Advanced CFD simulation of two-phase anion exchange membrane water electrolysis

被引:2
作者
Lee, Donggyun [1 ]
Kim, Minsu [2 ]
Kim, Jeongdong [1 ]
Moon, Il [1 ]
Kim, Junghwan [1 ]
机构
[1] Yonsei Univ, Dept Chem & Biomol Engn, 50 Yonsei Ro, Seoul 03722, South Korea
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
Anion exchange membrane water electrolysis; Computational fluid dynamics; Parameter estimation; Multiphase flow; Green hydrogen; FUEL-CELL; PEM ELECTROLYSIS; HIGH-PRESSURE; HYDROGEN; PERFORMANCE; OPERATION; MODEL; ANODE; HEAT; COST;
D O I
10.1016/j.ijhydene.2024.09.180
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
Anion exchange membrane (AEM) water electrolysis is a promising and inexpensive solution for hydrogen production and environmental problems. Owing to its low technical proficiency, AEM electrolysis necessitates high fidelity to improve its durability, reliability, and efficiency. Therefore, a CFD-based model for AEM electrolysis was developed to analyze the three-dimensional and two-phase phenomena inside the cell. The temperature, pressure, and gas generation profiles inside the cell were studied by combining electrochemical models with mass, momentum, and heat transfer models. Parameters were estimated using the experimental data from a high-accuracy model. The results showed that the applied voltage, which determined the exothermic/endothermic mode, significantly influenced the water electrolysis performance. Specifically, in the exothermic mode, with voltages exceeding the thermo-neutral voltage (1.48 V), the amount of hydrogen generated (15.53, 25.05, and 28.82 mol/m(3) at 1.6, 1.8, and 2.0 V, respectively) was higher than that in the endothermic mode (4.78 mol/m3 3 at 1.45 V). However, the increased gas generation caused a rapid increase in the temperature and pressure drop inside the cell, which adversely affected durability. The model developed in this study can be used in experiments of various scales to optimize serpentine designs and commercial AEM electrolysis stack developments.
引用
收藏
页码:322 / 332
页数:11
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