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Film levitation and central jet of droplet impact on nanotube surface at superheated conditions

Physical Review E 2020年第4期102卷 043108-043108页

作者： Dongdong Zhou Yuhui Zhang Yu Hou Xin Zhong Jian Jin Lidong Sun State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University Shaanxi 710049 China State Key Laboratory of Mechanical Transmission School of Materials Science and Engineering Chongqing University Chongqing 400044 China

Influences of surface nanotubes at high temperatures are investigated on droplet impact dynamics and Leidenfrost effect. Five distinct regimes of impact droplets are found on the nanotube surface, including contact boiling, film levitation, central jet levitation, central jet, and Leidenfrost phenomenon. The regimes of film levitation, central jet levitation, and central jet are characterized by either film levitation and/or liquid central jet. The regime of Leidenfrost phenomenon is characterized by droplet bounce-off behavior free of any liquid jets. Film levitation is driven by the vaporization of two parts of the droplet, with one as the droplet bottom layer over the contact area above the nanotube structure, and the other as the hemiwicking liquid in nanotubes. Both the vaporization is impaired by increasing the surface temperature, which is attributed to the reduced contact time and less extent of spread of the droplet at a higher surface temperature. The central jet phenomenon is driven by the vapor stream produced by hemiwicking liquid in the central area upon impact. It is enhanced and then suppressed by elevating the surface temperature, resulting from the collective effects of the vapor pressure in nanotubes which increases with the surface temperature, and the cross-sectional area of the vapor stream, which increases and then decreases with the surface temperature. At a high Weber number, the Leidenfrost temperature can be increased by 125∘C on the nanotube surface, implying a great potential in heat transfer enhancement for droplet-based applications.

关键词： Drop & bubble phenomena Drop breakup Multiphase flows

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Thermal-mechanical coupling behavior analysis of solid-state constrained component in advanced nuclear energy system

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Energy 2025年 330卷

作者： Yang, Xuan Li, Quan Zhang, Jing Wu, Yingwei He, Yanan Li, Chenxi Wang, Mingjun Guo, Kailun Wang, Chenglong Su, G.H. Tian, Wenxi Qiu, Suizheng State Key Laboratory of Multiphase Flow in Power Engineering School of Nuclear Science and Technology Xi'an Jiaotong University Xi'an710049 China Science and Technology on Reactor System Design Technology Laboratory Nuclear Power Institute of China Chengdu610213 China

With the advantage of phase change heat transfer, heat pipes have the potential to replace flowing coolants for removing fission heat from nuclear reactors. However, the solid-state constrained heat transfer configuration poses mutual constraints between mechanical properties and heat transfer, and their long-term thermal-mechanical coupling behavior requires further investigation. Currently, research on long-term behavior is limited to either individual/local system components or a single physical field. In this paper, an analysis method for coupled thermal-mechanical behavior is proposed and verified, comprehensively considering thermal-mechanical properties, interactions between components, and the fission gas release. This method is employed to analyze the operating characteristics of a solid-state constrained component. The results indicate that prolonged operation leads to complete contact between structural components, generating high contact pressure that enhances heat transfer but increases creep. The release of gaseous fission products, accumulated over operating time, results in a synchronous increase in both gap and external contact pressures, reaching 5.2 MPa and 4.8 MPa, respectively. This process reduces the gas gap conductance, leading to elevated system peak temperatures and a reduction in temperature safety margins by 43 K. After heat pipe failure, continued operation significantly increases the local creep strain, up to 3.9 times that under normal conditions. The gap size and fuel gap pressure should be optimized to enhance gap heat transfer and reduce component creep. Excessive fission gas release should be avoided in fuel configuration. Reducing the system power following a single heat pipe failure can mitigate component creep and extend the operational lifespan. © 2025 Elsevier Ltd

关键词： Electric heating

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Boosted Photocatalytic Co2 Reduction by Induced Electromotive Force in Rotating Magnetic Field

SSRN

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SSRN 2023年

作者： Lu, Danchen Ren, Yuqi Yang, Ya Cheng, Miao Wang, Ke Wang, Nan Liu, Maochang Zhou, Jiancheng Chen, Wenshuai Li, Naixu School of Chemistry and Chemical Engineering Southeast University No.2 Dongnandaxue Road Jiangsu Nanjing211189 China CAS Center for Excellence in Nanoscience Beijing Key Laboratory of Micro-nano Energy and Sensor Beijing Institute of Nanoenergy and Nanosystems Chinese Academy of Sciences Beijing101400 China Key Laboratory of Bio-Based Material Science and Technology Ministry of Education Northeast Forestry University No. 26 Hexing Road Harbin150040 China International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University No.28 Xianning West Road Shaanxi Xi'An710049 China

