Quantum interference and decoherence in hexagonal antidot lattices

The Altshuler–Aronov–Spivak (AAS) oscillations and the Aharonov–Bohm (AB) type oscillations both at low and high magnetic fields were observed in hexagonal antidot lattices fabricated from a GaAs/AlGaAs two-dimensional electron gas sample. The periodicities in the magnetic field and in the gate bias voltage, of the high field AB oscillation furnish information on the edge states localized around the antidots. The temperature dependences of these quantum oscillations are studied.     

All-electric-controlled spin current switching in single-molecule magnet-tunnel junctions

A single-molecule magnet (SMM) coupled to two normal metallic electrodes can both switch spin-up and spin-down electronic currents within two different windows of SMM gate voltage. Such spin current switching in the SMM tunnel junction arises from spin-selected single electron resonant tunneling via the lowest unoccupied molecular orbit of the SMM. Since it is not magnetically controlled but all-electrically controlled,the proposed spin current switching effect may have potential applications in future spintronics.     

Quantum phase interference and spin-parity in Mn12 single-molecule magnets

Magnetization measurements of Mn12 molecular nanomagnets with spin ground states of S=10 and S=19/2 show resonance tunneling at avoided energy level crossings. The observed oscillations of the tunnel probability as a function of the magnetic field applied along the hard anisotropy axis are due to topological quantum phase interference of two tunnel paths of opposite windings. Spin-parity dependent tunneling is established by comparing the quantum phase interference of integer and half-integer spin systems.     

Inelastic tunnelling and the pair-quasiparticle interference current in Josephson junctions

The contribution to the quasiparticle current and pair—quasiparticle interference current of inelastic tunnelling due to the excitation of a boson mode in the tunnelling barrier is evaluated.     

Current-induced conformational switching in single-molecule junctions

Current-induced conformational switching in single-molecule junctions constitutes a fundamental process in molecular electronics. Motivated by recent experiments on azobenzene derivatives, we study this process for molecules which exhibit two (meta)stable conformations in the neutral state but only a single stable conformation in the ionic state. We derive and analyze appropriate Fokker–Planck equations obtained from a density-matrix formalism starting from a generic model and present comprehensive analytical and numerical results for the switching dynamics in general and the quantum yield in particular.     

Multiple-beam Ramsey interference and quantum decoherence

We study the effect of photon scattering from a path of a four-beam atomic interference setup, which is based on a cesium atomic beam and two subsequent optical Ramsey pulses projecting the atoms onto a multilevel dark state. While in two-beam interference, any attempt to keep track of an interfering path reduces the fringe contrast, we demonstrate that photon scattering in a multiple-path arrangement cannot only lead to a decrease, but - under certain conditions - also to an increase of the interference contrast. The results are confirmed by a density-matrix calculation. We are aware that in all cases the “which-path” information carried away by the scattered photons leads to a loss of information that is contained in the atomic quantum state. An approach to quantify this “which-path” information using observed fringe signals is presented; it allows for an appropriate measure of quantum decoherence in multiple-path interference. Received: 27 July 2000 / Published online: 6 December 2000     

Controlled decoherence in multiple beam Ramsey interference

We have scattered photons from an interfering path of a multiple beam Ramsey interference experiment realized with a cesium atomic beam. It is demonstrated that in multiple beam interference the decoherence from photon scattering cannot only lead to a decrease but, under certain conditions, also to an increase of the Michelson fringe contrast. In all cases, the atomic quantum state loses information with photon scattering, as "which-path" information is carried away by the photon field. We outline an approach to quantify this which-path information from observed fringe signals, which allows for an appropriate measure of decoherence in multiple path interference.     

Vibrationally induced two-level systems in single-molecule junctions

Single-molecule junctions are found to show anomalous spikes in dI/dV spectra. The position in energy of the spikes is related to local vibration mode energies. A model of vibrationally induced two-level systems reproduces the data very well. This mechanism is expected to be quite general for single-molecule junctions. It acts as an intrinsic amplification mechanism for local vibration mode features and may be exploited as a new spectroscopic tool.     

Role of inter-tube coupling and quantum interference on electrical transport in carbon nanotube junctions

Due to excellent transport properties, Carbon nanotubes (CNTs) show a lot of promise in sensor and interconnect technology. However, recent studies indicate that the conductance in CNT/CNT junctions are strongly affected by the morphology and orientation between the tubes. For proper utilization of such junctions in the development of CNT based technology, it is essential to study the electronic properties of such junctions. This work presents a theoretical study of the electrical transport properties of metallic Carbon nanotube homo-junctions. The study focuses on discerning the role of inter-tube interactions, quantum interference and scattering on the transport properties on junctions between identical tubes. The electronic structure and transport calculations are conducted with an Extended Hückel Theory-Non Equilibrium Green's Function based model. The calculations indicate conductance to be varying with a changing crossing angle, with maximum conductance corresponding to lattice registry, i.e. parallel configuration between the two tubes. Further calculations for such parallel configurations indicate onset of short and long range oscillations in conductance with respect to changing overlap length. These oscillations are attributed to inter-tube coupling effects owing to changing π orbital overlap, carrier scattering and quantum interference of the incident, transmitted and reflected waves at the inter-tube junction.     

