A Chemical Approach To Break the Planar Configuration of Ag Nanocubes into Tunable Two-Dimensional Metasurfaces.

A Chemical Approach To Break the Planar Configuration of Ag Nanocubes into Tunable Two-Dimensional Metasurfaces.
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DOI:
10.1021/acs.nanolett.6b01388
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发表时间:
2016-05
期刊:
影响因子:
10.8
通讯作者:
Yijie Yang;Yih Hong Lee;I. Phang;R. Jiang;Howard Yi Fan Sim;Jianfang Wang;X. Ling
Yijie Yang;Yih Hong Lee;I. Phang;R. Jiang;Howard Yi Fan Sim;Jianfang Wang;X. Ling
中科院分区:
材料科学1区
文献类型:
--
作者:
Yijie Yang;Yih Hong Lee;I. Phang;R. Jiang;Howard Yi Fan Sim;Jianfang Wang;X. Ling

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Current plasmonic metasurfaces of nanocubes are limited to planar configurations, restricting the ability to create tailored local electromagnetic fields. Here, we report a new chemical strategy to achieve tunable metasurfaces with nonplanar nanocube orientations, creating novel lattice-dependent field localization patterns. We manipulate the interfacial behaviors of Ag nanocubes by controlling the ratio of hydrophilic/hydrophobic molecules added in a binary thiol mixture during the surface functionalization step. The nanocube orientation at an oil/water interface can consequently be continuously tuned from planar to tilted and standing configurations, leading to the organization of Ag nanocubes into three unique large-area metacrystals, including square close-packed, linear, and hexagonal lattices. In particular, the linear and hexagonal metacrystals are unusual open lattices comprising nonplanar nanocubes, creating unique local electromagnetic field distribution patterns. Large-area "hot hexagons" with significant delocalization of hot spots form in the hexagonal metacrystal. With a lowest packing density of 24%, the hexagonal metacrystal generates nearly 350-fold stronger surface-enhanced Raman scattering as compared to the other denser-packing metacrystals, demonstrating the importance of achieving control over the geometrical and spatial orientation of the nanocubes in the metacrystals.