共查询到20条相似文献，搜索用时 15 毫秒
1.
Wonjoo Lee Seung Yong Lee Robert M. Briber Oded Rabin 《Advanced functional materials》2011,21(18):3424-3429
The fabrication of surface‐enhanced Raman spectroscopy (SERS) substrates that are optimized for use with specific laser wavelength–analyte combinations is addressed. In order to achieve large signal enhancement, temporal stability, and reproducibility over large substrate areas at low cost, only self‐assembly and templating processes are employed. The resulting substrates consist of arrays of gold nanospheres with controlled diameter and spacing, properties that dictate the optical response of the structure. Tunability of the extended surface plasmon resonance is observed in the range of 520–1000 nm. It is demonstrated that the enhancement factor is maximized when the surface plasmon resonance is red‐shifted with respect to the SERS instrument laser line. Despite relying on self‐organization, site‐to‐site enhancement factor variations smaller than 10% are obtained. 相似文献
2.
Haibin Tang Guowen Meng Qing Huang Zhuo Zhang Zhulin Huang Chuhong Zhu 《Advanced functional materials》2012,22(1):218-224
A new, highly sensitive and uniform three‐dimensional (3D) hybrid surface‐enhanced Raman scattering (SERS) substrate has been achieved via simultaneously assembling small Ag nanoparticles (Ag‐NPs) and large Ag spheres onto the side surface and the top ends of large‐scale vertically aligned cone‐shaped ZnO nanorods (ZnO‐NRs), respectively. This 3D hybrid substrate manifests high SERS sensitivity to rhodamine and a detection limit as low as 10?11 M to polychlorinated biphenyl (PCB) 77—a kind of persistent organic pollutants as global environmental hazard. Three kinds of inter‐Ag‐NP gaps in 3D geometry create a huge number of SERS “hot spots” that mainly contribute to the high SERS sensitivity. Moreover, the supporting chemical enhancement effect of ZnO‐NRs and the better enrichment effect ascribed to the large surface area of the substrate also help to achieve a lower detection limit. The arrays of cone‐shaped ZnO‐NRs decorated with Ag‐NPs on their side surface and large Ag spheres on the top ends have potentials in SERS‐based rapid detection of trace PCBs. 相似文献
3.
Giuseppe V. Bianco Maria M. Giangregorio Maria Losurdo Pio Capezzuto Giovanni Bruno 《Advanced functional materials》2012,22(24):5081-5088
A novel dry plasma methodology for fabricating directly stabilized substrate‐supported gold nanoparticle (NP) ensembles for near infrared surface enhanced Raman scattering (NIR SERS) is presented. This maskless stepwise growth exploits Au‐sulfide seeds by plasma sulfidization of gold nuclei to produce highly faceted Au NPs with a multiple plasmon resonance that can be tuned from the visible to the near infrared, down to 1400 nm. The role of Au sulfidization in modifying the dynamics of Au NPs and of the corresponding plasmon resonance is discussed. The tunability of the plasmon resonance in a broad range is shown and the effectiveness as substrates for NIR SERS is demonstrated. The SERS response is investigated by using different laser sources operating both in the visible and in the NIR. SERS mapping of the SERS enhancement factor is carried out in order to evaluate their effectiveness, stability, and reproducibility as NIR SERS substrates, also in comparison with gold NPs fabricated by conventional sputtering and with the state‐of‐the‐art in the current literature. 相似文献
4.
Due to the surface‐enhanced Raman scattering (SERS) effect, SERS labels based on noble‐metal nanoparticles loaded with Raman‐active molecules are good candidates for ultrasensitive multiplexed assays and in vitro/in vivo imaging. However, understanding how to maximize the brightness of such labels is of paramount importance for their widespread application. The effective differential Raman scattering cross‐section (dσR/dΩ) of SERS labels made of pegylated gold nanoparticles loaded with various Raman active molecules (Raman reporters) is studied. It is found that proper choice of the Raman reporter and of nanoparticle size can enhance the dσR/dΩ by several orders of magnitude. The experimental results are understood by considering the molecular cross‐section for resonant Raman scattering and the local electromagnetic enhancement factor (GSERS) in the nearby of gold nanoparticles. These results are useful to guide the design of SERS labels with improved performances and to provide a reference for the comparison of the absolute value of the dσR/dΩ of SERS labels based on metal nanoparticles. 相似文献
5.
