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Although metal oxide nanocrystals are often highly active, rapid aggregation (particularly in water) generally precludes detailed solution‐state investigations of their catalytic reactions. This is equally true for visible‐light‐driven water oxidation with hematite α‐Fe2O3 nanocrystals, which bridge a conceptual divide between molecular complexes of iron and solid‐state hematite photoanodes. We herein...
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