DNA self-assembly-based fabrication of metallic nanostructures and related nanophotonics

Zhang Yi-Nan; Wang Li-Hua; Liu Hua-Jie; Fan Chun-Hai

doi:10.7498/aps.66.147101

Abstract

Nanophotonics focuses on the study of the behavior of light and the interaction between light and matter on a nanometer scale. It has often involved metallic nanostructures which can concentrate and guide the light beyond the diffraction limit due to the unique surface plasmons (SPs). Manipulation of light can be accomplished through controlling the morphologies and components of metallic nanostructures to incur special surface plasmons. However, it is still a severe challenge to achieve exquisite control over the morphologies or components of metallic nanostructures: chemical methods can provide anisotropic but highly symmetric metallic nanostructures; lithographic methods have a limited resolution, especially for three-dimensional metallic nanostructures. By comparison, DNA self-assembly-based fabrication of metallic nanostructures is not restricted to these confinements. With the high-fidelity Waston-Crick base pairing, DNA can self-assemble into arbitrary shapes ranging from the simplest double strands to the most sophisticated DNA origami. Due to the electrostatic interactions between negatively charged phosphate backbones and positively charged metal ions, DNA of any shapes can affect the metal ions or atoms to a certain degree. Depending on the shape and base, DNA self-assembly nanostructures can exert different influences on the growth of metallic nanoparticles, which in turn gives rise to deliberately controllable metallic nanostructures. Besides, DNA self-assembly nanostructures can act as ideal templates for the organization of metallic nanoparticles to construct special metallic nanostructures. In this case, DNA-modified metallic nanoparticles are immobilized on DNA self-assembly nanostructures carrying complementary sticky ends. The geometry and component arrangements of metallic nanostructures both can be precisely dictated on the DNA nanostructures by programming the sticky end arrays. Complicated metallic nanostructures which can be hardly fabricated with conventional chemical or lithographic methods have been readily prepared with the DNA self-assembly-based fabrication method, thereby greatly promoting the development of nanophotonics. Therefore, the studies of DNA self-assembly-based fabrication of metallic nanostructures and related nanophotonics have received rapidly growing attention in recent years. This review first gives a brief introduction of the mechanism for breaking the diffraction limit of light with metallic nanostructures based on SPs. Then we give a systematic review on DNA self-assembly-based fabrication of metallic nanostructures and related nanophotonics, which is divided into several parts according to the different pathways by which DNA self-assembly can influence the morphologies or components of metallic nanostructures. Finally, the remaining problems and limitations for the existing DNA self-assembly-based fabrication of metallic nanostructures are presented and an outlook on the future trend of the field is given as well.

Keywords:

Authors and contacts

1.
Division of Physical Biology and Bioimaging Center, Shanghai Synchrotron Radiation Facility; CAS Key Laboratory of Interfacial Physics and Technology; Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China;
2.
University of Chinese Academy of Sciences, Beijing 100049, China

Corresponding author: Liu Hua-Jie, liuhuajie@sinap.ac.cn;fchh@sinap.ac.cn ; Fan Chun-Hai, liuhuajie@sinap.ac.cn;fchh@sinap.ac.cn

Funds: Project supported by the National Basic Research Program of China (Grant No. 2013CB932803), the National Natural Science Foundation of China (Grant Nos. 21473236, 31371015), and the Youth Innovation Promotion Association of Chinese Academy of Sciences.

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Cited By

[1]	Schuller J A, Barnard E S, Cai W, Jun Y C, White J S, Brongersma M L 2010 Nat. Mater. 9 193
[2]	Braun E, Eichen Y, Sivan U, Ben-Yoseph G 1998 Nature 391 775
[3]	Wang Z, Tang L, Tan L H, Li J, Lu Y 2012 Angew. Chem. Int. Ed. 51 9078
[4]	Lee J H, Kim G H, Nam J M 2012 J. Am. Chem. Soc. 134 5456
[5]	Song T, Tang L, Tan L H, Wang X, Satyavolu N S, Xing H, Wang Z, Li J, Liang H, Lu Y 2015 Angew. Chem. Int. Ed. 54 8114
[6]	Alivisatos A P, Johnsson K P, Peng X, Wilson T E, Loweth C J, Bruchez M P, Schultz Jr P G 1996 Nature 382 609
[7]	Mirkin C A, Letsinger R L, Mucic R C, Storhoff J J 1996 Nature 382 607
[8]	Pinheiro A V, Han D, Shih W M, Yan H 2011 Nat. Nanotechnol. 6 763
[9]	Chao J, Zhang Y, Zhu D, Liu B, Cui C, Su S, Fan C, Wang L 2016 Sci. China: Chem. 59 730
[10]	Lan X, Lu X, Shen C, Ke Y, Ni W, Wang Q 2015 J. Am. Chem. Soc. 137 457
[11]	Acuna G, Moller F, Holzmeister P, Beater S, Lalkens B, Tinnefeld P 2012 Science 338 506
[12]	Murphy C J, Thompson L B, Chernak D J, Yang J A, Sivapalan S T, Boulos S P, Huang J Y, Alkilany A M, Sisco P N 2011 Curr. Opin. Colloid Interf. Sci. 16 128
[13]	Feng L, Romulus J, Li M, Sha R, Royer J, Wu K T, Xu Q, Seeman N C, Weck M, Chaikin P 2013 Nat. Mater. 12 747
[14]	Hedrick J L, Brown K A, Kluender E J, Cabezas M D, Chen P C, Mirkin C A 2016 ACS Nano 10 3144
[15]	Kumar A, Hwang J H, Kumar S, Nam J M 2013 Chem. Commun. 49 2597
[16]	Tan S J, Campolongo M J, Luo D, Cheng W 2011 Nat. Nanotechnol. 6 268
[17]	Kuzyk A, Schreiber R, Fan Z, Pardatscher G, Roller M, Hogele A, Simmel F, Govorov O, Liedl T 2012 Nature 483 311
[18]	Thacker V V, Herrmann L O, Sigle D O, Zhang T, Liedl T, Baumberg J J, Keyser U F 2014 Nat. Commun. 5 3448
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Vol. 66, Issue 14 - 2017-07-20

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