A Cr() supramolecular network composite membrane with high water stability and proton conductivity

Proton exchange membranes have attracted considerable attention as the core component of fuel cells. Among them, the blending matrix membrane will result in a composite membrane with the advantages of individual components. Chitosan (CS) has a strong binding capacity to Cr 3+ ions, and it combines w...

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Published inCrystEngComm Vol. 25; no. 13; pp. 23 - 21
Main Authors Zhou, Shu-Fang, Zhang, Hong-Jie, Zhang, Chen-Xi, Wang, Qing-Lun
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 27.03.2023
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Summary:Proton exchange membranes have attracted considerable attention as the core component of fuel cells. Among them, the blending matrix membrane will result in a composite membrane with the advantages of individual components. Chitosan (CS) has a strong binding capacity to Cr 3+ ions, and it combines with polyvinylpyrrolidone (PVP) to form a rich network of hydrogen bonds. Hence, the composite membrane of blending hydrophilic polymer CS-PVP matrix and metal-hydrogen-organic frameworks (MHOFs) [Cr 2 (DBPZ) 2 (μ-OH) 2 ] 1 (H 2 DBPZ) = bis(3,5-dicarboxypyrazol-1-yl)dicarboxylic acid were fabricated. The Cr 3+ ion is six-coordinated by four oxygen atoms and two nitrogen atoms to form an octahedron configuration. Two DBPZ 2− ligands connected two Cr 3+ ions forming a dimeric unit, and an adjacent dimeric core are further connected by a hydrogen bond to form a 3D supramolecular framework. The proton conductivity of 1 @CS/PVP-10 reached up to 8.64 × 10 −2 S cm −1 at 363 K and 98% RH, which is about 10 times higher than that of 1 . The blending matrix membrane with highly efficient double proton conduction pathways has been synthesized. The value of 1 @CS/PVP-10 is ten times higher than that of 1 .
Bibliography:Electronic supplementary information (ESI) available: Tables S1-S4, Fig. S1-S11. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
2083244
https://doi.org/10.1039/d2ce01610a
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ISSN:1466-8033
1466-8033
DOI:10.1039/d2ce01610a