Directed Liquid Phase Assembly of Highly Ordered Metallic Nanoparticle Arrays
Source abstract
Abstract
Directed assembly of nanomaterials is a promising route for the synthesis of nanoscale materials. In this paper, we demonstrate the directed-assembly of highly ordered two-dimensional arrays of hierarchical nanostructures with tunable size, spacing and composition. The directed assembly is achieved on lithographically patterned metal films that are subsequently pulse-laser melted; during the brief liquid lifetime, the pattened nanostructures assemble into highly ordered primary and secondary nanoparticles, with sizes below that which was originally patterned. Complementary fluid-dynamics simulations emulate the resultant patterns and show how the competition of capillary forces and liquid metal-solid substrate interaction potential drives the directed assembly. As an example of the enhanced functionality, a full-wave electromagnetic analysis has been performed to identify the nature of the supported plasmonic resonances.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fluid Dynamics and Thin Films · nanoparticles nucleation surface interactions · Nanomaterials and Printing Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, The University of Tennessee, Knoxville, Tennessee 37996, United States
Department of Mathematical Sciences, New Jersey Institute of Technology, Newark, New Jersey 07102, United States
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37381, United States
Charles M. Bowden Research Laboratory, National Research Council−AMRDEC, Redstone Arsenal, Huntsville, Alabama 35898, United States
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