Coherent transfer by adiabatic passage in two-dimensional lattices

Coherent tunneling by adiabatic passage (CTAP) is a well-established technique for robust spatial transport of quantum particles in linear chains. Here we introduce two exactly-solvable models where the CTAP protocol can be extended to two-dimensional lattice geometries. Such bi-dimensional lattice models are synthesized from time-dependent second-quantization Hamiltonians, in which the bosonic field operators evolve adiabatically like in an ordinary three-level CTAP scheme thus ensuring adiabatic passage in Fock space.     

Heavy-Atom Tunneling in Semibullvalenes: How Driving Force,Substituents, and Environment Influence the Tunneling Rates

The Cope rearrangement of selectively deuterated isotopomers of 1,5-dimethylsemibullvalene 2 a and 3,7-dicyano-1,5-dimethylsemibullvalene 2 b were studied in cryogenic matrices. In both semibullvalenes the Cope rearrangement is governed by heavy-atom tunneling. The driving force for the rearrangements is the small difference in the zero-point vibrational energies of the isotopomers. To evaluate the effect of the driving force on the tunneling probability in 2 a and 2 b , two different pairs of isotopomers were studied for each of the semibullvalenes. The reaction rates for the rearrangement of 2 b in cryogenic matrices were found to be smaller than the ones of 2 a under similar conditions, whereas differences in the driving force do not influence the rates. Small curvature tunneling (SCT) calculations suggest that the reduced tunneling rate of 2 b compared to that of 2 a results from a change in the shape of the potential energy barrier. The tunneling probability of the semibullvalenes strongly depends on the matrix environment; however, for 2 a in a qualitatively different way than for 2 b .     

Semiclassical transition state theory/master equation kinetics of HO + CO: Performance evaluation

Previously, master equation (ME) simulations using semiclassical transition state theory (SCTST) and high-accuracy extrapolated ab initio thermochemistry (HEAT) predicted rate constants in excellent agreement with published experimental data over a wide range of pressure and temperatures ≳250 K, but the agreement was not as good at lower temperatures. Possible reasons for this reduced performance are investigated by (a) critically evaluating the published experimental data and by investigating; (b) three distinct ME treatments of angular momentum, including one that is exact at the zero- and infinite-pressure limits; (c) a hindered-rotor model for HOCO that implicitly includes the cis- and trans-conformers; (d) possible empirical adjustments of the thermochemistry; (e) possible empirical adjustments to an imaginary frequency controlling tunneling; (f) including or neglecting the prereaction complex PRC1; and (g) its possible bimolecular reactions. Improvements include better approximations to factors in SCTST and using the Hill and van Vleck treatment of angular momentum coupling. Evaluation of literature data does not reveal any specific shortcomings, but the stated uncertainties may be underestimated. All ME treatments give excellent fits to experimental data at T ≥ 250 K, but the discrepancy at T < 250 K persists. Note that each ME model requires individual empirical energy transfer parameters. Thermochemical adjustments were unable to match the experimental H/D kinetic isotope effects. Adjusting an imaginary frequency can achieve good fits, but the adjustments are unacceptably large. Whether PRC1 and its possible bimolecular reactions are included had little effect. We conclude that none of the adjustments is an improvement over the unadjusted theory. Note that only one set of experimental data exists in the regime of the discrepancy with theory, and data for DO + CO are scanty.     

The self-assemblies of a newly designed star-shaped molecule end-capped with bromine atoms studied by scanning tunneling microscopy

A new star-shaped molecule StOF-Br_3 containing oligofluorenes and halogen atoms(Bromine) has been synthesized and studied by Scanning Tunneling Microscopy(STM) at the highly oriented pyrolytic graphite(HOPG) surface.We have obtained the high-resolution self-assembled STM images,from which the highly ordered and closely packed non-porous arrangements of the StOF-Br_3 molecular selfassemblies at the heptanoic acid/HOPG surface could be observed.The molecular models and selfassembled StOF-Br_3 architectures have been given in the following text.Besides,we have also figured out the surface free energy by the density functional theory(DFT) calculation,which proved that the halogen...halogen interaction was strong enough to stabilize the ordered molecular self-assemblies.This work verifies the existence of bromine...bromine interactions,and meanwhile provides a kind of effective approach for quickly building ordered molecular nanoarchitectures with large areas and different geometries.     

