Novel methods for fabrication of non-close-packed structures through colloidal self-assembly

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2010. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 141-154). === Colloidal dispersions are usually stabilized by interparticle electrostatic repulsion. However...

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Main Author: Sharma, Vyom
Other Authors: Yet-Ming Chiang and W. Craig Carter.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2010
Subjects:
Online Access:http://hdl.handle.net/1721.1/59710
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-597102019-05-02T16:10:21Z Novel methods for fabrication of non-close-packed structures through colloidal self-assembly Sharma, Vyom Yet-Ming Chiang and W. Craig Carter. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Materials Science and Engineering. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2010. Cataloged from PDF version of thesis. Includes bibliographical references (p. 141-154). Colloidal dispersions are usually stabilized by interparticle electrostatic repulsion. However, strong electrostatic potentials prevent nucleation of new structures. When the electrostatic potential is strongly attractive, particles coagulate into a disordered structure; if it is strongly repulsive, known processes can order them into a closepacked structure. Driven by the need to make tailored structures, researchers have focused on circumventing electrostatics to nucleate and stabilize newer structures. Yet most colloidal systems of interest are strongly charged. Reducing the electrostatic potential of a system may create only unstable structures without long-range order. In this thesis, electrostatic interaction between strongly charged particles is exploited to make novel structures. It is shown that -with an added steric component in the interaction potential- oppositely charged particles, which undergo rapid coagulation otherwise, can be arranged into stable, long-range ordered structures. Compared to their like-charged counterparts, these structures have greater stability due to an attractive electrostatic potential. It is shown that an entire class of surfactants, amphiphilic non-ionic surfactants, can be used to stabilize an oppositely charged particle system. Stabilizing these systems, allows for the nucleation of newer structures. For instance, it is shown that a non-close-packed arrangement of positive particles can be obtained on a layer of negatively charged particles. Creating such non-close-packed 2D structures on a template is essential for creating 3D non-closepacked structures. Indeed, it is shown that at high Debye lengths, by varying the concentration of particles in a suspension of like-charged colloids, electrostatic repulsion among particles can stabilize "sparse" structures. In these structures, particles occupy only a few of the many sites that are available to them. Yet, they form an ordered structure. Nuclei of a sparser structure are assembled at higher Debye length and lower particle concentration. Monte Carlo simulations confirm that these structures are stabilized by electrostatic repulsion when particle concentration is low. It is shown that the remaining sites in a sparse structure can be filled by a different particle type. By replicating this process of 2D heterostructure formation, layer by layer, and removing one kind of particle in the last step of the process, a two-layer non-close-packed structure is obtained. by Vyom Sharma. Ph.D. 2010-10-29T18:18:58Z 2010-10-29T18:18:58Z 2010 2010 Thesis http://hdl.handle.net/1721.1/59710 668429546 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 154 p. application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Materials Science and Engineering.
spellingShingle Materials Science and Engineering.
Sharma, Vyom
Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2010. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 141-154). === Colloidal dispersions are usually stabilized by interparticle electrostatic repulsion. However, strong electrostatic potentials prevent nucleation of new structures. When the electrostatic potential is strongly attractive, particles coagulate into a disordered structure; if it is strongly repulsive, known processes can order them into a closepacked structure. Driven by the need to make tailored structures, researchers have focused on circumventing electrostatics to nucleate and stabilize newer structures. Yet most colloidal systems of interest are strongly charged. Reducing the electrostatic potential of a system may create only unstable structures without long-range order. In this thesis, electrostatic interaction between strongly charged particles is exploited to make novel structures. It is shown that -with an added steric component in the interaction potential- oppositely charged particles, which undergo rapid coagulation otherwise, can be arranged into stable, long-range ordered structures. Compared to their like-charged counterparts, these structures have greater stability due to an attractive electrostatic potential. It is shown that an entire class of surfactants, amphiphilic non-ionic surfactants, can be used to stabilize an oppositely charged particle system. Stabilizing these systems, allows for the nucleation of newer structures. For instance, it is shown that a non-close-packed arrangement of positive particles can be obtained on a layer of negatively charged particles. Creating such non-close-packed 2D structures on a template is essential for creating 3D non-closepacked structures. Indeed, it is shown that at high Debye lengths, by varying the concentration of particles in a suspension of like-charged colloids, electrostatic repulsion among particles can stabilize "sparse" structures. In these structures, particles occupy only a few of the many sites that are available to them. Yet, they form an ordered structure. Nuclei of a sparser structure are assembled at higher Debye length and lower particle concentration. Monte Carlo simulations confirm that these structures are stabilized by electrostatic repulsion when particle concentration is low. It is shown that the remaining sites in a sparse structure can be filled by a different particle type. By replicating this process of 2D heterostructure formation, layer by layer, and removing one kind of particle in the last step of the process, a two-layer non-close-packed structure is obtained. === by Vyom Sharma. === Ph.D.
author2 Yet-Ming Chiang and W. Craig Carter.
author_facet Yet-Ming Chiang and W. Craig Carter.
Sharma, Vyom
author Sharma, Vyom
author_sort Sharma, Vyom
title Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
title_short Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
title_full Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
title_fullStr Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
title_full_unstemmed Novel methods for fabrication of non-close-packed structures through colloidal self-assembly
title_sort novel methods for fabrication of non-close-packed structures through colloidal self-assembly
publisher Massachusetts Institute of Technology
publishDate 2010
url http://hdl.handle.net/1721.1/59710
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