Inoptics, anultrashort pulse, also known as anultrafast event, is anelectromagnetic pulse whose time duration is of the order of apicosecond (10⁻¹² second) or less. Such pulses have a broadbandoptical spectrum, and can be created bymode-locked oscillators. Amplification of ultrashort pulses almost always requires the technique ofchirped pulse amplification, in order to avoid damage to the gain medium of the amplifier.

They are characterized by a high peakintensity (or more correctly,irradiance) that usually leads to nonlinear interactions in various materials, including air. These processes are studied in the field ofnonlinear optics.

In the specialized literature, "ultrashort" refers to thefemtosecond (fs) andpicosecond (ps) range, although such pulses no longer hold the record for the shortest pulses artificially generated. Indeed, x-ray pulses with durations on theattosecond time scale have been reported.

The 1999Nobel Prize in Chemistry was awarded toAhmed H. Zewail, for the use of ultrashort pulses to observechemical reactions at the timescales on which they occur,^[1] opening up the field offemtochemistry.A further Nobel prize, the 2023Nobel Prize in Physics, was also awarded for ultrashort pulses. This prize was awarded toPierre Agostini,Ferenc Krausz, andAnne L'Huillier for the development of attosecond pulses and their ability to probe electron dynamics.^[2]

There is no standard definition of ultrashort pulse. Usually the attribute 'ultrashort' applies to pulses with a duration of a few tens of femtoseconds, but in a larger sense any pulse which lasts less than a few picoseconds can be considered ultrashort. The distinction between "Ultrashort" and "Ultrafast" is necessary as the speed at which the pulse propagates is a function of theindex of refraction of the medium through which it travels, whereas "Ultrashort" refers to the temporal width of the pulsewavepacket.^[3]

A common example is a chirped Gaussian pulse, awave whosefield amplitude follows aGaussianenvelope and whoseinstantaneous phase has afrequency sweep.

The real electric field corresponding to an ultrashort pulse is oscillating at an angular frequencyω₀ corresponding to the central wavelength of the pulse. To facilitate calculations, a complex fieldE(t) is defined. Formally, it is defined as theanalytic signal corresponding to the real field.

The central angular frequencyω₀ is usually explicitly written in the complex field, which may be separated as a temporal intensity functionI(t) and a temporal phase functionψ(t):

${\displaystyle E(t)=\sqrt{I(t)}{e}^{i{\omega }_{0}t}{e}^{i\psi (t)}}$

The expression of the complex electric field in the frequency domain is obtained from theFourier transform ofE(t):

${\displaystyle E(\omega )=\mathcal{F}(E(t))}$

Because of the presence of the${\displaystyle e^{i{\omega }_{0}t}}$ term,E(ω) is centered aroundω₀, and it is a common practice to refer toE(ω-ω₀) by writing justE(ω), which we will do in the rest of this article.

Just as in the time domain, an intensity and a phase function can be defined in the frequency domain:

${\displaystyle E(\omega )=\sqrt{S(\omega )}{e}^{i\varphi (\omega )}}$

The quantity${\displaystyle S(\omega )}$ is thepower spectral density (or simply, thespectrum) of the pulse, and${\displaystyle \varphi (\omega )}$ is thephase spectral density (or simplyspectral phase). Example of spectral phase functions include the case where${\displaystyle \varphi (\omega )}$ is a constant, in which case the pulse is called abandwidth-limited pulse, or where${\displaystyle \varphi (\omega )}$ is a quadratic function, in which case the pulse is called achirped pulse because of the presence of an instantaneous frequency sweep. Such a chirp may be acquired as a pulse propagates through materials (like glass) and is due to theirdispersion. It results in a temporal broadening of the pulse.

The intensity functions—temporal${\displaystyle I(t)}$ and spectral${\displaystyle S(\omega )}$ —determine the time duration and spectrum bandwidth of the pulse. As stated by theuncertainty principle, their product (sometimes called the time-bandwidth product) has a lower bound. This minimum value depends on the definition used for the duration and on the shape of the pulse. For a given spectrum, the minimum time-bandwidth product, and therefore the shortest pulse, is obtained by a transform-limited pulse, i.e., for a constant spectral phase${\displaystyle \varphi (\omega )}$. High values of the time-bandwidth product, on the other hand, indicate a more complex pulse.

