Lasers and Their Applications: Debabrata Goswami
Lasers and Their Applications: Debabrata Goswami
Abstract
Ever since the advent of the first LASER (acronym for Light Amplification by Stimulation Emission
of Radiation) in 1960, there has been a steady increase in the application of lasers. Applications have
kept on becoming more and more diverse as the capability of the lasers have increased. In this chapter
we will enumerate and classify many of the applications of lasers and then go on to discuss in more
detail some of the more modern applications.
1. Introduction
Lasers deliver coherent, monochromatic, well-controlled, and precisely directed light beams.
A priori, therefore, lasers would seem tobe poor choices for general-purpose illumination,
however, they are ideal for concentrating light in space, time, or particular wavelengths. Lasers
have been regularly used to measure, cut, drill, weld, read, write, send messages, solve crimes,
burn plaque out of arteries, and perform delicate eye operations. Over and over again the
laser has proved to be an extremely practical tool. Nevertheless, lasers have also proved their
usefulness in non-practical applications, especially in the realm of art and entertainment. Lasers
are involved in almost all aspects of these fields, from “light shows” to Compact Discs (CDs)
and Digital Video Discs (DVDs), to special effects in the movies. Some other commonplace
application of lasers are as Laser pointers, barcode scanners, laser printers, etc. Still, much
of the important modern day celebrated applications lie in the fiber-optic communication,
Lasers and their Applications 79
laser machining and fabrication, trace element detection, laser metrology and medical
imaging.
Figure 1: (Color online) Schematic diagram of the comparison between the CD, DVD and Blue-Ray
disk for data storage using different laser wavelengths.
Fiber-optic communication systems that transmit signals more than a few kilometers also
use semiconductor laser beams. The optical signals are sent at infrared wavelengths of 1.3 to
1.6 micrometers, where silica glass fibers are most transparent. This technology has become the
backbone of the global telecommunications network, and most telephone calls traveling beyond
the confines of a single town go part of the way through optical fibers.
Figure 2: (Color online) Schematic diagram of laser machining head and its machining action under
the comparison of long pulse versus femtosecond (10-15 second) laser pulse machining.
plane for construction workers installing walls or ceilings. Pulsed laser radar can measure distance
in the same manner as microwave radar by timing how long it takes a laser pulse to bounce back
from a distant object. For example, in 1969 laser radar precisely measured the distance from the
Earth to the Moon. Laser range finding is now widely used for remote sensing. Instruments flown
on aircraft can profile the layers of foliage in a forest, and the Mars Global Surveyor used a laser
altimeter to map elevations on the Martian surface.
Figure 3: (Color online) A train of stabilized laser pulses generates a comb of sharp spectral lines
defined by two radio frequencies: the comb spacing (frep) and an offset (f0).
Mode-locked femtosecond lasers emit tens of thousands of discrete laser lines with a
frequency-spacing precisely given by the laser repetition rate frep. Their output is thus commonly
referred to as a frequency comb where each tooth is essentially an integer multiple of frep. It is this
simplicity by which a frequency comb directly links the optical (hundreds of terahertz) and the
radio (hundreds of Mega-hertz) frequency domains separated by several decades that are practically
governed by very different technologies (Fig. 3),which has made frequency combs very powerful
and invaluable tools. The 2015 Physics Nobel Prize was awarded to Theodor Hänsch and John
Hall for developing this idea. Frequency combs enable precision optical frequency measurements
Lasers and their Applications 83
much in the same way as a ruler is used to measure a distance. They serve in many laboratories
worldwide to perform fundamental physics experiments such as measurements of the drift of
fundamental natural constants. They are used to perform massively parallel precision optical
spectroscopy or to synthesize microwave signals with unprecedentedly low phase-noise. Frequency
combs also support the development of novel superior optical atomic clocks, by functioning as
their clockwork, which may eventually lead to such practical advances as a more precise Global
Positioning System (GPS) navigation.
Figure 4: Schematic of Holography process where the laser beam is split into three components. First
two beams are needed to create the hologram which is viewed with the help of the third.
