Dynamic Neutron Imaging and Modeling of Cationic Impurities in Polymer Electrolyte Water Electrolyzer

被引:12
|
作者
Zlobinski, Mateusz [1 ]
Babic, Ugljesa [1 ]
Fikry, Meriem [1 ]
Gubler, Lorenz [1 ]
Schmidt, Thomas J. [1 ,2 ]
Boillat, Pierre [1 ,3 ]
机构
[1] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
[2] Swiss Fed Inst Technol, Lab Phys Chem, CH-8093 Zurich, Switzerland
[3] Paul Scherrer Inst, Lab Neutron Scattering & Imaging, Villigen, Switzerland
关键词
POWER-TO-GAS; LIQUID/GAS DIFFUSION LAYERS; OXYGEN EVOLUTION REACTION; HIGH-SURFACE-AREA; CURRENT COLLECTORS; ION CONTAMINATION; MEMBRANE; PERFORMANCE; HYDROGEN; CELLS;
D O I
10.1149/1945-7111/abc83b
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The high operation and capital costs of polymer electrolyte water electrolyzers (PEWE) are the major obstacles that have to be tackled for hydrogen to penetrate the market as a solution for renewable energy storage. Commercial stacks often suffer from cationic contamination of catalyst-coated membranes (CCMs) that comes from impure feed water and corrosion of system components, which can result in increasing operation costs and lowered lifetime. This study describes the behavior of the contaminants in the CCMs and their impact on performance under various operating conditions using Gd3+ as model contaminant imaged with neutron with a combination of high effective temporal (2 s) and spatial (30 mu m) resolutions. The presence of electric field directly affects the position of cations in the CCM leading to their accumulation near the cathode catalyst layer. The cationic impurities trigger multiple loss mechanisms, as the ohmic resistance increase does not scale linearly with the amount of occupied exchange groups in the membrane (10% resistance increase caused by 2.5% exchange groups occupation). A model has been developed that predicts the movement of the ions in the CCM under intermittently operating PEWE and was used as a basis to explain the hysteresis observed in the polarization curve of contaminated PEWEs.
引用
收藏
页数:9
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