Quantitative Analysis of Polarization-Controlled Tip-Enhanced Raman Imaging through the Evaluation of the Tip Dipole

被引:52
作者
Mino, Toshihiro [1 ]
Saito, Yuika [1 ]
Verma, Prabhat [1 ]
机构
[1] Osaka Univ, Dept Appl Phys, Suita, Osaka 5650871, Japan
关键词
polarization near-field; tip-enhanced Raman spectroscopy; defocused imaging; plasmon; nanoimaging; THIN-FILMS; FIELD; SPECTROSCOPY; ORIENTATION; SCATTERING; RESOLUTION; MOLECULES; RADIATION; EMISSION; PATTERN;
D O I
10.1021/nn5031803
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polarization analysis in tip-enhanced Raman spectroscopy (TERS) is of tremendous advantage, as it allows one to study highly directional intrinsic properties of a sample at the nanoscale. However, neither evaluation nor control of the polarization properties of near-field light in TERS is as straightforward as in usual far-field illumination, because of the random metallic nanostructure attached to the tip apex. In this study, we have developed a method to successfully analyze the polarization of near-field light in TERS from the scattering pattern produced by the induced dipole in the metallic tip. Under dipole approximation, we measured the image of the dipole at a plane away from the focal plane, where the information about the direction of the dipole oscillation was intact. The direction of the dipole oscillation was determined from the defocused pattern, and then the polarization of near-field light was evaluated from the oscillation direction by calculating the intensity distribution of near-field light through Green's function. After evaluating the polarization of some fabricated tips, we used those tips to measure TERS images from single-walled carbon nanotubes and confirmed that the contrast of the TERS image depended on the oscillation direction of the dipole, which were also found in excellent agreement with the calculated TERS images, verifying that the polarization of the near-field was quantitatively estimated by our technique. Our technique would lead to better quantitative analysis in TERS imaging with consideration of polarization impact, giving a better understanding of the behavior of nanomaterials.
引用
收藏
页码:10187 / 10195
页数:9
相关论文
共 48 条
[1]   Chirality changes in carbon nanotubes studied with near-field Raman spectroscopy [J].
Anderson, Neil ;
Hartschuh, Achim ;
Novotny, Lukas .
NANO LETTERS, 2007, 7 (03) :577-582
[2]   Tip-enhanced Raman spectroscopy - an interlaboratory reproducibility and comparison study [J].
Blum, Carolin ;
Opilik, Lothar ;
Atkin, Joanna M. ;
Braun, Kai ;
Kaemmer, Stefan B. ;
Kravtsov, Vasily ;
Kumar, Naresh ;
Lemeshko, Sergey ;
Li, Jian-Feng ;
Luszcz, Karol ;
Maleki, Teimour ;
Meixner, Alfred J. ;
Minne, Steve ;
Raschke, Markus B. ;
Ren, Bin ;
Rogalski, Jan ;
Roy, Debdulal ;
Stephanidis, Bruno ;
Wang, Xiang ;
Zhang, Dai ;
Zhong, Jin-Hui ;
Zenobi, Renato .
JOURNAL OF RAMAN SPECTROSCOPY, 2014, 45 (01) :22-31
[3]   Enhancing and redirecting carbon nanotube photoluminescence by an optical antenna [J].
Boehmler, Miriam ;
Hartmann, Nicolai ;
Georgi, Carsten ;
Hennrich, Frank ;
Green, Alexander A. ;
Hersam, Mark C. ;
Hartschuh, Achim .
OPTICS EXPRESS, 2010, 18 (16) :16443-16451
[4]   Orientation imaging of single molecules by wide-field epifluorescence microscopy [J].
Böhmer, M ;
Enderlein, J .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 2003, 20 (03) :554-559
[5]   Mechanism of Near-Field Raman Enhancement in One-Dimensional Systems [J].
Cancado, L. G. ;
Jorio, A. ;
Ismach, A. ;
Joselevich, E. ;
Hartschuh, A. ;
Novotny, L. .
PHYSICAL REVIEW LETTERS, 2009, 103 (18)
[6]   Tip-enhanced Raman spectroscopy of carbon nanotubes [J].
Cancado, Luiz Gustavo ;
Hartschuh, Achim ;
Novotny, Lukas .
JOURNAL OF RAMAN SPECTROSCOPY, 2009, 40 (10) :1420-1426
[7]   Multipolar radiation of quantum emitters with nanowire optical antennas [J].
Curto, Alberto G. ;
Taminiau, Tim H. ;
Volpe, Giorgio ;
Kreuzer, Mark P. ;
Quidant, Romain ;
van Hulst, Niek F. .
NATURE COMMUNICATIONS, 2013, 4
[8]   Plasmonic nanoantennas: Angular scattering properties of multipole resonances in noble metal nanorods [J].
Encina, Ezequiel R. ;
Coronado, Eduardo A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (26) :9586-9594
[9]   Rapid determination of the three-dimensional orientation of single molecules [J].
Fourkas, JT .
OPTICS LETTERS, 2001, 26 (04) :211-213
[10]   Single-molecule anisotropy imaging [J].
Harms, GS ;
Sonnleitner, M ;
Schütz, GJ ;
Gruber, HJ ;
Schmidt, T .
BIOPHYSICAL JOURNAL, 1999, 77 (05) :2864-2870