Direct observation of ultrafast surface transport of laser-driven fast electrons in a solid target Prashant Kumar Singh, Y. Q. Cui, Gourab Chatterjee, Amitava Adak, W. M. Wang, Saima Ahmed, Amit D. Lad, Z. M. Sheng, and G. Ravindra Kumar Citation: Physics of Plasmas (1994-present) 20, 110701 (2013); doi: 10.1063/1.4830101 View online: http://dx.doi.org/10.1063/1.4830101 View Table of Contents: http://scitation.aip.org/content/aip/journal/pop/20/11?ver=pdfcov Published by the AIP Publishing This article is copyrighted as indicated in the abstract. Reuse of AIP content is subject to the terms at: http://scitation.aip.org/termsconditions. Downloaded to IP: 158.144.29.202 On: Thu, 07 Nov 2013 16:20:00 PHYSICS OF PLASMAS 20, 110701 (2013) Direct observation of ultrafast surface transport of laser-driven fast electrons in a solid target Prashant Kumar Singh,1 Y. Q. Cui,2 Gourab Chatterjee,1 Amitava Adak,1 W. M. Wang,2 Saima Ahmed,1 Amit D. Lad,1 Z. M. Sheng,2,3,a) and G. Ravindra Kumar1,b) 1 Tata Institute of Fundamental Research, 1 Homi Bhabha Road, Mumbai 400005, India Beijing National Laboratory of Condensed Matter Physics, Institute of Physics, CAS, Beijing 100190, China 3 Key Laboratory for Laser Plasmas (MoE), Department of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai 200240, China 2 (Received 24 July 2013; accepted 26 September 2013; published online 7 November 2013) We demonstrate rapid spread of surface ionization on a glass target excited by an intense, ultrashort laser pulse at an intensity of 3 1017 W cm2. Time- and space-resolved reflectivity of the target surface indicates that the initial plasma region created by the pump pulse expands at c/7. The measured quasi-static megagauss magnetic field is found to expand in a manner very similar to that of surface ionization. Two-dimensional particle-in-cell simulations reproduce measurements of surface ionization and magnetic fields. Both the experiment and simulation convincingly demonstrate the role of self-induced electric and magnetic fields in confining fast electrons along C 2013 AIP Publishing LLC. [http://dx.doi.org/10.1063/1.4830101] the target-vacuum interface. V The gigantic strides in the development of tabletop intense ultrashort lasers provide a great impetus to study diverse areas such as relativistic optics,1 high-energy-density science,2 laboratory astrophysics,3 and novel compact highenergy charged4 or neutral particle accelerators.5 All these applications are basically driven by the laser-generated fast electron beams, which are facilitated by several collisionless absorption mechanisms.6 The transport of fast electrons is governed both by the self-generated azimuthal magnetic field (B)7 and the longitudinal electric field (E) present at the target-vacuum interface.8 These self-induced fields can redirect most of the energy far away from the laser focal spot by the well-known E B drift,9 causing significant surface transport. Self-induced magnetic fields can originate from hot electron streams and target return current,3,7,10 thermomagnetic phenomena,11 etc. Surface spreading of hot electrons can (a) critically compromise the efficacy of the laser plasma as a point x-ray source, (b) hinder energy-coupling into the bulk by deleterious transverse dissipation, and (c) prevent longitudinal transport by confining hot electrons at interfaces. Surface transport is therefore a crucial part of the overall transport process. Some previous experiments10,12,13 and numerical studies9,14 have investigated the role of selfgenerated magnetic fields in surface transport of fast electrons. Most previous measurements focused on the transport of fast electrons created by long laser pulses10,12,13,15 and/or used time-integrated methods such as the surface spread of Ka x-ray and ion emission16 for inferring the lateral transport. A recent study17 has probed surface heat transport in an aluminum target in the ultrashort pulse regime using optical reflectometry. However, there were no measurements of the self-induced fields at the surface. To clearly establish the role of self-induced electric and magnetic fields in the confinement of electrons along the surface, it is crucial to have a) Electronic mail: [email protected] Electronic mail: [email protected] b) 1070-664X/2013/20(11)/110701/4/$30.00 simultaneous measurements of the spatial extent of the fields and the ionization spots away from the laser-irradiated region. In this letter, we address the crucial physics of fast electron surface transport by a confluence of (i) time- and spaceresolved surface ionization measurement by