Quantum entanglement formation by repeated spin blockade measurements in a spin field-effect transistor structure embedded with quantum dots

We propose a method of operating a quantum state machine made of stacked quantum dots buried in adjacent to the channel of a spin field-effect transistor (FET) [S. Datta, B. Das, Appl. Phys. Lett. 56 (1990) 665; K. Yoh, et al., Proceedings of the 23rd International Conference on Physics of Semiconductors (ICPS) 2004; H. Ohno, K. Yoh et al., Jpn. J. Appl. Phys. 42 (2003) L87; K. Yoh, J. Konda, S. Shiina, N. Nishiguchi, Jpn. J. Appl. Phys. 36 (1997) 4134]. In this method, a spin blockade measurement extracts the quantum state of a nearest quantum dot through Coulomb blockade [K. Yoh, J. Konda, S. Shiina, N. Nishiguchi, Jpn. J. Appl. Phys. 36 (1997) 4134; K. Yoh, H. Kazama, Physica E 7 (2000) 440] of the adjacent channel conductance. Repeated quantum Zeno-like (QZ) measurements [H. Nakazato, et al., Phys. Rev. Lett. 90 (2003) 060401] of the spin blockade is shown to purify the quantum dot states within several repetitions. The growth constraints of the stacked InAs quantum dots are shown to provide an exchange interaction energy in the range of 0.01–1 meV [S. Itoh, et al., Jpn. J. Appl. Phys. 38 (1999) L917; A. Tackeuchi, et al., Jpn. J. Appl. Phys. 42 (2003) 4278]. We have verified that one can reach the fidelity of 90% by repeating the measurement twice, and that of 99.9% by repeating only eleven QZ measurements. Entangled states with two and three vertically stacked dots are achieved with the sampling frequency of the order of 100 MHz.     

Simulation of slow-motion CW EPR spectrum using stochastic Liouville equation for an electron spin coupled to two nuclei with arbitrary spins: matrix elements of the Liouville superoperator

An algorithm is developed that extends the well known nitroxide slow-motional continuous wave electron paramagnetic resonance (EPR) simulation technique developed originally by Meirovitch et al. [E. Meirovitch, D. Inger, E. Inger, G. Moro, J.H. Freed, J. Chem. Phys. 77 (1982) 3915-3938], and implemented by Schneider and Freed [D.J. Schneider, J.H. Freed, Calculating slow motional magnetic resonance spectra: a user's guide, in: Biological Magnetic Resonance, vol. 6, Plenum Publishing Corporation, 1989]. This paper deals with the more general case of coupling of one electron spin to two nuclear spins. A complete listing of the matrix elements of the Liouville superoperator for this extension has been included. This advance has been successfully tested by reproducing the observed spectral lineshapes of a solution of the novel radical Mes(*)(CH(3))P-PMes(*) [Mes(*)=2,4,6 (tBu)(3)C(2)H(2)] in tetrahydrofuran (THF), in which the radical is undergoing slow tumbling, with the coupling of one electron spin to two physically and magnetically inequivalent phosphorus ((31)P) nuclei.     

Determination of the Mode Grüneisen Parameter of AlN using different Fits on Experimental High Pressure Data

To investigate the pressure dependence of the AlN phonon frequencies Raman spectra of single-crystalline bulk AlN under hydrostatic pressure up to 10 GPa were recorded. The Raman peak positions of the A 1 (TO), E 1 (TO), E 2 (high), A 1 (LO) and quasi-longitudinal optical (QLO) phonons were plotted as a function of pressure. The experimental data was fitted using the traditional parabolic fit (M. Kuball et al . (2001) Appl. Phys. Lett., 78, 724 [1]) and fits to physical models, density, volume, etc. The mode Grüneisen parameters of the different phonons were determined for each fit and significant differences are found between the various fits. Results are compared with recent theoretical calculations (J.-M. Wagner et al . (2000) Phys. Rev. B, 62, 4526 [2]).     