Electron-vibration interaction in single-molecule junctions: from contact to tunneling regimes

Point contact spectroscopy on a H(2)O molecule bridging Pt electrodes reveals a clear crossover between enhancement and reduction of the conductance due to electron-vibration interaction. As single-channel models predict such a crossover at a transmission probability of tau=0.5, we used shot noise measurements to analyze the transmission and observed at least two channels across the junction where the dominant channel has a tau=0.51 +/- 0.01 transmission probability at the crossover conductance, which is consistent with the predictions for single-channel models.     

Quantum decoherence in the theory of open systems

Within the framework of the Lindblad theory for open quantum systems, we determine the degree of quantum decoherence of a harmonic oscillator interacting with a thermal bath. It is found that the system manifests a quantum decoherence which is more and more significant in time. We also calculate the decoherence time scale and analyze the transition from quantum to classical behavior of the considered system. The text was submitted by the author in English.     

Contact interference in molecular junctions

We highlight a new manifestation of quantum interference in transport through single-molecule junctions, owing to different charge transport pathways from the molecule through the contacts into the three-dimensional electrode. Such contact interference can be identified with characteristic features of the current–voltage curve, as dramatic as closing an otherwise open transport channel. Based on analysis of the necessary conditions for observation of this phenomenon, we conclude that this effect should be detectable in relatively small molecules, where a molecular site shares coupling to two electrodes, and an electrode surface site shares coupling to different molecular sites. The importance of the surface-molecule connectivity scheme implies that commonly used reduced models which couple different molecular sites to effectively independent electrodes, fail to account for this effect and must be corrected in order to properly capture contact interference.     

Thermoelectricity in B80-based single-molecule junctions: First-principles investigation

Thermoelectricity is a thermorelated property that is of great importance in single-molecule junctions. The electrical conductance (σ), electron-derived thermal conductance (κ_el) and Seebeck coefficient (S) of B₈₀-based single-molecule junctions are investigated by using density functional theory in combination with non-equilibrium Green’s function. When the distance between the left/right electrodes is 11.4 Å, the relationship between σ and κ_el obeys the Wiedemann–Franz law very well because of the strong hybridization between B₈₀ molecular orbitals and the surface states of Au electrodes. Furthermore, the calculated Lorenz number is close to the famous value in metal or degenerate semiconductors. In addition, S is only –19.09 μV/K at 300 K, thus leading to the smaller electron’s thermoelectric figure of merit (Z_elT = S²σT/κ_el). Interestingly, the strain and chemical potential can modulate B₈₀-based single-molecule junctions from n-type to p-type when the compressive strain reaches –0.6 Å or the chemical potential shifts to –0.16 eV. This might be attributed that S reflects the asymmetry in the electrical conductance with respect to the chemical potential and is proportional to the slopes of the transmission spectrum.     

Quantum coherence and decoherence of protons and muons in condensed matter

The coherence in quantum superposition states of protons (and chemically similar particles, the positive muons) has been studied in some condensed matter environments. It is shown that if the proton systems and the experimental techniques used to study them are carefully selected, it is possible to observe quantum delocalization states of single particles and to understand the mechanisms for their loss of coherence. Quantum correlated two- and multiparticle states of protons lose coherence very fast when coupled to condensed matter environments, but new sub-femtosecond techniques have made them accessible to experimental studies. The degree of decoherence can be measured as function of time and the decoherence mechanisms can, at least in certain cases, be identified. Although less clean than in corresponding studies of quantum optical systems, these studies can be seen as a first step towards understanding the conditions for preservation of quantum correlation and entanglement in massive systems. Some consequences and some suggestions for future work are discussed. Received 28 August 2002 Published online 7 January 2003     

On the environmental decoherence and spin interference in mesoscopic loop structures

Mechanisms of ‘environmental decoherence’ such as surface scattering, Elliot–Yafet process and precession mechanisms, as well as their influence on the spin phase relaxation are considered and compared. It is shown that the ‘spin ballistic’ regime is possible, when the phase relaxation length for the spin part of the wave function (L^(s)) is much greater than the phase relaxation length for the ‘orbital part’ (L^(e)). In the presence of an additional magnetic field, the spin part of the electron's wave function (WF) acquires a phase shift due to additional spin precession about that field. If the structure length L is chosen to be L^(s)>L>L^(e), it is possible to ‘wash out’ the quantum interference related to the phase coherence of the ‘orbital part’ of the WF, retaining at the same time that related to the phase coherence of the spin part and, hence, to reveal corresponding conductance oscillations.     

Asymmetric Berry-phase interference patterns in a single-molecule magnet

A Mn(4) single-molecule magnet displays asymmetric Berry-phase interference patterns in the transverse-field (H(T)) dependence of the magnetization tunneling probability when a longitudinal field (H(L)) is present, contrary to symmetric patterns observed for H(L)=0. Reversal of H(L) results in a reflection of the transverse-field asymmetry about H(T)=0, as expected on the basis of the time-reversal invariance of the spin-orbit Hamiltonian which is responsible for the tunneling oscillations. A fascinating motion of Berry-phase minima within the transverse-field magnitude-direction phase space results from a competition between noncollinear magnetoanisotropy tensors at the two distinct Mn sites.