pump-probe reflectometry, (ii) time- and space-resolved surface magnetic field measurements via polarimetry, (iii) surface electric field measurements via the energy of protons accelerated by the sheath field at the target front and finally, (iv) two-dimensional particle-in-cell (2D-PIC) simulations and their comparison with the experiments. Our temporal resolution on the femtosecond scale and spatial resolution on the micrometer scale enable clear delineation of the surface transport process. We observe the non-local nature of this surface ionization process attributable to the E B drift of the fast electrons. This multipronged approach establishes the physics of the ultrafast laserdriven electron transport correctly and unambiguously. The experiment was performed at the Tata Institute of Fundamental Research, Mumbai using a Ti:sapphire chirped pulse amplification laser system with a laser pulse (800 nm, 30 fs) depositing 32 mJ on target, focused by an f/4 off-axis parabola to a spot size of 20 lm. A p-polarized laser pulse, incident on a 5 mm thick BK7 glass target at 40 , was used to excite the target at a peak intensity of 3 1017 W cm2 (nanosecond contrast 3 106). A pump-probe reflectometry set-up was used to map the temporal and spatial evolution of the hot dense plasma at the target surface. A small fraction extracted from the main pulse and frequency-doubled (400 nm) served as a probe. The time-delayed probe was focused on target front to a spot of 60 lm of intensity of 1011 W cm2. The reflected signal was fed into a CCD to capture time- and space-resolved information. To understand the surface transport, it is essential to map out the time evolution of electron density in the transverse plane. We address this by capturing spatially resolved snapshots of the reflected probe at different time delays 20, 110701-1 C 2013 AIP Publishing LLC V This article is copyrighted as indicated in the abstract. Reuse of AIP content is subject to the terms at: http://scitation.aip.org/termsconditions. Downloaded to IP: 158.144.29.202 On: Thu, 07 Nov 2013 16:20:00 110701-2 Singh et al. FIG. 1. Space-resolved snapshots of reflected probe at different time delays. R(a.u.): Reflected signal in arbitrary units. (Fig. 1). At early time (t ¼ 0.1 ps), we see a bright blob of size similar to that of the pump spot, the spatial overlapped region of pump and probe. Soon after, the highly reflecting area spreads rapidly, indicating a massive and ultrafast ionization of the area well beyond the initially irradiated region. For a quantitative measure of the extent of surface ionization, an integrated line-out is plotted in the inset of Fig. 2. At t ¼ 0.1 ps, the signal level is nearly flat across the probe dimensions. At 0.1 ps a high-reflectivity peak appears at position of 22 lm, indicated by leftmost vertical yellow line. After 0.4 ps a second peak appears 18 lm away from the initially excited area (shown by middle yellow line), an indication of non-local nature of surface transport. Close to 0.7 ps, the entire probe region is excited to high reflectivity, indicating that hot electrons have expanded to a region thrice the originally excited region. The speed of this surface ionization was calculated to be 4.5 109 cm/s (c/7). Measurements performed (Fig. 2) with much bigger probe, FIG. 2. Temporal evolution of the surface excitation captured with much bigger probe (snapshots not shown here). Inset shows line profile of reflected probe of Fig. 1, along the vertical direction after averaging pixels along horizontal axis, at different time delays. Each normalized to its peak value. Phys. Plasmas 20, 110701 (2013) FIG. 3. Temporal evolution of front side reflectivity from experiment (green square) and simulation (red circle), compared with (1–A), (blue star), where A denotes the resonance absorptivity. Inset: temporal evolution of simulated y-averaged electron density profile. L: electron-density scale length. of sampling size of 300 lm, show similar expansion speed of c/7 up to 0.6 ps after which it saturates. To see the entire transition of this ultrafast plasma dynamics, the temporal evolution of the spatially integrated reflectivity signal is presented in Fig. 3. Consistent with Fig. 1, there is a sharp rise in the reflectivity just after the pump arrival followed by a decay which lasts up to 6 ps. The reflectivity drops at later times due to absorption in the evolving plasma. To simulate the observation, a 2D-PIC simulation was performed using our PIC code KLAPS (Refs. 18 and 19) with ionization module and binary collisions included.20 The simulation parameters