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131.
M. -L. Tan Y. H. Qian I. Goldhirsch S. A. Orszag 《Journal of statistical physics》1995,81(1-2):87-103
Many continuum theories for granular flow produce an equation of motion for the fluctuating kinetic energy density (granular temperature) that accounts for the energy lost in inelastic collisions. Apart from the presence of an extra dissipative term, this equation is very similar in form to the usual temperature equation in hydrodynamics. It is shown how a lattice-kinetic model based on the Bhatnagar-Gross-Krook (BGK) equation that was previously derived for a miscible two-component fluid may be modified to model the continuum equations for granular flow. This is done by noting that the variable corresponding to the concentration of one species follows an equation that is essentially analogous to the granular temperature equation. A simulation of an unforced granular fluid using the modified model reproduces the phenomenon of clustering instability, namely the spontaneous agglomeration of particles into dense clusters, which occurs generically in all granular flows. The success of the continuum theory in capturing the gross features of this basic phenomenon is discussed. Some shear flow simulations are also presented. 相似文献
132.
Layered image coding using the DCT pyramid 总被引:2,自引:0,他引:2
A block-based subband image coder that exploits the ability to perform decimation in the discrete cosine transform (DCT) domain to effect a pyramidal data structure is described. The proposed "DCT pyramid" has a distinct feature of improved image rendition properties without the associated blocking artifacts at low bit-rates. 相似文献
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136.
Yanwei Zhu Wenfang Deng Yueming Tan Jianqiao Shi Jingcheng Wu Wenbo Lu Jianfeng Jia Shuangyin Wang Yuqin Zou 《Advanced functional materials》2023,33(45):2304985
Photocatalytic selective oxidation of 5-hydroxymethylfurfural (HMF) coupled H2 production offers a promising approach to producing valuable chemicals. Herein, an efficient in situ topological transformation tactic is developed for producing porous O-doped ZnIn2S4 nanosheets for HMF oxidation cooperative with H2 evolution. Aberration-corrected high-angle annular dark-field scanning TEM images show that the hierarchical porous O-ZIS-120 possesses abundant atomic scale edge steps and lattice defects, which is beneficial for electron accumulation and molecule adsorption. The optimal catalyst (O-ZIS-120) exhibits remarkable performance with 2,5-diformylfuran (DFF) yields of 1624 µmol h−1 g−1 and the selectivity of >97%, simultaneously with the H2 evolution rate of 1522 µmol h−1 g−1. Mechanistic investigations through theoretical calculations show that O in the O-ZIS-120 lattice can reduce the oxidation energy barrier of hydroxyl groups of HMF. In situ attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) results reveal that DFF* (C4H2(CHO)2O*) intermediate has a weak interaction with O-ZIS-120 and desorb as the final product. This study elucidates the topotactic structural transitions of 2D materials simultaneously with electronic structure modulation for efficient photocatalytic DFF production. 相似文献
137.
Yeshu Tan Jianrui Feng Haobo Dong Longxiang Liu Siyu Zhao Feili Lai Tianxi Liu Ying Bai Ivan P. Parkin Guanjie He 《Advanced functional materials》2023,33(4):2209967
Platinum (Pt) is regarded as a promising electrocatalyst for hydrogen evolution reaction (HER). However, its application in an alkaline medium is limited by the activation energy of water dissociation, diffusion of H+, and desorption of H*. Moreover, the formation of effective structures with a low Pt usage amount is still a challenge. Herein, guided by the simulation discovery that the edge effect can boost local electric field (LEF) of the electrocatalysts for faster proton diffusion, platinum nanocrystals on the edge of transition metal phosphide nanosheets are fabricated. The unique heterostructure with ultralow Pt amount delivered an outstanding HER performance in an alkaline medium with a small overpotential of 44.5 mV and excellent stability for 80 h at the current density of −10 mA cm−2. The mass activity of as-prepared electrocatalyst is 2.77 A mg−1Pt, which is 15 times higher than that of commercial Pt/C electrocatalysts (0.18 A mg−1Pt). The density function theory calculation revealed the efficient water dissociation, fast adsorption, and desorption of protons with hybrid structure. The study provides an innovative strategy to design unique nanostructures for boosting HER performances via achieving both synergistic effects from hybrid components and enhanced LEF from the structural edge effect. 相似文献
138.
