Browsing by Author "Zhao, Lei"

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    Analyzing the Molecular Kinetics of Water Spreading on Hydrophobic Surfaces via Molecular Dynamics Simulation
    Zhao, Lei; Cheng, Jiangtao (Springer Nature, 2017-09-07)
    In this paper, we report molecular kinetic analyses of water spreading on hydrophobic surfaces via molecular dynamics simulation. The hydrophobic surfaces are composed of amorphous polytetrafluoroethylene (PTFE) with a static contact angle of similar to 112.4 degrees for water. On the basis of the molecular kinetic theory (MKT), the influences of both viscous damping and solid-liquid retarding were analyzed in evaluating contact line friction, which characterizes the frictional force on the contact line. The unit displacement length on PTFE was estimated to be similar to 0.621 nm and is similar to 4 times as long as the bond length of C-C backbone. The static friction coefficient was found to be similar to 10(-3) Pa.s, which is on the same order of magnitude as the dynamic viscosity of water, and increases with the droplet size. A nondimensional number defined by the ratio of the standard deviation of wetting velocity to the characteristic wetting velocity was put forward to signify the strength of the inherent contact line fluctuation and unveil the mechanism of enhanced energy dissipation in nanoscale, whereas such effect would become insignificant in macroscale. Moreover, regarding a liquid droplet on hydrophobic or superhydrophobic surfaces, an approximate solution to the base radius development was derived by an asymptotic expansion approach.
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    Computational investigation of the flow field contribution to improve electricity generation in granular activated carbon-assisted microbial fuel cells
    Zhao, Lei; Li, Jian; Battaglia, Francine; He, Zhen (Elsevier, 2016-11-30)
    Microbial fuel cells (MFCs) offer an alternative approach to treat wastewater with less energy input and direct electricity generation. To optimize MFC anodic performance, adding granular activated carbon (GAC) has been proved to be an effective way, most likely due to the enlarged electrode surface for biomass attachment and improved mixing of the flow field. The impact of a flow field on the current enhancement within a porous anode medium (e.g., GAC) has not been well understood before, and thus is investigated in this study by using mathematical modeling of the multi-order Butler-Volmer equation with computational fluid dynamics (CFD) techniques. By comparing three different CFD cases (without GAC, with GAC as a nonreactive porous medium, and with GAC as a reactive porous medium), it is demonstrated that adding GAC contributes to a uniform flow field and a total current enhancement of 17%, a factor that cannot be neglected in MFC design. However, in an actual MFC operation, this percentage could be even higher because of the microbial competition and energy loss issues within a porous medium. The results of the present study are expected to help with formulating strategies to optimize MFC with a better flow pattern design. (C) 2016 Elsevier B.V. All rights reserved.
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    Dynamics and Statics of Three-Phase Contact Line
    Zhao, Lei (Virginia Tech, 2019-09-17)
    Wetting, which addresses either spontaneous or forced spreading of liquids on a solid surface, is a ubiquitous phenomenon in nature and can be observed by us on a daily basis, e.g., rain drops falling on a windshield and lubricants protecting our corneas. The study of wetting phenomena can be traced back to the observation of water rising in a capillary tube by Hauksbee in 1706 and still remains as a hot topic, since it lays the foundation for a wide spectrum of applications, such as fluid mechanics, surface chemistry, micro/nanofluidic devices, and phase change heat transfer enhancement. Generally, wetting is governed by the dynamic and static behaviors of the three-phase contact line. Therefore, a deep insight into the dynamics and statics of three-phase contact line at nanoscale is necessary for the technological advancement in nanotechnology and nanoscience. This dissertation aims to understand the dynamic wetting under a molecular kinetic framework and resolve the reconfiguration of liquid molecules at the molecular region of contact line. Water spreading on polytetrafluoroethylene surfaces is selected as a classical example to study the dynamic behaviors of three-phase contact line. To accommodate the moving contact line paradox, the excess free energy is considered to be dissipated in the form of molecular dissipation. As-formed contact line friction/dissipation coefficient is calculated for water interacting with PTFE surfaces with varying structures and is found to be on the same order of magnitude with dynamic viscosity. From an ab initio perspective, contact line friction is decomposed into contributions from solid-liquid retarding and viscous damping. A mathematical model is established to generalize the overall friction between a droplet and a solid surface, which is able to clarify the static-to-kinetic transition of solid-liquid friction without introducing contact angle hysteresis. Moreover, drag reduction on lotus-leaf-like surface is accounted for as well. For the first time, the concept of contact line friction is used in the rational design of a superhydrophobic condenser surface for continuous dropwise condensation. We focus on the transport and reconfiguration of liquid molecules confined by a solid wall to shed light on the morphology of the molecular region of a three-phase contact line. A governing equation, which originates from the free energy analysis of a nonuniform monocomponent system, is derived to describe the patterned oscillations of liquid density. By comparing to the Reynolds transport theorem, we find that the oscillatory profiles of interfacial liquids are indeed governed in a combined manner by self-diffusion, surface-induced convection and shifted glass transition. Particularly for interfacial water, the solid confining effects give rise to a bifurcating configuration of hydrogen bonds. Such unique configuration consists of repetitive layer-by-layer water sheets with intra-layer hydrogen bonds and inter-layer defects. Molecular dynamics simulations on the interfacial configuration of water on solid surfaces reveal a quadratic dependence of adhesion on solid-liquid affinity, which bridges the gap between macroscopic interfacial properties and microscopic parameters.
