Amino-acid- and peptide-directed synthesis of chiral plasmonic gold nanoparticles

手性(物理) 纳米颗粒 材料科学 化学 胶体金 等离子纳米粒子 纳米技术 对映选择合成 等离子体子 表面等离子共振 手征对称破缺 有机化学 催化作用 物理 对称性破坏 光电子学 量子力学 Nambu–Jona Lasinio模型
作者
Hye‐Eun Lee,Hyo‐Yong Ahn,Jungho Mun,Yoon Young Lee,Minkyung Kim,Nam Heon Cho,Kiseok Chang,Wook Sung Kim,Junsuk Rho,Ki Tae Nam
出处
期刊:Nature [Nature Portfolio]
卷期号:556 (7701): 360-365 被引量:1010
标识
DOI:10.1038/s41586-018-0034-1
摘要

Understanding chirality, or handedness, in molecules is important because of the enantioselectivity that is observed in many biochemical reactions 1 , and because of the recent development of chiral metamaterials with exceptional light-manipulating capabilities, such as polarization control2-4, a negative refractive index 5 and chiral sensing 6 . Chiral nanostructures have been produced using nanofabrication techniques such as lithography 7 and molecular self-assembly8-11, but large-scale and simple fabrication methods for three-dimensional chiral structures remain a challenge. In this regard, chirality transfer represents a simpler and more efficient method for controlling chiral morphology12-18. Although a few studies18,19 have described the transfer of molecular chirality into micrometre-sized helical ceramic crystals, this technique has yet to be implemented for metal nanoparticles with sizes of hundreds of nanometres. Here we develop a strategy for synthesizing chiral gold nanoparticles that involves using amino acids and peptides to control the optical activity, handedness and chiral plasmonic resonance of the nanoparticles. The key requirement for achieving such chiral structures is the formation of high-Miller-index surfaces ({hkl}, h ≠ k ≠ l ≠ 0) that are intrinsically chiral, owing to the presence of 'kink' sites20-22 in the nanoparticles during growth. The presence of chiral components at the inorganic surface of the nanoparticles and in the amino acids and peptides results in enantioselective interactions at the interface between these elements; these interactions lead to asymmetric evolution of the nanoparticles and the formation of helicoid morphologies that consist of highly twisted chiral elements. The gold nanoparticles that we grow display strong chiral plasmonic optical activity (a dis-symmetry factor of 0.2), even when dispersed randomly in solution; this observation is supported by theoretical calculations and direct visualizations of macroscopic colour transformations. We anticipate that our strategy will aid in the rational design and fabrication of three-dimensional chiral nanostructures for use in plasmonic metamaterial applications.
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