scholarly journals Color from hierarchy: Diverse optical properties of micron-sized spherical colloidal assemblies

2015 ◽  
Vol 112 (35) ◽  
pp. 10845-10850 ◽  
Author(s):  
Nicolas Vogel ◽  
Stefanie Utech ◽  
Grant T. England ◽  
Tanya Shirman ◽  
Katherine R. Phillips ◽  
...  

Materials in nature are characterized by structural order over multiple length scales have evolved for maximum performance and multifunctionality, and are often produced by self-assembly processes. A striking example of this design principle is structural coloration, where interference, diffraction, and absorption effects result in vivid colors. Mimicking this emergence of complex effects from simple building blocks is a key challenge for man-made materials. Here, we show that a simple confined self-assembly process leads to a complex hierarchical geometry that displays a variety of optical effects. Colloidal crystallization in an emulsion droplet creates micron-sized superstructures, termed photonic balls. The curvature imposed by the emulsion droplet leads to frustrated crystallization. We observe spherical colloidal crystals with ordered, crystalline layers and a disordered core. This geometry produces multiple optical effects. The ordered layers give rise to structural color from Bragg diffraction with limited angular dependence and unusual transmission due to the curved nature of the individual crystals. The disordered core contributes nonresonant scattering that induces a macroscopically whitish appearance, which we mitigate by incorporating absorbing gold nanoparticles that suppress scattering and macroscopically purify the color. With increasing size of the constituent colloidal particles, grating diffraction effects dominate, which result from order along the crystal’s curved surface and induce a vivid polychromatic appearance. The control of multiple optical effects induced by the hierarchical morphology in photonic balls paves the way to use them as building blocks for complex optical assemblies—potentially as more efficient mimics of structural color as it occurs in nature.

Soft Matter ◽  
2021 ◽  
Author(s):  
Jiawei Lu ◽  
Xiangyu Bu ◽  
Xinghua Zhang ◽  
Bing Liu

The shapes of colloidal particles are crucial to the self-assembled superstructures. Understanding the relationship between the shapes of building blocks and the resulting crystal structures is an important fundamental question....


Molecules ◽  
2019 ◽  
Vol 24 (23) ◽  
pp. 4307 ◽  
Author(s):  
Gabriele Magna ◽  
Donato Monti ◽  
Corrado Di Natale ◽  
Roberto Paolesse ◽  
Manuela Stefanelli

The interest in assembling porphyrin derivatives is widespread and is accounted by the impressive impact of these suprastructures of controlled size and shapes in many applications from nanomedicine and sensors to photocatalysis and optoelectronics. The massive use of porphyrin dyes as molecular building blocks of functional materials at different length scales relies on the interdependent pair properties, consisting of their chemical stability/synthetic versatility and their quite unique physicochemical properties. Remarkably, the driven spatial arrangement of these platforms in well-defined suprastructures can synergically amplify the already excellent properties of the individual monomers, improving conjugation and enlarging the intensity of the absorption range of visible light, or forming an internal electric field exploitable in light-harvesting and charge-and energy-transport processes. The countless potentialities offered by these systems means that self-assembly concepts and tools are constantly explored, as confirmed by the significant number of published articles related to porphyrin assemblies in the 2015–2019 period, which is the focus of this review.


Soft Matter ◽  
2015 ◽  
Vol 11 (19) ◽  
pp. 3913-3919 ◽  
Author(s):  
E. Edlund ◽  
O. Lindgren ◽  
M. Nilsson Jacobi

Patchy colloidal particles are promising candidates for building blocks in directed self-assembly.


2019 ◽  
Vol 2 (1) ◽  
pp. 1900085
Author(s):  
Heng Zhang ◽  
Xiuming Bu ◽  
SenPo Yip ◽  
Xiaoguang Liang ◽  
Johnny C. Ho

Science ◽  
2020 ◽  
Vol 369 (6506) ◽  
pp. 950-955
Author(s):  
Carla Fernández-Rico ◽  
Massimiliano Chiappini ◽  
Taiki Yanagishima ◽  
Heidi de Sousa ◽  
Dirk G. A. L. Aarts ◽  
...  

Understanding the impact of curvature on the self-assembly of elongated microscopic building blocks, such as molecules and proteins, is key to engineering functional materials with predesigned structure. We develop model “banana-shaped” colloidal particles with tunable dimensions and curvature, whose structure and dynamics are accessible at the particle level. By heating initially straight rods made of SU-8 photoresist, we induce a controllable shape deformation that causes the rods to buckle into banana-shaped particles. We elucidate the phase behavior of differently curved colloidal bananas using confocal microscopy. Although highly curved bananas only form isotropic phases, less curved bananas exhibit very rich phase behavior, including biaxial nematic phases, polar and antipolar smectic-like phases, and even the long-predicted, elusive splay-bend nematic phase.


