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Paul Leiderer

Publications and source records attributed to Paul Leiderer.

6 recordsLinked to original sources

Nonmonotonic temperature dependence of the thermopower of atomic-size gold contacts

We report measurements of the thermopower of atomic-size gold contacts realized by the mechanically controllable break junction (MCBJ) technique over a temperature range from 18 K to 295 K. A thermometer included in the lithographic structure close to the constriction provides a direct measurement of the temperature increase generated by heating one side of the contact with a focused laser beam. While the conductance histograms confirm the quantum nature of the transport, we observe a nonmonotonic temperature dependence of the ensemble-averaged thermopower with a minimum of $-2\,\mu$VK$^{-1}$ at about 150 K. The values for the thermopower obtained at the lowest and the high temperature are compatible with values reported in the literature, but the nonmonotonic behavior in between disagrees with the expected linear dependence for quantum coherent conductors described by the Landauer formula. We develop a theoretical model based on an energy dependent transmission function that qualitatively reproduces the nonmonotonic behavior, but fails quantitatively. We therefore interpret our data as a result of phonon contributions to the thermopower beyond the Landauer model and with opposite sign than the classical phonon drag known from bulk systems. Our findings show that, firstly, the thermopower gives important insight into the transport properties of atomic-size structures and second that the linear approximation of the Landauer model has to be used with caution when studying more complex transport properties even for atomic contacts from free-electron metals.

cond-mat.mes-hall

Lane formation in gravitationally driven colloid mixtures consisting of up to three different particle sizes

Brownian dynamics simulations are utilized to study segregation phenomena far from thermodynamic equilibrium. In the present study, we expand upon the analysis of binary colloid mixtures and additionally introduce a third particle species to further our understanding of colloidal systems. Gravitationally driven, spherical colloids immersed in an implicit solvent are confined in two-dimensional linear microchannels. The interaction between the colloids is modeled by the Weeks-Chandler-Andersen potential, and the confinement of the colloids is realized by hard walls based on the solution of the Smoluchowski equation in half space. In binary and ternary colloidal systems, a difference in the driving force is achieved by differing colloid sizes, but fixed mass density. We observe for both the binary and ternary systems that a driving force difference induces a nonequilibrium phase transition to lanes. For ternary systems, we study the tendency of lane formation in dependence of the diameter of the medium-sized colloids. Here, we find a sweetspot for lane formation in ternary systems. Furthermore, we study the interaction of two differently sized colloids at the channel walls. Recently, we observed that driven large colloids push smaller colloids to the walls. This results in small particle lanes at the walls at early simulation times. In this work, we additionally find that thin lanes are unstable and dissolve over very long time frames. Furthermore, we observe a connection between lane formation and the nonuniform distribution of particles along the channel length. This nonuniform distribution occurs either alongside lane formation or in shared lanes (i.e. lanes consisting of two colloid types).

cond-mat.soft

Peaked bulk crystal nucleation in charged sphere melts from salt concentration dependent crystallization experiments at very low metastability

We determined bulk crystal nucleation rates in aqueous suspensions of charged spheres at low metastability. Experiments were performed in dependence on electrolyte concen-tration and for two different particle number densities. The time-dependent nucleation rate shows a pronounced initial peak, while post-solidification crystal size distributions are skewed towards larger crystallite sizes. At each concentration, the nucleation rate density initially drops exponentially with increasing salt concentration. The complete data set, however, shows an unexpected scaling of the nucleation rate densities with met-astability times the number density of particles. Parameterization of our results in terms of Classical Nucleation Theory reveals unusually low interfacial free energies of the nu-cleus surfaces and nucleation barriers well below the thermal energy. We tentatively attribute our observations to the presence of doublets introduced by the employed con-ditioning technique and acting as nucleation seeds.

cond-mat.soft

Climbing two hills is faster than one: collective barrier-crossing by colloids driven through a microchannel

Ohm's law is one of the most central transport rules stating that the total resistance of sequential single resistances is additive. While this rule is most commonly applied to electronic circuits, it also applies to other transport phenomena such as the flow of colloids or nanoparticles through channels containing multiple obstacles, as long as these obstacles are sufficiently far apart. Here we explore the breakdown of Ohm's law for fluids of repulsive colloids driven over two energetic barriers in a microchannel, using real-space microscopy experiments, particle-resolved simulations, and dynamical density functional theory. If the barrier separation is comparable to the particle correlation length, the resistance is highly non-additive, such that the resistance added by the second barrier can be significantly higher or lower than that of the first. Surprisingly, in some cases the second barrier can even add a {\it negative} resistance, such that two identical barriers are easier to cross than a single one. We explain this counterintuitive observation in terms of the structuring of particles trapped between the barriers.

cond-mat.soft

Transport Measurements of Strongly-Correlated Electrons on Helium in a Classical Point-Contact Device

We present transport measurements of electrons on the surface of liquid helium in a microchannel device in which a constriction may be formed by a split-gate electrode. The surface electron current passing through the microchannel first decreases and is then completely suppressed as the split-gate voltage is swept negative. The current decreases in a steplike manner, due to changes in the number of electrons able to pass simultaneously through the constriction. We investigate the dependence of the electron transport on the AC driving voltage and the DC potentials applied to the sample electrodes, in order to understand the electrostatic potential profile of the constriction region. Our results are in good agreement with a finite element modeling analysis of the device. We demonstrate that the threshold of current flow depends not only on the applied potentials but also on the surface electron density. The detailed understanding of the characteristics of such a device is an important step in the development of mesoscopic experiments with surface electrons on liquid helium.

cond-mat.mes-hall

Colloidal Micromotors: Controlled Directed Motion

Here we demonstrate a synthetic micro-engine, based on long-range controlled movement of colloidal particles, which is induced by a local catalytic reaction. The directed motion at long timescales was achieved by placing specially designed magnetic capped colloids in a hydrogen peroxide solution at weak magnetic fields. The control of the motion of the particles was provided by changes of the concentration of the solution and by varying the strength of the applied magnetic field. Such synthetic objects can then be used not only to understand the fundamental driving processes but also be employed as small motors in biological environments, for example, for the transportation of molecules in a controllable way.

cond-mat.stat-mech