Transcript Slide 1
UNIVERSITY OF MARYLAND AT COLLEGE PARK
Trapping and destruction of long range high
intensity optical/plasma filaments by molecular
quantum wakes
S. Varma, Y.-H. Chen, and H. M. Milchberg
Institute for Research in Electronics and Applied Physics
Dept. of Electrical and Computer Engineering
Dept. of Physics
HEDLP - 2008
Support: DoE, NSF, JHU-APL
Some applications of filaments
• directed energy
• triggering and guiding of lightening
• remote detection: LIDAR, LIBS
• directed, remote THz generation
Introduction to Filamentation
•
High power, femtosecond laser beams propagating through air form
extremely long filaments due to nonlinear self-focusing ((3)) dynamically
balanced by ionization and defocusing.
0
neff = n0 + ngas + nplasma
Pcr ~ 2/8n0n2
What does a filament look like?
5 mm
0.8Pcr
1.3Pcr
1.8Pcr
2.3Pcr
2.8Pcr
3.5 mJ
Filament images at increasing power
(Pcr occurs at 1.25 mJ for a 130fs pulse)
“prompt” and “delayed” optical
response of air constituents
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Atoms: 1% argon
Laser polarization
Prompt electronic response
Delayed inertial response
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Molecules: 78% nitrogen, 21% oxygen
Laser field alignment of linear gas molecules
Classical picture
E
p
induced
dipole
moment
molecular axis
p/ /
-laser field applies a net
torque to the molecule
-molecular axis aligns along
the E field
-delayed response (ps)
due to inertia
intense laser field
(~1013 W/cm2)
random
orientation
E
“some” alignment
time-dependent
refractive index shift
n(t )
2 N
1
cos2 t
n0
3
degree of alignment
cos2 1/ 3
cos2 1/ 3
< >t : time-dependent ensemble average
n0=n(random orientation)
Field alignment and “revivals” of rotational wavepacket
Quantum description
of rigid rotor
j, m exp(i jt )
eigenstate
even
where
j E j / 2πcBj( j 1) (j: ≥0 integer)
B h(8 2cI )1 (“rotational constant”)
I : moment of inertia
Rotational wavepacket
j ,m a j ,m j , m exp(i j t )
An intense fs laser pulse “locks” the
relative phases of the rotational states in
the wavepacket
Quantum revival of rotational response
The time-delayed nonlinear response is composed of many
quantized rotational excitations which coherently beat.
t = Tbeat
t=0
We can expect the index of refraction
to be maximally disturbed at each beat.
Single-shot Supercontinuum Spectral Interferometry
(SSSI) – Imagine a streak camera with 10fs resolution!
A pump pulse generates transient
refractive index n (r, t)
x
Pump pulse
Imaging lens
Probe Ref.
z
medium
y
Probe
Ref.
CCD
Imaging
spectrometer
Probe and Ref.
• Temporally stretched (chirp) for long
temporal field of view (~ 2 ps).
• ~100 nm bandwidth supercontinuum
gives ~10 fs resolution.
Extract probe (x, t) to obtain n(x, t).
Experimental setup and sample interferogram
0 ps
~ 2 ps
Sample interferogram
250 mm
N2O gas
652nm
723nm
Chen, Varma, York and Milchberg, Opt. Express 15, 11341 (2007)
Rotational wavepacket of D2 and H2 molecules
P=7.8 atm
I=4.4x1013 W/cm2
room temperature
Rotational quantum “wakes” in air
TN2 , ¾TO2
Vg pump
vg pump
SSSI measurement showing alignment and anti-alignment “wake”
traveling at the group velocity of the pump pulse.
Pump-probe filament experiment
2m
filament
f/300 focusing
Object
plane
Polarizing
beamsplitter
CCD
Filaments are trapped/enhanced or destroyed
TN2 , ¾TO2
A
5 mm
B
C
8.08.0
D
8.4
8.4
8.8 8.8(ps)
(ps)
Trapped filaments are ENHANCED
White light generation, filament length and spectral
broadening are enhanced.