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(a) (b)
Figure 5: (Color online) (a) Schematic of Laser Eye Surgery. (b) Laser energy delivery to precise spots
in joints for arthroscopic surgery.
Laser light can be delivered to places within the body that the beams could not otherwise
reach through optical fibers similar to the tiny strands of glass that carry information in telephone
systems. One important example involves threading a fiber through the urethra and into the kidney
so that the end of the fiber can deliver intense laser pulses to kidney stones. The laser energy splits
the stones into fragments small enough to pass through the urethra without requiring surgical
incisions. Fibers also can be inserted through small incisions to deliver laser energy to precise
spots in the knee joint during arthroscopic surgery (Fig. 5b). Another medical application for
lasers is in the treatment of skin conditions. Pulsed lasers can bleach certain types of tattoos as
well as dark-red birthmarks called port-wine stains. Cosmetic lasertreatments include removing
unwanted body hair and wrin-kles.
(a) (b)
Figure 6: (Color online) Schematic of a (a) confocal microscope showing the critical placement of
confocal pinhole to ensure all out of plane light is blocked before the detector to result in a
sharp image from a thick specimen. (b) For two-photon microscopy, self-aperture occurs.
It uses UV or visible light for the single photon excitation of fluorophore from ground state
to the excited state followed by deactivation through fluorescence emission which is detected
through high quantum efficiency photomultiplier tube (PMT) in the range of near ultraviolet, visible
and near infrared spectral region. The basic difference of confocal Light Scanning Microscope
with the conventional optical microscope is the confocal aperture arranged in a plane conjugate
to the intermediate image plane and thus, to the object plane of the microscope. The PMT can
only detect the light that passed the pinhole. As the laser beam is focused to a diffraction limited
spot, which illuminates only a point of the object at a time, the point illuminated and the point
observed are situated in conjugate planes, i.e. they are focused onto each other. The perfection
of focused beam which is connected to the resolution has always been a matter of concern in the
far-field fluorescence microscopy. Still, optical microscopy remains the best choice for monitoring
live specimens despite the resolution advantage of, say electron microscopes, since the energy
deposited in electron microscopy adversely affects the viability of live specimens. This practical
compromise implicitly sets resolution enhancement as one of the most important development in
optical microscopy. For a single fluorescent molecule, Ernst Abbe defined a minimum diffraction-
limited image having lateral (x,y) and axial (z) dimensions defined by the excitation wavelength
(l) refractive index of the imaging medium (η), and the angular aperture (α) of the microscope
objective as:
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l
Resolution x, y = 2 [ h ⋅ sin (a )] (1)
2l
Resolution x, y = [ h ⋅ sin (a )]2 (2)
where the combined term η • sin(α) is known as the objective numerical aperture (NA).
Objectives commonly used in microscopy have a numerical aperture that is less than 1.5 (although
new high-performance objectives closely approach this limit), restricting the term α in Equations
(1) and (2) to less than 70 degrees. Therefore, the theoretical resolution limit at the shortest
practical excitation wavelength (approximately 400 nanometers when using an objective having
a numerical aperture of 1.40) is around 150 nanometers in the lateral dimension and approaching
400 nanometers in the axial dimension. In practical terms for imaging living cells, these values
are approximately 200 and 500 nanometers, respectively. Thus, structures that lie closer than 200
to 250 nanometers cannot be resolved in the lateral plane using either a wide field or confocal
fluorescence microscope and is known as the Abbe’s resolution limit (Fig. 7a).
Figure 7: (Color online) (a) Schematic of Abbe’s diffraction resolution limit using the Rayleigh
criteria where the first diffraction minimum of the image of one source point coincides
with the maximum of another. (b) In stimulated emission depletion fluorescence (STED)
Microscope, the laser spot size is made smaller by using the depletion effect of fluorophore.
(c) In photoactivated localization microscopy (PALM), superresolution is achieved using
individual fluorophore that are photoactivated at different times as probe.
