journal article·2025-09-24

Activation of the Lattice Oxygen Mechanism in NiOOH as an Electrocatalyst for the Oxygen Evolution Reaction: The Role of Anion Intercalation

Xue Han, Siyi Chen, Jingxian Yu, Shengping Wang

ACS Applied Materials & Interfaces· Volume 17· Issue 38
Publisher page

Abstract

The lattice oxygen mechanism (LOM) of the oxygen evolution reaction (OER) offers significant kinetic advantages over the adsorbed oxygen mechanism. Anion intercalation induces the LOM in NiOOH by enhancing the covalency of lattice oxygen through the modulation of the metal–oxygen electronic state. The relationships between doping mechanisms, such as the size and valence state of anions and the kinetics of the OER, have been clarified. Phosphate-intercalated NiOOH (NiOOH-PO), which benefits from the activated LOM mechanism, has low overpotentials of 195 mV at 10 mA cm –2 and 274 mV at 50 mA cm –2 .
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications · Advanced battery technologies research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Faculty of Materials Science and Chemistry

China University of Geosciences

Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering

Guilin University of Technology

School of Chemistry, Physics and Earth Sciences

The University of Adelaide

Funding

Department of Science and Technology of Hubei Province · National Natural Science Foundation of China · Science and Technology Department of Guangxi Zhuang Autonomous Region

References (31)

Show source-provided references
1. 10.1021/acsnano.3c0522410.1021/acsnano.3c05224 ↗
2. 10.1021/acscatal.3c0124310.1021/acscatal.3c01243 ↗
3. 10.1016/j.jechem.2024.09.06610.1016/j.jechem.2024.09.066 ↗
4. 10.1016/j.scib.2020.09.03710.1016/j.scib.2020.09.037 ↗
5. 10.1039/C4TA03789H10.1039/C4TA03789H ↗
6. 10.1039/D3QI02264A10.1039/D3QI02264A ↗
7. 10.1016/j.jcat.2022.03.02810.1016/j.jcat.2022.03.028 ↗
8. 10.1016/j.cej.2021.13087310.1016/j.cej.2021.130873 ↗
9. 10.1002/anie.20201433110.1002/anie.202014331 ↗
10. 10.1063/5.003601910.1063/5.0036019 ↗
11. 10.1016/j.apcatb.2023.12261210.1016/j.apcatb.2023.122612 ↗
12. 10.1002/celc.20230023510.1002/celc.202300235 ↗
13. 10.1002/anie.20220727910.1002/anie.202207279 ↗
14. 10.1016/j.apcatb.2022.12209110.1016/j.apcatb.2022.122091 ↗
15. 10.1016/j.jcis.2022.05.16210.1016/j.jcis.2022.05.162 ↗
16. 10.1016/j.nanoen.2022.10707110.1016/j.nanoen.2022.107071 ↗
17. 10.1039/D3EE02627B10.1039/D3EE02627B ↗
18. 10.1038/ncomms1105310.1038/ncomms11053 ↗
19. 10.1016/j.electacta.2019.13539510.1016/j.electacta.2019.135395 ↗
20. 10.1016/j.cej.2022.13910410.1016/j.cej.2022.139104 ↗
21. 10.1016/j.matchemphys.2013.10.01310.1016/j.matchemphys.2013.10.013 ↗
22. 10.1021/acs.langmuir.4c0120010.1021/acs.langmuir.4c01200 ↗
23. 10.1039/C9TA03882E10.1039/C9TA03882E ↗
24. 10.3390/catal1207068810.3390/catal12070688 ↗
25. 10.1039/C9CS00607A10.1039/C9CS00607A ↗
26. 10.1038/nchem.269510.1038/nchem.2695 ↗
27. 10.1021/acscatal.2c0100110.1021/acscatal.2c01001 ↗
28. 10.1039/c3sc50205h10.1039/c3sc50205h ↗
29. 10.1016/j.apsusc.2025.16328210.1016/j.apsusc.2025.163282 ↗
30. 10.1039/D1EE01277K10.1039/D1EE01277K ↗
31. 10.1002/anie.20230140810.1002/anie.202301408 ↗