Pincella Francesca, Isozaki Katsuhiro, Taguchi Tomoya, Song Yeji, Miki Kazushi
J Nanosci Nanotechnol. 2015 Feb;15(2):1171-9. doi: 10.1166/jnn.2015.9501.
In this research, we report the development, characterization and application of various plasmonic substrates (with localized surface plasmon resonance wavelength tunable by gold nanoparticle size) for two-photon absorption (TPA)-induced photodimerization of an anthracene derivative, anthracene carboxylic acid, in both surface and solution phase under incoherent visible light irradiation. Despite the efficient photoreaction property of anthracene derivatives and the huge number of publications about them, there has never been a report of a multiphoton photoreaction involving an anthracene derivative with the exception of a reverse photoconversion of anthracene photodimer to monomer with three-photon absorption. We examined the progress of the TPA-induced photoreaction by means of surface-enhanced Raman scattering, taking advantage of the ability of our plasmonic substrate to enhance and localize both incident light for photoreaction and Raman scattering signal for analysis of photoreaction products. The TPA-induced photoreaction in the case of anthracene carboxylic acid coated 2D array of gold nanoparticles gave different results according to the properties of the plasmonic substrate, such as the size of the gold nanoparticle and also its resultant optical properties. In particular, a stringent requirement to achieve TPA-induced photodimerization was found to be the matching between irradiation wavelength, localized surface plasmon resonance of the 2D array, and twice the wavelength of the molecular excitation of the target material (in this case, anthracene carboxylic acid). These results will be useful for the future development of efficient plasmonic substrates for TPA-induced photoreactions with various materials.
在本研究中,我们报告了各种等离子体基底(其局域表面等离子体共振波长可通过金纳米颗粒尺寸调节)的开发、表征及应用,用于在非相干可见光照射下,使蒽衍生物蒽羧酸在表面和溶液相中发生双光子吸收(TPA)诱导的光二聚反应。尽管蒽衍生物具有高效的光反应特性且关于它们的出版物数量众多,但除了通过三光子吸收将蒽光二聚体反向光转化为单体之外,从未有过涉及蒽衍生物的多光子光反应的报道。我们利用等离子体基底增强和定位用于光反应的入射光以及用于分析光反应产物的拉曼散射信号的能力,通过表面增强拉曼散射来研究TPA诱导的光反应进程。对于涂覆有蒽羧酸的二维金纳米颗粒阵列,TPA诱导的光反应根据等离子体基底的性质(如金纳米颗粒的尺寸及其产生的光学性质)给出了不同的结果。特别地,发现实现TPA诱导的光二聚反应的一个严格要求是照射波长、二维阵列的局域表面等离子体共振与目标材料(在这种情况下为蒽羧酸)分子激发波长的两倍之间的匹配。这些结果将有助于未来开发用于与各种材料进行TPA诱导光反应的高效等离子体基底。