4.8 Article

Light-Responsive Colloidal Crystals Engineered with DNA

Journal

ADVANCED MATERIALS
Volume 32, Issue 8, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201906600

Keywords

azobenzene; colloidal crystals; DNA-nanoparticle superlattices; light-responsive materials; optical patterning

Funding

  1. Air Force Office of Scientific Research [FA9550-17-1-0348, FA9550-18-1-0493]
  2. Vannevar Bush Faculty Fellowship program - Basic Research Office of Assistant Secretary of Defense for Research and Engineering
  3. Office of Naval Research [N00014-15-1-0043]
  4. Center for Bio-Inspired Energy Science, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0000989]
  5. Sherman Fairchild Foundation, Inc.
  6. National Cancer Institute of National Institutes of Health [U54CA199091]
  7. DOE Office of Science [DE-AC02-06CH11357]
  8. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF ECCS-1542205]
  9. Materials Research Science and Engineering Center [NSF DMR-1720139]
  10. State of Illinois
  11. Northwestern University

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A novel method for synthesizing and photopatterning colloidal crystals via light-responsive DNA is developed. These crystals are composed of 10-30 nm gold nanoparticles interconnected with azobenzene-modified DNA strands. The photoisomerization of the azobenzene molecules leads to reversible assembly and disassembly of the base-centered cubic (bcc) and face-centered cubic (fcc) crystalline nanoparticle lattices. In addition, UV light is used as a trigger to selectively remove nanoparticles on centimeter-scale thin films of colloidal crystals, allowing them to be photopatterned into preconceived shapes. The design of the azobenzene-modified linking DNA is critical and involves complementary strands, with azobenzene moieties deliberately staggered between the bases that define the complementary code. This results in a tunable wavelength-dependent melting temperature (T-m) window (4.5-15 degrees C) and one suitable for affecting the desired transformations. In addition to the isomeric state of the azobenzene groups, the size of the particles can be used to modulate the T-m window over which these structures are light-responsive.

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