A Novel Antenna Selection Scheme for Spatially Correlated Massive MIMO Uplinks with Imperfect Channel Estimation

We propose a new antenna selection scheme for a massive MIMO system with a single user terminal and a base station with a large number of antennas. We consider a practical scenario where there is a realistic correlation among the antennas and imperfect channel estimation at the receiver side. The proposed scheme exploits the sparsity of the channel matrix for the effective selection of a limited number of antennas. To this end, we compute a sparse channel matrix by minimising the mean squared error. This optimisation problem is then solved by the well-known orthogonal matching pursuit algorithm. Widely used models for spatial correlation among the antennas and channel estimation errors are considered in this work. Simulation results demonstrate that when the impacts of spatial correlation and imperfect channel estimation introduced, the proposed scheme in the paper can significantly reduce complexity of the receiver, without degrading the system performance compared to the maximum ratio combining.Comment: in Proc. IEEE 81st Vehicular Technology Conference (VTC), May 2015, 6 pages, 5 figure

Controlling Condensate Collapse and Expansion with an Optical Feshbach Resonance

We demonstrate control of the collapse and expansion of an 88Sr Bose-Einstein condensate using an optical Feshbach resonance (OFR) near the 1S0-3P1 intercombination transition at 689 nm. Significant changes in dynamics are caused by modifications of scattering length by up to +- ?10a_bg, where the background scattering length of 88Sr is a_bg = -2a0 (1a0 = 0.053 nm). Changes in scattering length are monitored through changes in the size of the condensate after a time-of-flight measurement. Because the background scattering length is close to zero, blue detuning of the OFR laser with respect to a photoassociative resonance leads to increased interaction energy and a faster condensate expansion, whereas red detuning triggers a collapse of the condensate. The results are modeled with the time-dependent nonlinear Gross-Pitaevskii equation.Comment: 5 pages, 3 figure

(E)-N-Butyl-3-(3,4-dihy­droxy­phen­yl)acryl­amide hemihydrate

In the title compound, C13H17NO3·0.5H2O, a new caffeic acid amide derivative, the solvent water mol­ecule lies on a twofold axis and the terminal ethyl group appears disordered with occupancy factors of 0.525 (6) and 0.475 (6). The benzene ring makes an angle of 17.3 (2)° with the C=C—C—O linker. The presence of an ethyl­enic spacer in the caffeic acid amide mol­ecule allows the formation of a conjugated system, strongly stabilized through π-electron delocalization. The C=C double bond in the linker is trans, similar to those previously reported in caffeic esters. The crystal is stabilized by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds. The mol­ecules of the caffeic acid amide form a supermolecular planar structure through O—H⋯O hydrogen bonds between a hy­droxy group of one caffeic acid mol­ecule and a carbonyl O atom of another. These planes inter­act via C—H⋯O, O—H⋯O and N—H⋯O hydrogen bonds to form a three-dimensional network

Transition metal oxides for high performance sodium ion battery anodes

Sodium-ion batteries (SIBs) are attracting considerable attention with expectation of replacing lithium-ion batteries (LIBs) in large-scale energy storage systems (ESSs). To explore high performance anode materials for SIBs is highly desired subject to the current anode research mainly limited to carbonaceous materials. In this study, a series of transition metal oxides (TMOs) is successfully demonstrated as anodes for SIBs for the first time. The sodium uptake/extract is confirmed in the way of reversible conversion reaction. The pseudocapacitance-type behavior is also observed in the contribution of sodium capacity. For Fe2O3anode, a reversible capacity of 386 mAh g-1at 100 mA g-1 is achieved over 200 cycles; as high as 233 mAhg-1is sustained even cycling at a large current-density of 5 A g-1