Abstract
Ternary hybrid membranes composed of sulfonated (poly ether ether ketone) (SPEEK), sulfonated polyvinylidene fluoride-co-hexafluoropropylene (SPVdF-HFP) and 1, 3, 5 or 7 wt% graphene oxide (GO) were fabricated using a facile solution casting method. The reinforcement due to the existence of SPVdF-HFP and GO afforded good mechanical and thermal stabilities to the hybrid membranes, which was confirmed by dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA). The surface morphological properties and roughness of the hybrid membranes were scrutinized using field emission scanning electron microscopy (FE-SEM) and atomic force microscopy (AFM), whereas the clenched structure with even intercalation of GO sheets in the polymer matrix was observed. The temperature dependent changes in proton conductivity, as well as the mass, length, and thickness of membranes were measured; the ternary hybrid exhibited more significant changes compared to other membranes. The chemical structure, intermolecular bond stretching, structural reorganization, and crystallinity of the membranes were analyzed using proton nuclear magnetic resonance spectroscopy (1H-NMR), Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), and X-ray diffraction (XRD) instrumentation techniques. In the ternary hybrid membranes, SPVdF-HFP increased the per cluster volume of SO3H groups and GO increased the number of directional hydrogen bonds (H-bonds), which collectively provided good impact in proton conductivity. At 90 °C, the peak proton conductivity attained by the SPEEK was 68 mS cm−1, while that of the ternary hybrid was 122 mS cm−1, 1.7 times better conductivity. Furthermore, the ternary hybrids exhibited much lower H2 permeability compared to that of SPEEK and Nafion-117 membranes.
| Original language | English |
|---|---|
| Pages (from-to) | 108851-108863 |
| Number of pages | 13 |
| Journal | RSC Advances |
| Volume | 6 |
| Issue number | 110 |
| Early online date | 28 Oct 2016 |
| DOIs | |
| Publication status | E-pub ahead of print - 28 Oct 2016 |
| Externally published | Yes |
Bibliographical note
This journal is © The Royal Society of Chemistry 2016Funder
This work was supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (No. 20164030201070).Funding
This work was supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (No. 20164030201070).