Remarkable impact of chain backbone on the performance of Poly(norbornene derivatives)-based anion exchange membranes

Abstract

Chemical stability and the trade-off between ion conductivity and dimensional stability are two primary challenges for the development of suitable anion exchange membranes (AEMs). Herein, a series of non-crosslinked poly(norbornene derivatives)-based AEMs containing a bulky steric hindrance hydrophobic arylene substituent were prepared by vinyl addition polymerization (VAP), ring-opening metathesis polymerization (ROMP), and ROMP followed post-hydrogenation, respectively. Compared with ROMP and hydrogenated type membranes, VAP-type membranes, especially the VAP-N-50, exhibited excellent dimensional stability with limited swelling ratio (SR = 27.9 %) while higher water uptake (WU = 213.8 %) at 80 °C, which is attributed to its rigid VAP-type cyclic chain backbone. Microtopography study demonstrated the existence of nanoscale phase separation in VAP-type AEMs and its association with water uptake and swelling behavior. VAP-N-60 showed excellent hydroxide conductivity up to 105.5 mS cm−1 at 80 °C, while exhibited superior alkaline stability that was not found in ROMP-type membrane ROMP-N-50 and the hydrogenated-type membrane H-ROMP-N-50. After being immersed in 2 M NaOH solution at 80 °C for 1200 h, the hydroxide conductivity loss of VAP-N-60 was only 3.0 %. Furthermore, a H2/O2 single cell using VAP-N-50 membrane achieved the highest peak power density of 722 mW cm−2 at 60 °C without back pressure.