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    Measurement of the B0 lifetime and flavor-oscillation frequency using hadronic decays reconstructed in 2019-2021 Belle II data
    Ablikim, M.; Achasov, M. N.; Adlarson, P.; Ahmed, S.; Albrecht, M.; Amoroso, A.; An, Q.; Bai, X. H.; Bai, Y.; Bakina, O.; Ferroli, R. Baldini; Balossino, I.; Ban, Y.; Begzsuren, K.; Bennett, J.; Berger, N.; Bertani, M.; Bettoni, D.; Bianchi, F.; Biernat, J.; Bloms, J.; Bortone, A.; Boyko, I.; Briere, R. A.; Cai, H.; Cai, X.; Calcaterra, A.; Cao, G. F.; Cao, N.; Cetin, S. A.; Chang, J. F.; Chang, W. L.; Chelkov, G.; Chen, D. Y.; Chen, G.; Chen, H. S.; Chen, M. L.; Chen, S. J.; Chen, X. R.; Chen, Y. B.; Cheng, W.; Cibinetto, G.; Cossio, F.; Cui, X. F.; Dai, H. L.; Dai, J. P.; Dai, X. C.; Dbeyssi, A.; de Boer, R. B.; Dedovich, D.; Deng, Z. Y.; Denig, A.; Denysenko, I.; Destefanis, M.; De Mori, F.; Ding, Y.; Dong, C.; Dong, J.; Dong, L. Y.; Dong, M. Y.; Du, S. X.; Fang, J.; Fang, S. S.; Fang, Y.; Farinelli, R.; Fava, L.; Feldbauer, F.; Felici, G.; Feng, C. Q.; Fritsch, M.; Fu, C. D.; Fu, Y.; Gao, X. L.; Gao, Y.; Gao, Y.; Gao, Y. G.; Garzia, I.; Gersabeck, E. M.; Gilman, A.; Goetzen, K.; Gong, L.; Gong, W. X.; Gradl, W.; Greco, M.; Gu, L. M.; Gu, M. H.; Gu, S.; Gu, Y. T.; Guan, C. Y.; Guo, A. Q.; Guo, L. B.; Guo, R. P.; Guo, Y. P.; Guskov, A.; Han, S.; Han, T. T.; Han, T. Z.; Hao, X. Q.; Harris, F. A.; He, K. L.; Heinsius, F. H.; Held, T.; Heng, Y. K.; Himmelreich, M.; Holtmann, T.; Hou, Y. R.; Hou, Z. L.; Hu, H. M.; Hu, J. F.; Hu, T.; Hu, Y.; Huang, G. S.; Huang, L. Q.; Huang, X. T.; Huesken, N.; Hussain, T.; Andersson, W. Ikegami; Imoehl, W.; Irshad, M.; Jaeger, S.; Ji, Q.; Ji, Q. P.; Ji, X. B.; Ji, X. L.; Jiang, H. B.; Jiang, X. S.; Jiang, X. Y.; Jiao, J. B.; Jiao, Z.; Jin, S.; Jin, Y.; Johansson, T.; Kalantar-Nayestanaki, N.; Kang, X. S.; Kappert, R.; Kavatsyuk, M.; Ke, B. C.; Keshk, I. K.; Khoukaz, A.; Kiese, P.; Kiuchi, R.; Kliemt, R.; Koch, L.; Kolcu, O. B.; Kopf, B.; Kuemmel, M.; Kuessner, M.; Kupsc, A.; Kurth, M. G.; Kuehn, W.; Lane, J. J.; Lange, J. S.; Larin, P.; Lavezzi, L.; Leithoff, H.; Lellmann, M.; Lenz, T.; Li, C.; Li, C. H.; Li, Cheng; Li, D. M.; Li, F.; Li, G.; Li, H. B.; Li, H. J.