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Identifying the microscopic nature of non-equilibrium energy transfer mechanisms among electronic, spin, and lattice degrees of freedom is central to understanding ultrafast phenomena such as manipulating magnetism on the femtosecond timescale. Here, we use time- and angle-resolved photoemission spectroscopy to go beyond the often-used ensemble-averaged view of non-equilibrium dynamics in terms of quasiparticle temperature evolutions. We show for ferromagnetic Ni that the non-equilibrium electron and spin dynamics display pronounced variations with electron momentum, whereas the magnetic exchange interaction remains isotropic. This highlights the influence of lattice-mediated scattering processes and opens a pathway toward unraveling the still elusive microscopic mechanism of spin-lattice angular momentum transfer.

Thermoelectric materials play a vital role in the pursuit of a sustainable energy system by allowing the conversion of waste heat to electric energy. Low thermal conductivity is essential to achieving high-efficiency conversion. The conductivity depends on an interplay between the phononic and electronic properties of the nonequilibrium state. Therefore, obtaining a comprehensive understanding of nonequilibrium dynamics of the electronic and phononic subsystems as well as their interactions is key for unlocking the microscopic mechanisms that ultimately govern thermal conductivity. A benchmark material that exhibits ultralow thermal conductivity is SnSe. We study the nonequilibrium phonon dynamics induced by an excited electron population using a framework combining ultrafast electron diffuse scattering and nonequilibrium kinetic theory. This in-depth approach provides a fundamental understanding of energy transfer in the spatiotemporal domain. Our analysis explains the dynamics leading to the observed low thermal conductivity, which we attribute to a mode-dependent tendency to nonconservative phonon scattering. The results offer a penetrating perspective on energy transport in condensed matter with far-reaching implications for rational design of advanced materials with tailored thermal properties.

Ultrafast demagnetization induced by femtosecond laser pulses in thin metallic layers is caused by the outflow of spin-polarized hot-electron currents describable by the superdiffusive transport model. These laser-generated spin currents can cross the interface into another magnetic layer and give rise to magnetization dynamics in magnetic spin valves with noncollinear magnetizations. To describe ultrafast transport and spin dynamics in such nanostructures, we develop here the superdiffusive theory for general noncollinear magnetic multilayers. Specifically, we introduce an Al/Ni/Ru/Fe/Ru multilayer system with noncollinear Ni and Fe magnetic moments and analyze how the ultrafast demagnetization and spin-transfer torque depend on the noncollinearity. We employ ab initio calculations to compute the spin-and energy-dependent transmissions of hot electrons at the interfaces of the multilayer. Taking into account multiple electron scattering at interfaces and spin mixing in the spacer layer, we find that the laser-induced demagnetization of the Ni layer and the magnetization change of the Fe layer strongly depend on the angle between their magnetizations. Similarly, the spin-transfer torques on the Ni and Fe layers and the total spin momentum absorbed in the Ni and Fe layer are found to vary markedly with the amount of noncollinearity. These results suggest that by changing the amount of noncollinearity in magnetic multilayers, one can efficiently control the hot-electron spin transport, which may open a way toward achieving fast, laser-driven spintronic devices.

Magnetic nanoparticles such as FePt in the L1(0) phase are the bedrock of our current data storage technology. As the grains become smaller to keep up with technological demands, the superparamagnetic limit calls for materials with higher magnetocrystalline anisotropy. This, in turn, reduces the magnetic exchange length to just a few nanometers, enabling magnetic structures to be induced within the nanoparticles. Here, we describe the existence of spin-wave solitons, dynamic localized bound states of spin-wave excitations, in FePt nanoparticles. We show with time-resolved x-ray diffraction and micromagnetic modeling that spin-wave solitons of sub-10 nm sizes form out of the demagnetized state following femtosecond laser excitation. The measured soliton spin precession frequency of 0.1 THz positions this system as a platform to develop novel miniature devices.

Ultrashort light pulses can selectively excite charges, spins, and phonons in materials, providing a powerful approach for manipulating their properties. Here we use femtosecond laser pulses to coherently manipulate the electron and phonon distributions, and their couplings, in the charge-density wave (CDW) material 1T-TaSe2. After exciting the material with a femtosecond pulse, fast spatial smearing of the laser-excited electrons launches a coherent lattice breathing mode, which in turn modulates the electron temperature. This finding is in contrast to all previous observations in multiple materials to date, where the electron temperature decreases monotonically via electron-phonon scattering. By tuning the laser fluence, the magnitude of the electron temperature modulation changes from similar to 200 K in the case of weak excitation, to similar to 1,000 K for strong laser excitation. We also observe a phase change of pi in the electron temperature modulation at a critical fluence of 0.7 mJ/cm(2), which suggests a switching of the dominant coupling mechanism between the coherent phonon and electrons. Our approach opens up routes for coherently manipulating the interactions and properties of two-dimensional and other quantum materials using light.

