ArticleNature communications2026
DNA-programmed galvanic Ostwald ripening in nanoparticle assemblies.
Article in Nature communications, 2026. 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- DNA-programmed galvanic Ostwald ripening in nanoparticle assemblies.Nature communications · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ostwald ripening of nanoparticles, where larger particles grow at the expense of smaller ones, is typically a thermodynamically driven process that is difficult to control. Here, we report contact-dependent, localized galvanic Ostwald ripening, a mechanism that can harness Ostwald ripening of nanoparticles as a programmable tool for nanofabrication. Using DNA origami to precisely control interparticle distances, we show that silver grows homogeneously on gold seeds until nanoparticle electrical contact triggers asymmetric ripening, driven by size-dependent electrochemical potentials. By programming when and where nanoparticles touch, we direct ripening pathways to create designer heterogeneous nanoparticle structures with enhanced plasmonic properties. In this work, we elucidate the origin of heterogeneous silver growth in nanoparticle clusters and establish design principles for engineering asymmetric nanostructures with predetermined morphologies, advancing both fundamental colloidal nanoscience and plasmonic device fabrication.
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Registered trials
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