Fluorescence background suppression in Raman spectroscopy using combined Kerr gated and shifted excitation Raman difference techniques

被引:96
作者
Matousek, P [1 ]
Towrie, M [1 ]
Parker, AW [1 ]
机构
[1] Rutherford Appleton Lab, CLRC, Cent Laser Facil, Didcot OX11 0QX, Oxon, England
关键词
D O I
10.1002/jrs.840
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
An exceptionally high level of fluorescence rejection from resonance Raman spectra was achieved using a combination of two techniques, namely Kerr gated temporal rejection with shifted excitation Raman difference spectroscopy. The method was able to recover the resonance Raman spectrum from the intense fluorescence background with a signal-to-noise ratio at least 10 times higher than that achievable with either of the two approaches used individually. To demonstrate the effectiveness of the technique we obtained the resonance Raman spectrum of the laser dye rhodamine 6G (1 X 10(-3) mol dm(-3)) in methanol by excitation at 532 nm and measuring under the maximum of fluorescence emission at 560-590 nm. The method reached the photon shot noise limit of the residual fluorescence providing a detection limit for Raman spectra 10(6) times lower than the original fluorescence intensity in an accumulation time of 800 s. A unique feature of the experiment was the way in which the optical parametric amplifier light source was configured to alternate automatically between the two excitation wavelengths using an optogalvanic mirror arrangement. The ultra-high sensitivity of the combined approach holds great promise for selective probing of complex biological systems using resonance Raman spectroscopy. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:238 / 242
页数:5
相关论文
共 33 条
[1]   COMPUTER-CONTROLLED INSTRUMENT FOR THE RECOVERY OF A RESONANCE RAMAN-SPECTRUM IN THE PRESENCE OF STRONG LUMINESCENCE [J].
ANGEL, SM ;
DEARMOND, MK ;
HANCK, KW ;
WERTZ, DW .
ANALYTICAL CHEMISTRY, 1984, 56 (14) :3000-3001
[2]   Analysis of luminescent samples using subtracted shifted Raman spectroscopy [J].
Bell, SEJ ;
Bourguignon, ESO ;
Dennis, A .
ANALYST, 1998, 123 (08) :1729-1734
[3]  
Benniston AC, 2000, J RAMAN SPECTROSC, V31, P503, DOI 10.1002/1097-4555(200006)31:6<503::AID-JRS565>3.0.CO
[4]  
2-L
[5]   Solvent effect on absolute fluorescence quantum yield of rhodamine 6G determined using transient thermal lens technique [J].
Bindhu, CV ;
Harilal, SS ;
Nampoori, VPN ;
Vallabhan, CPG .
MODERN PHYSICS LETTERS B, 1999, 13 (16) :563-576
[6]   FLUORESCENCE-FREE RESONANCE RAMAN-SPECTRA OF REDUCED NICOTINAMIDE ADENINE-DINUCLEOTIDE VIA ULTRAVIOLET EXCITATION [J].
BOWMAN, WD ;
SPIRO, TG .
JOURNAL OF RAMAN SPECTROSCOPY, 1980, 9 (06) :369-371
[7]   FOURIER-TRANSFORM RAMAN-SPECTROSCOPY [J].
CHASE, DB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (24) :7485-7488
[8]   Picosecond time-resolved resonance Raman probing of the light-switch states of [Ru(Phen)2dppz]2+ [J].
Coates, CG ;
Olofsson, J ;
Coletti, M ;
McGarvey, JJ ;
Önfelt, B ;
Lincoln, P ;
Norden, B ;
Tuite, E ;
Matousek, P ;
Parker, AW .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (50) :12653-12664
[9]  
Deffontaine A., 1985, TIME RESOLVED VIBRAT, P20
[10]   Picosecond time-resolved Raman spectroscopy of solids: Capabilities and limitations for fluorescence rejection and the influence of diffuse reflectance [J].
Everall, N ;
Hahn, T ;
Matousek, P ;
Parker, AW ;
Towrie, M .
APPLIED SPECTROSCOPY, 2001, 55 (12) :1701-1708