English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The mechanisms of CO oxidation on the Mg 0.2 Co 0.2 Ni 0.2 Cu 0.2 Zn 0.2 O high-entropy oxide were studied by means of operando soft X-ray absorption spectroscopy. We found that Cu is the active metal and that Cu(II) can be rapidly reduced to Cu(I) by CO when the temperature is higher than 130 °C. Co and Ni do not have any role in this respect. The Cu(II) oxidation state can be easily but slowly recovered by treatment of the sample with O 2 at ca. 250 °C. However, it should be noted that CuO is readily and irreversibly reduced to Cu(I) when it is treated with CO at T &gt; 100 °C. Thus, the main conclusion of this work is that the high configurational entropy of Mg 0.2 Co 0.2 Ni 0.2 Cu 0.2 Zn 0.2 O stabilizes the rock-salt structure and permits the oxidation/reduction of Cu to be reversible, thus permitting the catalytic cycle to take place.

the journal of physical chemistry letters

Stabilization by Configurational Entropy of the Cu(II) Active Site during CO Oxidation on Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O