Performance analysis of prioritized parallel transmission MAC protocol in all‐IP wireless WAN

Prioritized parallel transmission MAC (PPTM) protocol is proposed for all‐IP wireless wide area network (WAN). In this paper, we analyse its performance and compare it with modified channel load sensing protocol (MCLSP). We model PPTM as a non‐preemptive priority queueing system and obtain a close form of transmission time delay for each priority class, throughput of the scheme, and number of packets in the queue in the Poisson arrival case. We find that PPTM achieves less transmission time delay than MCLSP does for high priority data. Hence, the overall performance of the system using PPTM is significantly improved. We verify the conclusions with simulation via a simplified all‐IP wireless WAN. Copyright © 2006 John Wiley & Sons, Ltd.     

塔里木盆地中央隆起带：新元古代造山型基底拼合带——来自深钻孔的碎屑记录证据

在塔里木盆地巴楚隆起,新近有同1井、夏河1井和巴探5井在寒武系碳酸盐岩之下钻遇碎屑沉积岩。在对碎屑岩进行详细岩相学观测、碎屑组分统计和地球化学分析的基础上,深入探讨了碎屑岩源区及其形成的构造环境。砾岩和砂岩碎屑组成与泥岩地球化学特征共同表明,这3口井寒武系碳酸盐岩之下的碎屑岩物源区包括沉积岩、火成岩和变质岩,以中酸性火山岩和侵入岩为主。砾石及砂岩中碎屑颗粒棱角状-次圆状的外貌、砾石中易磨蚀风化组分（碳酸盐岩和片岩）的存在以及泥岩较低的Th/U比值都反映这些碎屑岩为成熟度较低的近源堆积物。通过碎屑成分、地球化学特征和碎屑锆石年龄结构对比,确定这些碎屑岩的碎屑组分主要源自其下伏基底。砾岩和砂岩碎屑模式、泥岩地球化学特征及碎屑锆石原位微量元素分析结果表明,碎屑源区（即下伏基底）在新元古代（峰期约790~730 Ma）处于大陆边缘弧构造环境。本文新获取的碎屑记录证据与前人对同1井底安山岩、英安岩及卡塔克隆起上塔参1井底闪长岩、花岗闪长岩形成时代及构造环境的研究结论完全一致,表明横亘塔里木盆地中部的中央隆起带是一条新元古代大陆边缘弧,塔里木盆地的基底是由新元古代造山作用形成的拼合基底。     

Peripheral Nerve‐Derived Matrix Hydrogel Promotes Remyelination and Inhibits Synapse Formation

Regeneration of injured nerve tissues requires intricate interplay of complex processes like axon elongation, remyelination, and synaptic formation in a tissue‐specific manner. A decellularized nerve matrix‐gel (DNM‐G) and a decellularized spinal cord matrix‐gel (DSCM‐G) are prepared from porcine sciatic nerves and spinal cord tissue, respectively, to recapitulate the microenvironment cues unique to the native tissue functions. Using an in vitro dorsal root ganglion–Schwann cells coculture model and proteomics analysis, it is confirmed that DNM‐G promotes far stronger remyelination activity and reduces synapse formation of the regenerating axons in contrast to DSCM‐G, Matrigel, and collagen I, consistent with its tissue‐specific function. Bioinformatics analysis indicates that the lack of neurotrophic factors and presence of some axon inhibitory molecules may contribute to moderate axonal elongation activity, while laminin β2, Laminin γ1, collagens, and fibronectin in DNM‐G promote remyelination. These results confirm that DNM‐G is a promising matrix material for peripheral nerve repair. This study provides more insights into tissue‐specific extracellular matrix components correlating to biological functions supporting functional regeneration.     

Remote‐Loaded Platelet Vesicles for Disease‐Targeted Delivery of Therapeutics

The recent emergence of biomimetic nanotechnology has facilitated the development of next‐generation nanodelivery systems capable of enhanced biointerfacing. In particular, the direct use of natural cell membranes can enable multivalent targeting functionalities. Herein, this study reports on the remote loading of small molecule therapeutics into cholesterol‐enriched platelet membrane‐derived vesicles for disease‐targeted delivery. Using this approach, high loading yields for two model drugs, doxorubicin and vancomycin, are achieved. Leveraging the surface markers found on platelet membranes, the resultant nanoformulations demonstrate natural affinity toward both breast cancer cells and methicillin‐resistant Staphylococcus aureus. In vivo, this translates to improved disease targeting, increasing the potency of the encapsulated drug payloads compared with free drugs and the corresponding nontargeted nanoformulations. Overall, this work demonstrates that the remote loading of drugs into functional platelet membrane‐derived vesicles is a facile means of fabricating targeted nanoformulations, an approach that can be easily generalized to other cell types in the future.     

