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利用热诱导晶核孪生产生表面增强拉曼散射活性的近红外金纳米胶囊。

NIR-Active Plasmonic Gold Nanocapsules Synthesized Using Thermally Induced Seed Twinning for Surface-Enhanced Raman Scattering Applications.

机构信息

School of Basic Sciences , Indian Institute of Technology Mandi , Kamand, Mandi 175005 , Himachal Pradesh , India.

Leibniz-Institut für Polymerforschung Dresden e.V., Institute of Physical Chemistry and Polymer Physics , Hohe Str. 6 , Dresden D-01069 , Germany.

出版信息

ACS Appl Mater Interfaces. 2018 Nov 14;10(45):39380-39390. doi: 10.1021/acsami.8b14445. Epub 2018 Nov 2.

Abstract

Hollow and porous core-shell nanostructures with defined interior nanogaps are of great significance in the field of surface-enhanced Raman scattering (SERS) applications because of the presence of intrinsic electromagnetic (EM) hot spots, multipolar resonances, and multiple facets. Further, nanomaterials having extinction in the near-infrared (NIR) region are particularly important for SERS and biomedical applications, and thus it is highly desirable to synthesize NIR-active plasmonic nanostructures. Herein, we report the synthesis of gold nanocapsules having a solid Au bead as core and a thin-porous rod-shaped shell with extinction in both NIR I and NIR II regions. Thermally induced twinned seeds were used for the silver-free synthesis of pentatwinned Au bead, which served as the foundation for the directed growth of Ag nanorods, which was finally converted to Au nanocapsules following galvanic replacement reaction (GRR). Detailed investigation was carried out to understand the effect of thermal treatment duration in the seed morphology and its subsequent growth to anisotropic Au beads. Ag overgrowth on Au beads yielded uniform Au-bead@Ag nanorods whose size can be tuned by varying the Ag precursor. Five different sized Au-bead@Ag nanorods were studied, and they were converted to Au nanocapsules following GRR. We explored the size-dependent SERS activity of the prepared Au nanocapsules along with their comparison with solid pentatwinned Au beads and found that the smallest sized Au nanocapsules were the best SERS performers. Finite-difference time-domain simulation revealed the presence of intense EM hot spots in the smallest sized Au nanocapsule and corroborated the experimental SERS data. Finally, we fabricated a simple flexible cellulose-based SERS substrate by using the smallest sized Au nanocapsules and investigated its SERS sensing ability for the detection of 2-napthalenethiol (2-NT), as a model analyte, and were able to achieve its detection down to 1 fM concentration.

摘要

具有定义的内部纳米间隙的中空和多孔核壳纳米结构在表面增强拉曼散射 (SERS) 应用领域具有重要意义,因为存在固有电磁 (EM) 热点、多极共振和多个面。此外,在近红外 (NIR) 区域具有消光的纳米材料对于 SERS 和生物医学应用尤为重要,因此合成近红外活性等离子体纳米结构是非常理想的。在此,我们报告了具有实心 Au 珠核和薄多孔棒状壳的金纳米胶囊的合成,其在 NIR I 和 NIR II 区域均具有消光。热诱导孪晶种子用于无银合成五重孪晶 Au 珠,其作为 Ag 纳米棒定向生长的基础,随后通过电置换反应 (GRR) 转化为金纳米胶囊。进行了详细的研究以了解种子形态及其随后的各向异性 Au 珠生长的热处理持续时间的影响。Au 珠上的 Ag 外延生长得到了尺寸可调的均匀 Au 珠@Ag 纳米棒,其尺寸可以通过改变 Ag 前体来调节。研究了五种不同尺寸的 Au 珠@Ag 纳米棒,并通过 GRR 将其转化为金纳米胶囊。我们探索了所制备的金纳米胶囊的尺寸依赖性 SERS 活性,并将其与实心五重孪晶 Au 珠进行了比较,发现最小尺寸的金纳米胶囊具有最佳的 SERS 性能。有限差分时域模拟显示最小尺寸的金纳米胶囊中存在强烈的 EM 热点,并证实了实验 SERS 数据。最后,我们使用最小尺寸的金纳米胶囊制造了一种简单的基于纤维素的 SERS 基底,并研究了其对 2-萘硫醇 (2-NT) 的检测能力,作为模型分析物,能够达到 1 fM 的检测浓度。

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