Direct Observation of Collective Dissolution Mechanisms in Iridium Oxide Nanocrystals
Iridium oxide (IrO<sub>2</sub>) is the state-of-the-art electrocatalyst for water oxidation in electrolyzers, yet it suffers from instability under operating conditions. Here, we combine first-principles modeling with in situ liquid-phase transmission electron microscopy and device-scale characterization to resolve the atomic-scale morphology and dissolution dynamics of IrO<sub>2</sub> nanocrystals. Our computational Wulff constructions uniquely incorporate high-index facets, providing new insights into thermodynamic facet-dependent stability under operating conditions. Atomically resolved studies reveal multiple distinct collective dissolution pathways, including high-index facet formation, monolayer reconstruction, step-edge formation, and monolayer delamination on {110} surfaces. Device-scale studies confirm that electrochemical operation results in high-index facet formation. Ab initio molecular dynamics simulations further show that initial dissolution kinetics are facet-dependent. These findings highlight how combining in situ imaging with first-principles modeling reveals atomic-scale dynamics that influence material performance.
Authors
- Aleksandra Vojvodić (ORCID: https://orcid.org/0000-0002-5584-6711)
- Ivan A. Moreno‐Hernandez (ORCID: https://orcid.org/0000-0001-6461-9214)
- Joseph Nicolas (ORCID: https://orcid.org/0000-0002-4669-6635)
- Achala Kankanamge
- Max Huang
- Matteo Fratarcangeli
- S. Avery Vigil
- Daniel Intriago
- Ziqing Lin
- Rachel Thatcher
Institutions
- Duke University (US)
- California University of Pennsylvania (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1021/jacs.5c18363
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00