Designing neighboring-site activation of single atom via tunnel ions for boosting acidic oxygen evolution

Realizing an efficient turnover frequency in the acidic oxygen evolution reaction by modifying the reaction configuration is crucial in designing high-performance single-atom catalysts. Here, we report a "single atom-double site" concept, which involves an activatable inert manganese atom redox chemistry in a single-atom Ru-Mn dual-site platform with tunnel Ni ions as the trigger. In contrast to conventional single-atom catalysts, the proposed configuration allows direct intramolecular oxygen coupling driven by the Ni ions intercalation effect, bypassing the secondary deprotonation step instead of the kinetically sluggish adsorbate evolution mechanism. The strong bonding of Ni ions activates the inert manganese terminal groups and inhibits the cross-site disproportionation process inherent in the Mn scaffolding, which is crucial to ensure the dual-site platform. As a result, the single-atom Ru-Ni-Mn octahedral molecular sieves catalyst delivers a low overpotential, adequate mass activity and good stability.

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Publication Details

Journal
Nature Communications
Published
2024-09-13
DOI
https://doi.org/10.1038/s41467-024-52410-6
Citations
71
Primary Topic
Electrochemical Analysis and Applications
Type
article
Field-Weighted Citation Impact
12.24

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article

Designing neighboring-site activation of single atom via tunnel ions for boosting acidic oxygen evolution

Chun‐Han Kuo, Wen‐Jing Zeng, Liming Deng, Zih‐Yi Lin et al.
71 citations
Nature Communications
Electrochemical Analysis and Applications
12.24
article

Designing neighboring-site activation of single atom via tunnel ions for boosting acidic oxygen evolution

Chun‐Han Kuo, Wen‐Jing Zeng, Liming Deng, Zih‐Yi Lin, Shengjie Peng, Sung‐Fu Hung, Feng Hu, Han‐Yi Chen, Linlin Li, Chenchen Zhang, Ye Wang, Ying Zhang, Luqi Wang, Yixin Hao
article en
71 citations

Abstract

Realizing an efficient turnover frequency in the acidic oxygen evolution reaction by modifying the reaction configuration is crucial in designing high-performance single-atom catalysts. Here, we report a "single atom-double site" concept, which involves an activatable inert manganese atom redox chemistry in a single-atom Ru-Mn dual-site platform with tunnel Ni ions as the trigger. In contrast to conventional single-atom catalysts, the proposed configuration allows direct intramolecular oxygen coupling driven by the Ni ions intercalation effect, bypassing the secondary deprotonation step instead of the kinetically sluggish adsorbate evolution mechanism. The strong bonding of Ni ions activates the inert manganese terminal groups and inhibits the cross-site disproportionation process inherent in the Mn scaffolding, which is crucial to ensure the dual-site platform. As a result, the single-atom Ru-Ni-Mn octahedral molecular sieves catalyst delivers a low overpotential, adequate mass activity and good stability.

Nature CommunicationsVol. 15(1)
Jiangnan University (CN), National Yang Ming Chiao Tung University (TW), National Tsing Hua University (TW), Nanjing University of Aeronautics and Astronautics (CN)
National Natural Science Foundation of China, Government of Jiangsu Province
Openalex Percentile: Top 0%
Electrochemical Analysis and Applications
12.24
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