Synthesis of MIL-101@g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> nanocomposite for enhanced adsorption capacity towards CO<Subscript>2</Subscript>

MIL-101@g-C₃N₄ nanocomposite was prepared by solvothermal synthesis and used for CO₂ adsorption. The parent materials (MIL-101 and g-C₃N₄) and the MIL-101@g-C₃N₄ were characterized by X-ray diffraction, argon adsorption/desorption, Fourier transform infrared spectroscopy, thermal analysis (TG/DTA), transmission electronic microscopy, and Energy-dispersive X-ray spectroscopy. The results confirmed the formation of well-defined MIL-101@g-C₃N₄ with interesting surface area and pore volume. Furthermore, both MIL-101 and MIL-101@g-C₃N₄ were accomplished in carbon dioxide capture at different temperatures (280, 288, 273 and 298 K) at lower pressure. The adsorption isotherms show that the nanocomposite has a good CO₂ adsorption affinity compared to MIL-101. The best adsorption capacity is about 1.6 mmol g^?1 obtained for the nanocomposite material which is two times higher than that of MIL-101, indicating strong interactions between CO₂ and MIL-101@g-C₃N₄. This difference in efficacy is mainly due to the presence of the amine groups dispersed in the nanocomposite. Finally, we have developed a simple route for the preparation of an effective and new adsorbent for the removal of CO₂, which can be used as an excellent candidate for gas storage, catalysis, and adsorption.     

Physical and electrochemical properties of spherical Li1+x(Ni1/3Co1/3Mn1/3)1−xO2 cathode materials

A (Ni_1/3Co_1/3Mn_1/3)CO₃ precursor with an uniform, spherical morphology was prepared by coprecipitation using a continuously stirred tank reactor method. The as-prepared spherical (Ni_1/3Co_1/3Mn_1/3)CO₃ precursor served to produce dense, spherical Li_1+x(Ni_1/3Co_1/3Mn_1/3)_1−xO₂ (0 ≤ x ≤ 0.15) cathode materials. These Li-rich cathodes were also prepared by a second synthesis route that involved the use of an M₃O₄ (M = Ni_1/3Co_1/3Mn_1/3) spinel compound, itself obtained from the carbonate (Ni_1/3Co_1/3Mn_1/3)CO₃ precursor. In both cases, the final Li_1+x(Ni_1/3Co_1/3Mn_1/3)_1−xO₂ products were highly uniform, having a narrow particle size distribution (10-μm average particle size) as a result of the homogeneity and spherical morphology of the starting mixed-metal carbonate precursor. The rate capability of the Li_1+x(Ni_1/3Co_1/3Mn_1/3)_1−xO₂ electrode materials, which was significantly improved with increased lithium content, was found to be better in the case of the denser materials made from the spinel precursor compound. This result suggests that spherical morphology, high density, and increased lithium content were key factors in enabling the high rate capabilities, and hence the power performances, of the Li-rich Li_1+x(Ni_1/3Co_1/3Mn_1/3)_1−xO₂ cathodes.     

Anti‐Oxygen Leaking LiCoO2

LiCoO₂ is a prime example of widely used cathodes that suffer from the structural/thermal instability issues that lead to the release of their lattice oxygen under nonequilibrium conditions and safety concerns in Li‐ion batteries. Here, it is shown that an atomically thin layer of reduced graphene oxide can suppress oxygen release from Li_xCoO₂ particles and improve their structural stability. Electrochemical cycling, differential electrochemical mass spectroscopy, differential scanning calorimetry, and in situ heating transmission electron microscopy are performed to characterize the effectiveness of the graphene‐coating on the abusive tolerance of Li_xCoO₂. Electrochemical cycling mass spectroscopy results suggest that oxygen release is hindered at high cutoff voltage cycling when the cathode is coated with reduced graphene oxide. Thermal analysis, in situ heating transmission electron microscopy, and electron energy loss spectroscopy results show that the reduction of Co species from the graphene‐coated samples is delayed when compared with bare cathodes. Finally, density functional theory and ab initio molecular dynamics calculations show that the rGO layers could suppress O₂ formation more effectively due to the strong C? O_cathode bond formation at the interface of rGO/LCO where low coordination oxygens exist. This investigation uncovers a reliable approach for hindering the oxygen release reaction and improving the thermal stability of battery cathodes.     

