RESUMO
Anion exchange membrane fuel cells (AEMFCs), which are more economical than proton exchange membrane fuel cells (PEMFCs), stand out in the context of the rapid development of renewable energy. Superacid-catalyzed ether-free aromatic polymers have recently received a lot of attention due to their exceptional performance, but their development has been hampered by the trade-off between the dimensional stability and ionic conductivity of anion exchange membranes (AEMs). Here, we introduced fluoroketones containing different numbers of fluorinated groups (x = 0, 3 and 6) in the main chain of p-terphenyl piperidine because of the favorable hydrophobic properties of fluorinated groups. The results show that fluorinated AEMs can enhance OH- conductivity by building more aggregated hydrophilic channels while ensuring dimensional stability. The PTF6-QAPTP AEM with more fluorinated groups has the most excellent performance at 80 °C with an OH- conductivity of 142.7 mS cm-1 and a swelling ratio (SR) of only 4.55 %. Additionally, it exhibits good alkali durability, with the OH- conductivity and quaternary ammonium (QA) cation retaining at 93.45% and 92.6%, respectively, after immersion in a 2 M NaOH solution at 80 °C for 1200 h. In addition, the power density of the PTF6-QAPTP based single cell reaches 849 mW cm-2 when the current density is 1600 mA cm-2. The PTF6-QAPTP based cell has a voltage retention of 88% after 80 h of stability testing at a constant current density of 300 mA cm-2 at 80 °C.
RESUMO
Anion exchange membrane fuel cells (AEMFCs) have emerged as a promising alternative to proton exchange membrane fuel cells (PEMFCs) due to their adaptability to low-cost stack components and non-noble-metals catalysts. However, the poor alkaline resistance and low OH- conductivity of anion exchange membranes (AEMs) have impeded the large-scale implementation of AEMFCs. Herein, the preparation of a new type of AEMs with crown ether macrocycles in their main chains via a one-pot superacid catalyzed reaction was reported. The study aimed to examine the influence of crown ether cavity size on the phase separation structure, ionic conductivity and alkali resistance of anion exchange membranes. Attributed to the self-assembly of crown ethers, the poly (crown ether) (PCE) AEMs with dibenzo-18-crown-6-ether (QAPCE-18-6) exhibit an obvious phase separated structure and a maximum OH- conductivity of 122.5 mS cm-1 at 80 °C (ionic exchange capacity is 1.51 meq g-1). QAPCE-18-6 shows a good alkali resistance with the OH- conductivity retention of 94.5% albeit being treated in a harsh alkali condition. Moreover, the hydrogen/oxygen single cell equipped with QAPCE-18-6 can achieve a peak power density (PPD) of 574 mW cm-2 at a current density of 1.39 A cm-2.
RESUMO
Poly(aryl piperidinium) (PAP) anion exchange membranes (AEMs) furnish an important avenue for the commercialization of anion exchange membrane fuel cells (AEMFCs), but their ionic conductivity and alkali resistance still need to be improved. Here, we report the synthesis of PAP AEMs with a branched structure by the acid-catalyzed reaction and compare them with the main-chain AEMs. The experimental results show that the branched AEMs have higher OH- conductivity and alkaline resistance than the poly(terphenyl piperidine) (PTPQ1) AEM. The alkaline stability and OH- conductivity of the AEMs were further improved by a flexible multi-cation crosslinker. The results show that the branched poly(p-terphenyl triphenylmethane 1-methyl piperidine) membrane crosslinked by multi-cation (PTTPQ4-40) shows an excellent OH- conductivity (155.3 mS cm-1) at 80 °C. The OH- conductivity of the PTTPQ4-40 membrane was maintained at 92.1% after soaking in 2 M NaOH for 1080 h at 80 °C. In addition, the peak power density (PPD) of the crosslinked PTTPQ4-40 membrane can reach 656.7 mW cm-2. Compared to the PTPQ1 AEM, the PPD of the crosslinked PTTPQ4-40 AEM is increased by 38.6% in H2-O2. All of the results confirm that the PTTPQ4-40 AEM has excellent fuel cell application prospects.
