ElBachraoui F, Aymé-Perrot D, Girault H H
Materials Science, Energy and Nanoengineering (MSN) Department, University Mohammed VI Polytechnic, Ben Guerir, Morocco.
TotalEnergies SE, OneTech, Paris, France.
Research (Wash D C). 2025 Aug 28;8:0788. doi: 10.34133/research.0788. eCollection 2025.
Water electrolysis is a key industrial process for producing green hydrogen. To avoid the use of noble metals and fluorinated polymer membranes, liquid water electrolysis is often carried out in alkaline conditions. It is common to distinguish between 3 processes: alkaline electrolysis at high electrolyte concentrations (≥7 M) with porous membranes, alkaline electrolysis at high electrolyte concentrations (≥7 M) with ion-solvating membranes, and alkaline electrolysis at moderate electrolyte concentrations (<2 M) with anion-exchange membranes. Here, we consider the fundamental aspects of water and ion fluxes and of conductivity across the 3 types of membranes. We discuss ionic currents governed by ion-ion interactions and those resulting from a Grotthuss mechanism. Furthermore, in the case of porous membranes made of a polymeric fabric with compressed inorganic fillers such as zirconia, which are negatively charged in the presence of KOH, and of ion-solvating membranes such as polybenzimidazole, which also become negatively charged by deprotonation at high pH, those membranes should be a weak cation exchanger. We here address this dichotomy. All in all, we show that in all 3 cases, the membrane is an anion exchanger where hydroxide ion mobility differs from that of adjacent aqueous solution due to confinement favoring a Grotthuss-type transport and a jump mechanism.
水电解是生产绿色氢气的关键工业过程。为避免使用贵金属和含氟聚合物膜,液态水电解通常在碱性条件下进行。通常可区分三种过程:使用多孔膜在高电解质浓度(≥7 M)下进行碱性电解、使用离子溶剂化膜在高电解质浓度(≥7 M)下进行碱性电解以及使用阴离子交换膜在中等电解质浓度(<2 M)下进行碱性电解。在此,我们考虑水和离子通量以及这三种类型膜的电导率的基本方面。我们讨论由离子 - 离子相互作用控制的离子电流以及由格罗特斯机制产生的离子电流。此外,对于由带有压缩无机填料(如氧化锆)的聚合物织物制成的多孔膜,在氢氧化钾存在下带负电荷,以及对于离子溶剂化膜(如聚苯并咪唑),在高pH值下也会因去质子化而带负电荷,这些膜应是弱阳离子交换剂。我们在此解决这种二分法。总而言之,我们表明在所有三种情况下,膜都是阴离子交换剂,由于限制有利于格罗特斯型传输和跳跃机制,氢氧根离子迁移率与相邻水溶液的迁移率不同。