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首页> 外文期刊>Spectroscopy Letters >Adsorption of bipyridine compounds on gold nanoparticle surfaces investigated by UV-vis absorbance spectroscopy and surface enhanced Raman scattering
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Adsorption of bipyridine compounds on gold nanoparticle surfaces investigated by UV-vis absorbance spectroscopy and surface enhanced Raman scattering

机译:通过紫外可见吸收光谱和表面增强拉曼散射研究联吡啶化合物在金纳米颗粒表面的吸附

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摘要

Adsorption behaviors of 2,2'-bipyridine (2,2'-BiPy), 2,4'-bipyridine (2,4'-BiPy), and 4,4'-bipyridine (4,4'-BiPy) on gold nanoparticle surfaces have been comparatively investigated by means of UV-vis absorbance spectroscopy and surface-enhanced Raman scattering (SERS). The three bipyridine compounds are assumed to have a standing geometry on Au surfaces as indicated from several spectral features and relative vibrational intensity factors on the basis of the electromagnetic (EM) selection rule. 2,4'-BiPy appears to adsorb on Au surfaces via the 4-pyridyl nitrogen atom as suggested from the stronger enhancement of the vibrational bands ascribed to the 4-pyridyl ring. The SERS intensities for the three bipyridine compounds on Au could be ascribed to both the electromagnetic (EM) and charge transfer (CT) enhancement mechanism. The charge transfer is assumed to be dissimilar for 2,2'-BiPy, 2,4'-BiPy, and 4,4'-BiPy due to their different positions of the nitrogen atoms as indicated from the disparate nu(8a) band enhancements upon adsorption on surfaces.
机译:2,2'-联吡啶(2,2'-BiPy),2,4'-联吡啶(2,4'-BiPy)和4,4'-联吡啶(4,4'-BiPy)的吸附行为纳米粒子表面已通过紫外可见吸收光谱和表面增强拉曼散射(SERS)进行了比较研究。根据电磁(EM)选择规则,从几个光谱特征和相对振动强度因子可以看出,这三种联吡啶化合物在Au表面具有固定的几何形状。正如由于归因于4-吡啶环的振动带的增强所表明的那样,2,4'-BiPy似乎通过4-吡啶基氮原子吸附在Au表面上。三种联吡啶化合物在Au上的SERS强度可归因于电磁(EM)和电荷转移(CT)增强机制。电荷转移被假定为对于2,2'-BiPy,2,4'-BiPy和4,4'-BiPy不一样,因为它们的氮原子位置不同,如不同的nu(8a)能带增强所表明的吸附在表面上。

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