Yuanhui Zheng Thibaut Thai Philipp Reineck Ling Qiu Yueming Guo Udo Bach 《Advanced functional materials》2013,23(12):1519-1526
The excitation of surface plasmons in metallic nanostructures provides an opportunity to localize light at the nanoscale, well below the scale of the wavelength of the light. The high local electromagnetic field intensities generated in the vicinity of the nanostructures through this nanofocusing effect are exploited in surface enhanced Raman spectroscopy (SERS). At narrow interparticle gaps, so‐called hot‐spots, the nanofocusing effect is particularly pronounced. Hence, the engineering of substrates with a consistently high density of hot‐spots is a major challenge in the field of SERS. Here, a simple bottom‐up approach is described for the fabrication of highly SERS‐active gold core‐satellite nanostructures, using electrostatic and DNA‐directed self‐assembly. It is demonstrated that well‐defined core‐satellite gold nanostructures can be fabricated without the need for expensive direct‐write nanolithography tools such as electron‐beam lithography (EBL). Self‐assembly also provides excellent control over particle distances on the nanoscale. The as‐fabricated core‐satellite nanostructures exhibit SERS activities that are superior to commercial SERS substrates in signal intensity and reproducibility. This also highlights the potential of bottom‐up self‐assembly strategies for the fabrication of complex, well‐defined functional nanostructures with future applications well beyond the field of sensing. 相似文献
6.
用金纳米粒子(Au NPs)作为基底,基于罗丹明6G(R6G)探针分子拉曼特征峰随pH的变化,构建了一种具有表面增强拉曼散射(SERS)信号输出的pH传感器。由于(闭)开环形式下存在的(去)质子化R6G分子吸附于增强基底表面的倾斜度取向不同,R6G在不同pH下表现出了不同的SERS活性。根据寻找到的R6G在1363 cm-1和1314 cm-1位置处的SERS光谱峰面积比与pH的线性关系,设计出pH传感器。实验结果表明:R6G的SERS信号在室温下可以稳定2 h以上;当样品溶液pH在7和3之间转换时,传感器表现出了较好的恢复性。在pH检测过程中引入其他金属阳离子后,该探针表现出了对H+较好的选择性。通过检测实际样品的pH发现,该探针的分析性能良好,适于在酸性介质中检测pH。 相似文献
7.
用二次氧化的方法制得了孔径均一、排列规则的阳极氧化铝模板（AAO,anodic aluminumoxide）。利用磁控溅射的方法,银纳米颗粒被溅射在模板的表面以及孔洞里面,在模板的一面形成一层粗糙的银表面,当把模板放入一定浓度的NaOH溶液中,反面的Al2O3模板被部分地溶解后露出针尖状的银纳米线阵列。用结晶紫作为探针分子,在粗糙银表面（正面）和针尖状的银纳米线阵列面（反面）得到了不同的表面增强拉曼散射（SERS,surface enhanced Raman scattering）光谱,从而证明了两面具有不同的SERS机制。分析表明：正面粗糙的银表面是吸附增强,而反面在存在吸附增强的同时起主要作用的是针尖状的银纳米线阵列构成的天线模型所产生的非吸附的增强。针尖末端的曲率半径极小,会产生极强的局域电磁场,处于这个场中的分子的信号就被大大增强了。 相似文献
8.
Shaorong Si Wenkai Liang Yinghui Sun Jing Huang Weiliang Ma Zhiqiang Liang Qiaoliang Bao Lin Jiang 《Advanced functional materials》2016,26(44):8137-8145
The fabrication of ultrasmall nanogaps (sub‐1 nm) with high density is of significant interest and importance in physics, chemistry, life science, materials science, surface science, nanotechnology, and environmental engineering. However, it remains a challenge to generate uncovered and clean sub‐1‐nm gaps with high density and uniform reproducibility. Here, a facile and low‐cost approach is demonstrated for the fabrication of high‐density sub‐1‐nm gaps from Au nanoparticle monolayers as reproducible surface‐enhanced Raman scattering (SERS) substrates. Au nanoparticles with larger diameters possess lower surface charge, thus the obtained large‐area nanoparticle monolayer generates a high‐density of sub‐1‐nm gaps. In addition, a remarkable SERS performance with a 1011 magnitude for the Raman enhancement is achieved for 120 nm Au nanoparticle monolayers due to the dramatic increase in the electromagnetic field enhancement when the obtained gap is smaller than 0.5 nm. The Au nanoparticle monolayer is also transferred onto a stretchable PDMS substrate and the structural stability and reproducibility of the high‐density sub‐1‐nm gaps in Au monolayer films are illustrated. The resultant Au nanoparticle monolayer substrates with an increasing particle diameter exhibit tunable plasmonic properties, which control the plasmon‐enhanced photocatalytic efficiency for the dimerization of p‐aminothiophenol. The findings reported here offer a new opportunity for expanding the SERS application. 相似文献
9.
