Browsing by Author "Masuhara, H."

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Enhanced optical confinement of dye-doped dielectric nanoparticles using a picosecond-pulsed near-infrared laser
(2014-07-01)
Kittiravechote, A.
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Chiang, W-Y
;
Usman, A.
;
Liau, I.
;
Masuhara, H.
We demonstrate a novel strategy to increase the capability of confining numerous dye-doped polymeric nanobeads (diameter 100 nm) with laser trapping. Unlike most classical works of optical trapping that address mainly the stiffness of the optical trap, our work concerns an increase in the number of particles confined near the laser focus. We developed an imaging system of light scattering in which a condenser lamp was employed to illuminate the focal plane of the objective lens, and the scattering of the incoherent light was specifically measured to determine the number of confined nanobeads. In contrast to preceding work that used mainly continuous-wave or femtosecond-pulsed lasers, we employed a picosecond-pulsed laser with the half-wavelength of the laser particularly falling within the absorption band of the dopant. Our results show that the number of doped nanobeads held by the laser is significantly greater than that of the bare nanobeads of the same dimension. In striking contrast, the confinement of the nanobeads of the two types was comparable when a continuous-wave laser of the same wavelength and power was employed. The number of confined dye-doped nanobeads increased nonlinearly with the power of the pulsed laser; this dependence was fitted satisfactorily with a second-order polynomial. Supported by theoretical analysis, we attribute the enhanced confinement of doped nanobeads in part to an increased effective refractive index resulting from two-photon resonance between the optical field of the laser and the dopant of the nanobead. We envisage that our findings would evoke applications that benefit from controlled confinement or aggregation of nanomaterials with the employment of near-infrared pulsed lasers.
Fabrication of fluorescent nanoparticles of dendronized perylenediimide by laser ablation in water
(2008-10-01)
Yasukuni, R.
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Asahi, T.
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Sugiyama, T.
;
Masuhara, H.
;
Sliwa, M.
Highly fluorescent organic nanoparticles with size of about 300 nm were prepared by nanosecond laser ablation of micrometer-sized powder of dendronized perylenediimide dispersed in water. The nanoparticle colloidal solution provided a fluorescence quantum yield of 0.58. The absorption and emission spectral studies demonstrated that the bulky dendron groups at the side bays of perylenediimide chromophore efficiently suppress the interchromophoric interactions in the nanoparticles. Fluorescence measurement on several single nanoparticles underlines that the prepared nanoparticles are bright and photo-stable enough to be a useful probe for single particle fluorescence investigation.
Laser Fabrication and Spectroscopy of Organic Nanoparticles
(2008-12-01)
Asahi, T.
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Sugiyama, T.
;
Masuhara, H.
;
應用化學系
;
應用化學系分子科學碩博班
In working with nanoparticles, researchers still face two fundamental challenges: how to fabricate the nanoparticles with controlled size and shape and how to characterize them. In this Account, we describe recent advances in laser technology both for the synthesis of organic nanoparticles and for their analysis by single nanoparticle spectroscopy. Laser ablation of organic microcrystalline powders in a poor solvent has opened new horizons for the synthesis of nanoparticles because the powder sample is converted directly into a stable colloidal solution without additives and chemicals. By tuning laser wavelength, pulse width, laser fluence, and total shot number, we could control the size and phase of the nanoparticles. For example, we describe nanoparticle formation of quinacridone, a well-known red pigment, in water. By modifying the length of time that the sample is excited by the laser, we could control the particle size (30-120 nm) for nanosecond excitation down to 13 nm for femtosecond irradiation. We prepared beta- and gamma-phase nanoparticles from the microcrystal with beta-phase by changing laser wavelength and fluence. We present further results from nanciparticles produced from several dyes, C(60), and an anticancer drug. All the prepared colloidal solutions were transparent and highly dispersive. Such materials could be used for nanoscale device development and for biomedical and environmental applications. We also demonstrated the utility of single nanoparticle spectroscopic analysis in the characterization of organic nanoparticles. The optical properties of these organic nanoparticles depend on their size within the range from a few tens to a few hundred nanometers. We observed perylene nanoscrystals using single-particle spectroscopy coupled with atomic force microscopy. Based on these experiments, we proposed empirical equations explaining their size-dependent fluorescence spectra. We attribute the size effect to the change in elastic properties of the nanocrystal. Based on the results for nanoparticles of polymers and other molecules with flexible conformations, we assert that size-dependent optical properties are common for organic nanoparticles. While "electronic confinement" explains the size-dependent properties of inorganic nanoparticles, we propose "structural confinement" as an analogous paradigm for organic nanoparticles.
Light propagation in optical trapping assembling of colloidal particles at an interface
(2016-01-01)
Kudo, T.
;
Wang, S. F.
;
Yuyama, K.
;
Masuhara, H.
;
應用化學系
We conduct the optical trapping and assembling of polystyrene particles at the glass/solution interface by utilizing tightly focused 1064 nm laser of high power. Previously we reported that this leads to form the assembly sticking out horns consisting of single row of aligned particles through light propagation. Here, we demonstrate the laser power dependence of this phenomenon. With increasing the laser power, the particles are started to distribute around the focal spot and form the assembly larger than focal spot. The shape of the assembly becomes ellipse-like and the color at the central part of the assembly in transmission images is changed. This indicates that the assembly structure is changed, and trapping laser is started to propagate through the adjoining particles leading to horn formation. Strong laser power is necessary to elongate the horns and to align them straightly. We expect that this study will offer a novel experimental approach for assembling and crystallization of nanoparticles and molecules exclusively by optical trapping.
Nanoparticle preparation of quinacridone and beta-carotene using near-infrared laser ablation of their crystals
(2010-12-01)
Yuyama, K.
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Sugiyama, T.
;
Asahi, T.
;
Ryo, S.
;
Oh, I.
Quinacridone nanoparticles with a mean size of about 200 nm are successfully prepared using nanosecond near-infrared (NIR) laser ablation of its microcrystalline powders in heavy water. The absorption spectra of the formed colloidal solutions depend on the excitation wavelengths, which is eventually ascribed to number and energy of absorbed photons. beta-carotene has low photostability and is easily decomposed upon UV/VIS laser ablation of its solid, while its nanoparticles are prepared utilizing this NIR laser ablation technique. The advantage of nanoparticle preparation by NIR laser ablation is discussed.
Nanoparticle preparation of quinacridone and beta-carotene using near-infrared laser ablation of their crystals
(2010-12-01)
Yuyama, K.
;
Sugiyama, T.
;
Asahi, T.
;
Ryo, S.
;
Oh, I.
Quinacridone nanoparticles with a mean size of about 200 nm are successfully prepared using nanosecond near-infrared (NIR) laser ablation of its microcrystalline powders in heavy water. The absorption spectra of the formed colloidal solutions depend on the excitation wavelengths, which is eventually ascribed to number and energy of absorbed photons. beta-carotene has low photostability and is easily decomposed upon UV/VIS laser ablation of its solid, while its nanoparticles are prepared utilizing this NIR laser ablation technique. The advantage of nanoparticle preparation by NIR laser ablation is discussed.