ESSPR: an efficient secure routing scheme based on searchable encryption with vehicle proxy re-encryption for vehicular peer-to-peer social network

In this paper, we propose an Efficient Secure routing Scheme based on searchable encryption with vehicle Proxy Re-encryption, called ESSPR, for achieving privacy preservation of message in vehicular peer-to-peer social network (VP2PSN). Specifically, the proposed ESSPR scheme consists of six phases: system initializations phase, peer registration phase, document generation phase, document forwarding phase, vehicle proxy re-encryption phase, and document receiving phase. Based on rationale of QoS-based clustering strategy, public key encryption with keyword search, identity based aggregate signature, and proxy re-encryption, ESSPR provides privacy for keyword, privacy for resources, and authentication and data integrity of the demand’s source. In addition, ESSPR is robust against eavesdropping attack, wormhole attack, packet analysis attack, packet tracing attack, and replay attack. Through performance evaluation, we demonstrate the effectiveness of ESSPR in terms of delivery ratio, average delay, average fairness, and detection ratio under malicious peers proportions in VP2PSN.     

Fused ring and linking groups effect on overcharge protection for lithium-ion batteries

The derivatives of 1,3-benzodioxan (DBBD1) and 1,4-benzodioxan (DBBD2) bearing two tert-butyl groups have been synthesized as new redox shuttle additives for overcharge protection of lithium-ion batteries. Both compounds exhibit a reversible redox wave over 4 V vs Li/Li⁺ with better solubility in a commercial electrolyte (1.2 M LiPF₆ dissolved in ethylene carbonate/ethyl methyl carbonate (EC/EMC 3/7) than the di-tert-butyl-substituted 1,4-dimethoxybenzene (DDB). The electrochemical stability of DBBD1 and DBBD2 was tested under charge/discharge cycles with 100% overcharge at each cycle in MCMB/LiFePO₄ and Li₄Ti₅O₁₂/LiFePO₄ cells. DBBD2 shows significantly better performance than DBBD1 for both cell chemistries. The structural difference and reaction energies for decomposition have been studied by density functional calculations.     

Flow modelling of quasi-Newtonian fluids in two-scale fibrous fabrics

Permeability is the fundamental macroscopic material property needed to quantify the flow in a fibrous medium viewed as a porous medium. Composite processing models require the permeability as input data to predict flow patterns and pressure fields. In a previous work, the expressions of macroscopic permeability were derived in a double-scale porosity medium for both Newtonian and generalized Newtonian (shear-thinning) resins. In the linear case, only a microscopic calculation on a representative volume is required, implying as many microscopic calculations as there are representative microscopic volumes in the whole fibrous structure. In the non-linear case, and even when the porous microstructure can be described by a unique representative volume, a large number of microscopic calculations must be carried out as the microscale resin viscosity depends on the macroscopic velocity, which in turn depends on the permeability that results from a microscopic calculation. An original and efficient offline-online procedure was proposed for the solution of non-linear flow problems related to generalized Newtonian fluids in porous media. In this paper, this procedure is generalized to quasi-Newtonian fluids in order to evaluate the effect of extensional viscosity on the resulting upscaled permeability. This work constitutes a natural step forward in the definition of equivalent saturated permeabilities for linear and non-linear fluids.     

Construction and analytical characterization of Prussian-Blue-based carbon paste electrodes and their assembly as oxidase enzyme sensors

This paper reports on the development and characterization of Prussian Blue-modified carbon paste electrodes. New methods of matrix modification with Prussian Blue are reported. Two different carbon pastes have been prepared, using mineral oil or solid paraffin, thus obtaining different types of sensors whose behavior toward the electrochemical reduction of hydrogen peroxide has been fully characterized. Results obtained with Prussian Blue-modified electrodes showed a long operational lifetime, an excellent stability in a wide range of pH (3-9), a high sensitivity, and a fast response time. In addition, the coupling of solid carbon paste modified with Prussian Blue and the enzymes glucose oxidase and choline oxidase led to the assembling of biosensors that showed an optimum working range at alkaline pH.     

Scheduling with accurate communication delay model and scheduler implementation for multiprocessor system-on-chip

In multiprocessor system-on-chip, tasks and communications should be scheduled carefully since their execution order affects the performance of the entire system. When we implement an MPSoC according to the scheduling result, we may find that the scheduling result is not correct or timing constraints are not met unless it takes into account the delays of MPSoC architecture. The unexpected scheduling results are mainly caused from inaccurate communication delays and or runtime scheduler’s overhead. Due to the big complexity of scheduling problem, most previous work neglects the inter-processor communication, or just assumes a fixed delay proportional to the communication volume, without taking into consideration subtle effects like the communication congestion and synchronization delay, which may change dynamically throughout tasks execution. In this paper, we propose an accurate scheduling model of hardware/software communication architecture to improve timing accuracy by taking into account the effects of dynamic software synchronization and detailed hardware resource constraints such as communication congestion and buffer sharing. We also propose a method for runtime scheduler implementation and consider its performance overhead in scheduling. In particular, we introduce efficient hardware and software scheduler architectures. Furthermore, we address the issue of centralized implementation versus distributed implementation of the schedulers. We investigate the pros and cons of the two different scheduler implementations. Through experiments with significant demonstration examples, we show the effectiveness of the proposed approach.