Density matrix and eigenstates for an excess electron in water

We extend the molecular theory of the solvated electrons [Chandler, Singh and Richardson, J. Chem. Phys. 81, 1975 (1984)] to calculate the density matrix for an excess electron in water. Using this density matrix, the numerically obtained solvent induced interaction [Miura and Hirata, J. Phys. Chem. 98, 9649 (1994)] and our developed method [Sethia, Sanyal and Singh, J. Chem. Phys. 93, 7268 (1990)], we have calculated the eigenstates of the electron in water. These results show that the excees electron in water behaves almost like a free particle with effective mass m* in a constant potential well.     

A quasi-classical trajectory study of the Cl + H<Subscript>2</Subscript> (D<Subscript>2</Subscript>) reaction on a new BW3 potential energy surface

Molecular reaction dynamics of Cl + H₂ (D₂) has been studied on the latest analytical potential energy surface called BW3 using the Monte Carlo quasi-classical trajectory method. Excitation functions, differential cross sections and angular distributions of HCl and DCl products have been calculated. The excitation functions of the Cl (²P_3/2) + n-H₂ and Cl(²P_3/2) + n-D₂ reactions are also studied. The results are compared with those of quasi-classical trajectory [M. Alagia et al.: Phys. Chem. Chem. Phys. 2 (2000); F. J. Aoiz et al.: J. Phys. Chem. 100 (1996)], quantum mechanical (QM) calculations [F. J. Aoiz et al.:J. Chem. Phys. 115 (2001)] and experimental data [S. H. Lee et al.: J. Chem. Phys. 110 (1999); F. Dong et al.: J. Chem. Phys. 115 (2001)]. Discussions are given to some new results.     

Top Quark Flavor Changing Decay t

[1]R. Casalbuoani, A. Deandrea, and M. Oertel, JHEP 032(2004) 0402. [2]G. Hooft, In Search of the Ultimate Building Blocks, Cambridge University Press, Cambridge (1997). [3]J. Belazey, Searches for New Physics at Hadron Coliders,Northern Illinois University (2005). [4]N. Arkani-hamed, A.G. Cohen, and H. Georgi, Phys. Lett.B 513 (2001) 232 [hep-ph/0105239]. [5]I. Low, W. Skiba, and D. Smith, Phys. Rev. D 66 (2002)072001 [hep-ph/0207243]. [6]N. Arkani-hamed, A.G. Cohen, E. Katz, and A.E. Nelson,JHEP 0207 (2002) 304 [hep-ph/0206021]. [7]N. Arkani-hamed, A.G. Cohen, E. Katz, A.E. Nelson, T.Gregoire, and J. G. Wacker, JHEP 0208 (2002) 021 [hepph/0206020]. [8]T. Gregoire and J.G. Wacker, JHEP 0208 (2002) 019[hep-ph/0206023]. [9]For a recent review, see e.g., M. Schmaltz, Nucl. Phys. B (Proc. Suppl.) 117 (2003) 40. [10]N. Arkani-hamed, A.G. Cohen, T. Gregoire, and J.G.Jacker, JHEP 0208 (2002) 020 [hep-ph/0202089]. [11]or a recent review, see e.g., M. Schmaltz, Nucl. Phys.Proc. Suppl. 117 (2003) 40 [hep-ph/0210415]. [12]E. Katz, J. Lee, A.E. Nelson, and D.G. Walker, hepph/0312287. [13]M. Beneke, I. Efthymiopoulos, M.L. Mangano, et al., hepph/0003033. [14]D.O. Carlson and C.-P. Yuan, hep-ph/9211289. [15]R. Frey, D. Gerdes, and J. Jaros, hep-ph/9704243. [16]G. Eilam, J.L. Hewett, and A. Soni, Phys. Rev. D 44(1991) 1473; W.S. Hou, Phys. Lett. B 296 (1992) 179; K.Agashe and M. Graesser, Phys. Rev. D 54 (1996) 4445;M. Hosch, K. Whisnant, and B.L. Young, Phys. Rev. D56 (1997) 5725. [17]C.S. Li, R.J. Oakes, and J.M. Yang, Phys. Rev. D 49(1994) 293, Erratum-ibid. D 56 (1997) 3156; G. Couture,C. Hamzaoui, and H. Koenig, Phys. Rev. D 52 (1995)1713; G. Couture, M. Frank, and H. Koenig, Phys. Rev.D 56 (1997) 4213; G.M. de Divitiis, et al., Nucl. Phys. B 504 (1997) 45. [18]B. Mele, S. Petrarca, and A. Soddu, Phys. Lett. B 435(1998) 401. [19]B. Mele, hep-ph/0003064. [20]J.M. Yang and C.S. Li, Phys. Rev. D 49 (1994) 3412,Erratum, ibid. D 51 (1995) 3974; J.G. Inglada, hepph/9906517. [21]L.R. Xing, W.G. Ma, R.Y. Zhang, Y.B. Sun, and H.S.Hou, Commun. Theor. Phys. (Beijing, China) 41 (2004)241. [22]L.R. Xing, W.G. Ma, R.Y. Zhang, Y.B. Sun, and H.S.Hou, Commun. Theor. Phys. (Beijing, China) 40 (2003)171. [23]T. Han, H.E. Logan, B. McElrath, and L.T. Wang, Phys.Rev. D 67 (2003) 095004. [24]I. Low, W. Skiba, and D. Smith, Phys. Rev. D 66 (2002)072001. [25]T. Han, H.E. Logan, B. McElrath, and L.T. Wang, hepph/0302188. [26]A.J. Buras, A. Poschenrieder, and S. Uhlig, hepph/0410309. [27]S. Eidelman, et al., Phys. Lett. B 592 (2004) 1. [28]F. Legerlehner, DESY 01-029, hep-ph/0105283.     