Although optical devices also used for continuous light, like beam expanders and spatial filters, may be used for ultrashort pulses, several optical devices have been specifically designed for ultrashort pulses. One of them is thepulse compressor,^[4] a device that can be used to control the spectral phase of ultrashort pulses. It is composed of a sequence of prisms, or gratings. When properly adjusted it can alter the spectral phaseφ(ω) of the input pulse so that the output pulse is abandwidth-limited pulse with the shortest possible duration. Apulse shaper can be used to make more complicated alterations on both the phase and the amplitude of ultrashort pulses.

To accurately control the pulse, a full characterization of the pulse spectral phase is a must in order to get certain pulse spectral phase (such astransform-limited). Then, aspatial light modulator can be used in the 4f plane to control the pulse.Multiphoton intrapulse interference phase scan (MIIPS) is a technique based on this concept. Through the phase scan of the spatial light modulator, MIIPS can not only characterize but also manipulate the ultrashort pulse to get the needed pulse shape at target spot (such astransform-limited pulse for optimized peak power, and other specific pulse shapes). If the pulse shaper is fully calibrated, this technique allows controlling the spectral phase of ultrashort pulses using a simple optical setup with no moving parts. However the accuracy of MIIPS is somewhat limited with respect to other techniques, such asfrequency-resolved optical gating (FROG).^[5]

Several techniques are available to measure ultrashort optical pulses.

Intensityautocorrelation gives the pulse width when a particular pulse shape is assumed.

Spectral interferometry (SI) is a linear technique that can be used when a pre-characterized reference pulse is available. It gives the intensity and phase. The algorithm that extracts the intensity and phase from the SI signal is direct.Spectral phase interferometry for direct electric-field reconstruction (SPIDER) is a nonlinear self-referencing technique based on spectral shearing interferometry. The method is similar to SI, except that the reference pulse is a spectrally shifted replica of itself, allowing one to obtain the spectral intensity and phase of the probe pulse via a directFFT filtering routine similar to SI, but which requires integration of the phase extracted from the interferogram to obtain the probe pulse phase.

Frequency-resolved optical gating (FROG) is a nonlinear technique that yields the intensity and phase of a pulse. It is a spectrally resolved autocorrelation. The algorithm that extracts the intensity and phase from a FROG trace is iterative. Grating-eliminated no-nonsense observation of ultrafast incident laser light e-fields (GRENOUILLE) is a simplified version of FROG. (Grenouille is French for "frog".)

Chirp scan is a technique similar toMIIPS which measures the spectral phase of a pulse by applying a ramp of quadratic spectral phases and measuring second harmonic spectra. With respect to MIIPS, which requires many iterations to measure the spectral phase, only two chirp scans are needed to retrieve both the amplitude and the phase of the pulse.^[6]

Multiphoton intrapulse interference phase scan (MIIPS) is a method to characterize and manipulate the ultrashort pulse.

To partially reiterate the discussion above, theslowly varying envelope approximation (SVEA) of the electric field of a wave with central wave vector${\displaystyle {\mathbf{\text{K}}}_0}$ and central frequency${\displaystyle {\omega }_0}$ of the pulse, is given by:

${\displaystyle \mathbf{\text{E}}(\mathbf{\text{x}},t)=\mathbf{\text{A}}(\mathbf{\text{x}},t)\exp (i{\mathbf{\text{K}}}_0\mathbf{\text{x}}-i{\omega }_{0}t)}$

We consider the propagation for the SVEA of the electric field in a homogeneous dispersive nonisotropic medium. Assuming the pulse is propagating in the direction of the z-axis, it can be shown that the envelope${\displaystyle \mathbf{\text{A}}}$ for one of the most general of cases, namely a biaxial crystal, is governed by thePDE:^[7]

${\displaystyle \frac{\mathrm{\partial }\mathbf{\text{A}}}{\mathrm{\partial }z}=-{\beta }_1\frac{\mathrm{\partial }\mathbf{\text{A}}}{\mathrm{\partial }t}-\frac{i}{2}{\beta }_2\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }{t}^2}+\frac{1}{6}{\beta }_3\frac{{\mathrm{\partial }}^3\mathbf{\text{A}}}{\mathrm{\partial }{t}^3}+{\gamma }_x\frac{\mathrm{\partial }\mathbf{\text{A}}}{\mathrm{\partial }x}+{\gamma }_y\frac{\mathrm{\partial }\mathbf{\text{A}}}{\mathrm{\partial }y}}$

