Anode Catalysts in Anion-Exchange-Membrane Electrolysis without Supporting Electrolyte: Conductivity, Dynamics, and Ionomer Degradation.
Raina A KrivinaGrace A LindquistSarah R BeaudoinTimothy Nathan StovallWillow L ThompsonLiam P TwightDouglas MarshJoseph GrzybKevin FabrizioJames E HutchisonShannon W BoettcherPublished in: Advanced materials (Deerfield Beach, Fla.) (2022)
Anion-exchange-membrane water electrolyzers (AEMWEs) in principle operate without soluble electrolyte using earth-abundant catalysts and cell materials and thus lower the cost of green H 2 . Current systems lack competitive performance and the durability needed for commercialization. One critical issue is a poor understanding of catalyst-specific degradation processes in the electrolyzer. While non-platinum-group-metal (non-PGM) oxygen-evolution catalysts show excellent performance and durability in strongly alkaline electrolyte, this has not transferred directly to pure-water AEMWEs. Here, AEMWEs with five non-PGM anode catalysts are built and the catalysts' structural stability and interactions with the alkaline ionomer are characterized during electrolyzer operation and post-mortem. The results show catalyst electrical conductivity is one key to obtaining high-performing systems and that many non-PGM catalysts restructure during operation. Dynamic Fe sites correlate with enhanced degradation rates, as does the addition of soluble Fe impurities. In contrast, electronically conductive Co 3 O 4 nanoparticles (without Fe in the crystal structure) yield AEMWEs from simple, standard preparation methods, with performance and stability comparable to IrO 2 . These results reveal the fundamental dynamic catalytic processes resulting in AEMWE device failure under relevant conditions, demonstrate a viable non-PGM catalyst for AEMWE operation, and illustrate underlying design rules for engineering anode catalyst/ionomer layers with higher performance and durability.
Keyphrases
- highly efficient
- metal organic framework
- ion batteries
- ionic liquid
- reduced graphene oxide
- crystal structure
- transition metal
- room temperature
- single cell
- gold nanoparticles
- visible light
- magnetic resonance
- stem cells
- cell therapy
- magnetic resonance imaging
- genome wide
- carbon dioxide
- dna methylation
- solar cells
- tandem mass spectrometry
- liquid chromatography
- solid phase extraction