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Volcano-type relationship between oxidation states and catalytic activity of single-atom catalysts towards hydrogen evolution.


ABSTRACT: To date, the effect of oxidation state on activity remains controversial in whether higher or lower oxidation states benefit the enhancement of catalytic activity. Herein, we discover a volcanic relationship between oxidation state and hydrogen evolution reaction activity based on Os single-atom catalysts. Firstly, a series of Os SACs with oxidation states ranging from  + 0.9 to  + 2.9 are synthesized via modifying the coordination environments, including Os-N3S1, Os-N4, Os-S6, Os-C3, and Os-C4S2. A volcano-type relation between oxidation states and hydrogen evolution activity emerge with a summit at a moderate experimental oxidation state of  + 1.3 (Os-N3S1). Mechanism studies illustrate that with increasing oxidation states, the adsorption of H atoms on Os is strengthened due to increased energy level and decreased occupancy of anti-bonding states of Os-H bond until the anti-bonding states become empty. Further increasing the oxidation states weakens hydrogen adsorption because of the decreased occupancy of Os-H bonding states. In this work, we emphasize the essential role of oxidation state in manipulating activity, which offers insightful guidance for the rational design of single-atom catalysts.

SUBMITTER: Cao D 

PROVIDER: S-EPMC9532448 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Volcano-type relationship between oxidation states and catalytic activity of single-atom catalysts towards hydrogen evolution.

Cao Dong D   Xu Haoxiang H   Li Hongliang H   Feng Chen C   Zeng Jie J   Cheng Daojian D  

Nature communications 20221004 1


To date, the effect of oxidation state on activity remains controversial in whether higher or lower oxidation states benefit the enhancement of catalytic activity. Herein, we discover a volcanic relationship between oxidation state and hydrogen evolution reaction activity based on Os single-atom catalysts. Firstly, a series of Os SACs with oxidation states ranging from  + 0.9 to  + 2.9 are synthesized via modifying the coordination environments, including Os-N<sub>3</sub>S<sub>1</sub>, Os-N<sub>  ...[more]

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