Crossing the gap from p- to n-type doping: nature of the states near the chemical potential in La(2)-(x)Sr(x)CuO(4) and Nd(2-x)Ce(x)CuO(4-delta)

We report on an x-ray absorption and resonant photoemission study on single crystals of the high-T(c) cuprates La2-xSrxCuO4 and Nd(2-x)Ce(x)CuO(4-delta). Using an intrinsic energy reference, we find that the chemical potential of La2-xSrxCuO4 lies near the top of the La2CuO4 valence band whereas in Nd(2-x)Ce(x)CuO(4-delta) it is situated near the bottom of the Nd2CuO4 conduction band. The data clearly establish that the introduction of Ce in Nd2CuO4 results in electrons being doped into the CuO2 planes. We infer that the states closest to the chemical potential have a Cu 3d(10) singlet origin in Nd(2-x)Ce(x)CuO(4-delta) and a 3d(9)L singlet origin in La2-xSrxCuO4.     

Surface structure of TiO2(011)-(2x1)

A combined experimental and first principles study of the (2x1)-reconstructed rutile TiO2(011) surface is presented. Our results provide evidence that the surface structure is described by a model that includes onefold coordinated (titanyl) oxygen atoms giving rise to double bonded Ti=O species. These species should play a special role in the enhanced photocatalytic activity of the TiO2(011) surface.     

双层钙钛矿锰氧化物Nd_(2-2x)Ca_(1+2x)Mn_2O_7(x=0.4,0.5)的磁相变特性

利用固相反应法制备了Nd2-2x Ca1+2x Mn2O7(x=0.0-0.9)多晶样品,通过FULLPROF程序对样品X射线衍射图谱进行了精修,样品的空间群为14/mmm.测量了样品x=0.4,0.5的磁性(5K相似文献   

Anisotropic magnetoresistance in lightly doped La(2)-(x)Sr(x)CuO(4): impact of antiphase domain boundaries on the electron transport

Detailed behavior of the magnetoresistance (MR) is studied in lightly doped antiferromagnetic La(1.99)Sr(0.01)CuO(4), where, thanks to the weak-ferromagnetic moment due to spin canting, the antiferromagnetic (AF) domain structure can be manipulated by the magnetic field. The MR behavior demonstrates that CuO(2) planes indeed contain antiphase AF-domain boundaries in which charges are confined, forming antiphase stripes. The data suggest that a high magnetic field turns the antiphase stripes into in-phase stripes, and the latter appear to give better conduction than the former, which challenges the notion that the antiphase character of stripes facilitates charge motion.     

Orbital-selective Mott-insulator transition in Ca 2 - x Sr x RuO 4

The electronic structures of the metallic and insulating phases of the alloy series Ca_2-xSr_xRuO₄ ( 0 ? x ? 2) are calculated using LDA, LDA+U and Dynamical Mean-Field Approximation methods. In the end members the groundstate respectively is an orbitally non-degenerate antiferromagnetic insulator (x = 0) and a good metal (x = 2). For x > 0.5 the observed Curie-Weiss paramagnetic metallic state which possesses a local moment with the unexpected spin S = 1/2, is explained by the coexistence of localized and itinerant Ru-4d-orbitals. For 0.2 < x < 0.5 we propose a state with partial orbital and spin ordering. An effective model for the localized orbital and spin degrees of freedom is discussed. The metal-insulator transition at x = 0.2 is attributed to a switch in the orbital occupation associated with a structural change of the crystal. Received 27 July 2001     

Phase Manipulation between c(4 x 2) and p(2 x 2) on the Si(100) surface at 4.2 K

Phase manipulation between c(4x2) and p(2x2) on the Si(100) surface has been demonstrated at 4.2 K for the first time using a low-temperature scanning tunneling microscope. We have discovered that it is possible to change the c(4x2) surface into the p(2x2) surface, artificially, through a flip-flop motion of the buckling dimers by using a sample bias voltage control. Also, scanning at a negative bias voltage or applying a pulse voltage can restore the c(4x2) surface. The STM images as a function of bias voltage and tunneling current reveal the interesting dynamics of the buckling dimers on the long debated surface. Our results will show that energetic tunneling electrons are most likely responsible for the observed phase transition from c(4x2) to p(2x2).     

Strontium diffusion in Sr3−3x La2x □x(VO4)2 solid solutions

Layer-by-layer radiometric analysis in the temperature range 800–950 °C was used to measure the diffusion coefficients of ⁹⁰Sr, ⁴⁵Ca, ¹³³Ba radionuclides in Sr_3−3x La_2x □_x(VO₄)₂ (x=0,0.1,0.15,0.2,0.25) solid solutions. It was established that D _Ca ^* >D _Sr ^* >D _Ba ^* . An increase in the concentrations of vacancies (□) in the strontium sublattice leads to increased coefficients of diffusion of rare-earth metal cations. The activation energies for radionuclide diffusion were determined. It was shown that M²⁺ cations migrate via Sr(2) positions. Fiz. Tverd. Tela (St. Petersburg) 40, 223–226 (February 1998)