Use of a sample translation technique to minimize adverse effects of laser irradiation in surface-enhanced Raman spectrometry

被引:40
作者
De Jesús, MA [1 ]
Giesfeldt, KS [1 ]
Sepaniak, MJ [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
surface-enhanced Raman spectroscopy; SERS; sample translation; poly(dimethylsiloxane); PDMS; photolytic and thermal degradation; pyrrolysis;
D O I
10.1366/00037020360625970
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Surface-enhanced Raman spectroscopy (SERS) has proven to be a very powerful tool in the analysis of a wide range of compounds. However, continuous irradiation of the laser beam over the SERS substrate can promote the gross decomposition of the sample analytes and significantly broaden and diminish the intensities of observed spectral bands. In addition, the incident radiation can promote thermal or photolytic fragmentation of analytes, thereby altering the observable bands and possibly leading to a misinterpretation of analytical data. Finally, chemical or morphological changes in the SERS substrate are possible. This work presents the use of a sample translation technique (STT) as a means to minimize these adverse effects. By spinning the sample rapidly, the effective residence time of analytes and substrate within the irradiated zone is dramatically decreased without reduction of spectral acquisition time or the density of analyte in the zone. The technique is studied by acquiring SERS spectra of Naproxen USP, riboflavin, folic acid, Rhodamine 6G, and 4-aminothiophenol using silver islands on glass and silver-poly(dimethylsiloxane) composite substrates under various spinning and stationary conditions. In all cases, spectra show improvements upon spinning at laser powers as low as 4.2 (+/-0.1) mW. Specific differences in the appearance of the spectra and the potential use of STT for improved SERS qualitative and quantitative determinations are presented.
引用
收藏
页码:428 / 438
页数:11
相关论文
共 44 条
  • [1] How a resonant charge transfer mechanism determines the relative intensities in the SERS spectra of 4-methylpyridine
    Arenas, JF
    López-Tocón, I
    Centeno, SP
    Soto, J
    Otero, JC
    [J]. VIBRATIONAL SPECTROSCOPY, 2002, 29 (1-2) : 147 - 154
  • [2] Colthup N. B., 1990, INTRO INFRARED RAMAN, DOI [10.1016/B978-0-08-091740-5.50011-9, DOI 10.1016/B978-0-08-091740-5.50011-9]
  • [3] Corio P, 1997, J RAMAN SPECTROSC, V28, P235, DOI 10.1002/(SICI)1097-4555(199704)28:4<235::AID-JRS90>3.0.CO
  • [4] 2-#
  • [5] DINH TV, 1991, P SPIE INT SOC OPT E, V1435, P197
  • [6] VIBRATIONAL-SPECTRUM OF NAPHTHALENE ANION
    DODSON, CL
    GRAHAM, JF
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1973, 77 (24) : 2903 - 2906
  • [7] Single-molecule and single-nanoparticle SERS: Examining the roles of surface active sites and chemical enhancement
    Doering, WE
    Nie, SM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (02) : 311 - 317
  • [8] Dollish F. R., 1974, CHARACTERISTIC RAMAN, P27
  • [9] Dou XM, 1999, REV ANAL CHEM, V18, P285
  • [10] Chemical, microstructural and thermal analyses of a naphthalene-derived mesophase pitch
    Dumont, M
    Chollon, G
    Dourges, MA
    Pailler, R
    Bourrat, X
    Naslain, R
    Bruneel, JL
    Couzi, M
    [J]. CARBON, 2002, 40 (09) : 1475 - 1486