Fluorescence suppression in resonance Raman spectroscopy using a high-performance picosecond Kerr gate

被引:154
作者
Matousek, P [1 ]
Towrie, M
Ma, C
Kwok, WM
Phillips, D
Toner, WT
Parker, AW
机构
[1] Rutherford Appleton Lab, Cent Laser Facil, CLRC, Didcot OX11 0QX, Oxon, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AY, England
[3] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
关键词
D O I
10.1002/jrs.784
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
A high-performance Kerr gate designed for the suppression of fluorescence in both time-resolved and steady-state resonance Raman spectroscopy is described and its performance illustrated. This is an improved version of a system described recently, with superior extinction ratio, higher throughput and wider usable spectral range. Specially designed polarizers are an essential feature of the system. The gate opens for similar to4 ps at 1 kHz repetition rate, throughput in the open state is up to similar to40% (excluding Fresnel losses on optical elements), the extinction ratio in the closed state is 10(-5) and the usable spectral range is 300-700 nm with a single set of polarizers. The Kerr gate is driven by similar to500 muJ, 1 kHz, 1 ps laser pulses at 800 run and we believe that it is currently the most powerful device in operation for the temporal rejection of fluorescence from Raman spectra. It increases the general applicability of Raman spectroscopy as illustrated by picosecond time-resolved resonance Raman spectra of the intramolecular charge transfer state of 4-dimethylaminobertzonitrile and by the ground-state Raman spectrum of unleaded petrol at 400 run probe wavelength. Copyright (C) 2001 John Wiley Sons, Ltd.
引用
收藏
页码:983 / 988
页数:6
相关论文
共 30 条
[1]   DYNAMICS OF ULTRAFAST DECAY PROCESSES OF ERYTHROSIN MOLECULE IN DIFFERENT SOLVENTS [J].
ALFANO, RR ;
SHAPIRO, SL .
IEEE JOURNAL OF QUANTUM ELECTRONICS, 1972, QE 8 (06) :528-&
[2]   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
[3]   Analysis of luminescent samples using subtracted shifted Raman spectroscopy [J].
Bell, SEJ ;
Bourguignon, ESO ;
Dennis, A .
ANALYST, 1998, 123 (08) :1729-1734
[4]   Excited state structure of 4-(dimethylamino)benzonitrile studied by femtosecond mid-infrared spectroscopy and ab initio calculations [J].
Chudoba, C ;
Kummrow, A ;
Dreyer, J ;
Stenger, J ;
Nibbering, ETJ ;
Elsaesser, T ;
Zachariasse, KA .
CHEMICAL PHYSICS LETTERS, 1999, 309 (5-6) :357-363
[5]  
COATES CG, UNPUB J PHYS CHEM B
[6]  
Deffontaine A., 1985, TIME RESOLVED VIBRAT, P20
[7]   ON THE SOURCE OF THE ANOMALOUS FLUORESCENCE OF 4-(DIALKYLAMINO)BENZONITRILE IN AROMATIC HYDROCARBON SOLVENTS - THE ROLE OF EXCIPLEXES [J].
DELANGE, MCC ;
LEESON, DT ;
VANKUIJK, KAB ;
HUIZER, AH ;
VARMA, CAGO .
CHEMICAL PHYSICS, 1993, 174 (03) :425-440
[8]  
DUNGUAY MA, 1969, APPL PHYS LETT, V15, P192
[9]  
EVERALL N, IN PRESS APPL SPECTR
[10]   OBSERVATION OF RESONANCE RAMAN-SPECTRA OF S-1, T-1, AND S-0 PYRENE IN SOLUTION - APPLICATION OF A FLUORESCENCE REJECTION TECHNIQUE [J].
FUJII, T ;
KAMOGAWA, K ;
KITAGAWA, T .
CHEMICAL PHYSICS LETTERS, 1988, 148 (01) :17-20