Nickel@Nickel Oxide Core–Shell Electrode with Significantly Boosted Reactivity for Ultrahigh‐Energy and Stable Aqueous Ni–Zn Battery

The main bottlenecks of aqueous rechargeable Ni–Zn batteries are their relatively low energy density and poor cycling stability, mainly arising from the low capacity and inferior reversibility of the current Ni‐based cathodes. Additionally, the complicated and difficult‐to‐scale preparation procedures of these cathodes are not promising for large‐scale energy storage. Here, a facile and cost‐effective ultrasonic‐assisted strategy is developed to efficiently activate commercial Ni foam as a robust cathode for a high‐energy and stable aqueous rechargeable Ni–Zn battery. 3D Ni@NiO core–shell electrode with remarkably boosted reactivity and an area of 300 cm² is readily obtained by this ultrasonic‐assisted activation method (denoted as SANF). Benefiting from the in situ formation of electrochemically active NiO and porous 3D structure with a large surface area, the as‐fabricated SANF//Zn battery presents ultrahigh capacity (0.422 mA h cm^?2) and excellent cycling durability (92.5% after 1800 cycles). Moreover, this aqueous rechargeable SANF//Zn battery achieves an impressive energy density of 15.1 mW h cm^?3 (0.754 mW h cm^?2) and a peak power density of 1392 mW cm^?3, outperforming most reported aqueous rechargeable energy‐storage devices. These findings may provide valuable insights into designing large‐scale and high‐performance 3D electrodes for aqueous rechargeable batteries.     

Lateral‐Polarity Structure of AlGaN Quantum Wells: A Promising Approach to Enhancing the Ultraviolet Luminescence

Aluminum‐gallium‐nitride alloys (Al _x Ga_{1– x} N, 0 ≤ x ≤ 1) can emit light covering the ultraviolet spectrum from 210 to 360 nm. However, these emitters have not fulfilled their full promise to replace the toxic and fragile mercury UV lamps due to their low efficiencies. This study demonstrates a promising approach to enhancing the luminescence efficiency of AlGaN multiple quantum wells (MQWs) via the introduction of a lateral‐polarity structure (LPS) comprising both III and N‐polar domains. The enhanced luminescence in LPS is attributed to the surface roughening, and compositional inhomogeneities in the N‐polar domain. The space‐resolved internal quantum efficiency (IQE) mapping shows a higher relative IQE in N‐polar domains and near inversion domain boundaries, providing strong evidence of enhanced radiative recombination efficiency in the LPS. These experimental observations are in good agreement with the theoretical calculations, where both lateral and vertical band diagrams are investigated. This work suggests that the introduction of the LPS in AlGaN‐based MQWs can provide unprecedented tunability in achieving higher luminescence performance in the development of solid state light sources.     

DOA estimation for sparse nested MIMO radar with velocity receive sensor array

Direction of arrival (DOA) estimation for sparse nested MIMO radar with velocity receive sensor array is studied, and an algorithm based on extended unitary root multiple signal classification (MUSIC) is proposed. The nested MIMO radar utilizes sparse transmit array and velocity receive array with nested inter-element distances, which can make the final virtual array to be a long and sparse velocity sensor array. After exploiting unitary transformation to transform the data into real-valued one, an extended root MUSIC based method is developed to decompose the angle estimation into high-resolution but ambiguous and low-resolution but unambiguous DOA estimations, which are automatically paired. Thereafter, the ambiguous estimation is used to recover all possible DOAs, and the unambiguous DOA estimation is used as a reference to resolve the estimation ambiguity problem. Compared to conventional methods, the proposed algorithm requires no peak search, maintains larger aperture and achieves better DOA estimation performance. The simulation results verify the effectiveness of our approach.     

π‐Conjugated Molecules Crosslinked Graphene‐Based Ultrathin Films and Their Tunable Performances in Organic Nanoelectronics

Graphene‐based ultrathin films with tunable performances, controlled thickness, and high stability are crucial for their uses. The currently existing protocols, however, could hardly simultaneously meet these requirements. Using amino‐substituted π‐conjugated compounds, including 1,4‐diaminobenzene (DABNH2), benzidine (BZDNH2), and 5,10,15,20‐tetrakis (4‐aminophenyl)‐21H,23H‐porphine (TPPNH2), as cross‐linkages, a new protocol through which graphene oxide (GO) nanosheets can be anchored on solid supports with a high stability and controlled thickness via a layer‐by‐layer method is presented. A thermal annealing leads to the reduction of the films, and the qualities of the samples can be inherited by the as‐produced reduced GO films (RGO). When RGO films are integrated as source/drain electrodes in OFETs, tunable performances can be realized. The devices based on the BZDNH2‐crosslinked RGO electrodes exhibit similar electrical behaviors as those based on the non‐π‐conjugated compound crosslinked electrodes, while improved performances can be gained when those crosslinked by DABNH2 are used. The performances can be further improved when RGO films crosslinked by TPPNH2 are employed. This work likely paves a new avenue for graphene‐based films of tunable performances, controlled thickness, and high stability.     

MoO2/Mo2C Heteronanotubes Function as High‐Performance Li‐Ion Battery Electrode

Instead of carbon, Mo₂C is used to modify the MoO₂ material for the first time. The presence of highly conductive and electrochemical inactive Mo₂C decreases the resistance of the charge transport and enhances the structural stability of MoO₂ nanoparticles upon lithiation and delithiation, ensuring the superior cycling stability and high rate capability of the heteronanotubes. Cycled at 200 and 1000 mA g^?1 for 140 cycles, the discharge capacities of the MoO₂/Mo₂C heteronanotubes remain to be 790 and 510 mAh g^?1, respectively. This work demonstrates the potential of the novel heteronanotubes for application as an electrode material for high‐performance Li‐ion batteries.