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dc.contributor.advisorMacfarlane, Robert J.
dc.contributor.advisorHart, A. John
dc.contributor.authorThrasher, Carl James
dc.date.accessioned2026-01-12T19:40:44Z
dc.date.available2026-01-12T19:40:44Z
dc.date.issued2025-09
dc.date.submitted2025-08-18T20:43:05.333Z
dc.identifier.urihttps://hdl.handle.net/1721.1/164501
dc.description.abstractThe ability to precisely organize matter across multiple length scales is a central challenge in modern materials science. In this dissertation, I develop a systems materials design approach to engineer hierarchically structured nanocomposite assemblies, integrating molecular recognition, supramolecular chemistry, colloidal assembly, and bulk processing into unified material platforms. At the molecular and nanoscale, I investigate how multivalent supramolecular interactions can be rationally programmed by controlling the architecture of polymer binders grafted to nanoparticle surfaces. Through systematic variations in polymer topology, recognition group density, and scaffold geometry, I demonstrate how polymer design dictates the thermodynamic strength and multivalency of nanoparticle superlattice assembly, enabling precise control of thermal stability, crystallographic symmetry, and collective bonding behaviors in massively multivalent systems. Building on these design principles, I develop a colloidal metallurgy framework to process selfassembled nanoparticle superlattices into dense macroscopic polycrystalline solids while preserving nanoscale order. By systematically studying the interplay of temperature, pressure, and time during colloidal sintering, I elucidate mechanisms of densification, defect evolution, and grain growth unique to colloidal systems, establishing processing–structure relationships that parallel but fundamentally diverge from atomic sintering. Finally, I extend these concepts to create stretchable nanocomposite supercrystals, embedding supramolecularly assembled superlattices into elastomeric matrices via co-engineered polymer chemistries that enable hierarchical strain transduction. These materials combine the nanoscale precision of supercrystals with mechanical robustness, reconfigurability, and stimuli-responsive optical properties, illustrating a scalable pathway to multifunctional metamaterials. Collectively, this work demonstrates how a systemslevel integration of molecular design, colloidal assembly, and bulk processing enables new paradigms for the synthesis of hierarchically ordered, functional nanocomposites.
dc.publisherMassachusetts Institute of Technology
dc.rightsIn Copyright - Educational Use Permitted
dc.rightsCopyright retained by author(s)
dc.rights.urihttps://rightsstatements.org/page/InC-EDU/1.0/
dc.titleSystems Materials Design of Ordered Nanocomposite Assemblies
dc.typeThesis
dc.description.degreePh.D.
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.orcidhttps://orcid.org/0000-0002-5074-293X
mit.thesis.degreeDoctoral
thesis.degree.nameDoctor of Philosophy


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