Light-induced interaction between graphene and magnetic film in a cavity

An interaction mechanism between graphene and magnetic film in cavity is presented in this work. The pseudospin in graphene can indirectly interact with the spins in magnetic film by the media of a circularly polarized photons under the conditions of high temperature and intense laser field. The interaction energy as well as the average values of pseudospin and spin components are calculated according to a generating functional approach. This interaction mechanism provides a scheme of detecting the pseudospin polarization effect.     

Anomalous transport effects for the metal and insulator doped La0.833K0.167MnO3 systems

The La_0.833K_0.167MnO₃:Ag₂O and the La_0.833K_0.167MnO₃:SrTiO₃ samples are fabricated by the sol–gel method. The microstructure, magnetic and transportation properties have been systematically studied. X-ray diffraction patterns show that the La_0.833K_0.167MnO₃:Ag₂O (abbreviated as LKMO/Ag) sample is a two-phase composite and consists of a magnetic La_0.833K_0.167MnO₃ (abbreviated as LKMO) perovskite phase and a nonmagnetic Ag metal phase, while the structure of the La_0.833K_0.167MnO₃:SrTiO₃ (abbreviated as LKMO/STO) sample is a homogeneous solid solution phase. Comparing with the pure LKMO sample, the room temperature magnetoresistance (MR) effect for the LKMO/Ag sample is enhanced significantly due to the addition of Ag metal. The MR ratio increases from ∼25% for the pure LKMO sample to 65% for the LKMO/Ag sample under a higher field of 5.5 T at 300 K. For the LKMO/STO sample, however, the room temperature MR effect is weakened dramatically and is almost close to zero due to the addition of SrTiO₃ insulator. In the low temperature regime below the Curie temperature, the MR behaviors are different from that of the room temperature; that is, the MR effect is decreased for the LKMO/Ag sample and increased for the LKMO/STO sample with temperature decrease. In fact, the low-field (μ₀H=0.5 T) MR decreases from 32% to 5% for the LKMO/Ag sample, while increasing from 0.07% to 25% for the LKMO/STO sample with decreasing temperature from 300 to 4 K. The relative change between the intrinsic and the extrinsic MR, and varied roles of the spin-polarized-tunneling and the spin-dependent scattering mechanisms in different temperature regimes are employed to interpret the anomalous transport behaviors.     

Resistance switching memory in perovskite oxides

The resistance switching behavior has recently attracted great attentions for its application as resistive random access memories (RRAMs) due to a variety of advantages such as simple structure, high-density, high-speed and low-power. As a leading storage media, the transition metal perovskite oxide owns the strong correlation of electrons and the stable crystal structure, which brings out multifunctionality such as ferroelectric, multiferroic, superconductor, and colossal magnetoresistance/electroresistance effect, etc. The existence of rich electronic phases, metal–insulator transition and the nonstoichiometric oxygen in perovskite oxide provides good platforms to insight into the resistive switching mechanisms.     

Localization or tunneling in asymmetric double-well potentials

An asymmetric double-well potential is considered, assuming that the wells are parabolic around the minima. The WKB wave function of a given energy is constructed inside the barrier between the wells. By matching the WKB function to the exact wave functions of the parabolic wells on both sides of the barrier, for two almost degenerate states, we find a quantization condition for the energy levels which reproduces the known energy splitting formula between the two states. For the other low-lying non-degenerate states, we show that the eigenfunction should be primarily localized in one of the wells with negligible magnitude in the other. Using Dekker’s method (Dekker, 1987), the present analysis generalizes earlier results for weakly biased double-well potentials to systems with arbitrary asymmetry.     

Effect of bias voltage and electrodes size on the Pd conductance histograms

Conductance histograms of palladium nanocontacts in ultra high vacuum (UHV) were experimentally studied at room temperature using scanning tunneling microscope (STM). Our results show that the resolution of the pure Pd peaks, at 1.8 and around 3G₀, in the histograms, depends on the bias voltage and the electrodes size. The size of the electrodes should be as small as possible to achieve the higher extraction of hydrogen from them and therefore preventing the diffusion of H from the bulk to the nanocontacts during the conductance measurements, particularly at low bias voltage. This could explain why peaks have not been observed previously in the Pd histograms, using STM techniques in UHV.