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首页> 外文期刊>The Journal of Chemical Physics >Second-harmonic spectroscopy of surface immobilized gold nanospheres above a gold surface supported by self-assembled monolayers
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Second-harmonic spectroscopy of surface immobilized gold nanospheres above a gold surface supported by self-assembled monolayers

机译:由自组装单分子层支撑的金表面上方的表面固定金纳米球的二次谐波光谱

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We have investigated linear and nonlinear optical properties of surface immobilized gold nanospheres (SIGNs) above a gold surface with a gap distance of a few nanometers. The nanogap was supported by amine or merocyanine terminated self-assembled monolayers (SAMs) of alkanethiolates. A large second-harmonic generation (SHG) was observed from the SIGN systems at localized surface plasmon resonance condition. The maximum enhancement factor of SHG intensity was found to be 3x10(5) for the SIGN system of nanospheres 100 nm in diameter with a gap distance of 0.8 nm. The corresponding susceptibility was estimated to be chi((2))=750 pm/V (1.8x10(-6) esu). In the SIGN system supported with the merocyanine terminated SAMs, the SHG response was also resonant to the merocyanine in the nanogap. It was found that the SHG response of the SIGN systems is strongly frequency dependent. This leads us to conclude that the large chi((2)) is caused by enhanced electric fields at the localized surface plasmon resonance condition and is not due to an increase of the surface susceptibility following from the presence of the gold nanospheres. The observed SHG was consistent with the theoretical calculations involving Fresnel correction factors, based on the quasistatic approximation. (c) 2006 American Institute of Physics.
机译:我们已经研究了在金表面上方具有几纳米间隙距离的表面固定金纳米球(SIGNs)的线性和非线性光学性质。纳米间隙由链烷硫醇盐的胺或部花青终止的自组装单层(SAM)支撑。在局部表面等离振子共振条件下,从SIGN系统观察到大量的二次谐波(SHG)。对于直径为100 nm,间隙距离为0.8 nm的纳米球的SIGN系统,SHG强度的最大增强因子为3x10(5)。相应的磁化率估计为chi((2))= 750 pm / V(1.8x10(-6)esu)。在由花菁封端的SAM支持的SIGN系统中,SHG响应也与纳米间隙中的花菁共振。已经发现,SIGN系统的SHG响应强烈地依赖于频率。这使我们得出结论,大chi((2))是由局部表面等离振子共振条件下增​​强的电场引起的,而不是由于金纳米球的存在而引起的表面磁化率的增加。观测到的SHG与基于准静态逼近的菲涅耳校正因子的理论计算相符。 (c)2006年美国物理研究所。

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