A cylindrical quadrupole ion trap in combination with an electrospray ion source for gas-phase luminescence and absorption spectroscopy

被引:47
作者
Stockett, Mark H. [1 ]
Houmoller, Jorgen [1 ]
Stochkel, Kristian [1 ]
Svendsen, Annette [1 ]
Nielsen, Steen Brondsted [1 ]
机构
[1] Aarhus Univ, Dept Phys & Astron, Aarhus, Denmark
关键词
LASER-INDUCED FLUORESCENCE; RESONANCE ENERGY-TRANSFER; CONFORMATIONAL DYNAMICS; PROTEIN CHROMOPHORES; MOLECULAR-IONS; PROBE; PHOTODISSOCIATION; EXCITATION; LIFETIMES; CATIONS;
D O I
10.1063/1.4948316
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
A relatively simple setup for collection and detection of light emitted from isolated photo-excited molecular ions has been constructed. It benefits from a high collection efficiency of photons, which is accomplished by using a cylindrical ion trap where one end-cap electrode is a mesh grid combined with an aspheric condenser lens. The geometry permits nearly 10% of the emitted light to be collected and, after transmission losses, approximately 5% to be delivered to the entrance of a grating spectrometer equipped with a detector array. The high collection efficiency enables the use of pulsed tunable lasers with low repetition rates (e.g., 20 Hz) instead of continuous wave (cw) lasers or very high repetition rate (e.g., MHz) lasers that are typically used as light sources for gas-phase fluorescence experiments on molecular ions. A hole has been drilled in the cylinder electrode so that a light pulse can interact with the ion cloud in the center of the trap. Simulations indicate that these modifications to the trap do not significantly affect the storage capability and the overall shape of the ion cloud. The overlap between the ion cloud and the laser light is basically 100%, and experimentally >50% of negatively charged chromophore ions are routinely photodepleted. The performance of the setup is illustrated based on fluorescence spectra of several laser dyes, and the quality of these spectra is comparable to those reported by other groups. Finally, by replacing the optical system with a channeltron detector, we demonstrate that the setup can also be used for gas-phase action spectroscopy where either depletion or fragmentation is monitored to provide an indirect measurement on the absorption spectrum of the ion. Published by AIP Publishing.
引用
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页数:9
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[41]   A MASS-SPECTROMETRIC INVESTIGATION OF THE GAS-PHASE ION-MOLECULE REACTIONS OF FULLERENE CATIONS AND DICATIONS WITH VARIOUS NEUTRAL MOLECULES [J].
STRY, JJ ;
GARVEY, JF .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1994, 138 :241-261
[42]   Ion chemistry of sulfuryl fluoride: An experimental and theoretical study on gas-phase reactions involving neutral and ionized SO2F2 [J].
Antoniotti, Paola ;
Benzi, Paola ;
Operti, Lorenza ;
Rabezzana, Roberto ;
Borocci, Stefano ;
Giordani, Maria ;
Grandinetti, Felice .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2013, 354 :46-53
[43]   Gas-Phase Reactivity of Peptide Thiyl (RS•),Perthiyl (RSS•), and Sulfinyl (RSO•) Radical Ions Formed from Atmospheric Pressure Ion/Radical Reactions [J].
Tan, Lei ;
Xia, Yu .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2013, 24 (04) :534-542
[44]   Guided-Ion-Beam and ab Initio Study of the Li+, K+, and Rb+ Association Reactions with Gas-Phase Butanone and Cyclohexanone in Their Ground Electronic States [J].
Lucas, J. M. ;
de Andres, J. ;
Lopez, E. ;
Alberti, M. ;
Bofill, J. M. ;
Bassi, D. ;
Ascenzi, D. ;
Tosi, P. ;
Aguilar, A. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2009, 113 (52) :14766-14773
[45]   Gas-phase fluorine migration reactions in the radical cations of pentafluorosulfanylbenzene (Aryl-SF5) and benzenesulfonyl fluoride (Aryl-SO2F) derivatives and in the 2,5-xylylfluoroiodonium ion [J].
Gao, Ying ;
Wang, Hao-Yang ;
Zhang, Xiang ;
Cheng, Jia-Shun ;
Zhang, Fang ;
Guo, Yin-Long .
JOURNAL OF MASS SPECTROMETRY, 2014, 49 (06) :481-489
[46]   Selected Ion Flow Tube Study of the Gas-Phase Reactions of CF+, CF2+, CF3+, and C2F4+ with C2H4, C2H3F, CH2CF2, and C2HF3 [J].
Simpson, Matthew J. ;
Tuckett, Richard P. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (31) :8119-8129