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Low-iridium doped single-crystalline hydrogenated titanates (H2Ti3O7) with large exposed {100} facets for enhanced oxygen evolution reaction under acidic conditions.
- Source :
-
Journal of Alloys & Compounds . Jun2023, Vol. 946, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- Development of efficient and stable electrocatalysts for oxygen evolution reaction (OER) under acidic conditions is desirable goal for commercializing proton exchange membrane (PEM) water electroyzer. Herein, we report iridium-doped hydrogenated titanate (Ir–HTO) nanobelts as a promising catalyst with a low-Ir content for the acidic OER. Addition of low-Ir (∼ 3.36 at%) into the single-crystalline HTO nanobelts with large exposed {100} facets significantly boost catalytic activity and stability for OER under acidic conditions. The Ir-HTO outperforms the commercial benchmark IrO 2 catalyst; an overpotential for delivering 10 mA cm−2 current density was reduced to about 25% for the Ir-HTO. Moreover, the catalytic performance of Ir-HTO is positioned as the most efficient electrocatalyst for the acidic OER. An improved intrinsic catalytic activity and stability are also confirmed for the Ir-HTO through in-depth electrochemical characterizations. Therefore, our results suggest that low-Ir doped single-crystalline HTO nanobelts can be a promising catalyst for efficient and durable OER under acidic conditions. • We developed an Ir-doped catalyst for the acidic oxygen evolution reaction (OER). • Ir was incorporated into a H 2 Ti 3 O 7 nanobelts (Ir–HTO) with large exposed {100} facets. • The single-crystalline nature of HTO increased the active sites for the OER. • The Ir-HTO nanobelts have a low Ir content (about 3–4 wt%) at the atomic scale. • The Ir-HTO nanobelts have high catalytic activity and durability for acidic OER. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09258388
- Volume :
- 946
- Database :
- Academic Search Index
- Journal :
- Journal of Alloys & Compounds
- Publication Type :
- Academic Journal
- Accession number :
- 162386314
- Full Text :
- https://doi.org/10.1016/j.jallcom.2023.169466