Comment on "Wide-field coherent anti-Stokes Raman scattering microscopy with non-phase-matching illumination"

We comment on a Letter by Toytman et al. [Opt. Lett.32, 1941 (2007)] in which a novel setup for wide-field imaging in coherent anti-Stokes Raman scattering (CARS) microscopy is demonstrated. There the authors state that our phase-matching implementation of a wide-field CARS system [Appl. Phys. Lett.84, 816 (2004); New J. Phys.8, 36 (2006)] suffers from a strong background from the bulk medium. However, our results show quite the contrary, i.e., that our setup provides a very good signal contrast, due to an almost vanishing background level from the bulk solvent.     

Parameter identification of chaos system based on unknown parameter observer

Parameter identification of chaos system based on unknown parameter observer is discussed generally. Based on the work of Guan et al. [X.P. Guan, H.P. Peng, L.X. Li, et al., Acta Phys. Sinica 50 (2001) 26], the design of unknown parameter observer is improved. The application of the improved approach is extended greatly. The works in some literatures [X.P. Guan, H.P. Peng, L.X. Li, et al., Acta Phys. Sinica 50 (2001) 26; J.H. Lü, S.C. Zhang, Phys. Lett. A 286 (2001) 148; X.Q. Wu, J.A. Lu, Chaos Solitons Fractals 18 (2003) 721; J. Liu, S.H. Chen, J. Xie, Chaos Solitons Fractals 19 (2004) 533] are only the special cases of our Corollaries 1 and 2. Some observers for Lü system and a new chaos system are designed to test our improved method, and simulations results demonstrate the effectiveness and feasibility of the improved approach.     

