Laser-Driven Transient Phase Oscillations in Individual Spin Crossover Particles.

An unusual expansion dynamics of individual spin crossover nanoparticles is studied by ultrafast transmission electron microscopy. After exposure to nanosecond laser pulses, the particles exhibit considerable length oscillations during and after their expansion. The vibration period of 50-100 ns is of the same order of magnitude as the time that the particles need for a transition from the low-spin to the high-spin state. The observations are explained in Monte Carlo calculations using a model where elastic and thermal coupling between the molecules within a crystalline spin crossover particle govern the phase transition between the two spin states. The experimentally observed length oscillations are in agreement with the calculations, and it is shown that the system undergoes repeated transitions between the two spin states until relaxation in the high-spin state occurs due to energy dissipation. Spin crossover particles are therefore a unique system where a resonant transition between two phases occurs in a phase transformation of first order.

Kinetics and wavelength dependence of thermal and excited-state population on lens effect induced in a Nd:YAG rod amplifier.

Using a wavefront sensor, we have measured the temporal evolution of the lens induced in a Nd:YAG rod amplifier under side pumping by laser diode bars centered around 808 nm in a quasi-continuous wave regime. The evolution of the induced lens is drastically different when measured with a probe pulse centered at 532 nm or 1064.5 nm. To explain this evolution, we developed a model that accounts for both the excited state population of the Nd3+ ions and the thermal contribution to the refractive index of the amplifier. This model, which takes into account amplification and wavelength shift of the probe pulse at 1064.5 nm, makes it possible to quantitatively describe the spectral and temporal evolution of the amplifier focal length. It also shows that the excited state population contribution is more important around 1064.5 nm and can partly compensate for the thermal lens induced in the amplifier.

High power ytterbium rod-type fiber laser delivering tunable picosecond pulses.

We designed an all-normal dispersion ytterbium rod-type fiber laser oscillator delivering picosecond pulses which are continuously tunable both in central wavelength and pulse duration. This system delivers self-mode-locked pulses with an average power up to 25 W. At a repetition rate of 78 MHz, it yields picosecond laser pulses, of which the central wavelength and pulse duration can be tuned between 1010 nm - 1060 nm and 4.5 ps - 1.8 ps, respectively. The tunability is obtained by adjusting the position and the width of a slit which acts as a spectral bandwidth filter, placed close to the center of a 4f-folded zero dispersion line inserted in the laser cavity. This oscillator delivers nearly Fourier limited pulses with at most a 1.2 time-bandwidth product. A numerical model accounts well for the behavior of this all-normal dispersion fiber oscillator.

Rational Direct Synthesis of RbMnFe Nanoparticles (RbMnFe = RbxMn[Fe(CN)6](2+x)/3·nH2O Prussian Blue Analogue).

In this paper, we report the chemical strategy followed to obtain, in a direct way, nanoparticles of the RbxMn[Fe(CN)6](x+2)/3·nH2O (RbMnFe) Prussian blue analogue with the aim of keeping the switching ability of this compound at the nanoscale. The switching properties come from a reversible electron transfer between the iron and manganese ions and depends on the rubidium content in the structure that has to be higher than 0.6. Despite the multifunctionality of this family of compounds and its interest in various applications, no systematic studies were performed to obtain well-defined nanoparticles. This paper relates to such an investigation. To draw relationship between size reduction, composition, and switching properties, a special attention was brought to the determination of the composition through elemental analysis and structure refinement of powder X-ray diffraction patterns together with infrared spectroscopy and elemental analysis. Several chemical parameters were explored to control both the size reduction and the composition following a direct synthetic approach. The results show that the smaller the particles, the lower the rubidium content. This observation might prevent the observation of switching properties on very small particles. Despite this antagonist effect, we achieved switchable particles of around 200 nm without any use of surfactant. Moreover, the size reduction is associated with the observation of the electron transfer down to 52% of rubidium in the nanoparticles against 64% in microparticles. This work is of particular interest in processing such nanoparticles into devices.

Photo-Thermal Switching of Individual Plasmonically Activated Spin Crossover Nanoparticle Imaged by Ultrafast Transmission Electron Microscopy.

Spin crossover (SCO) is a promising switching phenomenon when implemented in electronic devices as molecules, thin films or nanoparticles. Among the properties modulated along this phenomenon, optically induced mechanical changes are of tremendous importance as they can work as fast light-induced mechanical switches or allow to investigate and control microstructural strains and fatigability. The development of characterization techniques probing nanoscopic behavior with high spatio-temporal resolution allows to trigger and visualize such mechanical changes of individual nanoscopic objects. Here, ultrafast transmission electron microscopy (UTEM) is used to precisely probe the length changes of individual switchable nanoparticles induced thermally by nanosecond laser pulses. This allows revealing of the mechanisms of spin switching, leading to the macroscopic expansion of SCO materials. This study is conducted on individual pure SCO nanoparticles and SCO nanoparticles encapsulating gold nanorods that serve for plasmonic heating under laser pulses. Length changes are compared with time-resolved optical measurements performed on an assembly of these particles.

