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61.
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We present a measurement of the time-dependent CP-violating asymmetry in B(s)(0) → J/ψ? decays, using data collected with the LHCb detector at the LHC. The decay time distribution of B(s)(0) → J/ψ? is characterized by the decay widths Γ(H) and Γ(L) of the heavy and light mass eigenstates, respectively, of the B(s)(0) - B(s)(0) system and by a CP-violating phase ?(s). In a sample of about 8500 B(s)(0) → J/ψ? events isolated from 0.37 fb(-1) of pp collisions at sqrt[s] = 7 TeV, we measure ?(s) = 0.15 ± 0.18(stat) ± 0.06(syst) rad. We also find an average B(s)(0) decay width Γ(s) ≡ (Γ(L) + Γ(H))/2 = 0.657 ± 0.009(stat) ± 0.008(syst) ps(-1) and a decay width difference ΔΓ(s) ≡ Γ(L) - Γ(H) = 0.123 ± 0.029(stat) ± 0.011(syst) ps(-1). Our measurement is insensitive to the transformation (?(s),ΔΓ(s)) ? (π - ?(s), -ΔΓ(s)).  相似文献   
63.
We use time-resolved x-ray diffraction and magneto-optical Kerr effect to study the laser-induced antiferromagnetic to ferromagnetic phase transition in FeRh. The structural response is given by the nucleation of independent ferromagnetic domains (τ(1)~30 ps). This is significantly faster than the magnetic response (τ(2)~60 ps) given by the subsequent domain realignment. X-ray diffraction shows that the two phases coexist on short time scales and that the phase transition is limited by the speed of sound. A nucleation model describing both the structural and magnetic dynamics is presented.  相似文献   
64.
The time-resolved magnetic response of ultrathin epitaxial Fe(001) films grown on GaAs(001) and covered by Au, Pd, and Cr capping layers was investigated by time and spatially resolved Kerr effect measurements. The magnetization was excited by an in-plane magnetic field pulse using the transient internal field generated at a Schottky barrier while the wavelength of the excitation (resonant mode) was roughly 4 microm. Each of the three cap layers affected the spin relaxation in a unique way. Au cap layers resulted in the bulk Gilbert damping of the Fe film. Pd cap layers caused an additional Gilbert damping due to spin-pump or spin-sink effects. Cr cap layers lead to a strong extrinsic damping which can be described by two-magnon scattering. In this case the strength of the extrinsic damping can be controlled by a field induced shift of the spin wave manifold with respect to the excited k vector.  相似文献   
65.
We present a design study of 3D photonic poly‐Si microarchitectures on 2 µm periodically textured glass substrates for application as absorber layers in crystalline Si thin‐film solar cells. Different arrays of microholes and microcones were fabricated in a low‐cost process, by combining high rate electron beam evaporation, nanoimprint technology and self‐organized solid phase crystallization. Two promising designs exhibiting strong absorption enhancement were identified by optical analysis. High angular acceptance and calculated maximum achievable short‐circuit current density of 27.6 mA/cm2 for an effective Si thickness of 1.1 µm highlight the optical potential of these microarchitectures as broadband absorbers in polycrystalline Si thin‐film solar cells.

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Structured emission spectra have been observed from ND3 excited at 2139 Å and 2144 Å. The emission is short-lived (τ12 < 10?10 s) and has been assigned to the ND3(A) → ND3(X) fluorescence transition.  相似文献   
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69.
The palladium-catalyzed heteroannulation of N-carbobenzyloxy-o-iodoanilines with 1-phenylthio-1,3-butadiene afforded indolines 7, which were oxidized with DDQ to produce vinylogous 2-(phenylthio)indoles 8. The latter compounds underwent highly regioselective Diels-Alder cycloadditions with methyl propiolate in the presence of MeAlCl(2) or AlCl(3), with simultaneous elimination of benzenethiol, to afford methyl N-(carbobenzyloxy)carbazole-3-carboxylates 9 and, in some cases, the N-deprotected derivatives 11. This is the opposite regiochemistry of that observed previously with the corresponding sulfone analogues of 8. Thus, the regiochemistry of the cycloaddition can be effectively controlled by appropriate choice of oxidation state of the diene sulfur substituent.  相似文献   
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