Lasers and their Applications 87
The 2014 Nobel Prize celebrated the development of super-resolved fluorescence microscopy
that has made visible essential details and movements of the molecules of life. This development
conquered the physical limit, described by Ernst Abbe in 1873, implying that objects of smaller
dimensions than half of the wave length of light cannot be discerned by opticalmicroscopy. The
Prize recognized the very first two ways to surpass Abbe’s diffraction limit. The first method to
by-pass Abbe’s limit involved two laser beams shining on the structure of interest in a fluorescence
microscope. One beam excites the fluorescent molecules in a volume determined by Abbe’s limit
(Equations (1) and (2)). The other beam rapidly brings all the excited molecules, except those in
a volume that can be made arbitrarily small, to their ground state before they can emit a photon.
When both beams jointly scan the structure, an image with resolution better than Abbe’s limit
emerges. Stefen W. Hell demonstrated this experimentally in 2000 and called it STimulated
Emission Depletion (STED) microscopy (Fig. 7b). In the second approach, William Moerner
and Eric Betzig developed a method where the biological structure is labelled with optically
activatable Green Fluorescence Protein (GFP). A weak light pulse activates a small fraction of the
GFP molecules, so that all molecules in this fraction are further apart than Abbe’s limit, and thus
can be localized with super-precision. Then, yet another small fraction of the GFP molecules are
activated so that also they can be super-localized. This is repeated until a large number of such
images have been created. Finally, all these images are combined into one super-resolved image
with complete structural information. They demonstrated this method first in 2006 and called it
Photo Activated Localization Microscopy (PALM) (Fig. 7c).
spectroscopic study of a molecular dissociation using flashes of laser light that last for a few
femtoseconds. A reaction can be over in 1,000 femtoseconds, so lasers capable of emitting pulses
lasting a hundred femtoseconds or less are needed to probe the details of the process. In the 1970s,
Charles Shank and colleagues at Bell Laboratories (Murray Hill), New Jersey developed liquid
dye lasers capable of producing pulses of just a few hundred femtoseconds. Liquid dye lasers
use fluorescent organic dyes to produce laser light. For shorter the laser pulse required, the larger
the range of frequencies of light it must contain. Shank and his colleagues were able to restrict
the pulses to the very short timescales by using a range of dyes, each of which emits light of a
different frequency, and by the early 1980s, they furthered the technology to a level that pulses
of tens of femtoseconds were possible. Zewail built a version of the Bell Labs laser in 1987 that
was capable of producing pulses of 60 femtoseconds and applied it to study the dissociation of
iodine cyanide (ICN) into iodine and cyanide. ICN molecules absorb different frequencies of
light as the bond between the iodine atom and cyanide molecule stretches. Zewail took a series
of snapshots of the process by sending in probe pulses at different times after the initial pulse and
showed that the bond broke after around 200 femtoseconds, by which point the iodine atom and
cyanide molecule had been stretched by about 5 angstroms. In itself, that finding was of limited
interest, but the proof that femtosecond spectroscopy worked was a huge breakthrough. Twelve
years later, Zewail was awarded the 1999 Nobel Prize in chemistry. This simplest approach to
femtochemistry is known as the pump–probe spectroscopy where femtosecond lasers were used
as ‘cameras’ to study the intermediate stages of chemical reactions (Fig. 8).
Figure 8: (Color online) Schematic of Zewail pump-probe spectroscopy for (a) a generic molecular
dissociation model with (b) pump and probe pulses generated from the same laser that are
measured at different time delays between them.
In this general “pump-probe” method, two or more optical pulses with variable time delay
between them are used to investigate the processes happening during a chemical reaction. The
first pulse (pump) initiates the reaction, by breaking a bond or exciting one of the reactants. The
second pulse (probe) is then used to interrogate the progress of the reaction a certain period of
Lasers and their Applications 89
time after initiation. Every atom or molecule has a unique set of frequencies of light that it can
absorb, so by looking for frequencies that are missing from the pulse, chemists can determine what
chemical species are present, and in what quantities. Atoms or molecules can also re-emit light that
they have absorbed, again at specific frequencies. As the reaction progresses, the response of the
reacting system to the probe pulse will change. By continually scanning the time delay between
pump and probe pulses and observing the response, researchers can reconstruct the progress of
the reaction as a function of time. These techniques have given chemists new ways to understand
chemical physics though their application has now been expanded to many more research fields.
