CoIr Nanoalloy/N-Doped Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene 0D/2D Heterojunction as a Catalyst for the Electrochemical Oxygen Evolution Reaction
Developing high-efficiency oxygen evolution reaction (OER) electrocatalysts is essential for industrial application of sustainable energy conversion and storage systems, which can address energy and environmental challenges. We herein use an ultrasonic-assisted reduction strategy to design an efficient 0D/2D heterojunction by strongly coupling CoIr nanoalloys and N-doped Ti3C2Tx MXenes for the alkaline OER. The resulting CoIr/N-Ti3C2Tx heterojunction not only modifies the electronic structure of Ir sites but also enhances the exposure of active sites, thereby optimizing the adsorption strength of oxygen-related intermediates and significantly lowering the reaction energy barrier for the OER. The CoIr/N-Ti3C2Tx catalyst with a low Ir content (5.12 wt %) only requires a low activation energy of 30.66 kJ mol–1 and a small OER overpotential of 260 mVRHE at 10 mA cm–2, outperforming the commercial IrO2 catalyst. The as-made OER electrocatalyst also shows high catalytic stability for at least 30 h of testing, highlighting that constructing MXene-based heterojunctions is a promising route to achieve high-performance OER electrocatalysts.
Authors
- Tai Thien Huynh (ORCID: https://orcid.org/0000-0002-8280-7902)
- Anh Quoc Khuong Nguyen (ORCID: https://orcid.org/0000-0002-9319-9746)
- Hau Quoc Pham (ORCID: https://orcid.org/0000-0001-6022-0118)
- Quyen Huynh (ORCID: https://orcid.org/0009-0000-1503-4922)
Institutions
- Duy Tan University (VN)
- Trường ĐH Nguyễn Tất Thành (VN)
- Hanoi University of Natural Resources and Environment (VN)
- Institute of Applied Technology (CN)
- Advanced Materials and Devices (United States) (US)
Publication Details
- Journal
- ACS Applied Nano Materials
- Published
- 2025-03-06
- DOI
- https://doi.org/10.1021/acsanm.4c07121
- Citations
- 18
- Primary Topic
- MXene and MAX Phase Materials
- Type
- article
- Field-Weighted Citation Impact
- 9.32