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Copper complexes as catalyst precursors in the electrochemical hydrogen evolution reaction
Merle Kügler1, Julius Scholz2, Andreas Kronz3
1Georg-August-University Göttingen, Institute of Inorganic Chemistry, Tammannstrasse 4, D-37077 Göttingen, Germany. inke.siewert@chemie.uni-goettingen.de.
Copper complexes catalyze electrochemical hydrogen evolution in water. Under reaction conditions, these complexes decompose, forming active copper deposits on the electrode surface, independent of the ligands.
Area of Science:
- Coordination Chemistry
- Electrochemistry
- Catalysis
Background:
- Copper complexes are investigated for catalytic applications.
- Understanding ligand effects on metal ion speciation is crucial.
- Electrochemical proton reduction is a key area in sustainable energy.
Purpose of the Study:
- Synthesize and characterize copper(II) complexes with novel ligand scaffolds.
- Evaluate their performance in electrochemical hydrogen evolution reaction (HER).
- Investigate the role of ligands and complex speciation in catalysis.
Main Methods:
- Synthesis of copper(II) complexes with two distinct ligand types.
- pH-dependent speciation studies (mononuclear/dinuclear equilibrium).
- Electrochemical testing for hydrogen evolution reaction (HER) in aqueous media.
Main Results:
- Two water-soluble copper(II) complexes with N4-coordination environments were synthesized.
- Complex solutions exhibited high catalytic activity for HER in acidic water.
- Complex decomposition under catalytic conditions led to active copper(0) and Cu2O deposits.
Conclusions:
- The active HER catalysts are copper deposits formed in situ, not the intact complexes.
- Ligand presence or absence did not affect the catalytic activity of the solution or deposit.
- Insights into the stability and decomposition pathways of copper catalysts in aqueous HER were gained.
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