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Updated: Feb 12, 2026

Morris Water Maze Test: Optimization for Mouse Strain and Testing Environment
Published on: June 22, 2015
CO₂電気還元のための最適化された微小環境を有する透過性密着膜電極界面(純水中)
Zhilong Zheng1,2, Songhu Bi3, Xiangji Zhou3
1School of Physics, Huazhong University of Science and Technology, Wuhan, China.
Abstract:
Pure water-fed membrane electrode assembly (MEA) electrolyzers represent a significant advance for practical deployment of electrochemical CO2 reduction, yet suffer from poor reaction kinetics and high ohmic resistance due to the lack of alkali cations and low intrinsic ionic conductivity. Here, we address interfacial mass transport limitations arising from inefficient H2O and OH- transport in anion exchange membrane (AEM)-based pure water MEAs. A permeable intimate membrane (PIM) electrode is developed by casting ionomer emulsion directly onto the catalyst layer (CL) to form the anion exchange layer (AEL) in situ, which creates an intimately bonded CL/AEL interface and allows the ionomer to permeate the CL, establishing continuous internal channels for efficient H2O and OH- transport. Consequently, the PIM-based MEA achieves over 90% CO selectivity across a wide current density range under pure water conditions, with a system energy efficiency 1.35 times higher than conventional MEAs. Characterization reveals that the intimate catalyst-ionomer interface reconstructs the hydrogen-bonded network of interfacial water, accelerating the hydrogenation kinetics of the key *COO- intermediate.
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