On the Homogeneity of a Cobalt-Based Water Oxidation Catalyst.
Daan den BoerQuentin SiberieMaxime A SieglerThimo H FerberDominik C MoritzJan Philipp HofmannDennis G H HetterscheidPublished in: ACS catalysis (2022)
The homogeneity of molecular Co-based water oxidation catalysts (WOCs) has been a subject of debate over the last 10 years as assumed various homogeneous Co-based WOCs were found to actually form CoO x under operating conditions. The homogeneity of the Co(H L ) (H L = N , N -bis(2,2'-bipyrid-6-yl)amine) system was investigated with cyclic voltammetry, electrochemical quartz crystal microbalance, and X-ray photoelectron spectroscopy. The obtained experimental results were compared with heterogeneous CoO x . Although it is shown that Co(H L ) interacts with the electrode during electrocatalysis, the formation of CoO x was not observed. Instead, a molecular deposit of Co(H L ) was found to be formed on the electrode surface. This study shows that deposition of catalytic material is not necessarily linked to the decomposition of homogeneous cobalt-based water oxidation catalysts.
Keyphrases
- metal organic framework
- resting state
- highly efficient
- ionic liquid
- carbon nanotubes
- hydrogen peroxide
- reduced graphene oxide
- solid state
- high resolution
- single molecule
- functional connectivity
- visible light
- electron transfer
- gold nanoparticles
- magnetic resonance imaging
- magnetic resonance
- computed tomography
- nitric oxide
- binding protein
- high speed
- carbon dioxide