Assembly of three-dimensional binary superlattices from multi-flavored particles

Pretti, Evan; Zerze, Hasan; Song, Minseok; Ding, Yajun; Mahynski, Nathan A.; Hatch, Harold W.; Shen, Vincent K.; Mittal, Jeetain

doi:10.1039/c8sm00989a

Title: Assembly of three-dimensional binary superlattices from multi-flavored particles

Journal Article · Tue Jul 10 00:00:00 EDT 2018 · Soft Matter

DOI:https://doi.org/10.1039/c8sm00989a· OSTI ID:1540083

Pretti, Evan ^[1]; Zerze, Hasan ^[1]; Song, Minseok ^[1]; Ding, Yajun ^[1];

^[2]; Hatch, Harold W. ^[2]; Shen, Vincent K. ^[2];

^[1]

Lehigh University, Bethlehem, PA (United States)
National Institute of Standards and Technology (NIST), Gaithersburg, MD (United States)

Binary superlattices constructed from nano- or micron-sized colloidal particles have a wide variety of applications, including the design of advanced materials. Self-assembly of such crystals from their constituent colloids can be achieved in practice by, among other means, the functionalization of colloid surfaces with single-stranded DNA sequences. However, when driven by DNA, this assembly is traditionally premised on the pairwise interaction between a single DNA sequence and its complement, and often relies on particle size asymmetry to entropically control the crystalline arrangement of its constituents. The recently proposed “multi-flavoring” motif for DNA functionalization, wherein multiple distinct strands of DNA are grafted in different ratios to different colloids, can be used to experimentally realize a binary mixture in which all pairwise interactions are independently controllable. Here we use various computational methods, including molecular dynamics and Wang–Landau Monte Carlo simulations, to study a multi-flavored binary system of micron-sized DNA-functionalized particles modeled implicitly by Fermi–Jagla pairwise interactions. We show how self-assembly of such systems can be controlled in a purely enthalpic manner, and by tuning only the interactions between like particles, demonstrate assembly into various morphologies. Although polymorphism is present over a wide range of pairwise interaction strengths, we show that careful selection of interactions can lead to the generation of pure compositionally ordered crystals. Additionally, we show how the crystal composition changes with the like-pair interaction strengths, and how the solution stoichiometry affects the assembled structures.

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Research Organization:: Lehigh Univ., Bethlehem, PA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences & Engineering Division (MSE); National Science Foundation (NSF); USDOE Office of Science (SC), Basic Energy Sciences (BES)

Grant/Contract Number:: SC0013979; AC02-05CH11231

OSTI ID:: 1540083

Alternate ID(s):: OSTI ID: 1460583

Journal Information:: Soft Matter, Vol. 14, Issue 30; ISSN 1744-683X

Publisher:: Royal Society of ChemistryCopyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 13 works

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Using symmetry to elucidate the importance of stoichiometry in colloidal crystal assembly Mahynski, Nathan A.; Pretti, Evan; Shen, Vincent K. Nature Communications, Vol. 10, Issue 1 https://doi.org/10.1038/s41467-019-10031-4	journal	May 2019
Size-dependent thermodynamic structural selection in colloidal crystallization Pretti, Evan; Zerze, Hasan; Song, Minseok Science Advances, Vol. 5, Issue 9 https://doi.org/10.1126/sciadv.aaw5912	journal	September 2019

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