2019
DOI: 10.1039/c9se00318e
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Cross-linked sulfonated poly(ether ether ketone) electrolytes bearing pendent imidazole groups for high temperature proton exchange membrane fuel cells

Abstract: A series of ionic-covalently cross-linked SPEEK bearing imidazole groups have been synthesized for high temperature fuel cells.

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Cited by 36 publications
(27 citation statements)
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“…The reason behind the higher PA loading of the composite membranes than the pristine OPBI can be a cumulative effect of several factors. First, both PSM 1 and PSM 2 consist of hydrophilic "−SO 3 H" groups, and with the increase in the loading of PSM 1 and PSM 2 in the composites Second, the sulfonic acid groups interact with nitrogen in the imidazole ring of OPBI to produce a more regular structure (a certain order of crystallinity has been observed in the PXRD analysis) and a bigger space between the chains that can easily accommodate a larger amount of absorbed PA. 61 PA doping disturbs the original crystalline ordering 62 and decreases the peak intensities of the * marked peaks in the 2θ range between 25°and 30°for PA doped samples (see Figure S1a,b in the Supporting Information). This change in the crystallinity is accompanied with partial disruption of the pre-existing Hbonded structure and development of new H-bonds involving the newly absorbed PA molecules and the "−SO 3 H" groups and "N−H" groups already present in the membrane.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The reason behind the higher PA loading of the composite membranes than the pristine OPBI can be a cumulative effect of several factors. First, both PSM 1 and PSM 2 consist of hydrophilic "−SO 3 H" groups, and with the increase in the loading of PSM 1 and PSM 2 in the composites Second, the sulfonic acid groups interact with nitrogen in the imidazole ring of OPBI to produce a more regular structure (a certain order of crystallinity has been observed in the PXRD analysis) and a bigger space between the chains that can easily accommodate a larger amount of absorbed PA. 61 PA doping disturbs the original crystalline ordering 62 and decreases the peak intensities of the * marked peaks in the 2θ range between 25°and 30°for PA doped samples (see Figure S1a,b in the Supporting Information). This change in the crystallinity is accompanied with partial disruption of the pre-existing Hbonded structure and development of new H-bonds involving the newly absorbed PA molecules and the "−SO 3 H" groups and "N−H" groups already present in the membrane.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…However, due to the strong plasticization of PA molecules, high proton conductivity is usually at the expense of the mechanical strength of the membrane [14][15][16][17]. Besides, the preparation of a high-strength PA-PBI membrane requires high molecular weight of PBI, which exhibits poor solubility in organic solvents and makes it fairly hard to prepare uniform casting solution [18]. Therefore, to realize high-performance HT-PEMs and high-efficiency HT-PEMFCs, it is one of the important issues to settle the balance between proton conductivity and mechanical properties of phosphoric acid-doped polymer membranes.…”
Section: Introductionmentioning
confidence: 99%
“…For example, sulfonated poly(phenylene)s, 10,11 poly(ether ether ketone)s 12 , poly(arylene ether sulfone)s 13 and polyimides 14 can be found as proton-exchange membranes in the literature, and some of these have been applied as electrode binders. [15][16][17][18][19][20][21] Recently, E.…”
Section: Introductionmentioning
confidence: 99%