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Conversion efficiency based on the higher heating value (HHV) of hydrogen for the electrochemical water splitting reaction.

Efficient Water Electrolysis at Elevated Temperature using Commercial Cell Components

Decarbonization of the energy system across different sectors using power-to-X concepts relies heavily on the availability of low-cost hydrogen produced from renewable power by water electrolysis. Polymer electrolyte water electrolysis (PEWE) is a promising technology for hydrogen (and oxygen) production for distributed as a well as centralized operation. The total cost of hydrogen is dominated by the electricity cost. Therefore, increase of conversion efficiency is pivotal in improving the commercial viability of electrolytically produced hydrogen. In this study, we investigate the prospects of improving conversion efficiency by reducing the membrane thickness from 200 to 50 micron and increasing the cell temperature from 60 to 120°C.

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Example of a modulation excitation X-ray absorption spectrum and schematic representation of the structural site changes

In situ spectroscopy unveils the structural changes of the sites in single atom catalysts

To improve the performance of single atom catalysts (SACs),  the structure of their active sites under operative conditions needs to be better understood. For this, we have performed in situ X-ray absorption spectroscopy measurements using a modulation excitation approach selectively sensitive to the species involved in the electrochemical reactions. This has allowed us to study the structural changes undergone by two types of SACs, and to tie the observed differences to their catalytic activities.

 

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Electrolyte-dependent differences in current response to applied potential.

Versatile and Fast Methodology for Evaluation of Metallic Lithium Negative Battery Electrodes

Evaluating potential electrolyte candidates is typically a lengthy procedure requiring long-term cycling experiments. To speed this process up, we have investigated potentiostatic lithium plating as a potential method for fast electrolyte suitability investigation. The applications of this methodology is not limited to liquid electrolytes, - effects of solid-state electrolytes, coatings, and other modifications can be readily assessed.

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