电解
联轴节(管道)
压差
差速器(机械装置)
直接耦合
化学
环境科学
材料科学
物理
电气工程
冶金
工程类
机械
电极
热力学
物理化学
电解质
作者
Stephan Heuser,Lucas Hoof,Kevinjeorjios Pellumbi,Jan Niklas Oberndorf,L. H. Kramer,Dennis Blaudszun,Kai junge Puring,Michael Prokein,Nils Mölders,Andreas Kilzer,Marcus Petermann,Ulf‐Peter Apfel
出处
期刊:Chem catalysis
[Elsevier]
日期:2025-05-20
卷期号:5 (8): 101393-101393
被引量:2
标识
DOI:10.1016/j.checat.2025.101393
摘要
Pressurized electrochemical carbon dioxide reduction (CO2R) offers a pathway to enhance selectivity, current density, and process integration. While elevated pressures improve CO2R performance, differential pressure operation above 10 bar between cathode and anode remains underexplored. This study introduces an innovative test facility and a continuous high-pressure reactor with a zero-gap architecture, enabling gaseous CO2 electrolysis at a differential pressure of 40 bar(g). Using a bipolar membrane electrode assembly eliminates the need for CO2 humidification, and using ultrapure water as the sole proton source creates a salt-free environment without acid or base additives. This setup achieved a Faraday efficiency for CO of 81% at 500 mA cm-2, efficient CO2R with a CO2 excess (λCO2) below 4, and single-pass conversion rates up to 26% at 40 bar(g). The pressurized CO2R outlet streams have low CO2 content, enabling direct integration into downstream chemical processes. This marks a key advancement toward scalable, energy-efficient industrial CO2 electrolysis systems.
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