纳米结构分子吸附引起的表面增强拉曼散射研究 总被引：7，自引：7，他引：0
利用模板印刷技术,制备了具有不同局域表面等离子体共振(LSPR)峰的Au纳米空心半球壳结构,并以4-巯基苯胺(4-ATP)为探针分子研究了纳米结构表面吸附分子对表面增强拉曼散射(SERS)强度的影响。结果表明,当纳米结构的LSPR峰位处于激发光波长的短波长或\"马鞍型\"位置时,SERS强度随吸附分子数的增加而增大;当处于长波长位置时,SERS强度呈现先增大后减小的趋势。利用分子吸附理论和纳米结构表面局域场强度变化,对此现象进行了解释。 相似文献
10.
Hwan Chul Jeon Chul‐Joon Heo Su Yeon Lee Seung‐Man Yang 《Advanced functional materials》2012,22(20):4268-4274
A novel, highly uniform and tunable hybrid plasmonic array is created via ion‐milling, catalytic wet‐etching and electron‐beam evaporation, using a holographically featured structure as a milling mask. A simple and low‐cost prism holographic lithography (HL) technique is applied to create an unprecedentedly coordinated array of elliptic gold (Au) holes, which act as the silicon (Si) etching catalyst in the reaction solution used to fabricate an elliptic silicon nanowire (SiNW) array; here, the SiNWs are arrayed hierarchically in such a way that three SiNWs are triangularly coordinated, and the triangles are arranged hexagonally. After removing the polymeric mask and metal thin film, the highly anisotropic thick Au film is deposited on the SiNW arrays. This hybrid substrate shows tunable optical properties in the near‐infrared (NIR) region from 875 nm to 1030 nm and surface‐enhanced Raman scattering (SERS) activities; these characteristics depend on the catalytic wet etching time, which changes the size of the vertical gap between the Au thick films deposited separately on the SiNWs. In addition, lateral interparticle coupling induces highly intensified SERS signals with good homogeneity. Finally, the Au‐capped elliptical SiNW arrays can be hierarchically patterned by combining prism HL and conventional photolithography, and the highly enhanced fluorescence intensity associated with both the structural effects and the plasmon resonances is investigated. 相似文献
11.
Hwan Chul Jeon Chul‐Joon Heo Su Yeon Lee Seung‐Man Yang 《Advanced functional materials》2012,22(20):4399-4399
12.
自组装法制备团簇Ag纳米结构衬底及其SERS 总被引：2，自引：2，他引：0
采用自组装方法,在3-Aminopropyltrimethoxy silane(APS)分子修饰后的玻璃衬底表面,获得了二维Ag纳 米结构衬底。在波长为532nm激光激发下,研究了沉积在衬底表面的 Rhodamine 6G(Rh6G)分子的拉曼光谱特性。结 果表明,制备的二维Ag纳米结构衬底具有强的拉曼增强特性,增强因子可以达到 107 倍。这说明,在外光场作用下,制备的Ag纳米结构衬底表面能够形成的强局部电磁场分布, 可以有效提升探针分子的光谱辐射效率,从而获得高增强拉曼散射。 相似文献
13.
Ronghui Que Mingwang Shao Shujuan Zhuo Chunye Wen Suidong Wang Shuit‐Tong Lee 《Advanced functional materials》2011,21(17):3337-3343
A facile method based on capillarity‐assisted assembly is used to fabricate high‐performance surface‐enhanced Raman scattering (SERS) substrates employing clean Au nanoparticles (NPs). This method is better than micro‐channel way because the former may supply large‐area uniform assembly and overcome the uneven radial distribution. Such densely‐arranged assembly of Au NPs exhibits high reproducibility and large Raman enhancement factors of 3 × 1010, arising from strong electromagnetic field coupling induced by adjacent Au NPs. The spot‐to‐spot SERS signals show that the relative standard deviation (RSD) in the intensity of the main Raman vibration modes (1310, 1361, 1509, 1650 cm?1) of Rhodamine 6G at a concentration of 1 × 10?10 M are consistently less than 20%, demonstrating good spatial uniformity and reproducibility. The SERS signals of sudan dye at a 1 × 10?8 M concentration also shows high reproducibility with a low RSD of <20%. Further, the assembly substrate is stable, retaining excellent uniformity and sensitivity after storage for months. This assembly strategy integrating the advantages of low‐cost production, high sensitivity, and reproducibility would significantly facilitate practical SERS detection. 相似文献
14.
