4.8 Article

Low-Density 2D Superlattices Assembled via Directional DNA Bonding

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 35, 页码 19035-19040

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202105796

关键词

colloidal crystals; DNA; nanoparticle superlattice; nanoparticles; small-angle X-ray scattering

资金

  1. Air Force Office of Scientific Research [FA9550-17-1-0348, FA9550-16-1-0150]
  2. Center for Bio-Inspired Energy Science, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0000989]
  3. Air Force Research Laboratory [FA8650-152-5518]
  4. DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]
  5. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF) [ECCS-1542205]
  6. MRSEC program at the Materials Research Center [NSFDMR-1121262]
  7. International Institute for Nanotechnology (IIN)
  8. State of Illinois, through the IIN
  9. Sherman Fairchild Foundation, Inc

向作者/读者索取更多资源

The study focuses on assembling nanoparticles of different shapes using DNA on substrates and investigating their reorganization into two-dimensional crystalline films under thermal conditions. Two new low-density 2D structures were reported, including a honeycomb lattice based on octahedral nanoparticles.
It is critical to assemble nanoparticles (NPs) into superlattices with controlled symmetries and spacings on substrates for metamaterials applications, where such structural parameters dictate their properties. Here, we use DNA to assemble anisotropic NPs of three shapes-cubes, octahedra, and rhombic dodecahedra-on substrates and investigate their thermally induced reorganization into two-dimensional (2D) crystalline films. We report two new low-density 2D structures, including a honeycomb lattice based on octahedral NPs. The low-density lattices favored here are not usually seen when particles are crystallized via other bottom-up assembly techniques. Furthermore, we show that, consistent with the complementary contact model, a primary driving force for crystallization is the formation of directional, face-to-face DNA bonds between neighboring NPs and between NPs and the substrate. Our results can be used to deliberately prepare crystalline NP films with novel morphologies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据