In biological studies, for instance, application of femtochemistry has helped to elucidate the
conformational dynamics of stem-loop RNA structures.
Despite the wealth of discoveries made possible by femtosecond techniques, some aspects of
chemistry remain inaccessible. Whatever the probe pulse used, femtosecond techniques provide
little information about the position of electrons within their orbits. Electrons move a thousand
times faster than atomic nuclei, hence recording their motion requires thousand times shorter
(10-18 second), i.e., attosecond-scale, shutter time. According to classical theories, an electron can
orbit a hydrogen atom in a fraction of a femtosecond, so pulses of just a few hundred attoseconds
would be needed to track each electron. The lower limit for a pulse of visible light, defined by the
duration of a single cycle of the wave, is 3 femtoseconds. But X-rays have shorter wavelengths,
and pulses down to as little as 50 attoseconds are possible in principle. Some researchers believe
attochemistry may soon be possible from the analogy that just as the amplitude variation of a
femtosecond pulse triggers and probes nuclear motion in Zewail’s femtosecond photography,
an attosecond ultraviolet or X-ray pulse coming in synchrony with a few-cycle laser pulse of
controlled waveform pulse may be used for starting or capturing electronic motion in real time.
The role of the attosecond “starter gun” or “shutter” can alternatively be played by the central half
cycle of the controlled electric field of a few-cycle wave of visible light. This can, for instance,
liberate an electron from an atom, and an attosecond ultraviolet pulse can take snapshots of the
electronic motion unfolding inside the atom after its ionization. The snapshots in this case appear
in the form of energy distributions of the photons of the attosecond pulse transmitted through
ionized atoms, from which the instantaneous state of the electrons can be inferred. If desirable
attosecond pulses can be generated, a host of new phenomena will be open up. One example is
the movement of electrons in excited molecules. A molecule is more likely to react when one of
its electrons is in an excited state, however, the electron may fall back to its ground state before
the reaction occurs. A study of the movement of excited electrons may help explain why certain
reactions occur, whereas others fail. The latest in a line of advances that have redrawn the limits
of chemical sciences would be attochemistry. Interestingly, the immeasurable will have to be
redefined once again if attosecond techniques do become reality.
One of the other areas where researchers are using such femtosecond techniques are to control
chemical reactions. The enhanced knowledge of the molecular systems and dynamics as possible
through femtochemistry has rejuvenated the quest to control chemistry, especially molecular
dynamics in the later part of the twentieth century. Birth of coherent control was originally spurred
by the theoretical understanding of the quantum interferences that lead to energy randomization
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and experimental developments in ultrafast laser spectroscopy. Coherent control is the ability to
control the dynamics at various stages of a process as it evolves under the effect of a coherent
source. Many of the frequencies constituting the ultrafast pulse can simultaneously excite many
coherent transitions to the excited states, and a capability to manipulate them with the shaped
pulses lead to the interesting results. The theoretical predictions on control of reaction channels
or energy randomization processes are still more dramatic than the experimental demonstrations,
though this gap between the two has consistently reduced over the recent years with realistic
theoretical models and technological developments. Experimental demonstrations of arbitrary
optical pulse shaping have made some of the previously impracticable theoretical predictions
possible to implement. Starting with the simple laser modulation schemes to provide proof-of-
the-principle demonstrations, feedback loop pulse shaping systems have been developed that can
actively manipulate some atomic and molecular processes. This tremendous experimental boost
of optical pulse shaping developments (Fig. 9) has prospects and implications into many more
new directions, including terabit/sec data communications.
