Abstract

Molecular hydrogen has exceptionally high gravimetric energy density but low volumetric energy density at ambient conditions. This discrepancy requires technical measures to increase its volumetric energy density for widespread hydrogen applications. Compressed hydrogen and liquified hydrogen are the most established hydrogen storage technologies. In addition, thermocatalytic liquid organic hydrogen carriers (LOHC) have drawn significant attention in the last decade.[1] LOHC couples consist of a hydrogen-lean and a hydrogen-rich form that can be reversibly converted into each other on demand. So far, only a few approaches adapted this hydrogen storage concept to electrochemistry. However, there is strong interest in electrochemical liquid organic hydrogen carriers (EC-LOHC) as electrochemical processes offer significant advantages like flexible operation, device size, scalability, and system simplicity.[2] This contribution demonstrates the concept of acetone/isopropanol as an electrochemical liquid organic hydrogen carrier focusing on the electrochemical dehydrogenation of isopropanol in a polymer electrolyte membrane electrode assembly (PEM-MEA) setup. The isopropanol oxidation at a PtRu electrode shows two distinct oxidation peaks at 0.18 V vs. RHE and 0.75 V vs. RHE, whereby the first oxidation peak is associated with a selective oxidation of isopropanol to acetone, electrons and protons.[3] The produced protons travel from the PtRu anode through the PEM and recombine with the electrons at the Pt cathode to form hydrogen. Therewith, this configuration is an electrolysis cell that produces hydrogen out of isopropanol upon polarization above the reversible cell potential.The study investigates the influence of acetone/isopropanol concentrations, temperature, and flow rates on the I-V characteristics of the electrochemical dehydrogenation of isopropanol at voltages below 0.35 V, revealing its possible potential as EC-LOHC.

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