ArticleNature communications2025
On-surface synthesis of tailored organic platforms for single metal atoms.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- A dual-mode large language model assistant for on-surface reactionsChemical science · 2026Article
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Authors and funding
13 authors.
Funding
Abstract
Recent advances in nanomaterials have pushed the boundaries of nanoscale fabrication to the limit of single atoms, particularly in heterogeneous catalysis. Single atom catalysts, comprising minute amounts of transition metals dispersed on inert substrates, have emerged as prominent materials in this domain. However, overcoming the tendency of these single atoms to cluster beyond cryogenic temperatures and precisely arranging them on surfaces with desired local environments pose significant challenges. Employing organic templates for orchestrating and modulating the activity of single atoms holds promise. Here, we introduce an on-surface synthesis of a single atom platform wherein atoms are firmly anchored to specific coordination sites distributed along carbon-based polymers. These platforms exhibit atomic-level structural precision and stability, even at elevated temperatures, offering arrays of undercoordinated metal centers as model active sites for single-atom catalysis. We theoretically reveal the pronounced ability of these architectures to coordinate several gas molecules and experimentally visualize their interaction with CO and CO
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Registered trials
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