Abstract
Surface reconstruction is inevitable for oxygen evolution reaction (OER) electrocatalysts. Here, we report that pyrite-type iridium telluride (Ir3Te8) can undergo favorable surface reconstruction during the OER process in acid. Compared with a IrTe2 counterpart, the relatively weak Ir–Te bonds in Ir3Te8 facilitate the formation of a Ir3Te8/IrO2-TeO2 heterojunction. Strengthened orbital interaction between the reconstructed IrO2-TeO2 layer and Ir3Te8 optimizes the electronic structure to enhance the electrocatalytic activity. As a result, the reconstructed Ir3Te8 with a stable surface achieves a low overpotential of 467.8 mV at a current density of 1 A cm−2 and maintains stability over 1,000 h at 10 mA cm−2. Although surface reconstruction is inevitable, this work demonstrates that its positive impacts can be maximized through optimization of the structural characteristics of the initial iridium telluride polymorphs to customize the reconstruction process. This highlights a design strategy for advanced OER catalysts that operate in acidic environments, including Ir-based catalysts and beyond.
| Original language | English |
|---|---|
| Article number | 101580 |
| Journal | Chem Catalysis |
| Volume | 6 |
| Issue number | 2 |
| DOIs | |
| State | Published - 19 Feb 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- iridium telluride
- oxygen evolution reaction
- phase structure
- surface reconstruction
- water splitting
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