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通过二维/三维金银纳米片的缺陷引导生长增强表面增强拉曼散射性能用于化学传感和细胞成像应用

Enhanced SERS performance through defect-guided growth of 2D/3D AuAg nanoplates for chemical sensing and cellular imaging applications.

作者信息

Liu Kuan-Wen, Sie Pei-Yu, Chen Hsi-Ying, Ho Fong-I, Huang Po-Sheng, Wu Pin Chieh, Liao Mei-Yi

机构信息

Department of Applied Chemistry, National Pingtung University, Pingtung, 900, Taiwan.

Department of Photonics, National Cheng Kung University, Tainan, 701, Taiwan.

出版信息

Anal Chim Acta. 2025 Jun 1;1353:343940. doi: 10.1016/j.aca.2025.343940. Epub 2025 Mar 22.

Abstract

BACKGROUND

Surface-enhanced Raman scattering (SERS) is a powerful analytical technique that utilizes localized electromagnetic fields to amplify molecular vibrational signatures. The effectiveness of SERS substrates relies on the presence of "hot spots," where electromagnetic fields are highly concentrated. However, the fabrication of metal nanotemplates with optimal hot spot structures is often restricted by the continuous shell formation inherent in conventional synthesis methods, which limits the reproducibility and sensitivity of SERS-based analyses. This study addresses the significant challenge of developing a reliable method for creating SERS substrates with a high density of hot spots.

RESULTS

We developed two-dimensional/three-dimensional (2D/3D) AuAg nanoplates by controlling pore formation within silver templates. This method enabled the selective deposition of gold and silver atoms at high-energy defect sites. The resulting 3D AuAg nanoplates displayed distinctive island-like structures with optimized gap spacings in nanogranule assembly, which led to significant shifts in surface plasmon resonance (SPR). The SERS performance of these 3D AuAg nanoplates, characterized by in-plane absorption, was enhanced, achieving a detection limit of 0.008 ppm for 4-nitrothiophenol, with enhancement factors 2 to 4 times greater than those of conventional nanocube and nanosphere structures. Additionally, functionalization with NTP:4-mercaptophenylboronic acid (MPBA) in a 1:3 ratio demonstrated excellent biocompatibility (>80 % cell viability) and effective cancer-targeting imaging capabilities in both SERS and dark-field microscopy. These findings highlight the crucial role of template morphology in enhancing electromagnetic fields, leading to improved SERS sensitivity for chemical and biological sensing.

SIGNIFICANCE

This study conclusively demonstrates the importance of template morphology in optimizing SERS performance. It emphasizes the potential of 2D/3D AuAg nanoplates for advanced chemical sensing and biological diagnostics. The developed methodology provides a viable approach for creating highly sensitive and specific SERS probes, thereby advancing the field of analytical chemistry.

摘要

背景

表面增强拉曼散射(SERS)是一种强大的分析技术,它利用局部电磁场来放大分子振动信号。SERS 基底的有效性依赖于“热点”的存在,即电磁场高度集中的区域。然而,具有最佳热点结构的金属纳米模板的制备常常受到传统合成方法中固有的连续壳层形成的限制,这限制了基于 SERS 分析的可重复性和灵敏度。本研究解决了开发一种可靠方法来创建具有高密度热点的 SERS 基底这一重大挑战。

结果

我们通过控制银模板内的孔形成来制备二维/三维(2D/3D)金-银纳米板。该方法能够使金和银原子在高能缺陷位点选择性沉积。所得的 3D 金-银纳米板呈现出独特的岛状结构,在纳米颗粒组装中具有优化的间隙间距,这导致表面等离子体共振(SPR)发生显著位移。这些 3D 金-银纳米板以面内吸收为特征的 SERS 性能得到增强,对 4-硝基硫酚的检测限达到 0.008 ppm,增强因子比传统的纳米立方体和纳米球结构大 2 至 4 倍。此外,以 1:3 的比例用 NTP:4-巯基苯硼酸(MPBA)进行功能化,在 SERS 和暗场显微镜中均表现出优异的生物相容性(>80%细胞活力)和有效的癌症靶向成像能力。这些发现突出了模板形态在增强电磁场方面的关键作用,从而提高了用于化学和生物传感的 SERS 灵敏度。

意义

本研究最终证明了模板形态在优化 SERS 性能中的重要性。它强调了 2D/3D 金-银纳米板在先进化学传感和生物诊断方面的潜力。所开发的方法为创建高灵敏度和特异性的 SERS 探针提供了一种可行的途径,从而推动了分析化学领域的发展。

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