ArticleACS nano2026
Site Defects and Structural Alignment Enhance Interfacial Charge Mobility in Heterostructured Carbon Nitride Catalysts.
Article in ACS nano, 2026. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Activating Ionic Carbon Nitrides via Epitaxial Dyadic Coupling for Efficient Solar-Driven HAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Crystalline-amorphous homojunction engineering in carbon nitride for solar-driven nitrate into ammonia conversion.Chemical science · 2026Article
- Oxygen-oxygen bond cleavage enables efficient photocatalytic HNature communications · 2026Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Engineering interfaces between organic semiconductors is an effective way to tailor organic electronic device performance, as charge transport and light interaction efficiency are strongly influenced by electronic coupling at molecular interfaces. Scanning transmission electron microscopy is routinely used to analyze interfaces at the atomic scale; however, its use for organic materials is limited due to the electron beam sensitivity of organic molecules, buried interfaces, and the semicrystalline nature of organics. In this work, we developed a workflow to correlate charge behavior at organic interfaces with their chemistry and structure, even when interface components are chemically and structurally similar and mixed at the nanoscale. We used this workflow to reveal the nanoscale mechanism behind enhanced charge transfer at the heterojunction between two-dimensional carbon nitride catalysts (poly-heptazine imide (PHI) and poly-triazine imide (PTI)) during the oxygen reduction reaction. We found that PHI crystallites grow on PTI layers formed at the gas-liquid interface in the salt melt, following the [001]
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