假电容器
材料科学
卟啉
共价有机骨架
氧化还原
质子化
电化学
化学工程
超级电容器
储能
电极
光化学
有机化学
化学
物理化学
物理
复合材料
离子
工程类
功率(物理)
冶金
量子力学
多孔性
作者
Bidhan Chandra Patra,Santanu Bhattacharya
标识
DOI:10.1021/acs.chemmater.1c02973
摘要
Covalent organic frameworks (COFs) are of increasing interest in the field of materials science. Polymerizations of the topologically fitted monomers into two-dimensional (2D) structures with a periodic order often make them crystalline. The existence of this structural periodicity and regular pores makes them effective for facile ion transport and storage applications. We report herein a new porphyrin-based 2D COF using Schiff base condensation reaction between 5,10,15,20-tetrakis(para-amino phenyl) porphyrin (TAPP) and 1,1,2,2-tetrakis(4-formyl-(1,1′-biphenyl))-ethane (TFBE) under solvothermal conditions. The as-prepared porphyrin-tetraphenyl ethylene COF (PT-COF) possesses high crystallinity along with a large surface area of 1998 m2 g–1. The PT-COF electrode was used as a supercapacitive energy storage system with the combination of an electrochemical double-layer capacitor and pseudocapacitor. This COF showed a maximum specific capacitance of 1443 F g–1 at a current density of 1 A g–1 in 0.5 M H2SO4 with 91% capacity retention after 3000 cycles. The presence of the porphyrin unit inside the framework causes good redox activity in the acidic media. During the cathodic scan, the porphyrin unit [H2P] got protonated, followed by 2e– reduction to form a 20π-electronic system [H4P]. Thus, the reversible proton accepting capability of the redox-active porphyrin-decorated PT-COF could allow for use as an energy storage material as a supercapacitor under acidic conditions. A high power density of 7.3 kW kg–1 was observed at a high scan rate, which outperforms most of the other COF-based electrode materials used for high storage performance.
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