Unveiling transport mechanisms of cesium and water in operando zero-gap CO2 electrolyzers

被引:17
作者
Joensen, Bjort Oladottir [1 ]
Zeledon, Jose A. Zamora [2 ]
Trotochaud, Lena [2 ]
Sartori, Andrea [3 ]
Mirolo, Marta [3 ]
Moss, Asger Barkholt [1 ]
Garg, Sahil [1 ]
Chorkendorff, Ib [1 ]
Drnec, Jakub [3 ]
Seger, Brian [1 ]
Xu, Qiucheng [1 ]
机构
[1] Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis SurfCat Sect, DK-2800 Lyngby, Denmark
[2] Twelve Benefit Corp, Berkeley, CA USA
[3] European Synchrotron Radiat Facil, Expt Div, Grenoble, France
关键词
X-RAY; REDUCTION; SYSTEMS;
D O I
10.1016/j.joule.2024.02.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In zero-gap CO2 2 electrolyzers, maintaining the balance of water and cations is crucial. Excessive accumulation at the cathode causes performance degradation, leading to flooding and salt precipitation. Using operando wide-angle X-ray scattering and X-ray fluorescence techniques, we observed the dynamic evolution of H2O 2 O and Cs+ + inside a membrane electrode assembly. Our findings indicate that Cs+ + movement across the membrane from the anode to the cathode is governed by migration and drags H2O 2 O via electroosmosis. H2O 2 O diffusion then allows Cs+ + diffusion further within the gas diffusion electrode. When decreasing the applied voltage, the concentration gradient causes Cs+ + to quickly diffuse back to the anode. The H2O 2 O content in the macro-porous layer remains at the same level, thus showcasing an origin of gas diffusion electrode (GDE) flooding. By regulating the electrolyte concentration, we deconvolute the correlation of water and cations for selectivity changes. Our work underscores the significance of water/cation management strategies in zero-gap electrolyzers.
引用
收藏
页码:1754 / 1771
页数:19
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