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2021-01-28 17:46
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2021年1月28日发(作者:垂体)



Industrial femtosecond lasers


and material processing


01/22/2019



NORMAN HODGSON, MICHAEL LAHA, TONY S. LEE, ALBRECHT


STEINKOPFF,


and


SEBASTIAN HEMING



Over the last five years, material processing with femtosecond pulses in the range of


300 to 900 fs has gained in popularity due to the small heat- affected zone (HAZ) and


increased energy penetration depth resulting from the high laser pulse intensity.


Industrial ultrashort-pulse (USP) diode-pumped solid-state and fiber lasers are now


being used to cut foils for flat panel displays, to cut stents, and to drill fuel injector


nozzles, as well as for wafer scribing and surface microstructuring.


The first industrial use of femtosecond laser pulses for microprocessing dates back to


the late 1990s, where titanium sapphire (Ti:sapphire) amplifiers were used to repair


lithography masks in integrated circuit fabrication. At that time, the only choice in


commercial laser sources were


Q


-switched, neodymium (Nd)-doped solid-state lasers


delivering pulse duration of tens of nanoseconds, and ultrafast Ti:sapphire amplifiers


that exhibited pulse durations of 100 fs and provided output power at the 1 W level at


1 kHz (FIGURE 1). The small feature size of the chromium layer on top of the fused


silica substrate prohibited the use of nanosecond pulses due to thermal damage of the


chromium, and even the substrate. The necessity for a small HAZ outweighed the


high cost of a Ti:sapphire amplifier system, which was about $$300,000.



FIGURE 1.


Lithography mask repair using a 100 fs Ti:sapphire laser is shown,


where a chromium layer on a fused silica substrate is ablated; width of the ablated


lines is 750 nm.


1



Today, many different femtosecond lasers are available, providing output pulse


energies of up to 200 ?


J, with average output powers in the kilowatt range. Especially


over the last decade, a large variety of femtosecond solid-state laser and fiber laser


architectures have entered the material processing field, all of them based on


ytterbium (Yb)-doped gain materials. Average output powers of up to 100 W are


currently employed in industrial applications, with pulse durations between 300 and


900 fs and repetition rates of up to 2 MHz. Compared to the original Ti:sapphire


amplifier systems, the output powers have increased by two orders of magnitude,


while system cost has been considerably decreased at the same time.


A majority of the low-power lasers have been deployed in ophthalmic applications. In


the 2000s, Nd:glass regenerative amplifiers were used to cut the corneal flap in


LASIK surgery by generating a bubble plane inside the cornea. These Nd:glass


systems were later replaced by Yb:fiber master-oscillator power-amplifiers (MOPAs),


which allowed higher repetition rates at a lower cost (FIGURE 2). Typical pulse


energies required for flap cutting are 2



4 ?


J at repetition rates of 50 to 200 kHz and


pulse durations of around 300 fs. A second, more recently emerging ophthalmic


application is lens dissection as part of cataract surgery. In this case, the pulse


energies employer are in the range of 20 to 40 ?


J at repetition rates of 50 to 100 kHz,


and pulse durations are preferably below 800 fs.



FIGURE 2.



The evolution of the deployment of femtosecond lasers in


microprocessing applications is shown; Ti:sapphire regenerative amplifiers for mask


repair have been replaced by picosecond Nd:YVO


4


lasers and Nd:glass regenerative


amplifiers by femtosecond Yb fiber MOPAs.



According to a forecast by Strategies Unlimited in 2016, the total market in 2019 for


femtosecond and picosecond lasers used for material processing (including


ophthalmic applications) is projected to be $$460 million (TABLE 1).


2


Half of this


revenue is generated by picosecond lasers, which have been widely used in


microelectronic manufacturing. The other half is split between ophthalmic


femtosecond lasers ($$136 million) and femtosecond lasers for non-biological material


processing ($$98 million).



TABLE 1.


The 2016 Revenue Forecast of femtosecond and picosecond lasers in


material processing is shown, where values for 2014 and 2015 are actual revenues;


femtosecond lasers include ophthalmic lasers.


2



Mechanism and benefits of femtosecond laser processing


The interaction of femtosecond and picosecond pulses with matter is governed by the


absorption of the light by the electrons and subsequent energy transfer to the lattice.


In the case of metals, the photons are absorbed by the electron gas, which increases its


temperatures to values of several 10,000°


C. The electrons will transfer their energy to


the lattice within the electron-phonon relaxation time, which for most materials is in


the range of 100 fs to 1 ps at room temperature. The lattice has about 100X higher


heat capacity compared to the electrons. This leads to a substantial delay between the


incidence of the laser pulse and the time when the lattice has reached melting


temperature (FIGURE 3). For high laser fluences, the ablation of the heated material


occurs several tens of picoseconds after the laser pulse is absorbed.



FIGURE 3.



Interaction of ultrafast pulses with a metal is shown. The electron gas


absorbs the laser light, leading to a hot, thermalized electron distribution within 100


fs; the lattice will heat up with a delay of 4 to 30 ps.



The light-matter interaction for ultrashort laser pulses can be mathematically


described by the Two-Temperature Model, which provides the temporal and spatial


evolution of the temperature of electron gas and lattice by incorporating the coupling


between both systems via the electron



phonon relaxation time.