Manipulation of magnetic domain walls via a helicity-independent laser pulse has recently been experimentally demonstrated and various physical mechanisms leading to domain wall dynamics have been discussed. Spin-dependent superdiffusive transport of hot electrons has been identified as one of the possible ways to affect a magnetic domain wall. Here, we develop a model based on superdiffusive spin-dependent transport to study the laser-induced transport of hot electrons through a smooth magnetic domain wall. We show that the spin transfer between neighboring domains can enhance ultrafast demagnetization in the domain wall. More importantly, our calculations reveal that when the laser pulse is properly focused onto the vicinity of the domain wall, it can excite sufficiently strong spin currents to generate a spin-transfer torque that can rapidly move the magnetic domain wall by several nanometers in several hundred femtoseconds, leading to a huge nonequilibrium domain wall velocity.

Femtosecond laser pulses can induce ultrafast demagnetization as well as generate bursts of hot-electron spin currents. In trilayer spin valves consisting of two metallic ferromagnetic layers separated by a nonmagnetic one, hot-electron spin currents excited by an ultrashort laser pulse propagate from the first ferromagnetic layer through the spacer, reaching the second magnetic layer. When the magnetizations of the two magnetic layers are noncollinear, this spin current exerts a torque on magnetic moments in the second ferromagnet. Since this torque is acting only within the subpicosecond timescale, it excites coherent high-frequency magnons, as recently demonstrated in experiments. Here, we calculate the temporal shape of the hot-electron spin currents using the superdiffusive transport model and simulate the response of the magnetic system to the resulting ultrashort spin-transfer torque pulse by means of atomistic spin-dynamics simulations. Our results confirm that the acting spin-current pulse is short enough to excite magnons with frequencies beyond 1 THz, a frequency range out of reach for current-induced spin-transfer torques. We demonstrate the formation of thickness-dependent standing spin waves during the first picoseconds after laser excitation. In addition, we vary the penetration depth of the spin-transfer torque to reveal its influence on the excited magnons. Our simulations clearly show a suppression effect of magnons with short wavelengths already for penetration depths in the range of 1 nm, confirming experimental findings reporting penetration depths below 2 nm.

The dynamics of electrons and phonons in metals upon laser excitation are often described by the two-temperature model, which assumes that both subsystems are individually in thermal equilibrium. However, recent experiments show that this description is not sufficient to describe the out-of-equilibrium dynamics on ultrashort timescales. Here, assuming a thermalized electronic system, we extend and apply a parameter-free microscopic out-of-equilibrium model to describe the ultrafast laser-induced phonon and electron temperature dynamics of various metallic systems such as gold, aluminum, iron, nickel, and cobalt. We report strong deviations from the two-temperature model on the picosecond timescale for all the materials studied, even for those where the assumption of separate thermal equilibrium seemed less restrictive, like in gold. Furthermore, we demonstrate the importance of the mode dependence of the electron-phonon coupling for the relaxation process and reveal the significance of this channel in the lattice equilibration.

Femtosecond laser excitation of solid-state systems creates out-of-equilibrium hot electrons that cool down by transferring their energy to other degrees of freedom and ultimately to lattice vibrations of the solid. By combining ab initio calculations with ultrafast diffuse electron scattering, we gain a detailed understanding of the complex nonequilibrium energy transfer between electrons and phonons in laser-excited Ni metal. Our experimental results show that the wave-vector-resolved population dynamics of phonon modes is distinctly different throughout the Brillouin zone and are in remarkable agreement with our theoretical results. We find that zone-boundary phonon modes become occupied first. As soon as the energy in these modes becomes larger than the average electron energy, a backflow of energy from lattice to electronic degrees of freedom occurs. Subsequent excitation of lower-energy phonon modes drives the thermalization of the whole system on the picosecond time scale. We determine the evolving nonequilibrium phonon occupations, which we find to deviate markedly from thermal occupations.

A material's magnetic state and its dynamics are of great fundamental research interest and are also at the core of a wide plethora of modern technologies. However, reliable access to magnetization dynamics in materials and devices on the technologically relevant ultrafast timescale, and under realistic device-operation conditions, remains a challenge. Here, we demonstrate a method of ultrafast terahertz (THz) magnetometry, which gives direct access to the (sub-)picosecond magnetization dynamics even in encapsulated materials or devices in a contact-free fashion, in a fully calibrated manner, and under ambient conditions. As a showcase for this powerful method, we measure the ultrafast magnetization dynamics in a laser-excited encapsulated iron film. Our measurements reveal and disentangle distinct contributions originating from (i) incoherent hot-magnon-driven magnetization quenching and (ii) coherent acoustically-driven modulation of the exchange interaction in iron, paving the way to technologies utilizing ultrafast heat-free control of magnetism. High sensitivity and relative ease of experimental arrangement highlight the promise of ultrafast THz magnetometry for both fundamental studies and the technological applications of magnetism.