Figure 9: (Color online) Schematic diagram of a Fourier Transform pulse shaper with AOM (acousto-
optic modulator) with a pump probe experimental setup on a sample.
Lasers and their Applications 91
The fundamental aspects of laser-matter interactions using arbitrary pulse shaping has been
intriguing andultrafast laser pulse shaping applications have been inves-tigated in gaseous and
liquid phase molecular dynamics, optoelectronics, nonli-near optics and optical communication,
biologically relevant multi-photon fluo-rescence microscopy and optical trapping. These diverse
fields have been knit together for quantum information processing. The importance of laser pulse
mani-pulation for controlled molecular interactions has resulted in the development of more
pragmatic goals and approaches to the age-old dream of “laser-selective chemistry”. Availability of
powerful ultrafast laser sources over a wide range of wavelengths and experimental developments
of arbitrary optical pulse shaping have been key technological factors in providing proof-of-
principle demonstra-tions. Pulse shaping essentially involves control over the amplitude, phase,
fre-quency and/or inter-pulse separation. Complex pulse shaping aims to control one or more
of the above-mentioned parameters in a programmable manner, such that the user has complete
control. In other words, complex pulse shaping allows gen-eration of complicated ultrafast optical
waveforms according to user specification.
An ultrafast laser pulse can be represented as a coherent superposition of many monochromatic
light waves within a range of frequencies that is inversely propor-tional to the duration of the
pulse. Thus, for instance, a 40fs pulse at 800nm that is commercially available has a spectrum as
broad as 30nm. Possibilities of manipulating such an ultrafast coherent bandwidth are nontrivial
as it lasts for such an ultrashort duration wherein no modulators work. A creative solution to the
problem of slow modulators is the indirect pulse shaping in the frequency domain. In the time
domain the filter is characterized by a time response function g(t). The output of the filter Eout(t)
in response to an input pulse Ein(t) is given by the convolution of Ein(t) and g(t), such that, Eout(t)
= Ein(t) ⊗ g(t). In the frequency domain, the filter is characterized by its frequency response
G(ω), i.e., Eout(ω) × Ein(ω) × G(ω), where Ein(t), Eout(t) and g(t) and Ein(ω), Eout(ω) and G(ω),
respectively are Fourier transform pairs. With a delta function input pulse, the input spectrum
Ein(ω) is unity and the output spectrum is equal to the frequency response of the filter, and thus,
due to Fourier transform relations generation of a desired output waveform can be accomplished
by implementing a filter with the required frequency response. Control of molecular reaction
directs vibronically excited molecular systems into specific reaction pathways. Failure through
such molecular control through laser selective excitation arises from decoherence and dephasing
of coherence. Minimizing decoherence is also an important challenge towards realizing quantum
computing and quantum information. Typical molecular vibrations occur in picoseconds. So it is
important to have control parameters in femtoseconds. Population transfer in molecules involves
multiple states besides the radiative coupled two labels which undergo quantum interferences
resulting in decoherences. Coupling to the non-radiative channels can however be minimized to
robustly controlled decoherence through destructive quantum interference between the multiple
excitation pathways.
Another attractive approach is the use of simple chirped pulses, which, by con-trast, have
been produced routinely at very high intensities and at various different wavelengths for many
applications, including selective excitation of molecules in coherent control. Demonstration of
control over a symmetric dissociation reaction of dicyclopentadiene into two cyclopentadiene
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molecules was successful simply with the help of linearly chirped pulses inducing the multiphoton
dissociation process in the gas phase (Fig. 10). Typical condensed phase reactions involving
solvents are much more complicated and require more complex pulse shaping as discussed.
Figure 10: (Color online) Linear frequency chirped laser pulse induced control showed in the gas phase
dissociation of dicyclopentadiene: (a) Photo-dissociation reaction. (b) The mass fragments
corresponding to the reactant and products. (c) Evidence of control as the negative chirp is
more efficient in dissociation reaction as compared to the positive chirp.
