Synergetic Modulation of Electronic Properties of Cobalt Oxide via “Tb” Single Atom for Uphill Urea and Water Electrolysis
Abstract
Exploring single-atom (SA) catalysts in hybrid urea-assisted water electrolysis offers a viable alternative to both Hydrogen (H 2 ) generation and polluted water treatment. However, the unfavorable electronic stabilization, low SA content, intrinsically slow kinetics, and imbalanced adsorption-desorption steps are the bottleneck for its scale-up implementation. Herein, a rare-earth Terbium single atom (Tb SA ) is topologically stabilized on defect-rich Co 3 O 4 (Tb SA @d-Co 3 O 4 ) by Tb─O co-ordination for urea oxidation reaction (UOR) and H 2 evolution reaction (HER). Benefitting from the strong Tb SA interaction with the d-Co 3 O 4, the Tb SA @d-Co 3 O 4 achieves a 10 mA cm -2 current density at 1.27 V and -35 mV for UOR and HER, respectively. Remarkably, when Tb SA @d-Co 3 O 4 is applied as a bi-functional catalyst in a two-electrode system, it merely requires 1.22 V to acquire 10 mA cm -2 with excellent operational stability for 100 h. The hybrid electrolyzer can be successfully empowered by the triboelectric nanogenerator, AA battery, and solar panel with a nominal potential of 1.5 V. The mechanistic investigation predicts "Tb SA " insertion in d-Co 3 O 4 lowered the potential determining step, attributed to balanced reaction energetics for adsorption-desorption of intermediates and favorable charge transfer characteristics for UOR. This work offers a new paradigm to explore the catalytic properties of rare-earth "f-block" elements to create advanced electrocatalysts vi…
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Cobalt facilitates the cleavage of N-H bonds and the oxidation of adsorbed intermediates like *CO and *NHx, which are critical steps in the UOR pathway.
“Additionally, cobalt's presence at the interface of heterostructures induces local electrophilic and nucleophilic regions. This spatial charge separation promotes the adsorption and decomposition of urea molecules [19] and facilitates the cleavage of N–H bonds and the oxidation of adsorbed intermediates like *CO and *NHx, which are critical steps in the UOR pathway [20].”
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Boosting urea electrooxidation on oxyanion-engineered nickel sites via inhibited water oxidation
Gao, X., Bai, X., Wang, P., Jiao, Y., Davey, K., Zheng, Y., & Qiao, S.-Z. (2023) · Nature Communications · doi:10.1038/s41467-023-41588-w · Cited by 306 · see citing works
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González-Lavín, J., Rey-Raap, N., Arenillas, A., Espinosa-Lagunes, F. I., Arriaga, L. G., & Ledesma-García, J. (2026) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2026.155094 · Cited by 1 · see citing works
- Authors
- Ajmal, S., Rasheed, A., Sheng, W., Dastgeer, G., Nguyen, Q. A. T., Wang, P., Chen, P., Liu, S., Bui, V. Q., Zhu, M., Li, P., & Wang, D.
- Affiliations
- Anhui University (CN)
- Sejong University (KR)
- University of Da Nang (VN)
- Tsinghua University (CN)
- Corresponding author
- Liu, Shoujie
- Bui, Viet Q.
- Li, Peng
- ORCID
- Venue
- Advanced Materials
- Publisher
- Wiley
- Published
- 2024-11-11
- Volume
- 37
- Issue
- 1
- Pages
- e2412173-e2412173
- ISSN
- 0935-9648 (ISSN-L)
- 1521-4095
- OpenAlex
- W4404245263
- Cited by
- 72
- References
- 1
- Citations by year
- 2026: 40 · 2025: 32
- FWCI
- 4.80
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Advanced Materials (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Anhui University (S202418001/078, S202418001/077)
- National Natural Science Foundation of China (12475323)
- Natural Science Foundation of Anhui Province (2108085MB55)
- Topics
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Electrocatalysts for Energy Conversion
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › CO2 Reduction Techniques and Catalysts
- Physical Sciences › Materials Science › Materials Chemistry › Catalytic Processes in Materials Science
- Keywords
- cobalt oxide, urea oxidation reaction, hydrogen evolution reaction, bifunctional electrocatalysts, triboelectric nanogenerator, charge transfer
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