${\displaystyle +i{\gamma }_{tx}\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }t\mathrm{\partial }x}+i{\gamma }_{ty}\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }t\mathrm{\partial }y}-\frac{i}{2}{\gamma }_{xx}\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }{x}^2}-\frac{i}{2}{\gamma }_{yy}\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }{y}^2}+i{\gamma }_{xy}\frac{{\mathrm{\partial }}^2\mathbf{\text{A}}}{\mathrm{\partial }x\mathrm{\partial }y}+\cdots }$

where the coefficients contains diffraction and dispersion effects which have been determined analytically withcomputer algebra and verified numerically to within third order for both isotropic and non-isotropic media, valid in the near-field and far-field.${\displaystyle {\beta }_1}$ is the inverse of the group velocity projection. The term in${\displaystyle {\beta }_2}$ is the group velocitydispersion (GVD) or second-order dispersion; it increases the pulse duration and chirps the pulse as it propagates through the medium. The term in${\displaystyle {\beta }_3}$ is a third-order dispersion term that can further increase the pulse duration, even if${\displaystyle {\beta }_2}$ vanishes. The terms in${\displaystyle {\gamma }_x}$ and${\displaystyle {\gamma }_y}$ describe the walk-off of the pulse; the coefficient${\displaystyle {\gamma }_x({\gamma }_y)}$ is the ratio of the component of the group velocity${\displaystyle x(y)}$ and the unit vector in the direction of propagation of the pulse (z-axis). The terms in${\displaystyle {\gamma }_{xx}}$ and${\displaystyle {\gamma }_{yy}}$ describe diffraction of the optical wave packet in the directions perpendicular to the axis of propagation. The terms in${\displaystyle {\gamma }_{tx}}$ and${\displaystyle {\gamma }_{ty}}$ containing mixed derivatives in time and space rotate the wave packet about the${\displaystyle y}$ and${\displaystyle x}$ axes, respectively, increase the temporal width of the wave packet (in addition to the increase due to the GVD), increase the dispersion in the${\displaystyle x}$ and${\displaystyle y}$ directions, respectively, and increase the chirp (in addition to that due to${\displaystyle {\beta }_2}$) when the latter and/or${\displaystyle {\gamma }_{xx}}$ and${\displaystyle {\gamma }_{yy}}$ are nonvanishing. The term${\displaystyle {\gamma }_{xy}}$ rotates the wave packet in the${\displaystyle x-y}$ plane. Oddly enough, because of previously incomplete expansions, this rotation of the pulse was not realized until the late 1990s but it has beenexperimentally confirmed.^[8] To third order, the RHS of the above equation is found to have these additional terms for the uniaxial crystal case:^[9]

${\displaystyle \cdots +\frac{1}{3}{\gamma }_{txx}\frac{{\mathrm{\partial }}^3\mathbf{\text{A}}}{\mathrm{\partial }{x}^2\mathrm{\partial }t}+\frac{1}{3}{\gamma }_{tyy}\frac{{\mathrm{\partial }}^3\mathbf{\text{A}}}{\mathrm{\partial }{y}^2\mathrm{\partial }t}+\frac{1}{3}{\gamma }_{ttx}\frac{{\mathrm{\partial }}^3\mathbf{\text{A}}}{\mathrm{\partial }{t}^2\mathrm{\partial }x}+\cdots }$

The first and second terms are responsible for the curvature of the propagating front of the pulse. These terms, including the term in${\displaystyle {\beta }_3}$ are present in an isotropic medium and account for the spherical surface of a propagating front originating from a point source. The term${\displaystyle {\gamma }_{txx}}$ can be expressed in terms of the index of refraction, the frequency${\displaystyle \omega }$ and derivatives thereof and the term${\displaystyle {\gamma }_{ttx}}$ also distorts the pulse but in a fashion that reverses the roles of${\displaystyle t}$ and${\displaystyle x}$ (see reference of Trippenbach, Scott and Band for details).So far, the treatment herein is linear, but nonlinear dispersive terms are ubiquitous to nature. Studies involving an additional nonlinear term${\displaystyle {\gamma }_{nl}|A{|}^{2}A}$ have shown that such terms have a profound effect on wave packet, including amongst other things, aself-steepening of the wave packet.^[10] The non-linear aspects eventually lead tooptical solitons.