3


This model has been


used very successfully over the last decades to calculate damage threshold fluence,


ablation rates, and HAZ for ultrashort pulse processing (FIGURE 4).


4-8


The main


results are that for pulses that are shorter than 10 ps, the damage threshold fluence


remains constant, while for larger pulse durations, the threshold fluence increases in


proportion to the square-root of the pulse duration, independent of incident laser pulse


wavelength.



FIGURE 4.



Calculated temporal temperature distribution of electron gas (left) and


lattice for copper after irradiation with a 100 fs pulse at an average fluence of 0.14


J/cm


2


and a wavelength of 800 nm.


7



Similarly, the HAZ remains constant for pulse durations below 10 ps, again


independent of the wavelength of the laser light. The basic reason for this behavior is


the delay in the temperature increase of the lattice and of heat conduction into the


material. This regime of pulsed laser- matter interaction is therefore referred to as cold


ablation, since the lattice stays cold during irradiation by the laser pulse. This name is


a bit misleading, though, since the material will have to reach melting temperature to


induce ablation.


The most interesting effect of ultrashort pulse interaction, however, is the increase in


the energy penetration depth and ablation depth with decreasing pulse duration.


Decreasing the pulse duration at a given energy fluence leads to an increase in the


temperature of the electron gas and a simultaneous increase of the electron-phonon


relaxation time.


In a more mechanical model, this can be easily understood: the velocity of the


electrons traveling through the lattice can become as high as 100,000 m/s for


femtosecond pulses due to the very high intensity, and this high speed results in


deeper penetration of the electron into the lattice without transferring energy to the


lattice.


8




The material processing efficiency and quality depends on the duration of the laser


pulses. For pulses in the nanosecond regime, the absorption of the laser pulse is


determined by the linear optical absorption depth of the laser light and the energy


dissipation is a result of heat conduction into the material (FIGURE 5). For pulses that


are shorter than 10 ps, the initial energy penetration depends strongly on the light


intensity and leads to deeper penetration depth for femtosecond pulses. In addition,


the lack of thermal conduction during the pulse and the time of lattice heating results


in a very low HAZ. For metals, HAZ of less than 5 ?


m can be achieved, while for


plastic materials, the HAZ is typically in the range of 30 to 50 ?


m.



FIGURE 5.


Absorption of a laser pulse in a medium is shown, where energy


penetration is represented in blue and volume heated via heat conduction in red.



The increase of the penetration depth for shorter pulses leads to an increase in the


maximum ablation rates when the pulses become shorter than about 20 ps (as shown


in FIGURE 6 for aluminum). As will be discussed subsequently, at any pulse duration


the maximum ablation rate is achieved at a pulse fluence of about 7.5X the ablation


threshold fluence. Compared to


Q


-switched laser pulses with pulse durations of tens


of nanoseconds, the increased electron velocity in the material leads to ablation rates


for sub- picosecond pulses that are only a factor of three lower.



FIGURE 6.


Maximum ablation rates of aluminum with Coherent's measured values


(red dots) and using values taken from data published by Breitling et al. (blue dots).


9



For pulsed lasers, ablation becomes most efficient at a pulse energy fluence equal to


e


2


times the threshold fluence. This is a result of the saturation of the ablated volume


with increasing pulse fluence. At a fixed output power, more volume can therefore be


ablated if the energy fluence is lowered, while simultaneously increasing pulse


repetition rate and therefore throughput (FIGURE 7). The maximum value is achieved


at the optimum fluence. The ablation rate, C (in mm


3


/W/min), is given by:



where


F


is the peak fluence in J/mm


2


,


F


th


is the peak threshold fluence, and


d


is the


energy penetration depth per pulse in millimeters.


10


Typical values for the energy


penetration depth per pulse are in the range of


20 to 100 nm for metals,


semiconductors, and plastics, and >500 nm for glasses and transparent crystals.



FIGURE 7.


Ablated volume per pulse (blue curve) and ablated volume per second


(green curve) at constant laser power are shown.


10



FIGURE 8 shows the measured ablation rates for Nitinol as a function of the average


pulse fluence for various pulse durations. Nitinol is used to manufacture stents and


requires femtosecond pulses to increase the throughput. The laser was a 1035 nm


modelocked fiber MOPA, where the settings of the compressor were changed to


implement different pulse durations, and external second- and third-harmonic


generation (SHG and THG, respectively) stages could be added to access wavelengths


of 517 and 345 nm. A rectangular area of about 0.5 ×


1.5 mm was ablated to a depth


of about 200 ?


m using a spot diameter of 20 ?


m with a spot overlap of 60% in both


directions. Decreasing the pulse duration to 400 fs resulted in an increase in the


ablation rate by a factor of two compared to 19 ps pulses. This increase in ablation


efficiency for femtosecond pulses is common amongst metals and semiconductors.


For transparent dielectrics, however, the ablation rate is higher for picosecond pulses.


This is due to the lack of free electrons, which requires high threshold fluences to


ablate the material. For femtosecond pulses, the resulting peak powers are too high


and lead to optical breakdown and decreased ablation rates.

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