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Yayın Behavior of quantum fisher information of bell pairs under decoherence channels(Polish Acad Sciences Inst Physics, 2014-02) Özaydın, Fatih; Altıntaş, Azmi Ali; Buğu, Sinan; Yeşilyurt, CanQuantum Fisher information has recently been an essential tool for analyzing the phase sensitivity of the quantum states in various quantum tasks, requiring high precision, such as quantum clock synchronization, positioning and many applications which include quantum interferometers. Due to the interactions with the environment, all quantum systems are subject to various decoherence effects. Therefore the research on quantum Fisher information under decoherence has been recently attracting more attention. In this work, analyzing the quantum Fisher information, we study the phase sensitivity of bipartite quantum correlations, in particular four Bell pairs amplitude damping channels. For a specific Bell state we arrive at similar results of Greenberger-Horne-Zeilinger (GHZ) states (as expected). For the other three Bell states, we present our results which point the interesting behavior of quantum Fisher information with respect to the decoherence rate. We also find the regions where the quantum Fisher information exhibits discontinuities.Yayın Design science perspective on NFC research: Review and research agenda(Slovensko Drustvo Informatika, 2013) Aydın, Mehmet Nafiz; Özdenizci Köse, BüşraNear Field Communication (NFC), as one of the emerging and promising technological developments, provides means to short range contactless communication for mobile phones and other devices alike. NFC has become an attractive design science research area for many academicians due to its exploding growth and its promising applications and related services. A better understanding of the current status of NFC research is necessary to maintain the advancement of knowledge in NFC research and to identify the gap between theory and practice. In this paper, we present a literature review on NFC. To facilitate the analysis of the literature, we propose a research framework and organize the NFC literature into four major categories (theory and development, applications and services, infrastructure, ecosystem). We contend that due to the nature of NFC (industry high stakes, multidisciplinary research, artifacts development), the design science research paradigm serves an appropriate ground to investigate an extent to which relevance and rigor is achieved. By employing the proposed research framework and design science perspective, we set up a research agenda (research directions and promising research questions) which may help practitioners and academics to achieve a substantial progress in NFC.Yayın An essential approach to the architecture of diatomic molecules: 1.Basic theory(Optical Soc Amer, 2004-11) Yarman, Nuh TolgaWe consider the quantum-mechanical description of a diatomic molecule of electronic mass m(0e), internuclear distance R-0, and total electronic energy E-0e. We apply to it the Born-Oppenheimer approximation, together with the relation E(0e)m(0e)R(0)(2) similar to h(2) (which we established previously), written for the electronic description (with fixed nuclei). Our approach yields an essential relationship for T-0,T- the classical vibration period, at the total electronic energy E-0e; i.e., T-0 = [4pi(2)/(rootn(1)n(2)h)] rootgM(0)m(e) R-0(2). Here, At,0 is the reduced mass of the nuclei; m(e) is the mass of the electron; g is a dimensionless and relativistically invariant coefficient. roughly around unity (this quantity is associated with the particular electronic structure under consideration; thus, it remains practically the same for bonds bearing similar electronic configurations); and n(1) and n(2) are the principal quantum numbers of electrons making up the bond(s) of the diatomic molecule in hand: because of quantum defects, they are not integer numbers. The above relationship holds generally, although the quantum numbers n(1) and n(2) need to be refined. This task is undertaken in our next article, yielding a whole new systematization regarding all diatomic molecules.Yayın An essential approach to the architecture of diatomic molecules: 2. how are size, vibrational period of time, and mass interrelated?(Optical Soc Amer, 2004-11) Yarman, Nuh TolgaIn our previous article, we arrived at an essential relationship for T the classical vibrational period of a given diatomic molecule, at the total electronic energy E-, i.e., T = [4pi(2)/(rootn(1)n(2)h)] rootgM(0)m(e) R-2, where M-0 to is the reduced mass of the nuclei; m(3) is the mass of the electron; R is the internuclear distance: g is a dimensionless and relativistically invariant coefficient, roughly around unity; and n(1) and n(2) are the principal quantum numbers of electrons making up the bond(s) of the diatomic molecule, which, because of quantum defects. are not integer numbers. The above relationship holds generally. It essentially yields T similar to R 2 for the classical vibrational period versus the square of the internuclear distance in different electronic states of a given molecule. which happens to be an approximate relationship known since 1925 but not understood until now. For similarly configured electronic states, we determine n(1)n(2) to be R/R-0, where R is the internuclear distance in the given electronic state and R-0 is the internuclear distance in the ground state. Furthermore. from the analysis of H-2 spectroscopic data, we found out that the ambiguous states of this molecule are configured like alkali hydrides and Li-2. This suggests that, quantum mechanically, on the basis of an equivalent H-2 excited state. we can describe well, for example, the ground state of Li-2. On the basis of this interesting finding, herein we propose to associate the quantum numbers n(1) and n2 With the bond electrons of the ground state of any diatomic molecule belonging to a given chemical family in reference to the ground state of a diatomic molecule still belonging to this family but bearing, say, the lowest classical vibrational period, since g, depending only on the electronic configuration. will stay nearly constant throughout. This allows us to draw up a complete systematization of diatomic molecules given that g (appearing to be dependent purely on the electronic structure of the molecule) stays constant for chemically alike molecules and n(1)n(2) can be identified to be R-0/R-00 for diatomic molecules whose bonds are electronically configured in the same way, R-00 then being the internuclear distance of the ground state of the molecule chosen as the