Optical damage limit of efficient spintronic THz emitters.

THz pulses are generated from femtosecond pulse-excited ferromagnetic/nonmagnetic spintronic heterostructures via inverse spin Hall effect. The highest possible THz signal strength from spintronic THz emitters is limited by the optical damage threshold of the corresponding heterostructures at the excitation wavelength. For the thickness-optimized spintronic heterostructure, the THz generation efficiency does not saturate with the excitation fluence even up till the damage threshold. Bilayer (Fe, CoFeB)/(Pt, Ta)-based ferromagnetic/nonmagnetic (FM/NM) spintronic heterostructures have been studied for an optimized performance for THz generation when pumped by sub-50 fs amplified laser pulses at 800 nm. Among them, CoFeB/Pt is the best combination for an efficient THz source. The optimized FM/NM spintronic heterostructure having α-phase Ta as the nonmagnetic layer shows the highest damage threshold as compared to those with Pt, irrespective of their generation efficiency. The damage threshold of the Fe/Ta heterostructure on a quartz substrate is ∼85 GW/cm2.

Electro-optic comb pumped optical parametric oscillator with flexible repetition rate at GHz level.

We present a gigahertz (GHz)-repetition-rate optical parametric oscillator (OPO) pumped by an electro-optic comb at 1.03 µm, delivering sub-picosecond signal pulses across 1.5-1.7 µm from a MgO-doped periodically poled LiNbO3 crystal. Using a pump power of 5 W at 14.2 GHz repetition rate, 378 mW of signal power is obtained at 1.52 µm from a subharmonic cavity, corresponding to a signal extraction efficiency of 7.6%. By cascading a Mach-Zehnder modulator, the pump pulse repetition rate can be divided by any integer number from one to 14, allowing the OPO to operate with a flexible repetition rate from 1 to 14.2 GHz. A strategy leading to quasi-continuous repetition rate tunability of the OPO is also discussed.

Enhancement in optically induced ultrafast THz response of MoSe2MoS2 heterobilayer.

THz conductivity of large area MoS2 and MoSe2 monolayers as well as their vertical heterostructure, MoSe2MoS2 is measured in the 0.3-5 THz frequency range. Compared to the monolayers, the ultrafast THz reflectivity of the MoSe2MoS2 heterobilayer is enhanced many folds when optically excited above the direct band gap energies of the constituting monolayers. The free carriers generated in the heterobilayer evolve with the characteristic times found in each of the two monolayers. Surprisingly, the same enhancement is recorded in the ultrafst THz reflectivity of the heterobilayer when excited below the MoS2 bandgap energy. A mechanism accounting for these observations is proposed.

Conical versus Gaussian terahertz emission from two-color laser-induced air plasma filaments.

In this Letter, we demonstrate that the far-field terahertz (THz) beam generated from a Ti:Sapphire two-color laser-induced filament can exhibit a conical or Gaussian distribution, depending on the filtering experimental conditions. Using both an incoherent Golay cell detector and a two-dimensional coherent electro-optic detection covering the 0.2-2.6 THz spectral range, in our experimental conditions, we provide evidence that the conical emission is due to photo-induced carriers in the silicon filter, typically used to block the remaining pump laser light. Moreover, the low-frequency THz beam retrieves an almost $ {{\rm TEM}_{00}} $TEM00 Gaussian spatial distribution when the silicon filter is preceded by a large bandgap ceramic filter, which stops the pump beam, thus preventing the carrier generation in the silicon filter.

Study of the Photoswitching of a Fe(II) Chiral Complex through Linear and Nonlinear Ultrafast Spectroscopy.

Photoswitching the physical properties of molecular systems opens large possibilities for driving materials far from equilibrium toward new states. Moreover, ultrashort pulses of light make it possible to induce and to record photoswitching on a very short time scale, opening the way to fascinating new functionalities. Among molecular materials, Fe(II) complexes exhibit an ultrafast spin-state transition during which the spin state of the complex switches from a low spin state (LS, S = 0) to a high spin state (HS, S = 2). The latter process is remarkable: It takes place within ∼100 fs with a quantum efficiency of ∼100%. Moreover, the spin-state switching induces an important shift of the broad metal-to-ligand absorption band of the complex, and it results in large modifications of the physical and chemical properties of the compounds. But because most of the Fe(II) complexes crystallize in centrosymmetric space groups, this prevents them from exhibiting piezoelectric, ferroelectric, as well as second-order nonlinear optical properties such as second-harmonic generation (SHG). This considerably limits their potential applications. We have recently synthesized [Fe(phen)3] [Δ-As2(tartrate)2] chiral complexes that crystallize in a noncentrosymmetric 32 space group. Hereafter, upon the excitation of a thin film of these complexes by a femtosecond laser pulse and performing simultaneously transient absorption (TRA) and time-resolved SHG (TRSH) measurements, we have recorded the ultrafast LS to HS switching. Whereas a single TRA measurement gives only partial information, we demonstrate that TRSH readily reveals the different mechanisms in play during the HS-to-LS state relaxation. Moreover, a simple model makes it possible to evaluate the relaxation times as well as the hyperpolarizabilities of the different excited states through which the system travels during the spin-state transition.

