ArticleACS nano2025
Template-Free Ultrafast Directed Self-Assembly Using Biaxial Toggled Magnetic Fields.
Article in ACS nano, 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.
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Who cites it
1 citing paper in PubMed.
- Roadmap collaborative research on structured magnetic elastomers and their material behavior-bridging from fundamental and materials science to educational science.The European physical journal. E, Soft matter · 2026Review
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Speeding up the directed self-assembly of functional nanomaterials is a rapidly advancing area of research. Traditional self-assembly methods can be slow and limited by kinetic barriers. In this study, we demonstrate that the process can be dramatically accelerated for magnetic colloids when biaxial toggled magnetic fields (BTFs) are used. In this field configuration, a transversal pulsed magnetic field is superimposed perpendicular to the primary toggled magnetic field, facilitating faster phase separation in a model magnetic colloid. This approach offers enhanced control over aggregation dynamics by adjusting the field's frequency and intensity and does not require any physical templates. Beyond structure control, the aggregation kinetics can also be precisely tuned. Within the context of magnetic materials, this method enables the formation of diverse and tunable structures such as chains, columns, depercolated aggregates, and percolating bands. BTFs further promote the formation of highly crystalline domains, enhancing the properties of the resulting self-assembled materials. While this technique is specifically tailored for magnetic systems, its versatility makes it relevant for the design and fabrication of functional nanomaterials. The ability to tune aggregation kinetics and achieve a range of structures may be beneficial for applications in photonics, electronics, and biomedicine.
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Registered trials
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