Alvi Afaaf Rahat, Vezzù Keti, Lanero Francesco, Sgarbossa Paolo, Nale Angeloclaudio, Di Noto Vito
Department of Industrial Engineering, Section of Chemistry for Technology, University of Padova, Via F. Marzolo 9, I-35131, Padova, Italy.
UDR di Padova, INSTM, Via F. Marzolo 9, I-35131, Padova, Italy.
ChemSusChem. 2025 Jul 17;18(14):e202402765. doi: 10.1002/cssc.202402765. Epub 2025 May 5.
Anion exchange membranes (AEMs) have been proposed as potential alternatives to proton exchange membranes in electrochemical energy conversion and storage devices. Herein, the synthesis of a series of AEMs based on random piperazinium-methyl N-substituted poly[ethylene pyrrole/ethylene ketone/propylene ketone] (P-FPKK) and their structural characterization together with the elucidation of the ion conduction mechanism are reported. Different copolymers are prepared by a Paal-Knorr reaction of a poly(ethylene ketone/propylene ketone) copolymer precursor with 1-(2-aminoethyl) piperazine, modulating the molar ratios amine/(1,4-diketonic repeat units of copolymer) from ¼ to 3. The composition and structure are investigated by elemental analysis, attenuated total reflectance-Fourier transform infrared spectroscopy, nuclear magnetic resonance, and X-ray diffraction. The degree of functionalization, f, plays a crucial role in controlling the thermal, morphological, and electrochemical properties of the P-FPKK(I) and P-FPKK(OH) membranes. P-FPKK(OH) displays an ionic conductivity of 11.3 mS cm at 60 °C. After alkaline aging (1 m KOH at 60 °C for 336 h), retaining its structural integrity and 25% of its initial ionic conductivity value, suggesting them as possible candidates for testing in alkaline energy conversion and storage devices. Furthermore, broadband electrical spectroscopy studies reveal that the long-range charge migration processes are modulated by the segmental motion of the backbone chains of the copolymer matrix.
阴离子交换膜(AEMs)已被提议作为电化学能量转换和存储设备中质子交换膜的潜在替代品。本文报道了一系列基于无规哌嗪鎓 - 甲基N - 取代聚[乙烯吡咯/乙烯酮/丙烯酮](P - FPKK)的AEMs的合成、其结构表征以及离子传导机制的阐明。通过聚(乙烯酮/丙烯酮)共聚物前体与1 - (2 - 氨基乙基)哌嗪的Paal - Knorr反应制备不同的共聚物,将胺/(共聚物的1,4 - 二酮重复单元)的摩尔比从1/4调节到3。通过元素分析、衰减全反射 - 傅里叶变换红外光谱、核磁共振和X射线衍射研究其组成和结构。官能化程度f在控制P - FPKK(I)和P - FPKK(OH)膜的热、形态和电化学性能方面起着关键作用。P - FPKK(OH)在60°C时显示出11.3 mS cm的离子电导率。在碱性老化(60°C下1 m KOH中336小时)后,保持其结构完整性和初始离子电导率值的25%,表明它们可能是用于碱性能量转换和存储设备测试的候选材料。此外,宽带电光谱研究表明,远程电荷迁移过程受共聚物基质主链链段运动的调节。