High performance cross-linked anion exchange membrane based on aryl-ether free polymer backbones for anion exchange membrane fuel cell application
Literature Information
HongMei Yu, Jinkai Hao, Zhigang Shao
Anion exchange membrane fuel cells (AEMFCs) have attracted growing interest in recent years due to the favored electrochemical kinetics of the oxygen reduction reaction (ORR) and potential low cost, and development of high performance AEMs is always an urgent issue. In this work, a series of cross-linked AEMs with different diamine cross-linkers and various degrees of crosslinking based on the aryl-ether free tri-block copolymer SEBS were prepared using an in situ crosslinking method. FT-IR, XRF and EDS spectra confirm the structures and the degree of crosslinking of the AEMs. Moreover, the cross-linked AEMs demonstrated good mechanical properties and dimensional stability; the tensile strength reached 18.43 MPa (ca. 4.5 times higher than that of the membrane without crosslinking), and the swelling ratios of the cross-linked AEMs were only ca. 10%, which meet the requirement of the AEMFC application. In addition, the cross-linked AEMs demonstrated high ionic conductivity at relatively low IECs and water uptake, and the results of SAXS and TEM verified that the high conductivity could be attributed to the good hydrophilic/hydrophobic phase separation microstructure. Furthermore, in the test of H2/O2 AEMFCs, the MEAs fabricated using the cross-linked membranes displayed good fuel cell performance, especially for the C4-CQASEBS membrane, and the fuel cell realized a peak power density of 585 mW cm−2 at 60 °C. The results indicated that the cross-linked AEMs based on SEBS are a promising candidate material for fuel cell application.
Recommended Journals

Journal of Peptide Science

Organic Process Research & Development

Journal of Natural Medicines

Chemistry Education Research and Practice

Journal of Saudi Chemical Society

Russian Chemical Bulletin

Saudi Pharmaceutical Journal

Russian Journal of General Chemistry

Acta Materialia

Russian Journal of Bioorganic Chemistry
Related Literature
Enhanced π⋯π interactions in α,β-unsaturated carbonyls
Lisa D. Harris, James A. Platts, Nicholas C. O. Tomkinson
DOI: 10.1039/B210497K
Tetracyclic pyrazine-fused furazans as insensitive energetic materials: syntheses, structures, and properties
Qi Sun, Xin Li, Qiuhan Lin, Ming Lu
DOI: 10.1039/C8OB02155D
The reactions of cytidine and 2′-deoxycytidine with SO4˙− revisited. Pulse radiolysis and product studies
Charuvila T. Aravindakumar, Man Nien Schuchmann, Balijepalli S. M. Rao, Justus von Sonntag
DOI: 10.1039/B209626A
Synthesis of (R)-2-methyl-4-deoxy and (R)-2-methyl-4,5-dideoxy analogues of 6-phosphogluconate as potential inhibitors of 6-phosphogluconate dehydrogenase
Christophe Dardonville, Ian H. Gilbert
DOI: 10.1039/B210606J
One-pot synthesis of monodisperse dual-functionalized polyethylene glycols through macrocyclic sulfates
Xiaoyan Lv, Xing Zheng, Zhigang Yang, Zhong-Xing Jiang
DOI: 10.1039/C8OB02392A
Immune responses against Lewis Y tumor-associated carbohydrate antigen displayed densely on self-assembling nanocarriers
Yuji Yamazaki, Yukiko Nambu, Masashi Ohmae, Manabu Sugai, Shunsaku Kimura
DOI: 10.1039/C8OB01955J
Transition metal free decarboxylative fluoroalkylation of N-acrylamides with 3,3,3-trifluoro-2,2-dimethylpropanoic acid (TFDMPA)
Yingkun Shi, Hongqing Xiao, Xiu-Hua Xu, Yangen Huang
DOI: 10.1039/C8OB02457J
A general microcantilever surface modification method using a multilayer for biospecific recognition
Xiaodong Yan, Yuri Lvov, Hai-Feng Ji, Alok Singh, Thomas Thundat
DOI: 10.1039/B209944F
HIV-1 protease: mechanism and drug discovery
Ashraf Brik, Chi-Huey Wong
DOI: 10.1039/B208248A
Syntheses and anti-cancer activity of CO-releasing molecules with targeting galactose receptors
Jili Li, Jinlong Zhang, Qiuping Zhang, Zhongjie Bai, Quanyi Zhao, Dian He, Zhen Wang, Yonglin Chen, Bin Liu
DOI: 10.1039/C8OB01921E
You might also like
Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?
4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...
What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?
(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...
How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?
1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...
What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?
(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...
What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?
When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...
How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?
(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...
What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?
Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...
What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?
2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...
What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?
The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...
Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?
1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...

![3-(6-Nitrobenzo[d][1,3]dioxol-5-yl)acrylic acid structure 3-(6-Nitrobenzo[d][1,3]dioxol-5-yl)acrylic acid structure](https://static.chemtradehub.com/structs/631/6315-90-8-6b36.webp)


![1-{2-[(4-Chlorobenzyl)sulfanyl]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole structure 1-{2-[(4-Chlorobenzyl)sulfanyl]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole structure](https://static.chemtradehub.com/structs/613/61318-90-9-6785.webp)
![5-Fluoro-4-(4-fluoro-2-methoxyphenyl)-N-{4-[(S-methylsulfonimidoyl)methyl]-2-pyridinyl}-2-pyridinamine structure 5-Fluoro-4-(4-fluoro-2-methoxyphenyl)-N-{4-[(S-methylsulfonimidoyl)methyl]-2-pyridinyl}-2-pyridinamine structure](https://static.chemtradehub.com/structs/161/1610358-53-6-afd1.webp)