A Real-Time Error Detection (RTD) architecture and its use for reliability and post-silicon validation for F/F based memory arrays

This work proposes in-situ Real-Time Error Detection (RTD): embedding hardware in a memory array for detecting a fault in the array when it occurs, rather than when it is read. RTD breaks the serialization between data access and error-detection and, thus, it can speed-up the access-time of arrays that use in-line error-correction. The approach can also reduce the time needed to root-cause array related bugs during post-silicon validation and product testing. The paper introduces a two-dimensional error-correction scheme based on RTD and, also, presents a proactive error-correction method that combines RTD with demand-scrubbing. The work describes how to build RTD into a memory array with flip-flops to track in real-time the column-parity. A comparison of the proposed two-dimensional ECC scheme, as compared to single-error-correction-double-error-detection, shows that the RTD design has comparable error-detection-and-correction strength and, depending on the array dimensions and configuration, RTD reduces access time by 4% to 26% at an area and power overhead (negative is a reduction) between -7% to 33% and -42% to 86% respectively.Peer ReviewedPostprint (author's final draft

The troubadour Marcabru and his public

Vanadium(V)-containing oxides show superior intercalation properties for alkaline ions, although the performance of the material strongly depends on its surface morphology. In this work, intercalation activity of LiV$_{3}$O$_{8}$, prepared by a conventional solid state synthesis, is demonstrated for the first time in non-aqueous Li,Na-ion hybrid batteries with Na as negative electrode, and different Na/Li ratios in the electrolyte. In the pure Na-ion cell, one Na per formula unit of LiV$_{3}$O$_{8}$ can be reversibly inserted at room temperature via a two-step process, while further intercalation leads to gradual amorphisation of the material, with a specific capacity of 190 mAhg$^{−1}$ after 10 cycles in the potential window of 0.8–3.4 V. Hybrid Li,Na-ion batteries feature simultaneous intercalation of Li$^+$ and Na$^+$ cations into LiV$_{3}$O$_{8}$, resulting in the formation of a second phase. Depending on the electrolyte composition, this second phase bears structural similarities either to Li$_{0.7}$Na$_{0.7}$V$_{3}$O$_{8}$ in Na-rich electrolytes, or to LiV$_{3}$O$_{8}$ in Li-rich electrolytes. The chemical diffusion coefficients of Na+ and Li+ in crystalline LiV$_{3}$O$_{8}$ are very close, hence explaining the co-intercalation of these cations. As DFT calculations show, once formed, the Li$_{0.7}$Na$_{0.7}$V$_{3}$O$_{8}$-type structure favors intercalation of Na$^+$, whereas the LiV$_{3}$O$_{8}$-type prefers to accommodate Li$^+$ cations

(CaxNd11-x)Ru4O24 (x = 4.175)

Single crystals of the title compound, calcium neodymium ruthenate, (CaxNd11-x)Ru4O24 (x = 4.175), have been grown by the flux method. The structure consists of two crystallographically independent RuO6 octa­hedra, which are isolated from each other and embedded in a matrix composed of the Ca and Nd atoms. There are seven M sites which accommodate the Ca and Nd atoms with different populations. Four M sites at general positions are enriched with Nd, whereas the remaining three M sites on twofold rotation axes are enriched with Ca. The coordination numbers of O atoms to the M sites range from 6 to 9. The mean oxidation state of Ru was estimated at +4.79 from the composition analysis. The title compound is non-centrosymmetric and potentially multiferroic

Anomalous electric conductions in KSbO3-type metallic rhenium oxides

Single crystals of KSbO3-type rhenium oxides, La4Re6O$19, Pb6Re6O19, Sr2Re3O9 and Bi3Re3O11, were synthesized by a hydrothermal method. Their crystal structures can be regarded as a network of three-dimensional orthogonal-dimer lattice of edge-shared ReO6 octahedra. All of them exhibit small magnitude of Pauli paramagnetism, indicating metallic electronic states without strong electron correlations. The resistivity of these rhenates, except Bi3Re3O11, have a temperature dependence of$rho(T)=\rho_{0}+AT^{n}$$(n \approx 1.6)$ in a wide temperature range between 5 K and 300 K, which is extraordinary for three-dimensional metals without strong electron correlations. The resistivity of Bi3Re3O11 shows an anomaly around at 50 K, where the magnetic susceptibility also detects a deviation from ordinary Pauli paramagnetism.Comment: 13 pages, 7 figures. J. Phys. Soc. Japan, in pres

Crystal structures of spinel-type Na2MoO4and Na2WO4 revisited using neutron powder diffraction

