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Cited by 363

The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.

Locking the lattice oxygen in RuO2 to stabilize highly active Ru sites in acidic water oxidation

Open access
Ping, Xinyu, Liu, Yongduo, Zheng, Lixia, Song, Yang, Guo, Lin, Chen, Siguo, Wei, Zidong·2024·Nature Communications

Abstract

Ruthenium dioxide is presently the most active catalyst for the oxygen evolution reaction (OER) in acidic media but suffers from severe Ru dissolution resulting from the high covalency of Ru-O bonds triggering lattice oxygen oxidation. Here, we report an interstitial silicon-doping strategy to stabilize the highly active Ru sites of RuO 2 while suppressing lattice oxygen oxidation. The representative Si-RuO 2−0.1 catalyst exhibits high activity and stability in acid with a negligible degradation rate of ~52 μV h−1 in an 800 h test and an overpotential of 226 mV at 10 mA cm−2. Differential electrochemical mass spectrometry (DEMS) results demonstrate that the lattice oxygen oxidation pathway of the Si-RuO 2−0.1 was suppressed by ∼95% compared to that of commercial RuO 2, which is highly responsible for the extraordinary stability. This work supplied a unique mentality to guide future developments on Ru-based oxide catalysts’ stability in an acidic environment.

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Metadata

Authors
Ping, X., Liu, Y., Zheng, L., Song, Y., Guo, L., Chen, S., & Wei, Z.
Venue
Nature Communications
Published
2024-03-20
Volume
15
Issue
1
Pages
2501-2501
ISSN
2041-1723 (ISSN-L)
OpenAlex
W4392984079
Cited by
363
References
56
FWCI
23.99
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Locking the lattice oxygen in RuO2 to stabilize highly active Ru sites in acidic water oxidation. https://app.cochat.ai/papers/10.1038/s41467-024-46815-6
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Ping, X., Liu, Y., Zheng, L., Song, Y., Guo, L., Chen, S., & Wei, Z. (2024). Locking the lattice oxygen in RuO2 to stabilize highly active Ru sites in acidic water oxidation. Nature Communications. https://doi.org/10.1038/s41467-024-46815-6

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