Surface Segregation Acts as Surface Engineering for the Oxygen Evolution Reaction on Perovskite Oxides in Alkaline Media
Source abstract
Abstract
La1–xSrxCoO3-δ perovskites are potential catalysts for the anodic reaction of alkaline water electrolyzers, i.e., the oxygen evolution reaction (OER). It is well-known that La1–xSrxCoO3−δ perovskites can easily display strontium surface segregation, but how this influences the performance of La1–xSrxCoO3−δ perovskites as anodic electrode in alkaline water electrolyzers, particularly in terms of OER activity, has not been unveiled yet. This study focuses on La0.2Sr0.8CoO3−δ, which shows relatively high activity for the OER, and reveals the influence of the preparation temperature on the amount and morphology of segregated strontium-containing islands. Thin film samples were prepared at different temperatures by using pulsed laser deposition. Those samples were then characterized with synchrotron-based X-ray photoelectron spectroscopy “as prepared” and after being immersed in ultrapure water. We found that higher preparation temperatures enhance the segregation of strontium, which is then almost quantitatively removed by washing the samples with ultrapure water. After immersion in water, the samples expose a cobalt-rich surface. Investigating the OER activity as a function of the perovskite deposition temperature, it has been found that the higher the deposition temperature (i.e., the more extended the strontium segregation), the higher the OER activity. Such an effect has been linked to the higher amount of cobalt accessible after removing the strontium segregated islands.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electrocatalysts for Energy Conversion · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Paul Scherrer Institut, Forschungsstrasse 111, CH-5232 Villigen PSI, Switzerland
Laboratory of Physical Chemistry, ETH Zürich, CH-8093 Zürich, Switzerland
Funding
Paul Scherrer Institut
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