Photonics of Template-Mediated Lattices of Colloidal Clusters.

Langmuir

Department of Chemical Engineering , Technion-Israel Institute of Technology, Haifa 32000 , Israel.

Published: March 2019

The recent progress in microfluidic microfabrication enables mass production of "colloidal molecules" with a preprogrammed geometry (e.g., dumbbells, tetrahedrons, etc.). Such colloids can be used as elementary building blocks in the fabrication of colloidal crystals with unique optical properties. Anisotropic clusters, however, cannot be readily assembled into regular lattices. In this paper, we study photonic properties of compact cubic templates of microdrops encapsulating complex "colloidal molecules". Because monodisperse droplets can be easily packed into dense cubic lattices and encapsulation techniques (e.g., using microfluidics) are well developed, such a material is experimentally feasible. The rationale behind such a methodology is that for a particular alignment of the encapsulated "colloidal molecules" (e.g., by applying an external magnetic or electric field), the resulting structures resemble a diamond lattice, which is known to exhibit a wide complete photonic band gap. The photonic properties of two cubic templates encapsulating dumbbells (symmetric and asymmetric) and tetrahedrons are investigated numerically. In particular, we show the emergence of the complete 3D band gap (∼8% wide for the dielectric contrast ε = 14) for symmetric dumbbells embedded within a face-centered cubic template and oriented along the space diagonal of the elementary cubic cell.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.langmuir.8b03714DOI Listing

Publication Analysis

Top Keywords

"colloidal molecules"
12
photonic properties
8
cubic templates
8
band gap
8
cubic
5
photonics template-mediated
4
template-mediated lattices
4
lattices colloidal
4
colloidal clusters
4
clusters progress
4

Similar Publications

In this study, we explore the self-assembly of various colloidal symmetric dumbbell (DB) isomers, including dipole Janus, cis-Janus, trans-Janus, apolar-inward and polar-inward perpendicular Janus, and alternating perpendicular Janus DBs. Using dissipative particle dynamics (DPD) simulations under conditions mimicking experimental setups, we investigate cluster formation driven by emulsion droplet evaporation. Our findings reveal a diverse set of cluster structures, which are in good agreement with experimental and simulation results reported in the literature while also predicting the formation of novel cluster configurations.

View Article and Find Full Text PDF

In-situ isomerization and reversible self-assembly of photoresponsive polymeric colloidal molecules enabled by ON and OFF light control.

J Colloid Interface Sci

February 2025

Institute for Advanced Study, Shenzhen University, Nanhai Avenue 3688, Shenzhen 518060, China. Electronic address:

Photocatalytic colloids enable light-triggered nonequilibrium interactions and are emerging as key components for the self-assembly of colloidal molecules (CMs) out of equilibrium. However, the material choices have largely been limited to inorganic substances and the potential for reconfiguring structures through dynamic light control remains underexplored, despite light being a convenient handle for tuning nonequilibrium interactions. Here, we introduce photoresponsive N,O-containing covalent organic polymer (NOCOP) colloids, which display multi-wavelength triggered fluorescence and switchable diffusiophoretic interactions with the addition of triethanolamine.

View Article and Find Full Text PDF

Coacervation, the phase separation of liquid induced by polymeric solutes, sometimes results in the formation of oligomeric clusters of droplets. The morphology of the clusters is non-uniform because the clustering is a consequence of the random collisions of the drifting droplets. Here we report distinctively organized coacervation, yielding colloidal molecules with monodisperse size, morphological symmetry, and compositional heterogeneity.

View Article and Find Full Text PDF
Article Synopsis
  • Colloidal molecules are structures made from micro- and nanoparticles that help us study molecular behavior and create materials with adjustable properties.
  • This research presents a method for creating colloidal molecules, where a central active particle is surrounded by passive particles that interact via chemical reactions and electric fields.
  • The study showcases the ability to design various particle structures and control their assembly in real time, leading to innovative applications in adaptive micro-nanomachines.
View Article and Find Full Text PDF

Impact of non-reciprocal interactions on colloidal self-assembly with tunable anisotropy.

J Chem Phys

August 2024

Institute for Theoretical Physics, Technical University of Berlin, Hardenbergstr. 36, 10623 Berlin, Germany.

Non-reciprocal (NR) effective interactions violating Newton's third law occur in many biological systems, but can also be engineered in synthetic, colloidal systems. Recent research has shown that such NR interactions can have tremendous effects on the overall collective behavior and pattern formation, but can also influence aggregation processes on the particle scale. Here, we focus on the impact of non-reciprocity on the self-assembly of a colloidal system (originally passive) with anisotropic interactions whose character is tunable by external fields.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!