arrow
Return

Ionic solids from common colloids

delete2020-04-22
delete0
PRE
AI
T
Theodore Hueckel
G
Glen M. Hocky
J
Jérémie Palacci
S
Stefano Sacanna *
DOI:10.1038/s41586-020-2205-0delete
deleteOriginal
deleteShare
deleteSave
Abstract

Abstract

En 中文
From rock salt to nanoparticle superlattices, complex structure can emerge from simple building blocks that attract each other through Coulombic forces1–4. On the micrometre scale, however, colloids in water defy the intuitively simple idea of forming crystals from oppositely charged partners, instead forming non-equilibrium structures such as clusters and gels5–7. Although various systems have been engineered to grow binary crystals8–11, native surface charge in aqueous conditions has not been used to assemble crystalline materials. Here we form ionic colloidal crystals in water through an approach that we refer to as polymer-attenuated Coulombic self-assembly. The key to crystallization is the use of a neutral polymer to keep particles separated by well defined distances, allowing us to tune the attractive overlap of electrical double layers, directing particles to disperse, crystallize or become permanently fixed on demand. The nucleation and growth of macroscopic single crystals is demonstrated by using the Debye screening length to fine-tune assembly. Using a variety of colloidal particles and commercial polymers, ionic colloidal crystals isostructural to caesium chloride, sodium chloride, aluminium diboride and K4C60 are selected according to particle size ratios. Once fixed by simply diluting out solution salts, crystals are pulled out of the water for further manipulation, demonstrating an accurate translation from solution-phase assembly to dried solid structures. In contrast to other assembly approaches, in which particles must be carefully engineered to encode binding information12–18, polymer-attenuated Coulombic self-assembly enables conventional colloids to be used as model colloidal ions, primed for crystallization. Oppositely charged colloidal particles are assembled in water through an approach that allows electrostatic interactions to be precisely tuned to generate macroscopic single crystals.

Journal

Nature cover
Nature
IF:
48.5
Papers:
3.4W
Citations:
96.7W

Organization

U
University of California San Diego
Scholars:
2.9K
Papers: 895
Citations: 0
N
New York University
Scholars:
1.2K
Papers: 596
Citations: 0
Cited Papers

Cited Papers

Electrostatic self-assembly of macroscopic crystals using contact electrification
err2003-03-23
err239
PREAI
errGrzybowski, BA; Winkleman, A; Wiles, JA; Brumer, Y; Whitesides, GM
errShare
errSave
errShare
errSave
Superlattice formation in binary mixtures of hard-sphere colloids
err1992-06-22
err0
PREAI
errP. Bartlett; R. H. Ottewill; P. N. Pusey
errShare
errSave
Patchy Particle Self-Assembly via Metal Coordination
err2013-09-17
err106
PREAI
errWang, Yufeng; Hollingsworth, Andrew D.; Yang, Si Kyung; Patel, Sonal; Pine, David J.; Weck, Marcus
errShare
errSave
Assembling oppositely charged lock and key responsive colloids: A mesoscale analog of adaptive chemistry
err2017-09-01
err43
errOAAI
errMihut, Adriana M.; Stenqvist, Bjorn; Lund, Mikael; Schurtenberger, Peter; Crassous, Jerome J.
errShare
errSave
DNA-guided crystallization of colloidal nanoparticles
errNature
IF48.5
err2008-01-01
err0
PREAI
errDmytro Nykypanchuk; Mathew M. Maye; Daniel van der Lelie; Oleg Gang
errShare
errSave
Lock and key colloids
err2010-03-01
err0
PREAI
errS. Sacanna; W. T. M. Irvine; P. M. Chaikin; D. J. Pine
errShare
errSave
Electrostatic Self-Assembly of Binary Nanoparticle Crystals with a Diamond-Like Lattice
errScience
IF45.8
err2006-01-01
err0
PREAI
errAlexander M. Kalsin; Marcin Fiałkowski; Maciej Paszewski; Stoyan K. Smoukov; Kyle J. M. Bishop; Bartosz A. Grzybowski
errShare
errSave
Ionic colloidal crystals of oppositely charged particles
errNature
IF48.5
err2005-09-01
err0
PREAI
errMirjam E. Leunissen; Christina G. Christova; Antti-Pekka Hynninen; C. Patrick Royall; Andrew I. Campbell; Arnout Imhof; Marjolein Dijkstra; René van Roij; Alfons van Blaaderen
errShare
errSave
researcher View more