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dc.contributor.authorMa, Le
dc.contributor.authorHuang, Hejin
dc.contributor.authorVargo, Emma
dc.contributor.authorHuang, Jingyu
dc.contributor.authorAnderson, Christopher L
dc.contributor.authorChen, Tiffany
dc.contributor.authorKuzmenko, Ivan
dc.contributor.authorIlavsky, Jan
dc.contributor.authorWang, Cheng
dc.contributor.authorLiu, Yi
dc.contributor.authorErcius, Peter
dc.contributor.authorAlexander-Katz, Alfredo
dc.contributor.authorXu, Ting
dc.date.accessioned2022-05-11T15:20:14Z
dc.date.available2022-05-11T15:20:14Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/142470
dc.description.abstractAlthough significant progress has been made in the self-assembly of nanostructures, present successes heavily rely on precision in building block design, composition, and pair interactions. These requirements fundamentally limit our ability to synthesize macroscopic materials where the likelihood of impurity inclusion escalates and, more importantly, to access molecular-to-nanoscopic-to-microscopic-to-macroscopic hierarchies, since the types and compositions of building blocks vary at each stage. Inspired by biological blends and high-entropy alloys, we hypothesize that diversifying the blend's composition can overcome these limitations. Increasing the number of components increases mixing entropy, leading to the dispersion of different components and, as a result, enhances interphase miscibility, weakens the dependence on specific pair interactions, and enables long-range cooperativity. This hypothesis is validated in complex blends containing small molecules, block copolymer-based supramolecules, and nanoparticles/colloidal particles. Hierarchically structured composites can be obtained with formulation flexibility in the filler selection and blend composition. It is worth noting that, by adding small molecules, we can solve the size constraint that plagues traditional block copolymer/nanoparticle blends. Detailed characterization and simulation further confirm that each component is distributed to locally mediate unfavorable interactions, cooperatively mitigate composition fluctuations, and retain structural fidelity. Furthermore, the blends have sufficient mobility to access tunable microstructures without compromising the order of the nanostructure. Besides establishing a kinetically viable pathway to release current constraints in the composite design and to navigate uncertainties during structure formation over multiple length scales, the present study demonstrates that entropy-driven behaviors can be realized in systems beyond high-entropy alloys despite inherent differences between metal alloys and organic/inorganic hybrids.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACSNANO.1C04606en_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 Internationalen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceOther Repositoryen_US
dc.titleDiversifying Composition Leads to Hierarchical Composites with Design Flexibility and Structural Fidelityen_US
dc.typeArticleen_US
dc.identifier.citationMa, Le, Huang, Hejin, Vargo, Emma, Huang, Jingyu, Anderson, Christopher L et al. 2021. "Diversifying Composition Leads to Hierarchical Composites with Design Flexibility and Structural Fidelity." ACS Nano, 15 (9).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.relation.journalACS Nanoen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-05-11T15:15:50Z
dspace.orderedauthorsMa, L; Huang, H; Vargo, E; Huang, J; Anderson, CL; Chen, T; Kuzmenko, I; Ilavsky, J; Wang, C; Liu, Y; Ercius, P; Alexander-Katz, A; Xu, Ten_US
dspace.date.submission2022-05-11T15:15:53Z
mit.journal.volume15en_US
mit.journal.issue9en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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