scholarly journals Measurement of the positronium 13S1–23S1interval by continuous-wave two-photon excitation

1993 ◽  
Vol 48 (1) ◽  
pp. 192-219 ◽  
Author(s):  
M. S. Fee ◽  
S. Chu ◽  
A. P. Mills ◽  
R. J. Chichester ◽  
D. M. Zuckerman ◽  
...  
Keyword(s):  
Continuous Wave ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

scholarly journals Continuous-wave two-photon excitation of individual CdS nanocrystallites

2001 ◽  
Vol 79 (6) ◽  
pp. 830-832 ◽  
Author(s):  
A. M. van Oijen ◽  
R. Verberk ◽  
Y. Durand ◽  
J. Schmidt ◽  
J. N. J. van Lingen ◽  
...  
Keyword(s):  
Continuous Wave ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

scholarly journals Measurement of the positronium13S1-23S1interval by continuous-wave two-photon excitation

1993 ◽  
Vol 70 (10) ◽  
pp. 1397-1400 ◽  
Author(s):  
M. S. Fee ◽  
A. P. Mills ◽  
S. Chu ◽  
E. D. Shaw ◽  
K. Danzmann ◽  
...  
Keyword(s):  
Continuous Wave ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

Two-Photon near Infrared Excitation in Living Cells

1997 ◽  
Vol 5 (1) ◽  
pp. 27-34 ◽  
Author(s):  
Karsten König
Keyword(s):  
Near Infrared ◽  
Continuous Wave ◽  
Cell Damage ◽  
Local Heating ◽  
Average Power ◽  
Two Photon ◽  
Photon Excitation ◽  
Non Linear ◽  
Linear Effects ◽  
Two Photon Excitation

Non-linear effects due to two-photon near infrared (NIR) excitation of endogenous and exogenous cellular chromophores allow novel techniques in tissue, cell and biomolecule diagnostics, as well as in intracellular micromanipulation (e.g. intracellular photochemistry). Two-photon NIR excitation may also result in cell damage effects. The high photon intensities (1024 photons cm−2 s−1) required for non-resonant two-photon excitation can be achieved by diffraction-limited focusing of continuous wave (cw) laser beams (cw microbeams) with powers in the mW range. For example, NIR traps (“laser tweezers”) used as force transducers and micromanipulation tools in cellular and molecular biology are sources of two-photon excitation. NIR traps can induce two-photon excited visible fluorescence and, in the case of <800 nm-traps, UVA-like cell damage. Multimode cw microbeams may enhance non-linear effects due to longitudinal mode-beating. To perform high scan rate two-photon fluorescence imaging, the application of ultrashort laser pulses of moderate peak power but low average power (pulsed microbeams) is required. In NIR femtosecond microscopes, non-destructive imaging of two-photon excited fluorophores in various human and culture cells was demonstrated for <2 mW average powers, <200 mW peak powers and 400 GW cm−2 intensities (700–800 nm, ∼150 fs, ∼100 MHz). However, higher average power levels may result in failed cell reproduction and cell death due to intracellular optical breakdown. In addition, destructive transient local heating and μN force generation may occur.

Two-photon excitation microscopy in cellular biophysics

1995 ◽  
Vol 53 ◽  
pp. 62-63
Author(s):  
David W. Piston ◽  
Brian D. Bennett ◽  
Robert G. Summers
Keyword(s):  
Confocal Microscopy ◽  
Laser Beam ◽  
Duty Cycle ◽  
Excited Electronic State ◽  
Input Power ◽  
Two Photon ◽  
Simultaneous Absorption ◽  
Photon Excitation ◽  
Very High ◽  
Two Photon Excitation