The subtle forces exerted by laser beams, i.e., radiation pressure or the photon flux has been
used to slow and trap atoms, molecules, and small particles. A technique pioneered by the Bell
Labs researcher, Arthur Ashkin, “optical tweezers” use a tightly focused horizontal laser beam to
trap atoms in the highest light intensity zone, is now used in a variety of research. Other research
has also shown that laser illumination can slow the motion of atoms if its wavelength is tuned to
a point slightly off the wavelength of peak absorption. The atoms repeatedly absorb photons from
the beam and then emit photons in random directions. The photon momentum slows the motion
toward the laser beam. Placing the atoms at the junction of six laser beams aimed at right angles
to each other slows their momentum in all directions, produces a clump of atoms less than 0.001
degree above absolute zero. Adding a magnetic field improves confinement and can reduce their
Lasers and their Applications 93
temperature to less than one-millionth degree above absolute zero. These techniques have led to
the creation of a new state of matter, called a Bose-Einstein condensate, which earned Steven Chu,
Claude Cohen-Tannoudji, and William D. Phillips the 1997 Nobel Prize for Physics.
One of the more recent developments have been an optical tweezer that is generated with
femtosecondlaser (Fig. 11), where the trapped particle is confined in space through temporally
instantaneous interaction and provides both spatial and temporal control in trapping. Even for
most of the high repetition rate lasers which have been employed for such tweezers (lasers with
~100 femtosecond pulse width at ~100MHz repetition), the light is absent for more often than it is
present, much of the observations from such a trapped object reflect the inertial stable condition.
Figure 11: (Color online) Femtosecond pulsed laser tweezer showing the trapped florophore coated
nanosphere glowing from two-photon fluorescence. Since it is a pulsed trap, the trap is only
present intermittantly. However, as long as the gap between the pulses are not so large that
the particle can drift away substantially, the particle remaines trapped.
The main advantage of using femtosecond laser is that in addition to the back-scattering signal
of the trapped object, it can generate multi-photon processes like two-photon fluorescence (TPF)
that can be used for background free imaging of the trapping process and can efficiently trap and
manipulate micro- and nano-objects including living cells, colloidal nano spheres, metallic nano
particles, quantum dots etc. in a non-invasive, non-contact fashion. The back ground free detection
of trapping is possible as TPF appears at a different wavelength as com-pared to the trapping
laser and so can be measured independent of interference of the incident trapping laser. Such
an approach has been recently shown to be very effective in measuring very small temperature
changes in nanoscale environments accurately.
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5. Conclusion
This chapter has provided a glimpse of some of the many applications of lasers. We have
deliberately provided more details on some of the recent applications that have been the highlighted
in recent literature. We just hope that this would increase the interest of the reader to keep up to
the many more laser applications that keep coming up with time.
Acknowledgments
DG thanks DST, MCIT, MHRD, ISRO (India) as well as Wellcome Trust International Senior
Research Fellowship for financial supports. Thanks are also due to the incessant support from the
PhD students for the re-search done in the lab and Mrs. S. Goswami for patient proof reading.
11. Goswami, T., Das D.K., and Goswami, D., Controlling the femtosecond laser-driven
transformation of dicyclopentadiene into cyclopentadiene. Chem. Phys. Lett. 558, 1-7
(2013)
12. Ashkin, A., Dziedzic, J.M., Bjorkholm, J.E., and Chu, S., Observation of a single-beam
gradient force optical trap for dielectric particles. Opt. Lett. 11, 288-290 (1986)
13. Phillips, W.D., Laser cooling and Trapping Neutral Atoms. Rev. Mod. Phys. 70, 721-741
(1998)
14. De, A.K. and Goswami, D., Towards controlling molecular motions in fluorescence
microscopy and optical trapping: a spatiotemporal approach. Int. Rev. Phys. Chem. 30(3),
275-299 (2011)
15. Mondal, D. and Goswami, D.,Controlling local temperature in water us-ing femtosecond
optical tweezer. Biomed. Express 6, 3190-3196 (2015)