E. Beaurepaire

Robust spin crossover and memristance across a single molecule

A nanoscale molecular switch can be used to store information in a single molecule. Although the switching process can be detected electrically in the form of a change in the molecules conductance, adding spin functionality to molecular switches is a key concept for realizing molecular spintronic devices. Here we show that iron-based spin-crossover molecules can be individually and reproducibly switched between a combined high-spin, high-conduction state and a low-spin, low-conduction state, provided the individual molecule is decoupled from a metallic substrate by a thin insulating layer. These results represent a step to achieving combined spin and conduction switching functionality on the level of individual molecules.

Giant magnetoresistance through a single molecule

Magnetoresistance is a change in the resistance of a material system caused by an applied magnetic field. Giant magnetoresistance occurs in structures containing ferromagnetic contacts separated by a metallic non-magnetic spacer, and is now the basis of read heads for hard drives and for new forms of random access memory. Using an insulator (for example, a molecular thin film) rather than a metal as the spacer gives rise to tunnelling magnetoresistance, which typically produces a larger change in resistance for a given magnetic field strength, but also yields higher resistances, which are a disadvantage for real device operation. Here, we demonstrate giant magnetoresistance across a single, non-magnetic hydrogen phthalocyanine molecule contacted by the ferromagnetic tip of a scanning tunnelling microscope. We measure the magnetoresistance to be 60% and the conductance to be 0.26G(0), where G(0) is the quantum of conductance. Theoretical analysis identifies spin-dependent hybridization of molecular and electrode orbitals as the cause of the large magnetoresistance.

Distinguishing the ultrafast dynamics of spin and orbital moments in solids

For an isolated quantum particle, such as an electron, the orbital (L) and spin (S) magnetic moments can change provided that the total angular momentum of the particle is conserved. In condensed matter, an efficient transfer between L and S can occur owing to the spin–orbit interaction, which originates in the relativistic motion of electrons. Disentangling the absolute contributions of the orbital and spin angular momenta is challenging, however, as any transfer between the two occurs on femtosecond timescales. Here we investigate such phenomena by using ultrashort optical laser pulses to change the magnetization of a ferromagnetic film and then probe its dynamics with circularly polarized femtosecond X-ray pulses. Our measurements enable us to disentangle the spin and orbital components of the magnetic moment, revealing different dynamics for L and S. We highlight the important role played by the spin–orbit interaction in the ultrafast laser-induced demagnetization of ferromagnetic films, and show also that the magneto-crystalline anisotropy energy is an important quantity to consider in such processes. Our study provides insights into the dynamics in magnetic systems as well as perspectives for the ultrafast control of information in magnetic recording media.

Coherent terahertz emission from ferromagnetic films excited by femtosecond laser pulses

It is shown that the laser induced ultrafast demagnetization of ferromagnetic films results in the emission of a terahertz electromagnetic pulse. This emission has been detected from Ni films using free-space electro-optic sampling. The radiated electric field E(t) is explained by Maxwell equations (radiation from a time dependent magnetic dipole), and is expected to be proportional to the second time derivative of the magnetization d2M/dt2, as measured in the far field. This technique opens appealing perspectives in the context of measuring and understanding the ultrafast spin dynamics as well as the interaction of electrons (both charge and spin) with electromagnetic fields.

Paramagnetism of the Co sublattice in ferromagnetic Zn1 xCoxO films

Using the spectroscopies based on x-ray absorption, we have studied the structural and magnetic properties of

Study of molecular spin-crossover complex Fe(phen)2(NCS)2 thin films

{\mathrm{Zn}}_{1\ensuremath{-}x}{\mathrm{Co}}_{x}\mathrm{O}

Direct observation of a highly spin-polarized organic spinterface at room temperature

films (

Experimental and theoretical investigation of the pre-peaks at the Ti K-edge absorption spectra in TiO2

x=0.1

Efficient metallic spintronic emitters of ultrabroadband terahertz radiation

and 0.25) produced by reactive magnetron sputtering. These films show ferromagnetism with a Curie temperature

Structural order related to the magnetic anisotropy in epitaxial (111) CoPt3 alloy films

{T}_{C}