; Li, J. L.; Li, J. Q.; Li, Ke; Li, L. K.; Li, Lei; Li, P. L.; Li, P. R.; Li, W. D.; Li, W. G.; Li, X. H.; Li, X. L.; Li, Z. B.; Li, Z. Y.; Liang, H.; Liang, H.; Liang, Y. F.; Liang, Y. T.; Liao, L. Z.; Libby, J.; Lin, C. X.; Liu, B.; Liu, B. J.; Liu, C. X.; Liu, D.; Liu, D. Y.; Liu, F. H.; Liu, Fang; Liu, Feng; Liu, H. B.; Liu, H. M.; Liu, Huanhuan; Liu, Huihui; Liu, J. B.; Liu, J. Y.; Liu, K.; Liu, K. Y.; Liu, Ke; Liu, L.; Liu, L. Y.; Liu, Q.; Liu, S. B.; Liu, T.; Liu, X.; Liu, Y. B.; Liu, Z. A.; Liu, Zhiqing; Long, Y. F.; Lou, X. C.; Lu, H. J.; Lu, J. D.; Lu, J. G.; Lu, X. L.; Lu, Y.; Lu, Y. P.; Luo, C. L.; Luo, M. X.; Luo, P. W.; Luo, T.; Luo, X. L.; Lusso, S.; Lyu, X. R.; Ma, F. C.; Ma, H. L.; Ma, L. L.; Ma, M. M.; Ma, Q. M.; Ma, R. Q.; Ma, R. T.; Ma, X. N.; Ma, X. X.; Ma, X. Y.; Ma, Y. M.; Maas, F. E.; Maggiora, M.; Maldaner, S.; Malde, S.; Malik, Q. A.; Mangoni, A.; Mao, Y. J.; Mao, Z. P.; Marcello, S.; Meng, Z. X.; Messchendorp, J. G.; Mezzadri, G.; Min, T. J.; Mitchell, R. E.; Mo, X. H.; Mo, Y. J.; Muchnoi, N. Yu; Muramatsu, H.; Nakhoul, S.; Nefedov, Y.; Nerling, F.; Nikolaev, I. B.; Ning, Z.; Nisar, S.; Olsen, S. L.; Ouyang, Q.; Pacetti, S.; Pan, Y.; Pan, Y.; Papenbrock, M.; Pathak, A.; Patteri, P.; Pelizaeus, M.; Peng, H. P.; Peters, K.; Pettersson, J.; Ping, J. L.; Ping, R. G.; Pitka, A.; Poling, R.; Prasad, V.; Qi, H.; Qi, M.; Qi, T. Y.; Qian, S.; Qiao, C. F.; Qin, L. Q.; Qin, X. P.; Qin, X. S.; Qin, Z. H.; Qiu, J. F.; Qu, S. Q.; Rashid, K. H.; Ravindran, K.; Redmer, C. F.; Rivetti, A.; Rodin, V.; Rolo, M.; Rong, G.; Rosner, Ch; Rump, M.; Sarantsev, A.; Savrie, M.; Schelhaas, Y.; Schnier, C.; Schoenning, K.; Shan, W.; Shan, X. Y.; Shao, M.; Shen, C. P.; Shen, P. X.; Shen, X. Y.; Shi, H. C.; Shi, R. S.; Shi, X.; Shi, X. D.; Song, J. J.; Song, Q. Q.; Song, Y. X.; Sosio, S.; Spataro, S.; Sui, F. F.; Sun, G. X.; Sun, J. F.; Sun, L.; Sun, S. S.; Sun, T.; Sun, W. Y.; Sun, Y. J.; Sun, Y. K.; Sun, Y. Z.; Sun, Z. T.; Tan, Y. X.; Tang, C. J.; Tang, G. Y.; Thoren, V.; Tsednee, B.; Uman, I.; Wang, B.; Wang, B. L.; Wang, C. W.; Wang, D. Y.; Wang, H. P.; Wang, K.; Wang, L. L.; Wang, M.; Wang, M. Z.; Wang, Meng; Wang, W. P.; Wang, X.; Wang, X. F.; Wang, X. L.; Wang, Y.; Wang, Y.; Wang, Y. D.; Wang, Y. F.; Wang, Y. Q.; Wang, Z.; Wang, Z. Y.; Wang, Ziyi; Wang, Zongyuan; Weber, T.; Wei, D. H.; Weidenkaff, P.; Weidner, F.; Wen, H. W.; Wen, S. P.; White, D. J.; Wiedner, U.; Wilkinson, G.; Wolke, M.; Wollenberg, L.; Wu, J. F.; Wu, L. H.; Wu, L. J.; Wu, Z.; Xia, L.; Xiao, S. Y.; Xiao, Y. J.; Xiao, Z. J.; Xie, Y. G.; Xie, Y. H.; Xing, T. Y.; Xiong, X. A.; Xu, G. F.; Xu, J. J.; Xu, Q. J.; Xu, W.; Xu, X. P.; Yan, L.; Yan, W. B.; Yan, W. C.; Yang, H. J.; Yang, H. X.; Yang, L.; Yang, R. X.; Yang, S. L.; Yang, Y. H.; Yang, Y. X.; Yang, Yifan; Yang, Zhi; Ye, M.; Ye, M. H.; Yin, J. H.; You, Z. Y.; Yu, B. X.; Yu, C. X.; Yu, G.; Yu, J. S.; Yu, T.; Yuan, C. Z.; Yuan, W.; Yuan, X. Q.; Yuan, Y.; Yue, C. X.; Yuncu, A.; Zafar, A. A.; Zeng, Y.; Zhang, B. X.; Zhang, Guangyi; Zhang, H. H.; Zhang, H. Y.; Zhang, J. L.; Zhang, J. Q.; Zhang, J. W.; Zhang, J. Y.; Zhang, J. Z.; Zhang, Jianyu; Zhang, Jiawei; Zhang, L.; Zhang, Lei; Zhang, S.; Zhang, S. F.; Zhang, T. J.; Zhang, X. Y.; Zhang, Y.; Zhang, Y. H.; Zhang, Y. T.; Zhang, Yan; Zhang, Yao; Zhang, Yi; Zhang, Z. H.; Zhang, Z. Y.; Zhao, G.; Zhao, J.; Zhao, J. Y.; Zhao, J. Z.; Zhao, Lei; Zhao, Ling; Zhao, M. G.; Zhao, Q.; Zhao, S. J.; Zhao, Y. B.; Zhao, Z. G.; Zhemchugov, A.; Zheng, B.; Zheng, J. P.; Zheng, Y.; Zheng, Y. H.; Zhong, B.; Zhong, C.; Zhou, L. P.; Zhou, Q.; Zhou, X.; Zhou, X. K.; Zhou, X. R.; Zhu, A. N.; Zhu, J.; Zhu, K.; Zhu, K. J.; Zhu, S. H.; Zhu, W. J.; Zhu, X. L.; Zhu, Y. C.; Zhu, Z. A.; Zou, B. S.; Zou, J. H. (American Physical Society, 2023-05-15)
    We measure the B0 lifetime and flavor-oscillation frequency using B0→D(∗)-π+ decays collected by the Belle II experiment in asymmetric-energy e+e- collisions produced by the SuperKEKB collider operating at the ϒ(4S) resonance. We fit the decay-time distribution of signal decays, where the initial flavor is determined by identifying the flavor of the other B meson in the event. The results, based on 33000 signal decays reconstructed in a data sample corresponding to 190 fb-1, are τB0=(1.499±0.013±0.008) ps, Δmd=(0.516±0.008±0.005) ps-1, where the first uncertainties are statistical and the second are systematic. These results are consistent with the world-average values.