Qijun Li Yukun Qin Dengke Cheng Ming Cheng Hongjia Zhao Lvzhou Li Songnan Qu Jing Tan Jianning Ding 《Advanced functional materials》2023,33(15):2211013
Moisture-enabled electricity generation (MEG) is highly promising in next-generation energy conversion. However, the practical applications of existing MEG devices are limited due to their low current and voltage outputs, strong dependence on high moisture, and inflexible nature. Herein, an efficient MEG integrated with flexible, all-weather, and scalable fabrication characteristics based on the rational combination of carbonized polymer dots (CPDs) and liquid metal (LM) active electrodes is developed for the first time. Remarkably, the fabricated MEG device can produce a stable voltage output of 800 mV and a record high current density of 1640 µA cm−2. Even at a low air humidity of 15%, the MEG device can provide a high voltage output of 0.65 V and a considerable current density of 12 µA cm−2. The prompted diffusion of hydrogen ions in CPDs and the additional metal ions ionized from the LM electrode contribute synergistically to the high electricity generation. Additionally, the device can be easily integrated on various flexible substrates and generate an ultrahigh voltage of 210 V to power commercial electronics, showing great potential in large-scale fabrication and application. 相似文献
139.
Panpan Xu Darren H. S. Tan Binglei Jiao Hongpeng Gao Xiaolu Yu Zheng Chen 《Advanced functional materials》2023,33(14):2213168
As the dominant means of energy storage technology today, the widespread deployment of lithium-ion batteries (LIBs) would inevitably generate countless spent batteries at their end of life. From the perspectives of environmental protection and resource sustainability, recycling is a necessary strategy to manage end-of-life LIBs. Compared with traditional hydrometallurgical and pyrometallurgical recycling methods, the emerging direct recycling technology, rejuvenating spent electrode materials via a non-destructive way, has attracted rising attention due to its energy efficient processes along with increased economic return and reduced CO2 footprint. This review investigates the state-of-the-art direct recycling technologies based on effective relithiation through solid-state, aqueous, eutectic solution and ionic liquid mediums and thoroughly discusses the underlying regeneration mechanism of each method regarding different battery chemistries. It is concluded that direct regeneration can be a more energy-efficient, cost-effective, and sustainable way to recycle spent LIBs compared with traditional approaches. Additionally, it is also identified that the direct recycling technology is still in its infancy with several fundamental and technological hurdles such as efficient separation, binder removal and electrolyte recovery. In addressing these remaining challenges, this review proposes an outlook on potential technical avenues to accelerate the development of direct recycling toward industrial applications. 相似文献
140.
Mingzhen Hu Zengjian Cai Shitu Yang Zhe Wang Fengyi Shen Xinhu Liang Guodong Sun Hao Ren Yanan Cao Botao Hu Shoujie Liu Haiyan Tan Kebin Zhou 《Advanced functional materials》2023,33(13):2212097
Due to the surface inhomogeneity of the solid supports, direct growth of uniform bimetallic nanoparticles (NPs) with controllable structure and size thereon is particularly challenging. Herein, a surface-confinement strategy is reported to directly prepare ultrafine bimetallic Pt M NPs (MFe, Cu, and Co) with structure of core-shell or intermetallic compounds on an N functionalized carbon support (NC). It is found that the N species of NC support can atomically disperse metal cations of precursors, which largely renders uniform nucleation and growth of bimetallic NPs and fine structure modulation of them. In another regard, metal transfer is confined to a narrow region on NC via N-mediation, hence greatly favoring localized particle growth and formation of ultrafine bimetallic NPs. Remarkably, the ultrafine 3.1 ± 0.7 nm intermetallic Pt3Fe NPs on NC displayed excellent catalytic activity and durability toward electrochemical hydrogen evolution reaction. 相似文献