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1.
We use molecular simulation to probe the connection between local structure and the unusual re-entrant dynamics observed for polydisperse hard-sphere liquids confined in thin slit pores. The local structure is characterised by calculating 2-D bond-orientational order parameters associated with square and hexatic order for particles in the layer adjacent to the confining walls. When the wall separation is commensurate with the average particle size, the particles primarily exhibit local hexatic order, whereas local square order increases in prevalence for incommensurate geometries. The relaxation time extracted from the ensemble-averaged mean-square displacement increases exponentially with the static correlation length associated with hexatic local order in strongly confined commensurate geometries, in agreement with theoretical predictions for dynamical slowing. Square order, by contrast, is not associated with a growing length scale for either commensurate or incommensurate geometries, indicating that it is strongly geometrically frustrated. Our results suggest that the influence of bond-orientational order on dynamical slowing may be altered by changing the extent of confinement. 相似文献
2.
Dr. Michael Peter Mercer Sam Affleck Dr. Edgardo Maximiliano Gavilán-Arriazu Dr. Alana Aragón Zülke Dr. Philip A. Maughan Shivam Trivedi Prof. Maximilian Fichtner Dr. Anji Reddy Munnangi Prof. Ezequiel P. M. Leiva Prof. Harry Ernst Hoster 《Chemphyschem》2022,23(5):e202100748
Sodium-ion batteries (NIBs) utilize cheaper materials than lithium-ion batteries (LIBs) and can thus be used in larger scale applications. The preferred anode material is hard carbon, because sodium cannot be inserted into graphite. We apply experimental entropy profiling (EP), where the cell temperature is changed under open circuit conditions. EP has been used to characterize LIBs; here, we demonstrate the first application of EP to any NIB material. The voltage versus sodiation fraction curves (voltage profiles) of hard carbon lack clear features, consisting only of a slope and a plateau, making it difficult to clarify the structural features of hard carbon that could optimize cell performance. We find additional features through EP that are masked in the voltage profiles. We fit lattice gas models of hard carbon sodiation to experimental EP and system enthalpy, obtaining: 1. a theoretical maximum capacity, 2. interlayer versus pore filled sodium with state of charge. 相似文献
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The ability to separate enzymes, nucleic acids, cells, and viruses is an important asset in life sciences. This can be realised by using their spontaneous asymmetric partitioning over two macromolecular aqueous phases in equilibrium with one another. Such phases can already form while mixing two different types of macromolecules in water. We investigate the effect of polydispersity of the macromolecules on the two-phase formation. We study theoretically the phase behavior of a model polydisperse system: an asymmetric binary mixture of hard spheres, of which the smaller component is monodisperse and the larger component is polydisperse. The interactions are modelled in terms of the second virial coefficient and are assumed to be additive hard sphere interactions. The polydisperse component is subdivided into sub-components and has an average size ten times the size of the monodisperse component. We calculate the theoretical liquid–liquid phase separation boundary (the binodal), the critical point, and the spinodal. We vary the distribution of the polydisperse component in terms of skewness, modality, polydispersity, and number of sub-components. We compare the phase behavior of the polydisperse mixtures with their concomittant monodisperse mixtures. We find that the largest species in the larger (polydisperse) component causes the largest shift in the position of the phase boundary, critical point, and spinodal compared to the binary monodisperse binary mixtures. The polydisperse component also shows fractionation. The smaller species of the polydisperse component favor the phase enriched in the smaller component. This phase also has a higher-volume fraction compared to the monodisperse mixture. 相似文献
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在工程应用的很多摩擦对偶中,往往有一方是锐形的,因此,研究锐形滑块的滚动与滑动具有重要的实用意义。以锐缘硬质轮在挤压铝和软钢两种平面试样表面的滚动和滑动为研究对象,考察了两种摩擦过程中材料的受力状况和变形状况,结果表明,要在同种金属试样表面造成相同宽度的槽痕,滚动法所需要的垂直负荷比滑动法所需要的大,然而滚动法所需要的切向牵引力却比滑动法所需要的小.对两种摩擦过程中界面上的应力与材料的强度性能之关系的分析讨论指出,滚动试验中接触界面上的正应力相应于变形材料的屈服应力,因而滚动试验可以作为材料硬度的一种测量方法;滑动试验中接触界面上的剪应力相应于变形材料的流动剪应力;但滚动试验中界面剪应力与材料的流动剪应力之间,以及滑动试验中界面正应力与材料的屈服应力之间却都没有直线关系. 相似文献
6.
磁头/磁盘滑动接触下磁盘温度及热退磁临界条件的研究 总被引:1,自引:1,他引:1
采用二维轴对称有限元模型计算磁头/磁盘滑动接触下,铝质磁盘的稳态温度和热应力场以及热退磁临界条件.结果表明:磁盘温度在极短时间内升至摩擦稳态值,然后缓慢线性升高到最终稳态值;经过充分热传导和热交换后磁盘的温度梯度较小,此时磁层内的热应力集中分布于磁盘固定端边缘附近;磁盘的稳态温度和热应力均随速度增大而增大,且载荷越大其值增大越快;热应力小于1.2 GPa时所对应的速度和载荷为安全工况;温升大于373 K时所对应的工况将导致磁盘退磁. 相似文献
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Muhammad Ejaz Bhanukiran Sunkara Lakhinder Kamboj Jibao He Vijay T. John Noshir S. Pesika Scott M. Grayson 《Journal of polymer science. Part A, Polymer chemistry》2013,51(15):3314-3322
An efficient and novel one‐pot process is developed to immobilize the atom transfer radical polymerization (ATRP) initiators onto the surface of fully pyrolyzed carbon hard spheres (CHSs) via a radical trapping process from the in situ thermal decomposition of bis(bromomethylbenzoyl)peroxide. The CHSs do not require any additional preparative treatment prior to the initiator immobilization. Styrene and methyl methacrylate are polymerized onto initiator‐immobilized CHSs by surface‐initiated atomic transfer radical polymerization (SI‐ATRP). Samples are characterized using Fourier transform infrared, thermogravimetric analysis, scanning electron microscopy, and transmission electron microscopy. These methods of characterization confirmed that all the CHSs are coated with a uniform layer of grafted polymer. This efficient, one‐pot immobilization of ATRP‐initiators represents an exceptionally simple route for the rapid preparation of various polymer‐coated carbon‐based nanomaterials using SI‐ATRP. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3314–3322 相似文献
10.
Energy spectrum of multi-radiation of X-rays in a low energy Mather-type plasma focus device 下载免费PDF全文
The multi-radiation of X-rays was investigated with special attention to their energy spectrum in a Mather-type plasma focus device (operated with argon gas). The analysis is based on the effect of anomalous resistances. To study the energy spectrum, a four-channel diode X-ray spectrometer was used along with a special set of filters. The filters were suitable for detection of medium range X-rays as well as hard X-rays with energy exceeding 30 keV. The results indicate that the anomalous resistivity effect during the post pinch phase may cause multi-radiation of X-rays with a total duration of 300 ± 50 ns. The significant contribution of Cu-Kα was due to the medium range X-rays, nonetheless, hard X-rays with energies greater than 15 keV also participate in the process. The total emitted X-ray energy in the forms of Cu-K and Cu-K/3 was around 0.14 ± 0.02 (J/Sr) and 0.04 ±0.01 (J/Sr), respectively. The total energy of the emitted hard X-ray (〉 15 keV) was around 0.12± 0.02 (J/Sr). 相似文献