Base tolerant polybenzimidazolium hydroxide membranes for solid alkaline-exchange membrane fuel cells
- Authors
- Lee, Ju Yeon; Lim, Dong-Hee; Chae, Ji Eon; Choi, Jieun; Kim, Bo Hyun; Lee, So Young; Yoon, Chang Won; Nam, Sang Yong; Jang, Jong Hyun; Henkensmeier, Dirk; Yoo, Sung Jong; Kim, Jin-Young; Kim, Hyoung-Juhn; Ham, Hyung Chul
- Issue Date
- Sep-2016
- Publisher
- Elsevier BV
- Keywords
- Poly(dibenzylated benzimidazolium) hydroxide; Solid alkaline membrane fuel cell; OH- ion conductivity; Density functional theory; Electron affinity
- Citation
- Journal of Membrane Science, v.514, pp 398 - 406
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Journal of Membrane Science
- Volume
- 514
- Start Page
- 398
- End Page
- 406
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/15263
- DOI
- 10.1016/j.memsci.2016.05.012
- ISSN
- 0376-7388
1873-3123
- Abstract
- Poly(dibenzylated benzimidazolium) bromides (Bz-PBI-Br) were converted successfully to OH- ion conducting poly(dibenzylated benzimidazolium) hydroxides (Bz-PBI-hydroxides) by the treatment of KOH. The Bz-PBI-hydroxides obtained in this study showed an excellent alkali tolerance compared to previously synthesized poly(dimethylated benzimidazolium) hydroxides (Me-PBI-hydroxides). According to H-1-NMR analysis, Me-PBI-hydroxides were decomposed during KOH treatment. In order to find out the reason, density functional theory (DFT) calculations of two benzimidazolium structures, e.g., di-methylated benzimidazolium (Me-BI+) and dibenzylated benzimidazolium (Bz-BI+), were performed. Bz-BI+ showed lower electron affinity and OH--binding energies at the C2 position of the benzimidazolium ring than Me-BI+ These DFT results strongly confirm that Bz-BI+ is less vulnerable to an OH attack than Me-BI+; this contributes to the enhanced stability and OH- ion conductivity of the Bz-PBI-hydroxides. (C) 2016 Elsevier B.V. All rights reserved.
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