Formation times of RbHe exciplexes on the surface of superfluid versus normal fluid helium nanodroplets

Nanodroplets of either superfluid 4He or normal fluid 3He are doped with Rb atoms that are bound to the surface of the droplets. The formation of RbHe exciplexes upon 5P(3/2) excitation is monitored in real time by femtosecond pump-probe techniques. We find formation times of 8.5 and 11.6 ps for Rb 4He and Rb 3He, respectively. A comparison to calculations based on a tunneling model introduced for these systems by Reho et al. [J. Chem. Phys. 113, 9694 (2000)]] shows that the proposed mechanism cannot account for our findings. Apparently, a different relaxation dynamics of the superfluid opposed to the normal fluid surface is responsible for the observed formation times.     

Predissociation induced by ungerade-gerade symmetry breaking in 6Li7Li molecule

In the recent sub-Doppler experiment on the B1Pi(u) state of the Li2 molecule by Bouloufa et al. [J. Chem. Phys. 111, 1926 (1999)], where the dissociation of vibrational levels due to the tunneling through the potential barrier was investigated, several vibrational levels with abnormally large dissociated rates were observed in the case of the 6Li7Li isotopomer. This dynamical effect cannot be explained by tunneling as in the case of 6Li2 or 7Li2. A simple model of coupling between B1Pi(u) and 1(1)Pi(g) states involving the u-g symmetry breaking for 6Li7Li is proposed. Rates of the B1Pi(u) predissociated levels due to this coupling are calculated. A good agreement with the experiment is found.     

Spectra of sonoluminescent rare-Gas bubbles

Sonoluminescence spectra of the heavy rare gases are calculated by combining the Hilgenfeldt et al. model of sonoluminescence [Phys. Fluids 11, 1318 (1999)] with quantum line-shape calculations of electron-neutral-atom bremsstrahlung spectra [L. Frommhold, Phys. Rev. E 58, 1899 (1998)]. Good agreement between theoretical and experimental spectra is obtained by choosing values of the ambient radius R0 and acoustic pressure amplitude P(a) that are compatible with diffusive equilibrium calculations.     

High pressure Raman spectroscopy of single-walled carbon nanotubes: Effect of chemical environment on individual nanotubes and the nanotube bundle

The pressure-induced tangential mode Raman peak shifts for single-walled carbon nanotubes (SWNTs) have been studied using a variety of different solvents as hydrostatic pressure-transmitting media. The variation in the nanotube response to hydrostatic pressure with different pressure transmitting media is evidence that the common solvents used are able to penetrate the interstitial spaces in the nanotube bundle. With hexane, we find the surprising result that the individual nanotubes appear unaffected by hydrostatic pressures (i.e. a flat Raman response) up to 0.7 GPa. Qualitatively similar results have been obtained with butanol. Following the approach of Amer et al. [J. Chem. Phys. 121 (2004) 2752], we speculate that this is due to the inability of SWNTs to adsorb some solvents onto their surface at lower pressures. We also find that the role of cohesive energy density in the solvent-nanotube interaction is more complex than previously thought.     

Study of thermal properties of the metastable supersaturated vapor with the restricted ensemble

The pressure and internal energy data at different densities of the supersaturated Argon vapor at the reduced temperatures 0.7 and 0.8 are obtained by the restricted canonical ensemble Monte Carlo simulation method [D.S. Corti, P. Debenedetti, Chem. Eng. Sci. 49 (1994) 2717]. In order to maintain the system in its one-phase state, different constraints on the density fluctuations have been imposed, varying with densities approaching and beyond the spinodal. The results are comparable with a molecular dynamics simulation study [A. Linhart, C.C. Chen, J. Vrabec, H. Hasse, J. Chem. Phys. 122 (2005) 144506] on the same system. The current study verifies the conclusion drawn by the simulation work that clustering of Argon atoms exists even in the vicinity of the spinodal. Compared with molecular dynamics simulations, our method can give the equilibrium properties of a metastable fluid, for example internal energies.     

