Programming Defects and Cavities into Colloidal Crystals Engineered With DNA

R Rachel R. Chan (Department of Chemistry and International Institute for Nanotechnology) K Kaitlin M. Landy (Department of Chemistry Northwestern University Evanston IL 60208 USA) K Kyle J. Gibson (Department of Chemistry Northwestern University Evanston IL 60208 USA) S Sachin P. Kulkarni (International Institute for Nanotechnology Northwestern University Evanston IL 60208 USA) J Junjing Deng (X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA) B Byeongdu Lee (X-ray Science Division) J Joseph McCourt (X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA) S Soenke Seifert (X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA) O Olivier J. G. L. Chevalier (Department of Chemistry Northwestern University Evanston IL 60208 USA) A Alexa M. Wong (Department of Chemistry Northwestern University Evanston IL 60208 USA) C Chaojian Chen (Department of Chemistry) P Peter H. Winegar (California Institute for Quantitative Biosciences (QB3 Institute)) K Koray Aydin (Department of Electrical and Computer Engineering) C Chad A. Mirkin

Abstract

AbstractTaking inspiration from seed‐mediated crystal growth in atomic and molecular systems, a strategy is developed for incorporating particle and volume defects into the interior of colloidal crystals consisting of programmable atom equivalents (PAEs, oligonucleotide‐functionalized nanoparticles) assembled with DNA. Discrete PAEs spanning a range of shapes, sizes, and compositions serve as nucleation sites for seed‐mediated colloidal crystal growth and are incorporated into the centers of colloidal crystal lattices as cavities. Importantly, seed PAE shapes or sizes that are geometrically mismatched with the colloidal crystal lattice symmetry introduce defects such as local lattice disorder and long‐range grain boundaries that arise through geometric frustration. Colloidal crystals synthesized with plasmonic seed particles exhibit near‐infrared (NIR) wavelength scattering cross‐sections that are highly dependent upon cavity/particle size and shape. Taken together, these findings establish a platform for the deliberate introduction of 2 and 3D defects into colloidal crystals, which may inform the design of structures and materials for thermal management, sensing, and catalysis.

Article Details

Volume / Issue Vol. 37, Issue 41
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

R

Rachel R. Chan

Department of Chemistry and International Institute for Nanotechnology

K

Kaitlin M. Landy

Department of Chemistry Northwestern University Evanston IL 60208 USA

K

Kyle J. Gibson

Department of Chemistry Northwestern University Evanston IL 60208 USA

S

Sachin P. Kulkarni

International Institute for Nanotechnology Northwestern University Evanston IL 60208 USA

J

Junjing Deng

X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA

B

Byeongdu Lee

X-ray Science Division

J

Joseph McCourt

X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA

S

Soenke Seifert

X‐ray Science Division Advanced Photon Source Argonne National Laboratory Lemont IL 60439 USA

O

Olivier J. G. L. Chevalier

Department of Chemistry Northwestern University Evanston IL 60208 USA

A

Alexa M. Wong

Department of Chemistry Northwestern University Evanston IL 60208 USA

C

Chaojian Chen

Department of Chemistry

P

Peter H. Winegar

California Institute for Quantitative Biosciences (QB3 Institute)

K

Koray Aydin

Department of Electrical and Computer Engineering

C

Chad A. Mirkin