Cargando…
IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media
A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192761/ https://www.ncbi.nlm.nih.gov/pubmed/34112770 http://dx.doi.org/10.1038/s41467-021-23907-1 |
Sumario: | A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(−2) at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm(−2) at least 800 h with a negligible degradation rate of ~4 μV h(−1). Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO(2))(n) clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO(2) clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers. |
---|