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Non-linear optical response by functionalized gold nanospheres: identifying design principles to maximize the molecular photo-release

机译:功能化金纳米球的非线性光学响应:确定设计原理以最大化分子的光释放

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摘要

In a recent study by Voliani et al. [Small, 2011, 7, 3271], the electromagnetic field enhancement in the vicinity of the gold nanoparticle surface has been exploited to achieve photocontrolled release of a molecular cargo conjugated to the nanoparticles via 1,2,3-triazole, a photocleavable moiety. The aim of the present study is to investigate the mechanism of the photorelease by characterizing the nanoparticle aggregation status within the cells and simulating the electric field enhancement in a range of experimentally realistic geometries, such as single Au nanoparticles, dimers, trimers and random aggregates. Two plasmon-enhanced processes are examined for triazole photocleavage, i.e. three-photon excitation and third-harmonic-generation (one-photon) excitation. Taking into account the absorption cross sections of the triazole, we conclude that the latter mechanism is more efficient, and provides a photocleavage rate that explains the experimental findings. Moreover, we determine which aggregate geometries are required to maximize the field enhancement, and the dependence of such enhancement on the excitation wavelength. Our results provide design principles for maximizing the multiphoton molecular photorelease by such functionalized gold nanoparticles.
机译:在Voliani等人的最新研究中。 [Small,2011,7,3271],已经利用金纳米颗粒表面附近的电磁场增强来实现通过1,2,3-三唑(一种可光裂解的部分)与纳米颗粒结合的分子货物的光控释放。本研究的目的是通过表征细胞内纳米颗粒的聚集状态并模拟一系列实验现实几何形状(例如单个Au纳米颗粒,二聚体,三聚体和无规聚集体)中的电场增强来研究光释放的机理。对于三唑的光裂解,检查了两个等离子体激元增强过程,即三光子激发和第三谐波产生(单光子)激发。考虑到三唑的吸收截面,我们得出的结论是后者的机制更有效,并提供了光解速率,可以解释实验结果。此外,我们确定需要哪些集合几何体来最大化场增强,以及这种增强对激发波长的依赖性。我们的结果提供了通过这种功能化的金纳米颗粒使多光子分子光释放最大化的设计原理。

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