Despite being rather common, the SVEA is not required to formulate a simple wave equation describing the propagation of optical pulses.In fact, as shown in,^[11] even a very general form of the electromagnetic second order wave equation can be factorized into directional components, providing access to a single first order wave equation for the field itself, rather than an envelope. This requires only an assumption that the field evolution is slow on the scale of a wavelength, and does not restrict the bandwidth of the pulse at all—as demonstrated vividly by.^[12]

High energy ultrashort pulses can be generated throughhigh harmonic generation in anonlinear medium. A high intensity ultrashort pulse will generate an array ofharmonics in the medium; a particular harmonic of interest is then selected with amonochromator. This technique has been used to produce ultrashort pulses in theextreme ultraviolet andsoft-X-ray regimes fromnear infraredTi-sapphire laser pulses.

The ability of femtosecond lasers to efficiently fabricate complex structures and devices for a wide variety of applications has been extensively studied during the last decade. State-of-the-art laser processing techniques with ultrashort light pulses can be used to structure materials with a sub-micrometer resolution. Direct laser writing (DLW) of suitable photoresists and other transparent media can create intricate three-dimensional photonic crystals (PhC), micro-optical components, gratings, tissue engineering (TE) scaffolds and optical waveguides. Such structures are potentially useful for empowering next-generation applications in telecommunications and bioengineering that rely on the creation of increasingly sophisticated miniature parts. The precision, fabrication speed and versatility of ultrafast laser processing make it well placed to become a vital industrial tool for manufacturing.^[13]

Among the applications of femtosecond laser, the microtexturization of implant surfaces have been experimented for the enhancement of the bone formation around zirconia dental implants. The technique demonstrated to be precise with a very low thermal damage and with the reduction of the surface contaminants. Posterior animal studies demonstrated that the increase on the oxygen layer and the micro and nanofeatures created by the microtexturing with femtosecond laser resulted in higher rates of bone formation, higher bone density and improved mechanical stability.^[14][15][16]

Multiphoton Polymerization (MPP) stands out for its ability to fabricate micro- and nano-scale structures with exceptional precision. This process leverages the concentrated power of femtosecond lasers to initiate highly controlled photopolymerization reactions, crafting detailed three-dimensional constructs.^[17] These capabilities make MPP essential in creating complex geometries for biomedical applications, including tissue engineering and micro-device fabrication, highlighting the versatility and precision of ultrashort pulse lasers in advanced manufacturing processes.

• Attosecond chronoscopy
• Bandwidth-limited pulse
• Femtochemistry
• Frequency comb
• Medical imaging: Ultrashort laser pulses are used in multiphotonfluorescence microscopes
• Optical communication (Ultrashort pulses) Filtering and Pulse Shaping.
• Terahertz (T-rays) generation and detection.
• Ultrafast laser spectroscopy
• Ultrashort pulse laser
• Wave packet

This "Further reading" sectionmay need cleanup. Please read theediting guide and help improve the section.(October 2014) (Learn how and when to remove this message)

• Hirlimann, C. (2004). "Pulsed Optics". In Rullière, Claude (ed.).Femtosecond Laser Pulses: Principles and Experiments (2nd ed.). New York: Springer.ISBN 0-387-01769-0.
• Andrew M. Weiner (2009).Ultrafast Optics. Hoboken, NJ: Wiley.ISBN 978-0-471-41539-8.
• J. C. Diels and W. Rudolph (2006).Ultrashort Laser Pulse phenomena. New York, Academic.ISBN 978-0-12-215493-5.

• The virtual femtosecond laboratoryLab2
• Animation on Short Pulse propagation in random medium (YouTube)
• Ultrafast Lasers:An animated guide to the functioning of Ti:Sapphire lasers and amplifiers.

• Nonlinear optics
• Laser science

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