Daniela Drescher Ingrid Zeise Heike Traub Peter Guttmann Stephan Seifert Tina Büchner Norbert Jakubowski Gerd Schneider Janina Kneipp 《Advanced functional materials》2014,24(24):3765-3775
By adding a gold core to silica nanoparticles (BrightSilica), silica‐like nanoparticles are generated that, unlike unmodified silica nanoparticles, provide three types of complementary information to investigate the silica nano‐biointeraction inside eukaryotic cells in situ. Firstly, organic molecules in proximity of and penetrating into the silica shell in live cells are monitored by surface‐enhanced Raman scattering (SERS). The SERS data show interaction of the hybrid silica particles with tyrosine, cysteine and phenylalanine side chains of adsorbed proteins. Composition of the biomolecular corona of BrightSilica nanoparticles differs in fibroblast and macrophage cells. Secondly, quantification of the BrightSilica nanoparticles using laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) micromapping indicates a different interaction of silica nanoparticles compared to gold nanoparticles under the same experimental conditions. Thirdly, the metal cores allow the investigation of particle distribution and interaction in the cellular ultrastructure by cryo nanoscale X‐ray tomography (cryo‐XT). In 3D reconstructions the assumption is confirmed that BrightSilica nanoparticles enter cells by an endocytotic mechanism. The high SERS intensities are explained by the beneficial plasmonic properties due to agglomeration of BrightSilica. The results have implications for the development of multi‐modal qualitative and quantitative characterization in comparative nanotoxicology and bionanotechnology. 相似文献
15.
Xuanhua Li Guangyu Chen Liangbao Yang Zhen Jin Jinhuai Liu 《Advanced functional materials》2010,20(17):2815-2824
A multifunctional Au‐coated TiO2 nanotube array is made via synthesis of a TiO2 nanotube array through a ZnO template, followed by deposition of Au particles onto the TiO2 surface using photocatalytic deposition and a hydrothermal method, respectively. Such arrays exhibit superior detection sensitivity with high reproducibility and stability. In addition, due to possessing stable catalytic properties, the arrays can clean themselves by photocatalytic degradation of target molecules adsorbed to the substrate under irradiation with UV light into inorganic small molecules using surface‐enhanced Raman spectroscopy (SERS) detection, so that recycling can be achieved. Finally, by detection of Rhodamine 6G (R6G) dye, herbicide 4‐chlorophenol (4‐CP), persistent organic pollutant (POP) dichlorophenoxyacetic acid (2,4‐D), and organophosphate pesticide methyl‐parathion (MP), the unique recyclable properties indicate a new route in eliminating the single‐use problem of traditional SERS substrates and show promising applications for detecting other organic pollutants. 相似文献
16.
Anna Lee Stanislav Dubinsky Ethan Tumarkin Mathieu Moulin Andrew A. Beharry Eugenia Kumacheva 《Advanced functional materials》2011,21(11):1959-1969
Polymer‐based porous hybrid materials (PHMs) carrying inorganic nanoparticles on the surface of pores have important applications in chemical and biological sensing, in chromatography, and in heterogeneous catalysis. This Feature Article provides an overview of the recent developments in the synthesis and fabrication of multifunctional PHMs using polymerization‐induced phase separation. Exemplary applications of a PHM coated with gold nanorods were demonstrated for the simultaneous detection of different analytes using surface enhanced Raman scattering (SERS) spectroscopy and fluorescence microscopy. 相似文献
17.
在银胶体系中罗丹明B单分子水平上拉曼光谱研究 总被引：1，自引：1，他引：0
采用表面增强托曼散射（SERS）技术,比较了单分子水平上银胶纳米体系中罗丹明B（RhB）浓度为10^-11mol／L以下的拉曼光谱和通常单分子水平上罗丹明6G（Rh6G）浓度在10^-11mol／L的拉曼光谱,无论自由沉积在玻璃表面还是在液体环境下的结果显示,单分子水平上Rh B的拉曼光谱灵敏度是Rh 6G的2倍多。因此,利用RhB作为探测试剂将能够提供更加丰富的信息,这对单分子的光谱研究以及高灵敏度探测试剂的应用研究具有重要的意义。 相似文献
18.
19.
Silicon nanowires (SiNWs) with tens of micrometer in length have been synthesized and modified with Ag nanoparticles,which were confirmed by X-ray diffractometer (XRD),scanning electron microscopy and ... 相似文献
20.
单壁碳纳米管表面增强拉曼散射的新方法 总被引：1，自引：1，他引：0
依据碳纳米管独特的力学性能,在银表面直接研磨单壁碳纳米管(SWCNTs),在形成纳米级粗糙银表面的同时,SWCNTs管也吸附在银表面上,在银表面粗糙程度和SWCNTs厚度适中的区域得到了高质量的表面增强拉曼散射(SERS)谱。理论分析和实验结果表明,该方法是正确可行的。 相似文献