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One‐Step Cationic Grafting of 4‐Hydroxy‐TEMPO and its Application in a Hybrid Redox Flow Battery with a Crosslinked PBI Membrane
By using a one‐step epoxide ring‐opening reaction between 4‐hydroxy‐2,2,6,6‐tetramethylpiperidine 1‐oxyl (4‐hydroxy‐TEMPO) and glycidyltrimethylammonium cation (GTMA+), we synthesized a cation‐grafted TEMPO (g+‐TEMPO) and studied its electrochemical performance against a Zn2+/Zn anode in a hybrid re...
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Published in: | ChemSusChem 2017-08, Vol.10 (16), p.3193-3197 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | By using a one‐step epoxide ring‐opening reaction between 4‐hydroxy‐2,2,6,6‐tetramethylpiperidine 1‐oxyl (4‐hydroxy‐TEMPO) and glycidyltrimethylammonium cation (GTMA+), we synthesized a cation‐grafted TEMPO (g+‐TEMPO) and studied its electrochemical performance against a Zn2+/Zn anode in a hybrid redox flow battery. To conduct Cl− counter anions, a crosslinked methylated polybenzimidazole (PBI) membrane was prepared and placed between the catholyte and anolyte. Compared to 4‐hydroxy‐TEMPO, the positively charged g+‐ TEMPO exhibits enhanced reaction kinetics. Moreover, flow battery tests with g+‐TEMPO show improved Coulombic, voltage, and energy efficiencies and cycling stability over 140 cycles. Crossover of active species through the membrane was not detected.
Grafting and crosslinking: Through cationic grafting of a redox active nitroxyl radical and crosslinking an anion‐exchange PBI (polybenzimidazole) membrane, we improve the cycling properties of a hybrid flow battery utilizing low‐cost components (organic active compound, zinc, anion‐exchange membrane). |
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ISSN: | 1864-5631 1864-564X |
DOI: | 10.1002/cssc.201701060 |