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1.
Phys Rev Lett ; 113(26): 266401, 2014 Dec 31.
Artículo en Inglés | MEDLINE | ID: mdl-25615359

RESUMEN

We investigate tunneling between two spinful Tomonaga-Luttinger liquids (TLLs) realized, e.g., as two crossed nanowires or quantum Hall edge states. When injecting into each TLL one electron of opposite spin, the dc current measured after the crossing differs for singlet, triplet, or product states. This is a striking new non-Fermi liquid feature because the (mean) current in a noninteracting beam splitter is insensitive to spin entanglement. It can be understood in terms of collective excitations subject to spin-charge separation. This behavior may offer an easier alternative to traditional entanglement detection schemes based on current noise, which we show to be suppressed by the interactions.

2.
J Comput Chem ; 31(16): 2967-70, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20928852

RESUMEN

We herein present the graphical user interface (GUI) TmoleX for the quantum chemical program package TURBOMOLE. TmoleX allows users to execute the complete workflow of a quantum chemical investigation from the initial building of a structure to the visualization of the results in a user friendly graphical front end. The purpose of TmoleX is to make TURBOMOLE easy to use and to provide a high degree of flexibility. Hence, it should be a valuable tool for most users from beginners to experts. The program is developed in Java and runs on Linux, Windows, and Mac platforms. It can be used to run calculations on local desktops as well as on remote computers.


Asunto(s)
Teoría Cuántica , Interfaz Usuario-Computador , Simulación de Dinámica Molecular
3.
Nat Commun ; 6: 6724, 2015 Apr 02.
Artículo en Inglés | MEDLINE | ID: mdl-25832200

RESUMEN

Interest in manipulating the magnetic order by ultrashort laser pulses has thrived since it was observed that such pulses can be used to alter the magnetization on a sub-picosecond timescale. Usually this involves demagnetization by laser heating or, in rare cases, a transient increase of magnetization. Here we demonstrate a mechanism that allows the magnetic order of a material to be enhanced or attenuated at will. This is possible in systems simultaneously possessing a low, tunable density of conduction band carriers and a high density of magnetic moments. In such systems, the thermalization time can be set such that adiabatic processes dominate the photoinduced change of the magnetic order--the three-temperature model for interacting thermalized electron, spin and lattice reservoirs is bypassed. In ferromagnetic Eu(1-x)Gd(x)O, we thereby demonstrate the strengthening as well as the weakening of the magnetic order by ~10% and within ≤3 ps by optically controlling the magnetic exchange interaction.

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