Temporal electronic structure of non-resonant Raman excited virtual state of P-nitroaniline by 514 nm excitation via bond polarisabilities

We have studied the temporal bond polarisabilities of para-nitroaniline from the Raman intensities by the algorithm proposed by Wu et al.in 1987 (Tian B,Wu G,Liu G 1987 J.Chem.Phys.87 7300).The bond polarisabilities provide much information concerning the electronic structure of the non-resonant Raman excited virtual state.At the initial moment by the 514.5 nm excitation,the tendency of the excited electrons (mapped out by the bond polarisabilities) is to spread to the molecular periphery,and the electronic structure of the Raman virtual state is close to the pseudo-quinonoidic state.When the final stage of relaxation is approached,the bond polarisabilities of those peripheral bonds relax faster than those closer to the molecular core,the phenyl ring.The molecule is in the benzenoidic form as demonstrated by the bond polarisabilities after relaxation.     

Phase transition of traffic states with on-ramp

We study the phase transition on a highway in a modified anisotropic continuum model with an on-ramp, which is recently developed by Gupta and Katiyar (J. Phys. A: Math. Nucl. Gen. 38 (2005) 4069]. To investigate whether this model can describe several distinct traffic states that are identified from real-traffic data [Kerner and Rehborn, Phys. Rev. Lett. 79 (1997) 4030; Kerner, Phys. Rev. Lett. 81 (1998) 3797], we carry out numerical simulations with an open boundary condition. The observed transition between free flow and various types of congested flow such as localized clusters, stop-and-go traffic and different kinds of synchronized traffic flow is obtained by applying a triggering pulse through an on-ramp in our simulation.We present the phase diagram for three representative values of the upstream boundary flux and for the whole range of the on-ramp flux. Several states like pinned localized cluster, triggered stop-and-go, recurring hump state, the oscillatory congested traffic and the homogeneous congested traffic are observed in phase transition from free flow to traffic-jam state. The phase diagram for our model near on-ramp is consistent with the results obtained by Lee et al. [Phys. Rev. E 59(5) (1999) 5101]. The results suggest that the modified model is able to describe all the three phases of traffic-flow theory developed by Kerner [Physica A 333 (2004) 379].     

Re-study of Nucleon Pole Contribution in J/

[1]V.D.Burkert,Phys.Lett.B 72 (1997) 109. [2]S.Capstick and W.Roberts,Prog.Part.Nucl.Phys.45 (2000) S241,and references therein. [3]B.S.Zou,Nucl.Phys.A 675 (2000) 167c; B.S.Zou,Nucl.Phys.A 684 (2001) 330; BES Collaboration (J.Z.Bai,et al.) Phys.Lett.B 510 (2001) 75; BES Collaboration (M.Ablikim,et al.),hep-ex/0405030. [4]R.Sinha and Susumu Okubo,Phys.Rev.D 30 (1984)2333. [5]W.H.Liang,P.N.Shen,B.S.Zou,and A.Faessler,Euro.Phys.J A 21 (2004) 487. [6]Particle Data Group,Euro.Phys.J.C 15 (2000) 1. [7]K.Tsushima,A.Sibrtsev,and A.W.Thomas,Phys.Lett.B 390 (1997) 29. [8]J.Kogut,Rev.Mod.Phys.51 (1979) 659; Rev.Mod.Phys.55 (1983) 775. [9]Q.Haider and L.C.Liu,J.Phys.G 22 (1996) 1187; L.C.Liu and W.X.Ma,J.Phys.G 26 (2000) L59. [10]V.G.J.Stoks,R.A.M.Klomp,C.P.F.Terheggen,and J.J.de Swart,Phys.Rev.C 49 (1994) 2950. [11]H.Haberzettl,C.Bennhold,T.Mart,and T.Feuster,Phys.Rev.C 58 (1998) R40. [12]Y.Oh,A.I.Titov,and T.-S.H.Lee,Phys.Rev.C 63(2001) 25201.     