were similar to that of the experiment, with the exception of hydrogen atoms being used as the target material instead of BK7 glass for reducing the requirement of computation resources. Different materials can result in different target density and atom species, which may change the electron transport processes. Obviously, the higher the target density, the slower the electron transport rate. In this sense, our simulation model with high density hydrogen instead of glass provides a qualitative picture of electron transport. From the view point of laser interaction including ionization in the simulation, it is adequate to use hydrogen instead of glass. In the simulation, the target was comprised of a slab of homogeneous neutral hydrogen atoms of 10nc with a thickness of 9.6 lm (between x ¼ 12 lm and 21.6 lm) and low density preplasma with a thickness of 3.2 lm in front of the slab (Fig. 5). Absorption boundary conditions are used for all sides of the simulation box, i.e., particles reaching the boundaries will escape from the simulation box. Moreover, there is no vacuum region in the target rear side to avoid possible refluxing effects in our relatively thin target. The simulated temporal evolution of the reflectivity of the probe pulse is shown in Fig. 3. The inset of Fig. 3 shows the simulated density profiles at different times, with the measured scale length L ¼ dx=dðln ne Þ at ne ¼ 4nc (nc and 4nc denote the critical density for 800 nm and 400 nm, respectively). This article is copyrighted as indicated in the abstract. Reuse of AIP content is subject to the terms at: http://scitation.aip.org/termsconditions. Downloaded to IP: 158.144.29.202 On: Thu, 07 Nov 2013 16:20:00 110701-3 Singh et al. Phys. Plasmas 20, 110701 (2013) FIG. 4. Snapshot of reflectivity (a) and magnetic field (b) at 0.4 ps time delay. (c) Temporal evolution of experimental and simulated magnetic field, (d) proton energy spectrum at front side of the target. Using the formula in Ref. 21, we calculated the resonance absorptivity, A with the scale lengths given in the inset, and found that the value (1–A) is in good agreement with the reflectivity. We have estimated the plasma expansion towards the vacuum by the temporal evolution of the simulated density profile (inset of Fig. 3), which is 3 107 cm/s. Even if we assume a similar speed for the plasma flow along the surface, it is still two orders of magnitude smaller than the speed of observed surface ionization (Figs. 1 and 2). This rules out any possible role of bulk plasma motion in the observed surface transport. The rapid spread of surface excitation is therefore clearly due to the lateral transport of the fast electrons. To ascertain the role of magnetic field, we have carried out time- and space-resolved surface magnetic field measurements using a two-pulse Cotton-Mouton polarimetry method (details described elsewhere3,22) simultaneous with the reflectivity measurements. Except the probe wavelength (800 nm), all other parameters were similar to the reflectivity experiment discussed earlier. For illustration, measurements of reflectivity and magnetic field at a time delay of 0.4 ps are shown in Figs. 4(a) and 4(b), respectively. Consistent with the rapid spread of the high reflectivity zone (which indicates ultrafast electron transport), the magnetic field shows a similar rapid transverse spread. At the same time, the magnetic field shows similar spatial features in form and extent. Furthermore, we also present temporal evolution of the spatially integrated magnetic field (Fig. 4(c)). The magnetic field rises in nearly 200 fs to its peak value of 8 MG and decreases exponentially with a decay constant of s 0.4 ps. The temporal evolution of simulated magnetic field is also shown in the same figure, matching very well with the measurements. The spatial extent of the surface ionization driven by the self-induced fields can be estimated by a simple E B drift picture.9 The drift speed (vd) is given23 as vd ¼ 108 (E/B), where vd, E, and B are in units of cm/s, V/cm, and Gauss, respectively. For an estimation of the target surface electric FIG. 5. Snapshots of electron density (a), electric field strength (b) at t ¼ 0.1 ps, 0.3 ps, 0.4 ps, and 1.3 ps. and magnetic field (c) from PIC simulation at t ¼ 0.15 ps, 0.4 ps, 0.58 ps, and 0.95 ps. The laser coming from left to right as marked by the white arrow in (a), excites the 9.6 lm thick target kept at x ¼ 12 lm. field, we carried out ion measurements at the target front under similar conditions. A high-resolution Thomson parabola spectrometer24 was used to measure the