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Over the past decades, optical manipulation of magnetization by ultrafast laser pulses has attracted extensive interest. It not only shows intriguing fundamental science arising from the interactions between spins, electrons, phonons, and photons, but also manifests the potential to process and store data at a speed that is three orders of magnitude faster than the current technologies. In this paper, all‐optical helicity‐dependent switching (AO‐HDS) in hybrid metal–ferromagnet thin films, which consist of Co/Pt multilayers with perpendicular magnetic anisotropy and an Au film capping layer on the top, is experimentally demonstrated. The switching behaviors of the hybrid Co/Pt–Au material, with various laser repetition rates, scanning speeds, and fluencies, are systematically studied. In comparison with bare Co/Pt multilayers, the hybrid metal–ferromagnet thin films show pronounced AO‐HDS when the number of laser pulses per μm along the scanning direction gradually increases. In addition, the AO‐HDS effect is very robust against laser fluences. A possible mechanism is further proposed based on numerical simulations of the optomagnetic coupling model. These findings promise a new material system that exhibits stable AO‐HDS phenomena, and hence can transform future magnetic storage devices, especially with the addition of plasmonic nanostructures made of noble metals.

 

Many small proteins move across cellular compartments through narrow pores. In order to thread a protein through a constriction, free energy must be overcome to either deform or completely unfold the protein. In principle, the diameter of the pore, along with the effective driving force for unfolding the protein, as well as its barrier to translocation, should be critical factors that govern whether the process proceeds via squeezing, unfolding/threading, or both. To probe this for a well-established protein system, we studied the electric-field–driven translocation behavior of cytochrome c (cyt c ) through ultrathin silicon nitride (SiN x ) solid-state nanopores of diameters ranging from 1.5 to 5.5 nm. For a 2.5-nm-diameter pore, we find that, in a threshold electric-field regime of ∼30 to 100 MV/m, cyt c is able to squeeze through the pore. As electric fields inside the pore are increased, the unfolded state of cyt c is thermodynamically stabilized, facilitating its translocation. In contrast, for 1.5- and 2.0-nm-diameter pores, translocation occurs only by threading of the fully unfolded protein after it transitions through a higher energy unfolding intermediate state at the mouth of the pore. The relative energies between the metastable, intermediate, and unfolded protein states are extracted using a simple thermodynamic model that is dictated by the relatively slow (∼ms) protein translocation times for passing through the nanopore. These experiments map the various modes of protein translocation through a constriction, which opens avenues for exploring protein folding structures, internal contacts, and electric-field–induced deformability.