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Superprotonic conductivity of ketoenamine covalent-organic frameworks grafted by imidazole-based units.
Zhang, Tao; Xia, Yu; Xie, Ya-Dian; Du, Hai-Jun; Shi, Zhi-Qiang; Hu, Hai-Liang; Zhang, Hong; Guo, Zhong-Cheng; Li, Gang.
Afiliación
  • Zhang T; Key Laboratory of Low-Dimensional Materials and Big Data, School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, PR China; Institute of Polyoxometalate Chemistry, Department of Chemistry, Northeast Normal University, Changchun, Jilin 130024, PR China.
  • Xia Y; Key Laboratory of Low-Dimensional Materials and Big Data, School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, PR China.
  • Xie YD; Key Laboratory of Low-Dimensional Materials and Big Data, School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, PR China.
  • Du HJ; Key Laboratory of Low-Dimensional Materials and Big Data, School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, PR China.
  • Shi ZQ; School of Chemistry and Chemical Engineering, Suzhou University, Suzhou 234000, PR China. Electronic address: kobeecho@163.com.
  • Hu HL; Key Laboratory of Low-Dimensional Materials and Big Data, School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, PR China. Electronic address: hlhu@gzmu.edu.cn.
  • Zhang H; Institute of Polyoxometalate Chemistry, Department of Chemistry, Northeast Normal University, Changchun, Jilin 130024, PR China.
  • Guo ZC; College of Chemistry and Green Catalysis Center, Zhengzhou University, Zhengzhou 450001, PR China.
  • Li G; College of Chemistry and Green Catalysis Center, Zhengzhou University, Zhengzhou 450001, PR China. Electronic address: gangli@zzu.edu.cn.
J Colloid Interface Sci ; 665: 554-563, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38552572
ABSTRACT
The achievement of covalent organic frameworks (COFs) with high stability and exceptional proton conductivity is of tremendous practical importance and challenge. Given this, we hope to prepare the highly stable COFs carrying CN connectors and enhance their proton conductivity via a post-modification approach. Herein, one COF, TpTta, was successfully synthesized by employing 1,3,5-triformylphloroglucinol (Tp) and 4,4',4″-(1,3,5-triazine-2,4,6-triyl)-trianiline (Tta) as starting materials, which has a ß-ketoenamine structure bearing a large amount of -NH groups and intramolecular H-bonds. TpTta was then post-modified by inserting imidazole (Im) and histamine (His) molecules, yielding the corresponding COFs, Im@TpTta and His@TpTta, respectively. As a result, their proton conductivities were surveyed under changeable temperatures (30-100 °C) and relative humidities (68-98 %), revealing a degree of temperature and humidity dependence. Impressively, under identical conditions, the optimum proton conductivities of the two post-modified COFs are 1.14 × 10-2 (Im@TpTta) and 3.45 × 10-3 S/cm (His@TpTta), which are significantly greater than that of the pristine COF, TpTta (2.57 × 10-5 S/cm). Finally, their proton conduction mechanisms were hypothesized based on the computed activation energy values, water vapor adsorption values, and structural properties of these COFs. Additionally, the excellent electrochemical stability of the produced COFs was expressed, as well as the prospective application value.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Colloid Interface Sci Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Colloid Interface Sci Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos