Highly Efficient and Durable Water Electrolysis at High KOH Concentration Enabled by Cationic Group-Free Ion Solvating Membranes in Free-standing Gel Form
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引用次数: 0
Abstract
The degradation of fixed cationic groups in most anion exchange membranes (AEMs) under alkaline environments limits their durability for alkaline water electrolysis (AWE). Ion-solvating membranes (ISMs) have emerged as a promising alternative to address this issue. Herein, a cationic group-free ion solvating membrane in a free-standing gel form (ISM-PBI-FG) is presented, created through a sol-to-gel transformation process followed by KOH imbibing. This approach yields a 3D porous microstructure composed of entangled polybenzimidazole (PBI) nanofibrils, achieving 89% porosity, which enables ultrahigh alkali uptake (346% in 6 M KOH) and exceptional ionic conductivity (763 mS cm−1 at 80 °C). The absence of cationic groups avoids the attack by OH−, thus ensures good alkaline stability with a conductivity retention rate of 91.6% over a 3120 h ex situ test in 6 M KOH. The resulting membrane delivered outstanding AWE performance with current densities of 5.5 A cm−2 using platinum-group-metal (PGM) catalysts and 2.2 A cm−2 using PGM-free catalysts at 2.0 V. Notably, the in situ electrolyzer device based on ISM-PBI-FG offers extensive operational flexibility ranging from 40–100 °C and demonstrates record durability in concentrated alkaline conditions, with a voltage decay rate of only 23.5µV h−1, outperforming most reported AEMs and ISMs.
大多数阴离子交换膜(AEMs)在碱性环境下固定阳离子基团的降解限制了其在碱性电解(AWE)中的耐久性。离子溶剂化膜(ISMs)已成为解决这一问题的一个有希望的替代方案。本文提出了一种游离凝胶形式的无阳离子基离子溶剂化膜(ISM - PBI - FG),该膜是通过溶胶-凝胶转化过程和KOH吸收形成的。该方法产生了由纠缠的聚苯并咪唑(PBI)纳米纤维组成的三维多孔结构,孔隙率达到89%,可实现超高的碱吸收率(在6 M KOH中为346%)和优异的离子电导率(80°C时为763 mS cm−1)。由于没有阳离子基团,避免了OH−的攻击,因此确保了良好的碱性稳定性,在6 M KOH中进行3120 h的非原位测试,电导率保持率为91.6%。采用铂族金属(PGM)催化剂和无铂族金属(PGM)催化剂制备的膜在2.0 V下电流密度分别为5.5 A cm - 2和2.2 A cm - 2,具有优异的AWE性能。值得注意的是,基于ISM - PBI - FG的原位电解槽装置提供了40-100°C范围内广泛的操作灵活性,并且在浓碱性条件下具有创纪录的耐久性,电压衰减率仅为23.5µV h - 1,优于大多数报道的AEMs和ISMs。
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