Metallic-Nanostructure-Enhanced Optical Trapping of Flexible Polymer Chains in Aqueous Solution As Revealed by Confocal Fluorescence Microspectroscopy

Metallic-Nanostructure-Enhanced Optical Trapping of Flexible Polymer Chains in Aqueous Solution As Revealed by Confocal Fluorescence Microspectroscopy
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DOI:
10.1021/jp305247a
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发表时间:
2012-06
影响因子:
3.7
通讯作者:
Mariko Toshimitsu;Yuriko Matsumura;T. Shoji;N. Kitamura;Mai Takase;K. Murakoshi;H. Yamauchi;S. Ito;H. Miyasaka;A. Nobuhiro;Y. Mizumoto;H. Ishihara;Yasuyuki Tsuboi
Mariko Toshimitsu;Yuriko Matsumura;T. Shoji;N. Kitamura;Mai Takase;K. Murakoshi;H. Yamauchi;S. Ito;H. Miyasaka;A. Nobuhiro;Y. Mizumoto;H. Ishihara;Yasuyuki Tsuboi
中科院分区:
化学3区
文献类型:
--
作者:
Mariko Toshimitsu;Yuriko Matsumura;T. Shoji;N. Kitamura;Mai Takase;K. Murakoshi;H. Yamauchi;S. Ito;H. Miyasaka;A. Nobuhiro;Y. Mizumoto;H. Ishihara;Yasuyuki Tsuboi

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Optical trapping of flexible polymer chains to a metallic nanostructured surface was explored by microscopic imaging and confocal fluorescence spectroscopy. A fluorescence-labeled poly(N-isopropylacrylamide) was targeted, being a representative thermo-responsive polymer. Upon resonant plasmonic excitation, it was clearly observed that polymers were assembled into the excitation area to form molecular assemblies. Simultaneously, fluorescence from the area was obviously intensified, indicating an increase in the number of polymer chains at the area. The excitation threshold of light intensity that was required for obvious trapping was 1 kW/cm2, which was much lower by a factor of 104 than that for conventional trapping using a focused laser beam. The morphology of the assemblies was sensitive to excitation intensity. We precisely evaluated temperature rise (ΔT) around the metallic nanostructure upon plasmonic excitation: ΔT ≈ 10 K at 1 kW/cm2 excitation. This temperature rise was an origin of a repulsive fo...