2020
DOI: 10.1039/d0ta01788d
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From polybenzimidazoles to polybenzimidazoliums and polybenzimidazolides

Abstract:

New and emerging technologies for electrochemical energy conversion processes and challenging separations have been major drivers for the tremendous development of new polybenzimidazole chemistries and materials in recent years.

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Cited by 168 publications
(147 citation statements)
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References 317 publications
(371 reference statements)
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“…Several authors reported the use of either acid doped polybenzimidazole (PBI) or modied versions of PBI, which have shown excellent selectivity, low self-discharge and thus high coulombic efficiency values up to nearly 100%. [16][17][18][19] A remaining challenge is the stability of current AEMs in the challenging environment of high concentrations of sulfuric acid as well as the highly oxidative VO 2 + species. Recently several groups have made tremendous efforts to improve the performance and stability of ionomers through methods such as crosslinking 18,20,21 and ionomer blending.…”
Section: Introductionmentioning
confidence: 99%
“…Several authors reported the use of either acid doped polybenzimidazole (PBI) or modied versions of PBI, which have shown excellent selectivity, low self-discharge and thus high coulombic efficiency values up to nearly 100%. [16][17][18][19] A remaining challenge is the stability of current AEMs in the challenging environment of high concentrations of sulfuric acid as well as the highly oxidative VO 2 + species. Recently several groups have made tremendous efforts to improve the performance and stability of ionomers through methods such as crosslinking 18,20,21 and ionomer blending.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, the design of hydrogen bonding to improve tensile strength of materials has received extensive attention in recent years. [ 17–19 ] 2‐(4‐aminophenyl)‐5‐aminobenzimidazole (PABZ), a diamine with benzimidazole ring, was introduced into PPTA as a monomer by Russian researchers. [ 20 ] The abundant hydrogen bonding sites on the benzimidazole ring greatly enhance the hydrogen bonding interaction in the aramid fiber and increase the tensile strength of PPTA by 20%.…”
Section: Introductionmentioning
confidence: 99%
“…According to the literature [ 33 , 34 , 35 ], 20 mL polyphosphoric acid (PPA) and 3,3′-diaminobenzidine 1 were added into a 50 mL flask and heated at 160 °C for 2 h. After they were completely dissolved, 3.0 mmol trans -butenedioic acid ( E -BA) 2 was added, and the mixture was heated to 170 °C for 48 h. After cooling to room temperature, the pH was adjusted to alkaline with NaOH solution, and then a blue–black solid was obtained by the filtration.…”
Section: Methodsmentioning
confidence: 99%