确的孔结构,碳化的PAF固体展现出优异的电化学性能,包括在6M KOH电解质中的高倍率性能和长期稳定性。值得注意的是,源自自牺牲模板法的比电容(294 F g-1)超过了包括自模板策略、纳米颗粒碳化和模板辅助策略在内的所有其他构建超微孔方法的性能。通过自牺牲模板路线合成超微孔碳为调整多孔结构以用于超级电容器的高性能应用开辟了一条有前景的途径。