Design and Study of Structural Linear and Nonlinear Optical Properties of Chiral [Fe(phen)3]2+ Complexes.

The dependence of nonlinear optical properties upon the spin state in molecular switches is still an unexplored area. Chiral [Fe( phen)3]2+ complexes are excellent candidates for those studies because they are expected to show nonlinear optical properties of interest and at the same time show photoconversion to a short-lived metastable high-Spin state by ultrafast optical pumping. Herein, we present the synthesis, crystallographic, and spectroscopic comparison of chiral [Fe( phen)3]2+ complexes obtained with chiral anions, a new lipophilic derivative of the D2-symmetric (As2(tartrate)2)2-, and D3-symmetric tris(catechol)phosphate(V) (TRISCAT), tris(catechol)arsenate(V) (TRISCAS), and 3,4,5,6-tetrachlorocatechol phosphate(V) (TRISPHAT). Complexes [Fe( phen)3]( rac-TRISCAT)2 (2) and [Fe( phen)3](X-TRISCAS)2 (X = rac (3), Δ (4), Λ (5)) were found to be isomorphous in the R32 Sohncke space group with twinning by inversion correlated with the starting chiral anion optical purity. The structures show the [Fe( phen)3]2+ complex interacting strongly along its 3-fold axis with two anions. Only the structure of a [Fe( phen)3]( rac-TRISPHAT)2 solvate (6) could be obtained, which showed no particular anion/cation interaction contrary to what was observed previously in solution. The [Fe( phen)3](X-As2(tartrate)2) (X = Δ (7), Λ (8), and racemic mixture (9)) crystallizes in enantiomorphic space groups P3121/ P3221 with the same solid-state packing. Dichroic electronic absorption studies evidenced racemization for all chiral complexes in solution due to ion pair dissociation, whereas the asymmetric induction is conserved in the solid state in KBr pellets. We evidenced on chiral complexes 4 and 5 strong nonlinear second harmonic generation, the intensity of which could be correlated with the complex electronic absorption.

Geometric phase shaping of terahertz vortex beams.

We propose a topological beam-shaping strategy of terahertz (THz) beams using geometric phase elements made of space-variant birefringent slabs. Quasi-monochromatic THz vortex beams are produced and characterized both in amplitude and phase from the reconstructed real-time two-dimensional imaging of the electric field. Nonseparable superpositions of such vortex beams are also obtained and characterized by two-dimensional polarimetric analysis. These results emphasize the versatility of the spin-orbit electromagnetic toolbox to prepare on-demand structured light endowed with polarization-controlled orbital angular momentum content in the THz domain, which should find many uses in future THz technologies.

Development of a wavefront sensor for terahertz pulses.

Wavefront characterization of terahertz pulses is essential to optimize far-field intensity distribution of time-domain (imaging) spectrometers or increase the peak power of intense terahertz sources. In this paper, we report on the wavefront measurement of terahertz pulses using a Hartmann sensor associated with a 2D electro-optic imaging system composed of a ZnTe crystal and a CMOS camera. We quantitatively determined the deformations of planar and converging spherical wavefronts using the modal Zernike reconstruction least-squares method. Associated with deformable mirrors, the sensor will also open the route to terahertz adaptive optics.

Terahertz-field-induced second harmonic generation through Pockels effect in zinc telluride crystal.

We report on the second harmonic generation (SHG) of a near-infrared pulse in a zinc telluride crystal through the Pockels effect induced by an intense terahertz pulse. The temporal and angular behaviors of the SHG have been measured and agree well with theoretical predictions. This phenomenon, so far overlooked, makes it possible to generate second harmonic through cascading of two second-order nonlinear phenomena in the near-infrared and terahertz ranges. We also show how this cascading process can be used to sample terahertz pulses.

Picosecond to femtosecond pulses from high power self mode-locked ytterbium rod-type fiber laser.

We have designed an ytterbium rod-type fiber laser oscillator with tunable pulse duration. This system that delivers more than 10 W of average power is self mode-locked. It yields femtosecond to picosecond laser pulses at a repetition rate of 74 MHz. The pulse duration is adjusted by changing the spectral width of a band pass filter that is inserted in the laser cavity. Using volume Bragg gratings of 0.9 nm and 0.07 nm spectrum bandwidth, this oscillator delivers nearly Fourier limited 2.8 ps and 18.5 ps pulses, respectively. With a 4 nm interference filter, one obtains picosecond pulses that have been externally dechirped down to 130 fs.