Influence of geometry on light harvesting in dendrimeric systems. II. nth-nearest neighbor effects and the onset of percolation

We explore the effect of imposing different constraints (biases, boundary conditions) on the mean time to trapping (or mean walklength) for a particle (excitation) migrating on a finite dendrimer lattice with a centrally positioned trap. By mobilizing the theory of finite Markov processes, we are able to obtain exact analytic expressions for site-specific walklengths as well as the overall walklength for both nearest-neighbor and second-nearest-neighbor displacements. This allows the comparison with and generalization of earlier results [A. Bar-Haim, J. Klafter, J. Phys. Chem. B 102 (1998) 1662; A. Bar-Haim, J. Klafter, J. Lumin. 76, 77 (1998) 197; O. Flomenbom, R.J. Amir, D. Shabat, J. Klafter, J. Lumin. 111 (2005) 315; J.L. Bentz, F.N. Hosseini, J.J. Kozak, Chem. Phys. Lett. 370 (2003) 319]. A novel feature of this work is the establishment of a connection between the random walk models studied here and percolation theory. The full dynamical behavior was also determined via solution of the stochastic master equation, and the results obtained compared with recent spectroscopic experiments.     

Rotational energy surface and quasiclassical analysis of the rotational energy level cluster formation in the ground vibrational state of PH3

We report and substantiate a method for constructing the rotational energy surface (RES) of a molecule as a pure classical object. For an arbitrary molecule we start from the potential energy surface rather than from a conventional “effective Hamiltonian”. The method is used for constructing the RES of the PH₃ molecule in its ground vibrational state. We have used an ab initio potential energy surface [D. Wang, Q. Shi, Q.-S. Zhu, J. Chem. Phys. 112 (2000) 9624-9631; S.N. Yurchenko, M. Carvajal, P. Jensen, F. Herregodts, T.R. Huet, Chem. Phys. 290 (2003) 59-67.]. The shape of the RES is shown not to change for J from 0 to 120. The procedure of quasiclassical quantization of the RES was also undertaken, yielding a set of quasiclassical critical values of the angular momentum. The results explain the structure of quantum rotational energy levels obtained by variational calculations [S.N. Yurchenko, W. Thiel, S. Patchkovskii, P. Jensen, Phys. Chem. Chem. Phys. 7 (2005) 573-582].     

Neutralization and Detachment in H^＋-H^- Collisions

The cross sections for neutralization and detachment in H^＋-H^- collisions in the energy range from 1.0 to lOO keV/u are calculated using the two-centre atomic orbital close-coupling （TC-AOCC） method. The results are compared with the available experimental and theoretical data. It is found that the neutralization cross section agrees well with the experimental data by Schon et al. [3. Phys. B 20 （1987） L759] and Melchert et al., [J. Phys. B 32 （1999） L139] especially at low energies. However, for the detachment process, our calculated cross section lies between the experimental data by Melchert et al. and by Peart et al. [J. Phys. B 9 （1976） 3047] for the energy below 15keV/u. Above this energy, our result is smaller than the two experimental data. It is worth pointing out that there exists a large difference between these two experimental data and it is difficult to judge which data is more accurate. Therefore, a high-precision measurement for detachment cross sections is expected to resolve this discrepancy and to test the theoretical calculations.     

Asymmetrically doped one-dimensional trans-polymers

More than 30 years ago [H. Shirakawa, E.J. Louis, A.G. MacDiarmid, C.K. Chiang, A.J. Heeger, J. Chem. Soc. Chem. Comm. 578 (1977); S. Etemad, A.J. Heeger, Ann. Rev. Phys. Chem. 33 (1982) 443] it was discovered that doped trans-polyacetylene (CH)_x, a one-dimensional (1D) conjugated polymer, exhibits electrical conductivity. In this work we show that an asymmetrically doped 1D trans-polymer has non-conventional properties, as compared to symmetrically doped systems. Depending on the level of asymmetry between the chemical potentials of the two involved fermionic species, the polymer can be in a partially or fully spin polarized state. Some possible experimental consequences of doped 1D trans-polymers used as 1D organic polarized conductors are discussed.