Two-photon excitation microscopy (TPEM) provides attractive advantages over confocal microscopy for three-dimensionally resolved fluorescence imaging and photochemistry. Two-photon excitation arises from the simultaneous absorption of two photons in a single quantitized event whose probability is proportional to the square of the instantaneous intensity. For example, two red photons can cause the transition to an excited electronic state normally reached by absorption in the ultraviolet. In practice, two-photon excitation is made possible by the very high local instantaneous intensity provided by a combination of diffraction-limited focusing of a single laser beam in the microscope and the temporal concentration of 100 femtosecond pulses generated by a mode-locked laser. Resultant peak excitation intensities are 106 times greater than the CW intensities used in confocal microscopy, but the pulse duty cycle of 10-5 maintains the average input power on the order of 10 mW, only slightly greater than the power normally used in confocal microscopy.

Two-photon excitation fluorescence microscopy in living systems

1993 ◽  
Vol 51 ◽  
pp. 154-155 ◽  
Author(s):  
David W. Piston
Keyword(s):  
Confocal Microscopy ◽  
Fluorescence Microscopy ◽  
Singlet State ◽  
Excited Electronic State ◽  
Input Power ◽  
Two Photon ◽  
Simultaneous Absorption ◽  
Photon Excitation ◽  
Very High ◽  
Two Photon Excitation

Two-photon excitation fluorescence microscopy provides attractive advantages over confocal microscopy for three-dimensionally resolved fluorescence imaging. Two-photon excitation arises from the simultaneous absorption of two photons in a single quantitized event whose probability is proportional to the square of the instantaneous intensity. For example, two red photons can cause the transition to an excited electronic state normally reached by absorption in the ultraviolet. In our fluorescence experiments, the final excited state is the same singlet state that is populated during a conventional fluorescence experiment. Thus, the fluorophore exhibits the same emission properties (e.g. wavelength shifts, environmental sensitivity) used in typical biological microscopy studies. In practice, two-photon excitation is made possible by the very high local instantaneous intensity provided by a combination of diffraction-limited focusing of a single laser beam in the microscope and the temporal concentration of 100 femtosecond pulses generated by a mode-locked laser. Resultant peak excitation intensities are 106 times greater than the CW intensities used in confocal microscopy, but the pulse duty cycle of 10−5 maintains the average input power on the order of 10 mW, only slightly greater than the power normally used in confocal microscopy.

Two‐photon excitation fluorescence microscopy using a semiconductor laser

Bioimaging ◽  
1995 ◽  
Vol 3 (2) ◽  
pp. 70-75 ◽  
Author(s):  
Pekka E Hänninen ◽  
Martin Schrader ◽  
Erkki Soini ◽  
Stefan W Hell
Keyword(s):  
Fluorescence Microscopy ◽  
Semiconductor Laser ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

Two-Photon Excitation Imaging of Glucose Metabolism in Living Tissue

1997 ◽  
Vol 3 (S2) ◽  
pp. 305-306
Author(s):  
David W. Piston
Keyword(s):  
Confocal Microscopy ◽  
Collection Efficiency ◽  
Three Dimensional ◽  
Spatial Filter ◽  
Input Power ◽  
Photon Absorption ◽  
Focal Volume ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

Two-photon excitation microscopy (TPEM) provides attractive advantages over confocal microscopy for three-dimensionally resolved fluorescence imaging and photochemistry. It provides three-dimensional resolution and eliminates background equivalent to an ideal confocal microscope without requiring a confocal spatial filter, whose absence enhances fluorescence collection efficiency. This results in inherent submicron optical sectioning by excitation alone. In practice, TPEM is made possible by the very high local instantaneous intensity provided by a combination of diffraction-limited focusing of a single laser beam in the microscope and the temporal concentration of 100 femtosecond pulses generated by a mode-locked laser. Resultant peak excitation intensities are 106 times greater than the CW intensities used in confocal microscopy, but the pulse duty cycle of 10−5 limits the average input power to less than 10 mW, only slightly greater than the power normally used in confocal microscopy. Because of the intensity-squared dependence of the two-photon absorption, the excitation is limited to the focal volume.

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