Charge separation plays a crucial role in semiconductor-based photocatalytic CO2 conversion. Herein, we report a unique induced electric field, which can actively manipulate carrier behavior at the minuscule, leading to significantly boosted photocatalytic CO2 reduction in H2O vapor. The success relies on the development a monolithic photocatalyst made of a copper foam substrate and nanosized ZnO/NiO/Au heterostructures that can effectively couple a special rotating magnetic field (RMF). Specifically, the copper foam cuts the magnetic induction line, leading to the periodic generation of induced electric field. This induced electric field could significantly increase the carriers' density by preventing their recombination. Moreover, NiO and Au as the active sites for oxidation and reduction, respective, synergistically magnify this effect. As a result, compared with the photocatalytic reaction without adding RMF, the utilization rate of photogenerated electrons increases by 5.24 times after coupling RMF, with the yield of CO and CH4 improved by 5.50 times and 5.18 times. This strategy by integrating unique RMF into the reaction system provides new insights for improving photocatalytic CO2 conversion. © 2023, The Authors. All rights reserved.

关键词： Carbon dioxide

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Mxene-Derived Ni/Tio2-X/Ti3c2 Catalyst for Enhanced Photothermal Co2 Methanation: Unraveling the Roles of Photoexcited Carriers

SSRN

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SSRN 2025年

作者： Sun, Fan Xin, Yu Xing, Xueli Lou, Jiahui Wang, Qiliang Hong, Hui International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Xi’an710049 China Institute of Engineering Thermophysics Chinese Academy of Sciences Beijing100190 China School of Aeronautics and Astronautics University of Chinese Academy of Sciences Beijing100049 China Huaneng Clean Energy Research Institute Beijing102209 China Shandong Institute of Advanced Technology Jinan250100 China Department of Architecture and Built Environment University of Nottingham NottinghamNG7 2RD United Kingdom Institute of Engineering Thermophysics China

Photothermal catalysis has emerged as a promising approach for CO2 conversion, which combines photo and thermal energy to drive catalytic reactions efficiently. While light can lower activation barriers and enhance reaction rates, the interplay between light and heat within the catalytic framework remains largely unexplored. In this study, we investigate the critical role of photoexcited carriers in enhancing catalytic performance under solar irradiation, unraveling their contribution to the CO2-to-CH4 conversion process. A multilayer accordion-like Ni/TiO2-x/Ti3C2 catalyst, which exhibits excellent photothermal and photoelectric response characteristics was fabricated for efficient photothermal CO2 methanation. Experimental results demonstrated that introduction of light during thermal catalysis markedly enhanced the CO2 conversion rate, with a 55% increase achieved at 275 ºC. Furthermore, the required temperature for maximum CO2 conversion rate was reduced by 50 ºC compared to the thermal-driven process. Meanwhile, the effects of concentrated ratio and incident wavelength on CO2 conversion were also examined, revealing a synergistic effect between photogenerated carriers and thermal energy. Further characterizations, including steady-state and transient photoluminescence spectroscopy, in-situ XPS, in-situ EPR, in-situ DRITFs, were employed to elucidate the enhancement mechanisms of photogenerated carriers in the catalytic reaction. At the same time, an outdoor experimental prototype was developed to verify the feasibility of photogenerated carrier-thermal synergistically driven CO2 methanation. The findings provide valuable insights into the role of photo-generated carriers in photothermal CO2 methanation, offering new perspectives for the design of efficient photothermal catalysts and advancing solar catalytic CO2 conversion technologies. © 2025, The Authors. All rights reserved.

关键词： Methanation

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Polarity switching from p- to n-type in a single thermoelectric donor-acceptor copolymer by p-type doping

Research Square

引用

Research Square 2021年

作者： Wang, Jing Wang, Yizhuo Li, Qing Li, Zhanchao Xu, Liqing Li, Kuncai Wang, Hong Frontier Institute of Science and Technology Xi’an Jiaotong University Xi’an710054 China State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Xi’an710054 China

The transport mechanism of organic materials is still far away from being well understood and controlled although conducting polymers have been discovered since 1977. It is rare to see conducting polyers possessing high bipolar (p- and n-type) electrical conductivities within a single bulk doped organic polymer without the assistant of gate voltage. Here, we report a novel approach to provide high performance n-type materials by p-type doping. More importantly, the bipolar electrical conductivities of the donor-acceptor conducting polymer are high, resulting high bipolar power factors among the solution-processable ambipolar D-A copolymers. A fully organic p-n junction is created in a planar film, exhibiting a high rectification ratio of 2 x 102 at ±5 V with a high current density of 3 A/cm2. Structural and spectroscopic tests have been performed to provide a fundamental understanding of the polarity switching mechanism. The results open the opportunity of making p- and n-type modules with a single conducting polymer for future modern organic electronics. © 2021, CC BY.

