95,200 research outputs found
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Reaction Mechanisms for Long-Life Rechargeable Zn/MnO 2 Batteries
Rechargeable aqueous Zn-ion batteries (ZIBs) are very promising for large-scale grid energy storage applications owing to their low cost, environmentally benign constituents, excellent safety, and relatively high energy density. Their usage, however, is largely hampered by the fast capacity fade. The complexity of the reactions has resulted in long-standing ambiguities of the chemical pathways of Zn/MnO 2 system. In this study, we find that both H + /Zn 2+ intercalation and conversion reactions occur at different voltages and that the rapid capacity fading can clearly be ascribed to the rate-limiting and irreversible conversion reactions at a lower voltage. By limiting the irreversible conversion reactions at â1.26 V, we successfully demonstrate ultrahigh power and long life that are superior to most of the reported ZIBs or even some lithium-ion batteries
An Online Approach to Dynamic Channel Access and Transmission Scheduling
Making judicious channel access and transmission scheduling decisions is
essential for improving performance as well as energy and spectral efficiency
in multichannel wireless systems. This problem has been a subject of extensive
study in the past decade, and the resulting dynamic and opportunistic channel
access schemes can bring potentially significant improvement over traditional
schemes. However, a common and severe limitation of these dynamic schemes is
that they almost always require some form of a priori knowledge of the channel
statistics. A natural remedy is a learning framework, which has also been
extensively studied in the same context, but a typical learning algorithm in
this literature seeks only the best static policy, with performance measured by
weak regret, rather than learning a good dynamic channel access policy. There
is thus a clear disconnect between what an optimal channel access policy can
achieve with known channel statistics that actively exploits temporal, spatial
and spectral diversity, and what a typical existing learning algorithm aims
for, which is the static use of a single channel devoid of diversity gain. In
this paper we bridge this gap by designing learning algorithms that track known
optimal or sub-optimal dynamic channel access and transmission scheduling
policies, thereby yielding performance measured by a form of strong regret, the
accumulated difference between the reward returned by an optimal solution when
a priori information is available and that by our online algorithm. We do so in
the context of two specific algorithms that appeared in [1] and [2],
respectively, the former for a multiuser single-channel setting and the latter
for a single-user multichannel setting. In both cases we show that our
algorithms achieve sub-linear regret uniform in time and outperforms the
standard weak-regret learning algorithms.Comment: 10 pages, to appear in MobiHoc 201
Realization of universal quantum cloning with SQUID qubits in a cavity
We propose a scheme to realize universal quantum cloning machine
(UQCM) with superconducting quantum interference device (SQUID) qubits, embeded
in a high-Q cavity. CNOT operations are derived to present our scheme, and the
two-photon Raman resonance processes are used to increase the operation rate.
Compared with previous works, our scheme has advantages in the experimental
realization and further utilization.Comment: 4 pages, 2 figure
Zero Modes of Matter Fields on Scalar Flat Thick Branes
Zero modes of various matters with spin 0, 1 and 1/2 on a class of scalar
flat thick branes are discussed in this paper. We show that scalar field with
spin 0 is localized on all thick branes without additional condition, while
spin 1 vector field is not localized. In addition, for spin 1/2 fermionic
field, the zero mode is localized on the branes under certain conditions.Comment: 11 pages,no figure
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Structure-Induced Reversible Anionic Redox Activity in Na Layered Oxide Cathode
Anionic redox reaction (ARR) in lithium- and sodium-ion batteries is under hot discussion, mainly regarding how oxygen anion participates and to what extent oxygen can be reversibly oxidized and reduced. Here, a P3-type Na0.6[Li0.2Mn0.8]O2 with reversible capacity from pure ARR was studied. The interlayer O-O distance (peroxo-like O-O dimer, 2.506(3) Å), associated with oxidization of oxygen anions, was directly detected by using a neutron total scattering technique. Different from Li2RuO3 or Li2IrO3 with strong metal-oxygen (M-O) bonding, for P3-type Na0.6[Li0.2Mn0.8]O2 with relatively weak Mn-O covalent bonding, crystal structure factors might play an even more important role in stabilizing the oxidized species, as both Li and Mn ions are immobile in the structure and thus may inhibit the irreversible transformation of the oxidized species to O2 gas. Utilization of anionic redox reaction (ARR) on oxygen has been considered as an effective way to promote the charge-discharge capacity of the layered oxide cathodes for lithium- or sodium-ion batteries. The detailed mechanism of ARR, in particular how crystal structure affects and coordinates with the ARR, is not yet well understood. In the present work, a combination of X-ray and neutron total scattering measurements has been performed to study the structure of the prototype P3-type layered Na0.6[Li0.2Mn0.8]O2 with pure ARR. Unique structural characteristics, rather than prevailing knowledge of covalency of metal-oxygen, enable the stabilization of the crystal structure of Na0.6[Li0.2Mn0.8]O2 along with the ARR. This work suggests that reversible ARR can be manipulated by proper structure designs, thus to achieve high lithium or sodium storage in layered oxide cathodes. For P3-type Na0.6[Li0.2Mn0.8]O2 with relatively weak Mn-O covalent bonding, crystal structure factors play an important role in stabilizing the oxidized species, inhibiting the irreversible transformation of the oxidized species to O2 gas. The finding is important for better design of layered oxide positive materials with higher reversible capacity via the introduction of a reversible anionic redox reaction
A semi-analytical method for nonlinear vibration of Euler-Bernoulli beams with general boundary conditions
This paper presents a new semianalytical approach for geometrically nonlinear vibration analysis of Euler-Bernoulli beams with different boundary conditions. The method makes use of Linstedt-Poincaré perturbation technique to transform the nonlinear governing equations into a linear differential equation system, whose solutions are then sought through the use of differential quadrature approximation in space domain and an analytical series expansion in time domain. Validation of the present method is conducted in numerical examples through direct comparisons with existing solutions, showing that the proposed semianalytical method has excellent convergence and can give very accurate results at a long time interval
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