Two processes for crosslinking polyvinyl alcohol (PVA) with sulfosuccinic acid (SSA) and thermal crosslinking were used to fabricate a proton exchange membrane (PEM). Such PEMs are used in different fields involving fuel cell applications. The crosslinking reaction between PVA and SSA was confirmed using Fourier-transform infrared (FTIR) spectroscopy. The characterization of the prepared membranes, namely, ion exchange capacity (IEC), thermal analyses, water uptake, and ionic conductivity, was carried out. The IEC of the prepared membranes was found to be between 0.084 and 2.086 mmol g-1, resulting in an essential increase in the ionic conductivity. It was observed that the ionic conductivity was in the range of 0.003-0.023 S cm-1, depending on both temperature and SSA content. From the thermogravimetric analysis (TGA) results, it was revealed that the thermal stability of the crosslinked membranes improved. Moreover, water uptake decreased with increasing SSA content. Positron annihilation lifetime spectroscopy (PALS) was used to study the microstructure of the PVA/SSA membranes and their distribution at different ambient temperatures and relative humidity (RH) values. At room temperature, no significant change was observed in the free-volume holes up to 15 wt% SSA; thereafter, the size of the free-volume holes increased with the SSA content. The PALS results show that at different humidity values, the size of the free-volume holes for crosslinked PVA/SSA membranes is lower than those for Nafion membranes, i.e., the gas permeability for the prepared PVA/SSA membranes is less than that for the Nafion membrane. In addition, a strong correlation between the water uptake, ionic conductivity, tensile strength, and free-volume holes was observed.
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http://dx.doi.org/10.1039/c8cp05301d | DOI Listing |
Int J Biol Macromol
January 2025
College of Materials Science and Engineering, Nanjing Tech University, Nanjing 211816, PR China. Electronic address:
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View Article and Find Full Text PDFInorg Chem
January 2025
Departamento de Química Física and Instituto de Biocomputación y Física de Sistemas Complejos (BIFI), Universidad de Zaragoza, Zaragoza 50009, Spain.
Nano Lett
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College of Materials Science and Engineering, Hunan Joint International Laboratory of Advanced Materials and Technology of Clean Energy, Hunan Province Key Laboratory for Advanced Carbon Materials and Applied Technology, Hunan University, Changsha 410082, China.
Sci Adv
January 2025
Department of Mechanical Engineering, University of Delaware, Newark, DE 19716, USA.
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Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
We present a strategy for enhancing Li conduction in block copolymer electrolytes by introducing trace amounts of Li salts into polystyrene--poly(ethylene oxide) (PS--PEO), wherein Li ions preferentially coordinate with the -OH end groups of the PEO chains, resulting in the formation of double primitive cubic (3̅) structures. Compared with TFSI anions in Li salts, smaller anions (PF and BF) could facilitate ion localization more effectively, expanding the salt concentration range for developing stable 3̅ structures. The 3̅ structures formed in PS--PEOs doped with LiBF at = 0.
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