Membrane-assisted direct seawater splitting (DSS) technologies are actively studied as a promising route to produce green hydrogen (H2), whereas the indispensable use of supporting electrolytes that help to extract water and provide electrochemically-accelerated reaction media results in a severe energy penalty, consuming up to 12.5% of energy input when using a typical KOH electrolyte. We bypass this issue by designing a zero-gap electrolyzer configuration based on the integration of cation exchange membrane and bipolar membrane assemblies, which protects stable DSS operation against the precipitates and corrosion in the absence of additional supporting electrolytes. The heterolytic water dissociation function of the bipolar membrane in-situ creates an asymmetric acidic-alkaline environment, kinetically facilitating H2 and O2 evolution reactions. When working in natural seawater without any chemical inputs, this zero-gap electrolyzer sustains nearly 100% Faradaic efficiency toward H2 for 120 h at a current density of 100 mA cm-2. With the high-integrity merit, our electrolyzer can be facilely scaled up into practical cell stacks with significantly increased active area and promising prospects for volume/space-sensitive application scenarios. This electrolyzer concept opens an underexplored design space for energy-saving H2 production from low-grade saline water sources, being complementary to, and potentially competitive with the pre-purification schemes.
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http://dx.doi.org/10.1002/anie.202422840 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Chinese Academy of Sciences Qingdao Industrial Energy Storage Technology Institute, Department of Energy Science and Energy Technology, Songling Road, 189, 266101, Qingdao City, CHINA.
Membrane-assisted direct seawater splitting (DSS) technologies are actively studied as a promising route to produce green hydrogen (H2), whereas the indispensable use of supporting electrolytes that help to extract water and provide electrochemically-accelerated reaction media results in a severe energy penalty, consuming up to 12.5% of energy input when using a typical KOH electrolyte. We bypass this issue by designing a zero-gap electrolyzer configuration based on the integration of cation exchange membrane and bipolar membrane assemblies, which protects stable DSS operation against the precipitates and corrosion in the absence of additional supporting electrolytes.
View Article and Find Full Text PDFACS Mater Lett
December 2024
Analytical Chemistry-Center for Electrochemical Sciences (CES), Faculty of Chemistry and Biochemistry, Ruhr University Bochum, Universitätsstr. 150, D-44780 Bochum, Germany.
Direct estimation of the reaction environment, e.g., local pH at the anode side of a membrane electrode assembly (MEA) of zero gap electrolyzer, is essential to understand possible key factors, which are influencing the sustainable operation of industrial electrolyzers.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Ruhr-Universität Bochum, Fakultät für Chemie und Biochemie, Anorganische Chemie I, Universitätsstraße 150, 44801 Bochum, Germany.
Metalloporphyrins are widely studied in the field of electrochemical CO reduction (COR), with the main focus on homogenous catalysis. Herein, six metalloporphyrins (M = Fe, Co, Ni, Cu, Zn, Ag) were incorporated in gas diffusion electrodes and used in zero-gap electrolyzers to reach varying FEs for CO of <1% (Fe,Ni), 11% (Cu), 37% (Zn), 75% (Co) and nearly 100% (Ag) at a current density of 50 mA cm.
View Article and Find Full Text PDFACS Appl Energy Mater
November 2024
Institute of Organic Chemistry, Laboratory for Sustainable Chemistry and Catalysis (LSusCat), Johannes Kepler University (JKU), Altenberger Straße 69, 4040 Linz, Austria.
In this study, we propose a practical approach for producing a heterobimetallic Ni(II)-Ce(III) diimine complex from an extended salen-type ligand (HL) to serve as an electrocatalyst for CO reduction and demonstrate an outstanding overall efficiency of 99.6% of the cerium-nickel complex and integrate it into applicable cell assemblies. We optimize not only the catalyst, but the operational conditions enabling successful CO electrolysis over extended periods at different current densities.
View Article and Find Full Text PDFNat Commun
November 2024
Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, Jiangsu, China.
CO electroreduction is a potential pathway to achieve net-zero emissions in the chemical industry. Yet, CO loss, resulting from (bi)carbonate formation, renders the process energy-intensive. Acidic environments can address the issue but at the expense of compromised product Faradaic efficiencies (FEs), particularly for multi-carbon (C) products, as rapid diffusion and migration of protons (H) favors competing H and CO production.
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