Rational Strain Engineering in Delafossite Oxides for Highly Efficient Hydrogen Evolution Catalysis in Acidic Media
arXiv:1903.10576 · doi:10.1038/s41929-019-0400-x
Abstract
The rational design of hydrogen evolution reaction (HER) electrocatalysts which are competitive with platinum is an outstanding challenge to make power-to-gas technologies economically viable. Here, we introduce the delafossites PdCrO, PdCoO and PtCoO as a new family of electrocatalysts for the HER in acidic media. We show that in PdCoO the inherently strained Pd metal sublattice acts as a pseudomorphic template for the growth of a strained (by +2.3%) Pd rich capping layer under reductive conditions. The surface modification continuously improves the electrocatalytic activity by simultaneously increasing the exchange current density j from 2 to 5 mA/cm and by reducing the Tafel slope down to 38 mV/decade, leading to overpotentials < 15 mV for 10 mA/cm, superior to bulk platinum. The greatly improved activity is attributed to the in-situ stabilization of a -palladium hydride phase with drastically enhanced surface catalytic properties with respect to pure or nanostructured palladium. These findings illustrate how operando induced electrodissolution can be used as a top-down design concept for rational surface and property engineering through the strain-stabilized formation of catalytically active phases.
References in corpus (4)
Cited by in corpus (6)
- Surface-Confined Two-Dimensional Crystal Growth on a Monolayer
- Emergent magnetism with continuous control in the ultrahigh conductivity layered oxide PdCoO2
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- Anomalous Hall effect in electrolytically reduced PdCoO thin films
- Dichotomy of electron-phonon interactions in the delafossite PdCoO: From weak bulk to polaronic surface coupling
- Layer-Resolved Many-Electron Interactions in Delafossite PdCoO2 from Standing-Wave Photoemission Spectroscopy