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Molecular active plasmonics: controlling plasmon resonances withmolecular machines

机译:分子活性等离子体:用分子机械控制等离子体共振

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The paper studies the molecular-level active control of localized surface plasmon resonances (LSPRs) of Au nanodisk arrays with molecular machines. Two types of molecular machines – azobenzene and rotaxane – have been demonstrated to enable the reversible tuning of the LSPRs via the controlled mechanical movements. Azobenzene molecules have the property of trans-cis photoisomerization and enable the photo-induced nematic (N)-isotropic (I) phase transition of the liquid crystals (LCs) that contain the molecules as dopant. The phase transition of the azobenzene-doped LCs causes the refractive-index difference of the LCs, resulting in the reversible peak shift of the LSPRs of the embedded Au nanodisks due to the sensitivity of the LSPRs to the disks' surroundings' refractive index. Au nanodisk array, coated with rotaxanes, switches its LSPRs reversibly when it is exposed to chemical oxidants and reductants alternatively. The correlation between the peak shift of the LSPRs and the chemically driven mechanical movement of rotaxanes is supported by control experiments and a time-dependent density functional theory (TDDFT)-based, microscopic model.
机译:本文用分子机械研究Au Nanodisk阵列的局部表面等离子体共振(LSPRS)的分子水平积极控制。已经证明了两种类型的分子机 - 偶氮苯和轮烷烷,以通过受控的机械运动来实现LSPRS的可逆调谐。偶氮苯分子具有反式顺式光致硅白化的性质,使得含有掺杂剂的液晶(LC)的光诱导的向毒液(N) - 滴度(I)相转变。偶氮介质掺杂LCS的相转变导致LCS的折射率差异,导致嵌入式Au纳米DANODisks的LSPRS的可逆峰值偏移,由于LSPRS对磁盘的周围环境的折射率的敏感性。 Au Nanodisk阵列涂有轮剑烷,在接触到化学氧化剂和还原剂时可逆地切换其LSPRS。通过对照实验支持LSPRS的峰值和旋尖的化学驱动机械运动之间的相关性和基于时间依赖的密度泛函理论(TDDFT)的微观模型。

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