Aligning filament (left) and probing
filament (right), misaligned
Both beams collinear, probe
filament coincident with alignment
wake of N2 and O2 in air
CCD camera saturation
Conclusions
• SSSI enables us to probe refractive index transients with
~10fs resolution over 2ps in a single shot, allowing us to
observe room-temperature molecular alignment.
• A high intensity laser filament propagating in the
quantum wake of molecular alignment can be
controllably and stably trapped and enhanced, or
destroyed.
• Applications: directed energy, remote sensing, etc...
Pump power
Response near t=0
A
0.68Pcr
1.12Pcr
1.72Pcr
A
2.20Pcr
2.60Pcr
(ps)
3.72Pcr
(ps)
Increasing aligning pulse energy
laser
scan (probe=3.4Pcr)
Spectral broadening
The spatio-temporally varying refractive index of the wake of
molecular alignment causes predictable spectral modulation and
broadening of the probe filament.
Filament spectrum v. delay
A
B
C
D
Alignment v. delay
E
C
E
A
B
D
Molecular rotational wavepacket revivals
mode-locking analogy: coherent sum of longitudinal modes
typ. spectrum
modes
pulse width ≈ (round trip time) / (# of modes)
T=8.2ps
T/2
Example:
N2
3T/4
T/4
nitrogen
ps
peak width ≈T / jmax(jmax+1) ~ 40 fs for N2
1D spatially resolved temporal evolution of O2 alignment
0T
0.5T
0.25T
• pump peak intensity:
2.7x1013 W/cm2
• 5.1 atm O2 at
room temperature
• T=11.6 ps
x
(mm)
(fs)
0.75T
1T
1.25T
x (mm)
(ps)
Introduction to Filamentation
• High power, femtosecond laser beams that propagate through air
form extremely long filaments due to nonlinear self-focusing ((3))
dynamically balanced by ionization and defocusing.
• Filaments can propagate through air up to 100s of meters, and are
useful for remote excitation, ionization and sensing.
Rotational wavepacket of H2 molecules at room temperature
Experiment:
Fourier
transform
BH 2=61.8 cm1
T=270 fs
Lineout at x=0
Calculation:
The pump intensity
bandwidth (~2.5x1013 s-1)
is even less adequate
than in D2 to populate j=2
and j=0 states.
Weaker rotational
wavepacket amplitude.
P=7.8 atm
I=4.4x1013 W/cm2
H2 0.3010-24 cm3
T
Charge density wave in N2 at 1 atm
vg
• Filament ionization fraction ~10-3 2x1016
cm3
• ~0.5% ponderomotive charge separation at
enhanced intensity ~5x1014 W/cm2 over 50100 fs alignment transient Ne~ 1014 cm-3
Quantum beat index bucket E~ 0.75 MV/cm
• Many meters of propagation
Experimental setup and sample interferogram
110 fs
high pressure
exp gas cell (up to ~8 atm)
1 kHz Ti:Sapphire
regenerative amplifier
~300 mJ
P: pinhole
BS: beamsplitter
HWP: /2 plate
SF4: dispersive material
xenon gas cell
(1-2 atm)
supercontinuum
(SC)
Michelson
interferometer
0 ps
~ 2 ps
Sample interferogram
250 mm
N2O gas
652nm
Optical Kerr effect ((3))
and the molecular rotational
response in the gas induce
spectral phase shift and
amplitude modulation on
the interferogram.
Both spectral phase and
amplitude information are
required to extract the
temporal phase (refractive
index).
723nm
Experimental setup and sample interferogram
110 fs
high pressure
exp gas cell (up to ~8 atm)
1 kHz Ti:Sapphire
regenerative amplifier
~300 mJ
P: pinhole
BS: beamsplitter
HWP: /2 plate
SF4: dispersive material
xenon gas cell
(1-2 atm)
supercontinuum
(SC)
Michelson
interferometer
0 ps
~ 2 ps
Sample interferogram
250 mm
N2O gas
652nm
Optical Kerr effect ((3))
and the molecular rotational
response in the gas induce
spectral phase shift and
amplitude modulation on
the interferogram.
Both spectral phase and
amplitude information are
required to extract the
temporal phase (refractive
index).
723nm