ArticleChemical science2024
Atomically dispersed dinuclear iridium active sites for efficient and stable electrocatalytic chlorine evolution reaction.
Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Identification of Ni-NJournal of the American Chemical Society · 2025Article
- Ultrafast Synthesis of IrBAngewandte Chemie (International ed. in English) · 2025Article
- Renaissance of Chlorine Evolution Reaction: Emerging Theory and Catalytic Materials.Angewandte Chemie (International ed. in English) · 2025Review
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9 authors.
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Abstract
The electrochemical chlorine evolution reaction (CER) is a critical anode reaction in chlor-alkali electrolysis. Although precious metal-based mixed metal oxides (MMOs) have long been used as CER catalysts, they suffer from high cost and poor selectivity due to the competing oxygen evolution reaction (OER). Single-atom catalysts (SACs), featuring high atom utilization efficiency, have captured widespread interest in diverse applications. However, the single-atom sites in SACs are generally recognized as independent motifs and the interplay of adjacent sites is largely overlooked. Herein, we report a "precursor-preselected" cage-encapsulated strategy to synthesize atomically dispersed dinuclear iridium active sites bridged by oxygen that are supported on nitrogen-doped carbon (Ir
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