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Ultrastable Covalent Triazine Organic Framework Based on Anthracene Moiety as Platform for High-Performance Carbon Dioxide Adsorption and Supercapacitors

Conductive and porous nitrogen-rich materials have great potential as supercapacitor electrode materials. The exceptional efficiency of such compounds, however, is dependent on their larger surface area and the level of nitrogen doping. To address these issues, we synthesized a porous covalent triaz...

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Detalles Bibliográficos
Autores principales: Mohamed, Mohamed Gamal, Sharma, Santosh U., Liu, Ni-Yun, Mansoure, Tharwat Hassan, Samy, Maha Mohamed, Chaganti, Swetha V., Chang, Yu-Lung, Lee, Jyh-Tsung, Kuo, Shiao-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8951433/
https://www.ncbi.nlm.nih.gov/pubmed/35328595
http://dx.doi.org/10.3390/ijms23063174
Descripción
Sumario:Conductive and porous nitrogen-rich materials have great potential as supercapacitor electrode materials. The exceptional efficiency of such compounds, however, is dependent on their larger surface area and the level of nitrogen doping. To address these issues, we synthesized a porous covalent triazine framework (An-CTFs) based on 9,10-dicyanoanthracene (An-CN) units through an ionothermal reaction in the presence of different molar ratios of molten zinc chloride (ZnCl(2)) at 400 and 500 °C, yielding An-CTF-10-400, An-CTF-20-400, An-CTF-10-500, and An-CTF-20-500 microporous materials. According to N(2) adsorption–desorption analyses (BET), these An-CTFs produced exceptionally high specific surface areas ranging from 406–751 m(2)·g(−1). Furthermore, An-CTF-10-500 had a capacitance of 589 F·g(−1), remarkable cycle stability up to 5000 cycles, up to 95% capacity retention, and strong CO(2) adsorption capacity up to 5.65 mmol·g(−1) at 273 K. As a result, our An-CTFs are a good alternative for both electrochemical energy storage and CO(2) uptake.