Ultrafast dynamics of metal complexes of tetrasulphonated phthalocyanines.

A promising material in medicine, electronics, optoelectronics, electrochemistry, catalysis, and photophysics, tetrasulphonated aluminum phthalocyanine (AlPcS(4)), is investigated by means of steady-state and time-resolved pump-probe spectroscopies. Absorption and steady-state fluorescence spectroscopy indicate that AlPcS(4) is essentially monomeric. Spectrally resolved pump-probe data are recorded on time scales ranging from femtoseconds to nanoseconds. The nature of these fast processes and pathways of the competing relaxation processes from the initially excited electronic states in aqueous and organic (dimethyl sulfoxide) solutions are discussed. The decays and bleaching recovery have been fitted in the ultrafast window (0-10 ps) and later time window extending to nanoseconds (0-1 ns). While the excited-state dynamics have been found to be sensitive to the solvent environment, we were able to show that the fast dynamics is described by three time constants in the ranges of 115-500 fs, 2-25 ps, and 150-500 ps. We were able to ascribe these three time constants to different processes. The shortest time constants have been assigned to vibrational wavepacket dynamics. The few picosecond components have been assigned to vibrational relaxation in the excited electronic states. Finally, the 150-500 ps components represent the decay from S(1) to the ground state. The experimental and theoretical treatment proposed in this paper provides a basis for a substantial revision of the commonly accepted interpretation of the Soret transition (B transition) that exists in the literature.

Mechanism for optical switching of the spin crossover [Fe(NH(2)-trz)(3)](Br)(2).3H(2)O compound at room temperature.

This paper reports on phase transition photo-induced by a nanosecond laser pulse in the molecular spin crossover material [Fe(NH(2)-trz)(3)] (Br)(2).3H(2)O (with NH(2)trz = 4-amino-1,2,4-triazole) around room temperature and in the close vicinity of the thermal hysteresis loop. The measurements are carried out using a time-resolved pump-probe experiment and by recording the reflectivity change at various temperatures and laser intensities. The dynamics of the optically induced reflectivity changes are presented and discussed. We propose a simple model that describes well the recorded phenomena. It takes into account the physical and optical properties of the sample that directly impact the amplitude and the dynamics of the laser-induced heating of the compound.

Nanoparticles of [Fe(NH2-trz)3]Br2.3H2O (NH2-trz=2-amino-1,2,4-triazole) prepared by the reverse micelle technique: influence of particle and coherent domain sizes on spin-crossover properties.

This paper describes the synthesis of iron(II) spin-crossover nanoparticles prepared by the reverse micelle technique by using the non-ionic surfactant Lauropal (Ifralan D0205) from the polyoxyethylenic family. By changing the surfactant/water ratio, the size of the particles of [Fe(NH2-trz)3]Br2.3H2O (with NH2trz=4-amino-1,2,4-triazole) can be controlled. On the macroscopic scale this complex exhibits cooperative thermal spin crossovers at 305 and 320 K. We find that when the size is reduced down to 50 nm, the spin transition becomes gradual and no hysteresis can be detected. For our data it seems that the critical size, for which the existence of a thermal hysteresis can be detected, is around 50 nm. Interestingly, the change of the particle size induces almost no change in the temperature of the thermal spin transition. A systematic determination of coherent domain size carried out on the nanoparticles by powder X-ray diffraction indicates that at approximately 30 nm individual particles consist of one coherent domain.

Tuning and focusing THz pulses by shaping the pump laser beam profile in a nonlinear crystal.

Spatially shaped femtosecond laser pulses are used to generate and to focus tunable terahertz (THz) pulses by Optical Rectification in a Zinc Telluride (ZnTe) crystal. It is shown analytically and experimentally that the focusing position and spectrum of the emitted THz pulse can be changed, in the intermediate field zone, by controlling the spatial shape of the near-infrared (NIR) femtosecond (fs) laser pump. In particular, if the pump consists of concentric circles, the emitted THz radiation is confined around the propagation axis, producing a THz pulse train, and focusing position and spectrum can be controlled by changing the number of circles and their diameter.

Nanoparticles of iron(II) spin-crossover.

We report the synthesis of spin crossover 69 nm spherical nanoparticles of [Fe(NH2-trz)3](Br)2.3H2O.0.03(surfactant) (NH2trz = 4-amino-1,2,4-triazole, surfactant = Lauropal), prepared by the reverse micelle technique, which exhibit at room temperature a thermal hysteresis characterized by magnetic, diffuse reflectivity and Raman studies.