The recent development of the vehicular ad hoc networks (VANETs) has motivated an increasing interest in vehicular services and applications, such as active safety service and the infotainment service. Effective data Dissemination has become more and more important in vehicular services sharing. In this paper, the connectivity characteristics of VANETs are theoretically analyzed and implemented to show the partial connections in vehicle to vehicle communication. Hence, we propose the connectivity-aware data dissemination (CADD) in partially connected VANETs will improve the data transmission capacity. In the CADD protocol, a new metric of the node forwarding capability estimation is introduced. The metric is designed by the combination the throughput function and the active connection time estimation. And then, the high efficiency data dissemination protocol is designed by the new metric. Simulation results show that the CADD protocol outperforms existing solutions in terms of the packet delivery ratio, the transmission delay, and the protocol overhead under the condition of the intermittent network connectivity.
Electrochemically driven carbon dioxide (CO2) conversion is an emerging research field due to the global warming and energy crisis. Carbon monoxide (CO) is one key product during electroreduction of CO2; however, this reduction process suffers from tardy kinetics due to low local concentration of CO2 on a catalyst's surface and low density of active sites. Herein, presented is a combination of experimental and theoretical validation of a Ni porphyrin‐based covalent triazine framework (NiPor‐CTF) with atomically dispersed NiN4 centers as an efficient electrocatalyst for CO2 reduction reaction (CO2RR). The high density and atomically distributed NiN4 centers are confirmed by aberration‐corrected high‐angle annular dark field scanning transmission electron microscopy and extended X‐ray absorption fine structure. As a result, NiPor‐CTF exhibits high selectivity toward CO2RR with a Faradaic efficiency of >90% over the range from ?0.6 to ?0.9 V for CO conversion and achieves a maximum Faradaic efficiency of 97% at ?0.9 V with a high current density of 52.9 mA cm?2, as well as good long‐term stability. Further calculation by the density functional theory method reveals that the kinetic energy barriers decreasing for *CO2 transition to *COOH on NiN4 active sites boosts the performance. 相似文献
Porous carbons, possessing exceptional stability, high surface area, and electric conductivity, are broadly used as superior adsorbent, supporter, or electrode material for environmental protection, industrial catalysis, and energy storage and conversion. The construction of such kinds of materials with designable structures and properties will extremely extend their potential applications, but remains a huge synthetic challenge. Herein, a bottom‐up approach is presented to synthesize one type of fully sp2 carbon–bonded frameworks by transition metal–catalyzed cross‐coupling of different polyphenylenes with electron‐withdrawing 9,9′‐bifluorenylidene (9,9′‐BF) through its 2,7‐position. The resulting porous polymeric carbons exhibit substantial semiconducting properties, such as strong light‐harvesting capabilities in the visible light region, likely due to their π‐extended backbones with donor–acceptor characters. Their electronic and porous structures can be finely tuned via the polyphenylene spacers. The intriguing properties allow these porous carbons to efficiently catalyze dye degradation under visible light or even natural sunlight with high reusability. Meanwhile, associated with their intrinsic structures, these porous carbons also exhibit highly selective degradation activities toward different dyes. In particular, the photodegradation mechanism involving oxygen and electron is elucidated for the first time for such kinds of materials, related to the presence of specific 9,9′‐BF units in their π‐conjugated skeletons. 相似文献
All organic charge‐transporting layer (CTL)‐featured perovskite solar cells (PSCs) exhibit distinct advantages, but their scaling‐up remains a great challenge because the organic CTLs underneath the perovskite are too thin to achieve large‐area homogeneous layers by spin‐coating, and their hydrophobic nature further hinders the solution‐based fabrication of perovskite layer. Here, an unprecedented anchoring‐based coassembly (ACA) strategy is reported that involves a synergistic coadsorption of a hydrophilic ammonium salt CA‐Br with hole‐transporting triphenylamine derivatives to acquire scalable and wettable organic hole‐extraction monolayers for p–i–n structured PSCs. The ACA route not only enables ultrathin organic CTLs with high uniformity but also eliminates the nonwetting problem to facilitate large‐area perovskite films with 100% coverage. Moreover, incorporation of CA‐Br in the ACA strategy can distinctly guarantee a high quality of electronic connection via the cations' vacancy passivation. Consequently, a high power‐conversion‐efficiency (PCE) of 17.49% is achieved for p–i–n structured PSCs (1.02 cm2), and a module with an aperture area of 36 cm2 shows PCE of 12.67%, one of the best scaling‐up results among all‐organic CTL‐based PSCs. This work demonstrates that the ACA strategy can be a promising route to large‐area uniform interfacial layers as well as scaling‐up of perovskite solar cells. 相似文献
Networks and Spatial Economics - Traffic networks are often perturbed by temporal events, which generally cause capacity on the links to drop. A capacity drop can lead to fluctuations in flows and... 相似文献
In this paper a numerical method is given for the solution of linear Fredholm integro-differential equation (FIDE) with piecewise intervals under the mixed conditions using the Bernoulli polynomials. The aim of this article is to present an efficient numerical procedure for solving linear FIDE with piecewise intervals. This method transforms linear FIDE with piecewise intervals and the given conditions into matrix equation which corresponds to a system of linear algebraic equation. Finally, some experiments and their numerical solutions are given. The results reveal that this method is reliable and efficient. 相似文献
Altimeter radar backscatter intensity, in terms of the normalized radar cross section (NRCS), is known to be modulated by surface wind forcing and the state of wind-sea development. Based on a data set of collocated altimeters (including Topex/Poseidon, Jason-1 and Jason-2) and in situ measurements, different responses to various wind speeds and wave ages (i.e. the state of wind-sea development) were illustrated for altimeter dual-frequency NRCSs (Ku-band at 13.6 Hz and C band at 5.4 Hz), which can facilitate the retrieval of wind speed and wave age parameters. A statistical parametric algorithm was developed to retrieve the two dynamic parameters from the altimeter dual-frequency NRCSs using the neutral network method. The wind-sea significant wave height (SWH) was estimated from wind speed and wave age parameters, which partitions the swell SWH from the altimeter SWH measurement. All newly derived parameters were well validated by comparison against in situ buoy measurements. A preliminary application of the method in examining the swell or wind-sea contributions to global waves was performed; it was found the swell dominance in an open ocean, and the wind-sea dominance in marginal and semi-enclosed seas. The methods would benefit other applications such as studies of air–sea interactions, validation of wave model, determination of swell decay rate and studies of wave climate. 相似文献