proton energy spectra (Fig. 4(d)). The maximum energy of the protons accelerated by the electric field at the target front was found to be nearly 20 keV. The maximum proton energy25 is given ¼ eELn , where e is the electron charge, E is as Eproton max the front side electric field and Ln is the plasma scale length. By taking a scale length of 0.5 lm at a delay of around 1 ps (Fig. 3 inset), we infer a maximum surface electric field of 0.4 GV/cm. With E ¼ 0.4 GV/cm and B ¼ 107 G (corresponding to 0.95 ps snapshot of Fig. 5(c)), the drift velocity vd comes to nearly 4 109 cm/s. Interestingly, this E B drift speed agrees very well with surface ionization expansion speed calculated in reflectivity measurements (Fig. 2). This article is copyrighted as indicated in the abstract. Reuse of AIP content is subject to the terms at: http://scitation.aip.org/termsconditions. Downloaded to IP: 158.144.29.202 On: Thu, 07 Nov 2013 16:20:00 110701-4 Singh et al. We now confirm all the above observations by 2D PIC simulations (computational details described earlier). Figure 5 shows snapshots of the spatial distributions of electron density, electric field and magnetic field at the same instant. The electric field at t ¼ 0.1 ps and magnetic field at t ¼ 0.15 ps are the components of the reflected laser pulse. The laser massively ionizes the target material within its penetration region of several micrometers, producing a high density plasma which reflects the laser. During the laser irradiation, a large flux of hot electrons is produced and they can penetrate into the neutral background. When the hot electrons move into the target, local charge separation fields and quasi-static magnetic fields are produced on both sides of the target. These fields tend to confine the hot electrons within the target so that they can only transport within the target along the surface. During the transport process, strong electric fields at the boundary and inside the target are generated, which are as large GV/cm. These fields continue to ionize the background media and produce more electrons, resulting in a much larger ionized area compared to the laser focal spot. The transverse expanding speed of the ionized area is estimated to be about ðc=2 2c=3Þ in the simulation, where c is the light speed in vacuum. This is somewhat larger than the experimental value. It can be partly attributed to the much thinner target used in the simulation, where the electric and the magnetic field at the backside of the target can confine the hot electrons inside the target, making the surface transport more efficient. Similar to our experimental observation, the spatial extent of the magnetic field and the electron density spread on the target surface are identical. In conclusion, we have presented a comprehensive investigation of the ultrafast surface transport of fast electrons created in a solid target by intense, femtosecond laser pulses. By a combination of experimental methods (pumpprobe spatio-temporal reflectometry, polarimetry, and proton acceleration measurements), we capture distinct images of non-local surface ionization and magnetic field and strength of the electric field at the surface. We establish that the nonlocal ionization at the target front surface is caused by the E B drift. Our experimental findings are strongly backed by 2D-PIC simulations. We believe that our results have significant implications for problems involving ultrafast surface transport of hot electrons, particularly energetic particle sources and fast ignition of laser fusion. Z.M.S. thanks the support by NSFC (Grant Nos. 11121504 and 11075105). Numerical simulation has been performed on the Magic Cube at Shanghai Supercomputer Center. G.R.K. Phys. Plasmas 20, 110701 (2013) acknowledges a J. C. Bose grant from the DST, Government of India. We thank M. Dalui, T. M. Trivikram, and M. Krishnamurthy for Thomson Parabola ion measurements. 1 G. A. Mourou, T. Tajima, and S. V. Bulanov, Rev. Mod. Phys. 78, 309 (2006). 2 R. P. Drake, High-Energy-Density Physics (Springer-Verlag, Berlin, Heidelberg, 2006). 3 S. Mondal, V. Narayanan, W. J. Ding, A. D. Lad, B. Hao, S. Ahmad, W. M. Wang, Z. M. Sheng, S. Sengupta, P. Kaw, A. Das, and G. R. Kumar, Proc. Natl. Acad. Sci. U.S.A. 109, 8011 (2012). 4 V. Malka, J. Faure, Y. A. Gauduel, E. Lefebvre, A. Rousse, and K. T. Phuoc, Nat. Phys. 4, 447–453 (2008). 5 R. Rajeev, T. M. Trivikram, K. P. M. Rishad, V. Narayanan, E. Krishnakumar, and M. Krishnamurthy, Nat. Phys. 9, 185 (2013). 6 S. C. Wilks, W. L. Kruer, M. Tabak, and A. B. 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