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首页> 外文期刊>ACS nano >Off-resonance surface-enhanced raman spectroscopy from gold nanorod suspensions as a function of aspect ratio: Not what we thought
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Off-resonance surface-enhanced raman spectroscopy from gold nanorod suspensions as a function of aspect ratio: Not what we thought

机译:金纳米棒悬浮液的非共振表面增强拉曼光谱与纵横比的关系:不是我们所想

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Design of nanoparticles for surface-enhanced Raman scattering (SERS) within suspensions is more involved than simply maximizing the local field enhancement. The enhancement at the nanoparticle surface and the extinction of both the incident and scattered light during propagation act in concert to determine the observed signal intensity. Here we explore these critical aspects of signal generation and propagation through experiment and theory. We synthesized gold nanorods of six different aspect ratios in order to obtain longitudinal surface plasmon resonances that incrementally spanned 600-800 nm. The Raman reporter molecule methylene blue was trap-coated near the surface of each nanorod sample, generating SERS spectra, which were used to compare Raman signals. The average number of reporter molecules per nanorod was quantified against known standards using electrospray ionization liquid chromatography mass spectrometry. The magnitude of the observed Raman signal is reported for each aspect ratio along with the attenuation due to extinction in suspension. The highest Raman signal was obtained from the nanorod suspension with a plasmon resonance blue-shifted from the laser excitation wavelength. This finding is in contrast to SERS measurements obtained from molecules dried onto the surface of roughened or patterned metal substrates where the maximum observed signal is near or red-shifted from the laser excitation wavelength. We explain these results as a competition between SERS enhancement and extinction, at the excitation and scattered wavelengths, on propagation through the sample.
机译:悬浮液中用于表面增强拉曼散射(SERS)的纳米颗粒的设计要比简单地最大化局部场增强更为复杂。纳米粒子表面的增强以及传播过程中入射光和散射光的消光共同作用,以确定观察到的信号强度。在这里,我们通过实验和理论探索信号生成和传播的这些关键方面。我们合成了六种不同长宽比的金纳米棒,以获取纵向跨越60-800 nm的表面等离振子共振。拉曼报道分子亚甲基蓝被捕获在每个纳米棒样品表面附近,产生SERS光谱,用于比较拉曼信号。使用电喷雾电离液相色谱质谱法,根据已知标准对每个纳米棒的平均报道分子数量进行定量。报告每个长宽比的观察到的拉曼信号的强度,以及由于悬浮中的消光而引起的衰减。从纳米棒悬浮液获得最高拉曼信号,其等离子体共振从激光激发波长蓝移。这一发现与SERS测量结果相反,SERS测量结果是从干燥到粗糙或有图案的金属基材表面上的分子获得的,在该表面上观察到的最大信号与激光激发波长相近或发生了红移。我们将这些结果解释为在激发和散射波长下,通过样品传播时SERS增强和消光之间的竞争。

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