Time-of-flight neutron powder diffraction data have been collected from Na2MoO4 and Na2WO4 to a resolution of sin ([theta])/[lambda] = 1.25 Å-1, which is substanti­ally better than the previous analyses using Mo K[alpha] X-rays, providing roughly triple the number of measured reflections with respect to the previous studies [Okada et al. (1974). Acta Cryst. B30, 1872-1873; Bramnik & Ehrenberg (2004). Z. Anorg. Allg. Chem. 630, 1336-1341]. The unit-cell parameters are in excellent agreement with literature data [Swanson et al. (1962). NBS Monograph No. 25, sect. 1, pp. 46-47] and the structural parameters for the molybdate agree very well with those of Bramnik & Ehrenberg (2004). However, the tungstate structure refinement of Okada et al. (1974) stands apart as being conspicuously inaccurate, giving significantly longer W-O distances, 1.819 (8) Å, and shorter Na-O distances, 2.378 (8) Å, than are reported here or in other simple tungstates. As such, this work represents an order-of-magnitude improvement in precision for sodium molybdate and an equally substantial improvement in both accuracy and precision for sodium tungstate. Both compounds adopt the spinel structure type. The Na+ ions have site symmetry .-3m and are in octa­hedral coordination while the transition metal atoms have site symmetry -43m and are in tetra­hedral coordination

Sodium vanadium titanium phosphate electrode for symmetric sodium-ion batteries with high power and long lifespan

Sodium-ion batteries operating at ambient temperature hold great promise for use in grid energy storage owing to their significant cost advantages. However, challenges remain in the development of suitable electrode materials to enable long lifespan and high rate capability. Here we report a sodium super-ionic conductor structured electrode, sodium vanadium titanium phosphate, which delivers a high specific capacity of 147 mA h g−1 at a rate of 0.1 C and excellent capacity retentions at high rates. A symmetric sodium-ion full cell demonstrates a superior rate capability with a specific capacity of about 49 mA h g−1 at 20 C rate and ultralong lifetime over 10,000 cycles. Furthermore, in situ synchrotron diffraction and X-ray absorption spectroscopy measurement are carried out to unravel the underlying sodium storage mechanism and charge compensation behaviour. Our results suggest the potential application of symmetric batteries for electrochemical energy storage given the superior rate capability and long cycle life

Exploring the Ni redox activity in polyanionic compounds as conceivable high potential cathodes for Na rechargeable batteries

Although nickel-based polyanionic compounds are expected to exhibit a high operating voltage for batteries based on the Ni2+/3+ redox couple activity, some rare experimental studies on the electrochemical performance of these materials are reported, resulting from the poor kinetics of the bulk materials in both Li and Na nonaqueous systems. Herein, the electrochemical activity of the Ni2+/3+ redox couple in the mixed-polyanionic framework Na4Ni3(PO4)2(P2O7) is reported for the first time. This novel material exhibits a remarkably high operating voltage when cycled in sodium cells in both carbonate- and ionic liquid-based electrolytes. The application of a carbon coating and the use of an ionic liquid-based electrolyte enable the reversible sodium ion (de-)insertion in the host structure accompanied by the redox activity of Ni2+/3+ at operating voltages as high as 4.8 V vs Na/Na+. These results present the realization of Ni-based mixed polyanionic compounds with improved electrochemical activity and pave the way for the discovery of new Na-based high potential cathode materials

Voltage, Stability and Diffusion Barrier Differences between Sodium-ion and Lithium-ion Intercalation Materials

To evaluate the potential of Na-ion batteries, we contrast in this work the difference between Na-ion and Li-ion based intercalation chemistries in terms of three key battery properties—voltage, phase stability and diffusion barriers. The compounds investigated comprise the layered AMO2 and AMS2 structures, the olivine and maricite AMPO4 structures, and the NASICON A3V2(PO4)3 structures. The calculated Na voltages for the compounds investigated are 0.18–0.57 V lower than that of the corresponding Li voltages, in agreement with previous experimental data. We believe the observed lower voltages for Na compounds are predominantly a cathodic effect related to the much smaller energy gain from inserting Na into the host structure compared to inserting Li. We also found a relatively strong dependence of battery properties on structural features. In general, the difference between the Na and Li voltage of the same structure, ΔVNa–Li, is less negative for the maricite structures preferred by Na, and more negative for the olivine structures preferred by Li. The layered compounds have the most negative ΔVNa–Li. In terms of phase stability, we found that open structures, such as the layered and NASICON structures, that are better able to accommodate the larger Na+ ion generally have both Na and Li versions of the same compound. For the close-packed AMPO4 structures, our results show that Na generally prefers the maricite structure, while Li prefers the olivine structure, in agreement with previous experimental work. We also found surprising evidence that the barriers for Na+ migration can potentially be lower than that for Li+ migration in the layered structures. Overall, our findings indicate that Na-ion systems can be competitive with Li-ion systems.United States. Office of Naval Research (Contract N00014-11-1-0212)United States. Dept. of Energy (Contract DE-FG02 96ER45571)United States. Dept. of Energy (BATT program under Contract DE-AC02-05CH11231