The evolution of cyclopropenium ions into functional polyelectrolytes

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作者
Yivan Jiang
Jessica L. Freyer
Pepa Cotanda
Spencer D. Brucks
Kato L. Killops
Jeffrey S. Bandar
Christopher Torsitano
Nitash P. Balsara
Tristan H. Lambert
Luis M. Campos
机构
[1] Columbia University,Department of Chemistry
[2] Joint Center for Artificial Photosynthesis,Department of Chemical and Biomolecular Engineering
[3] Lawrence Berkeley National Laboratory,Materials Sciences Division, Environmental Energy Technologies Division and Joint Center for Energy Storage
[4] University of California,undefined
[5] Edgewood Chemical Biological Center,undefined
[6] Aberdeen Proving Ground,undefined
[7] Lawrence Berkeley National Laboratory,undefined
来源
Nature Communications | / 6卷
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摘要
Versatile polyelectrolytes with tunable physical properties have the potential to be transformative in applications such as energy storage, fuel cells and various electronic devices. Among the types of materials available for these applications, nanostructured cationic block copolyelectrolytes offer mechanical integrity and well-defined conducting paths for ionic transport. To date, most cationic polyelectrolytes bear charge formally localized on heteroatoms and lack broad modularity to tune their physical properties. To overcome these challenges, we describe herein the development of a new class of functional polyelectrolytes based on the aromatic cyclopropenium ion. We demonstrate the facile synthesis of a series of polymers and nanoparticles based on monomeric cyclopropenium building blocks incorporating various functional groups that affect physical properties. The materials exhibit high ionic conductivity and thermal stability due to the nature of the cationic moieties, thus rendering this class of new materials as an attractive alternative to develop ion-conducting membranes.
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