Particle analogs of electrons in colloidal crystals

Author:

Girard Martin123ORCID,Wang Shunzhi34ORCID,Du Jingshan S.13ORCID,Das Anindita34ORCID,Huang Ziyin13ORCID,Dravid Vinayak P.13ORCID,Lee Byeongdu5ORCID,Mirkin Chad A.134ORCID,Olvera de la Cruz Monica1234ORCID

Affiliation:

1. Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.

2. Department of Physics and Astronomy, Northwestern University, Evanston, IL 60208, USA.

3. International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208, USA.

4. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.

5. X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Lemont, IL 60439, USA.

Abstract

Mobile particles in colloidal crystals The crystallization of nanoparticles can be controlled by functionalizing them with DNA strands that direct assembly through hybridization. The design rules for interactions between pairs of particles resemble those for ionic compounds. Inspired by molecular dynamics simulations, Girard et al. show that larger particles (∼10 nanometers in diameter) that have mutual repulsive interactions can form a stable lattice only if much smaller conjugate particles (∼1.5 nanometers in diameter) are present. These smaller particles are mobile and diffuse through the lattice, so the bonding interaction resembles the classical picture of electrons in metals. Science , this issue p. 1174

Funder

National Science Foundation

Office of Naval Research

U.S. Department of Energy

National Cancer Institute

Air Force Office of Scientific Research

Sherman Fairchild Foundation

Assistant Secretary of Defense for Research and Engineering

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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