TRACE-LEVEL QUANTITATION VIA TIME-RESOLVED 2-PHOTON-EXCITED FLUORESCENCE

被引:16
作者
LYTLE, FE
DINKEL, DM
FISHER, WG
机构
[1] Department of Chemistry, 1393 Brown Laboratories, Purdue University, West Lafayette
[2] Conoco Inc., Ponca City
[3] Oak Ridge National Laboratory, Oak Ridge
关键词
FLUORESCENCE; INSTRUMENTATION; 2-PHOTON; LASERS; TIME-RESOLVED SPECTROSCOPY;
D O I
10.1366/0003702934066389
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
With the use of a cavity-dumped, synchronously pumped dye laser for excitation, two-photon fluorescence cross sections are approximately eight orders of magnitude smaller than those for one-photon excitation. Thus, examination of dilute solutions has been achieved only with great difficulty. Any successful instrumentation will require that the blank be essentially eliminated. To this end, time-filtered detection has been combined with two-photon excitation and spatial filtering to produce fluorometric detection limits of 38 pM for 9,10-diphenylanthracene and 8.6 pM for alpha-NPO. It is believed that this latter value is the lowest concentration yet reported for two-photon spectroscopy in fluid solution. The instrumentation and data processing are described. Additionally, a comparison is made with the performance of other recent alternative approaches involving spatial filtering and second harmonic detection.
引用
收藏
页码:2002 / 2006
页数:5
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