Department of Chemistry, National University of Singapore , 3 Science Drive 3, Singapore 117543.
ACS Appl Mater Interfaces. 2014 Aug 13;6(15):13149-56. doi: 10.1021/am502988u. Epub 2014 Jul 10.
Plasmon coupling between noble metal nanoparticles has been known to dramatically enhance linear and nonlinear optical properties of nearby chromophores and metal nanoparticles themselves. The interparticle distance is expected to have significant influence on the coupling strength. Here we have prepared DNA tuned Au nanoparticle assemblies with well controlled separation distances from 2.0 to 12.2 nm to investigate plasmon coupling strength and particle size effects on two-photon photoluminescence (TPPL) enhancement. TPPL intensities of these DNA coupled nanoassemblies were found to increase rapidly as the separation distance decreases. The largest TPPL enhancement factors of 115 and 265 were achieved at the shortest available separation distance of 2.0 nm for 21 and 41 nm Au NPs-dsDNA assemblies, respectively. We have further utilized DNA induced coupling of Au NPs and TPPL enhancement to develop a two-photon sensing scheme for detection of DNA sequences. This TPPL based method displayed high sensitivity with a limit of detection of 2.9 pM and excellent selectivity against ssDNA with mismatched bases. A single mismatch can be easily differentiated at room temperature. Taking the unique advantages of two-photon excitation, this method could be potentially further extended to DNA detection inside cells or even in vivo. These findings can provide important insight for fundamental understanding of plasmon-coupling enhanced TPPL and development of various two-photon excitation based applications.
贵金属纳米粒子之间的等离子体耦合已被证实可以显著增强附近发色团和金属纳米粒子本身的线性和非线性光学性质。粒子间的距离预计会对耦合强度产生重大影响。在这里,我们制备了 DNA 调控的 Au 纳米粒子组装体,其分离距离可精确控制在 2.0 至 12.2nm 之间,以研究等离子体耦合强度和颗粒尺寸对双光子光致发光(TPPL)增强的影响。这些 DNA 耦合纳米组装体的 TPPL 强度发现随着分离距离的减小而迅速增加。在最短的可用分离距离为 2.0nm 时,对于 21nm 和 41nm Au NPs-dsDNA 组装体,TPPL 增强因子分别达到了 115 和 265。我们进一步利用 DNA 诱导的 Au NPs 耦合和 TPPL 增强,开发了一种双光子传感方案,用于检测 DNA 序列。这种基于 TPPL 的方法具有很高的灵敏度,检测限为 2.9pM,对具有错配碱基的单链 DNA 具有优异的选择性。在室温下,很容易区分单个错配。考虑到双光子激发的独特优势,这种方法可以进一步扩展到细胞内甚至活体的 DNA 检测。这些发现可以为理解等离子体耦合增强 TPPL 的基本原理和开发各种基于双光子激发的应用提供重要的见解。