reference molecule within the chemical fan-Lily under consideration. Our approach discloses the simple architecture of diatomic molecules, otherwise hidden behind a much too cumbersome quantum-mechanical description. This architecture, telling how the vibrational period of Lime. size. and mass are determined, is Lorentz-invariant and can be considered as the mechanism of the behavior of the quantities in question in interrelation with each other when the molecule is brought into uniform translational motion or transplanted into a gravitational field or, in fact, any field with which it can interact.Yayın Quantum fisher information of bipartitions of W states(Polish Acad Sciences Inst Physics, 2015-04-24) Özaydın, Fatih; Altıntaş, Azmi Ali; Yeşilyurt, Can; Buğu, Sinan; Erol, VolkanWe study the quantum Fisher information (QFI) of W states and W-like states under decoherence. In particular, we find that on the contrary to amplitude damping and depolarizing decoherence, a W-like state of 3 qubits obtained by discarding 1 qubit of a genuine W state of 4 qubits is more robust than a genuine W state of 3 qubits under amplitude amplifying and phase damping decoherence.Yayın Enhancing the W state fusion process with a toffoli gate and a CNOT gate via one-way quantum computation and linear optics(Polish Acad Sciences Inst Physics, 2015-04) Diker, Fırat; Özaydın, Fatih; Arık, MetinCreation of large-scale W state quantum networks is a key step for realization of various quantum information tasks. Regarding the photonics technology, a simple optical setup was proposed for the fusion of two W states. Recently it was shown that via a single Fredkin gate, this basic so-called "fusion setup" can be enhanced. However the main problem was that the probability of success of realization of Fredkin gate with linear optics is too low. In this work, we show that the same enhancement can be made possible via one Toffoli and one CNOT gate, instead of a Fredkin gate. Not only the probability of success of the combination of these two gates is much higher, than that of a single Fredkin gate via linear optics, but also there is another method for implementing our setup with current photonics technology, almost with a unity success probability: A hybrid circuit consisting of a Toffoli gate which can be implemented via one-way quantum computation on a weighted graph state of 8 qubits with a unity success probability and a linear optical CNOT gate which has a success probability close to unity. Therefore the preparation of polarization based encoded multi particle entangled W states of arbitrary sizes becomes considerably more efficient.Yayın Alpha head on collision with a fixed gold nucleus, taking into account the relativistic rest mass variation as implied by mass-energy equivalence(Polish Acad Sciences Inst Physics, 2014-02) Yarman, Nuh Tolga; Arık, Metin; Kholmetskii, Alexander; Altıntaş, Azmi Ali; Özaydın, FatihWe reformulate the Rutherford scattering of alpha particle for a head on collision, taking into account the rest mass variation of the particle, as implied by the energy conservation law. Our relativistic reformulation (which includes the energy conservation) constitutes a new example for the breakdown of the Lorentz invariance. Briefly speaking, even at rest or during the whole scattering process, the distance between the alpha particle and the gold nucleus is not invariant but depends on the frame of the observer attached to either object. According to our relativistic reformulation, we also provide a new set of Lorentz transformations.Yayın An essential approach to the architecture of diatomic molecules. 2. How size, vibrational period of time, and mass are interrelated?(Nauka/Interperiodica, 2004) Yarman, Nuh TolgaIn our previous article, we arrived at an essential relationship for T the classical vibrational period of a given diatomic molecule, at the total electronic energy E-, i.e., T = [4pi(2)/(rootn(1)n(2)h)] rootgM(0)m(e) R-2, where M-0 to is the reduced mass of the nuclei; m(3) is the mass of the electron; R is the internuclear distance: g is a dimensionless and relativistically invariant coefficient, roughly around unity; and n(1) and n(2) are the principal quantum numbers of electrons making up the bond(s) of the diatomic molecule, which, because of quantum defects. are not integer numbers. The above relationship holds generally. It essentially yields T similar to R 2 for the classical vibrational period versus the square of the internuclear distance in different electronic states of a given molecule. which happens to be an approximate relationship known since 1925 but not understood until now. For similarly configured electronic states, we determine n(1)n(2) to be R/R-0, where R is the internuclear distance in the given electronic state and R-0 is the internuclear distance in the ground state. Furthermore. from the analysis of H-2 spectroscopic data, we found out that the ambiguous states of this molecule are configured like alkali hydrides and Li-2. This suggests that, quantum mechanically, on the basis of an equivalent H-2 excited state. we can describe well, for example, the ground state of Li-2. On the basis of this interesting finding, herein we propose to associate the quantum numbers n(1) and n2 With the bond electrons of the ground state of any diatomic molecule belonging to a given chemical family in reference to the ground state of a diatomic molecule still belonging to this family but bearing, say, the lowest classical vibrational period, since g, depending only on the electronic configuration. will stay nearly constant throughout. This allows us to draw up a complete systematization of diatomic molecules given that g (appearing to be dependent purely on the electronic structure of the molecule) stays constant for chemically alike molecules and n(1)n(2) can be identified to be R-0/R-00 for diatomic molecules whose bonds are electronically configured in the same way, R-00 then being the internuclear distance of the ground state of the molecule chosen as the reference molecule within the chemical fan-Lily under consideration. Our approach discloses the simple architecture of diatomic molecules, otherwise hidden behind a much too cumbersome quantum-mechanical description. This architecture, telling how the vibrational period of Lime. size. and mass are determined, is Lorentz-invariant and can be considered as the mechanism of the behavior of the quantities in question in interrelation with each other when the molecule is brought into uniform translational motion or transplanted into a gravitational field or, in fact, any field with which it can interact.