Open Physics ◽  
2012 ◽  
Vol 10 (3) ◽  
Author(s):  
Achille Giacometti

AbstractMotivated by recent experimental findings in chemical synthesis of colloidal particles, we draw an analogy between self-assembly processes occurring in biological systems (e.g. protein folding) and a new exciting possibility in the field of material science. We consider a self-assembly process whose elementary building blocks are decorated patchy colloids of various types, that spontaneously drive the system toward a unique and predetermined targeted macroscopic structure. To this aim, we discuss a simple theoretical model — the Kern-Frenkel model — describing a fluid of colloidal spherical particles with a pre-defined number and distribution of solvophobic and solvophilic regions on their surface. The solvophobic and solvophilic regions are described via a short-range square-well and a hard-sphere potentials, respectively. Integral equation and perturbation theories are presented to discuss structural and thermodynamical properties, with particular emphasis on the computation of the fluid-fluid (or gas-liquid) transition in the temperaturedensity plane. The model allows the description of both one and two attractive caps, as a function of the fraction of covered attractive surface, thus interpolating between a square-well and a hard-sphere fluid, upon changing the coverage. By comparison with Monte Carlo simulations, we assess the pros and the cons of both integral equation and perturbation theories in the present context of patchy colloids, where the computational effort for numerical simulations is rather demanding.


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1114
Author(s):  
Petra Bačová ◽  
Dimitris G. Mintis ◽  
Eirini Gkolfi ◽  
Vagelis Harmandaris

We present an atomistic molecular dynamics study of self-assembled mikto-arm stars, which resemble patchy-like particles. By increasing the number of stars in the system, we propose a systematic way of examining the mutual orientation of these fully penetrable patchy-like objects. The individual stars maintain their patchy-like morphology when creating a mesoscopic (macromolecular) self-assembled object of more than three stars. The self-assembly of mikto-arm stars does not lead to a deformation of the stars, and their shape remains spherical. We identified characteristic sub-units in the self-assembled structure, differing by the mutual orientation of the nearest neighbor stars. The current work aims to elucidate the possible arrangements of the realistic, fully penetrable patchy particles in polymer matrix and to serve as a model system for further studies of nanostructured materials or all-polymer nanocomposites using the mikto-arm stars as building blocks.


2020 ◽  
Author(s):  
Shuai Zhang ◽  
Robert Alberstein ◽  
James De Yoreo ◽  
F. Akif Tezcan

Self-assembly of molecular building blocks into higher-order structures is exploited in living systems to create functional complexity and represents a powerful synthetic strategy for constructing new materials. As nanoscale building blocks, proteins offer unique advantages, including monodispersity and atomically tunable interactions. Yet, control of protein self-assembly has been limited compared to that of inorganic or polymeric nanoparticles, which lack such attributes. We report modular self-assembly of an engineered protein into four physicochemically distinct, precisely patterned 2D crystals via control of four classes of interactions acting locally, regionally and globally. We relate the resulting structures to the underlying free-energy landscape by combining in-situ atomic force microscopy observations of assembly with thermodynamic analyses of protein-protein and -surface interactions. Our results demonstrate rich phase behavior obtainable from a single, highly-patchy protein when interactions acting over multiple length scales are exploited and predict new bulk-scale properties for protein based materials that ensue from such control.<div> </div>


2021 ◽  
Author(s):  
Rivi Ratnaweera ◽  
Freddy Rodríguez Ortiz ◽  
Nicholas Gripp ◽  
Matthew Sheldon

Aligning large populations of colloidal nanorods (NRs) into ordered assemblies provides a strategy for engineering macroscopic functional materials with strong optical anisotropy. The bulk optical properties of such systems depend not only on the individual NR building blocks, but also on their meso- and macroscale ordering, in addition to more complex inter-particle coupling effects. Here, we investigate the dynamic alignment of colloidal CdSe/CdS NRs in the presence of AC electric fields by measuring concurrent changes in optical transmission. Our work identifies two distinct scales of interaction that give rise to the field-driven optical response: (1) the spontaneous mesoscale self-assembly of colloidal NRs into structures with increased optical anisotropy, and (2) the macroscopic ordering of NR assemblies along the direction of the applied AC field. By modeling the alignment of NR ensembles using directional statistics, we experimentally quantify the maximum degree of order in terms of the average deviation angle relative to the field axis. Results show a consistent improvement in alignment as a function of NR concentration—with a minimum average deviation of 18.7°—indicating that mesoscale assembly helps facilitate field-driven alignment of colloidal NRs.


Soft Matter ◽  
2018 ◽  
Vol 14 (39) ◽  
pp. 7954-7957 ◽  
Author(s):  
Liujun Song ◽  
Xiaolin Du ◽  
Li Zhong ◽  
Xinya Zhang ◽  
Zhengdong Cheng

The diagram shows a highly ordered periodic crystalline array, multilayer structure, Bragg diffraction phenomenon and well-patterned binary colloidal crystals, respectively.


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