关键词： Conducting polymers

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Non-Hermitian delocalization in a 2D photonic quasicrystal

arXiv

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arXiv 2023年

作者： Zhang, Zhaoyang Liang, Shun Septembre, Ismaël Yu, Jiawei Huang, Yongping Liu, Maochang Zhang, Yanpeng Xiao, Min Malpuech, Guillaume Solnyshkov, Dmitry Key Laboratory for Physical Electronics and Devices The Ministry of Education Shaanxi Key Lab of Information Photonic Technique School of Electronic Science and Engineering Faculty of Electronics and Information Xi’an Jiaotong University Xi’an710049 China Institut Pascal PHOTON-N2 Université Clermont Auvergne CNRS Clermont INP Clermont-FerrandF-63000 France International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Xi’an710049 China Department of Physics University of Arkansas FayettevilleAR72701 United States National Laboratory of Solid State Microstructures School of Physics Nanjing University Nanjing210093 China Paris75231 France

Quasicrystals show long-range order, but lack translational symmetry. So far, theoretical and experimental studies suggest that both Hermitian and non-Hermitian quasicrystals show localized eigenstates. This localization is due to the fractal structure of the spectrum in the Hermitian case and to the transition to diffusive bands via exceptional points in the non-Hermitian case. Here, we present an experimental study of a dodecagonal (12-fold) photonic quasicrystal based on electromagnetically-induced transparency in a Rb vapor cell. The transition to a quasicrystal is obtained by superposing two honeycomb lattices at 30◦ with a continuous tuning of their amplitudes. Non-Hermiticity is controlled independently. We study the spatial expansion of a probe wavepacket. In the Hermitian case, the wavepacket expansion is suppressed when the amplitude of the second lattice is increased (quasicrystal localization). We find a new regime, where increasing the non-Hermitian potential in the quasicrystal enhances spatial expansion, with the C12 symmetry becoming visible in the wavepacket structure. This real-space expansion is due to a k-space localization on specific quasicrystal modes. Our results show that the non-Hermitian quasicrystal behavior is richer than previously thought. The localization properties of the quasicrystals can be used for beam tailoring in photonics, but are also important in other fields. Copyright © 2023, The Authors. All rights reserved.

关键词： Quasicrystals

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Strengthening Chlorobenzene Catalytic Degradation Rate and Selectivity Over Laxsr1-Xmno3±Δ by Anchoring Interfacial Oxygen Vacancy

SSRN

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SSRN 2022年

作者： Li, Lu Tao, Dan Zhao, Qi Fu, Shuangshuang Min, Xin Chen, Changwei Tian, Mingjiao Shi, Jianwen He, Chi State Key Laboratory of Electrical Insulation and Power Equipment Center of Nanomaterials for Renewable Energy School of Electrical Engineering Xi’an Jiaotong University Shaanxi Xi’an710049 China State Key Laboratory of Multiphase Flow in Power Engineering School of Energy and Power Engineering Xi’an Jiaotong University Shaanxi Xi’an710049 China College of Geology and Environment Xi’an University of Science and Technology Shaanxi Xi’an710054 China Faculty of Electronic and Information Engineering Xi’an Jiaotong University Shaanxi Xi’an710049 China School of Environmental and Municipal Engineering Xi’an University of Architecture and Technology Shaanxi Xi’an710055 China School of Environmental Science and Engineering Shanghai Jiao Tong University 800 Dongchuan Road Shanghai200240 China

Surficial lattice oxygen in perovskite compounds is a common participant during chloroaromatic catalytic destruction. Herein, we proposed a facile oxygen vacancy construction strategy for preparing high active LaxSr1-xMnO3±δ (LSMO) via NaBH4 treatment. Results reveal that LSMO composites are not only reduced by NaBH4 under mild condition, but trigger a significant Sr segregation effect, which plays a key role in oxygen vacancy formation accounting to the electron donation from Sr to Mn acceptor and subsequent lattice oxygen activation. Moreover, the concentration of interfacial active oxygen species can be regulated by taming the La-Sr interaction with different Sr substitution proportions. The anchored oxygen vacancies (OVs) take advantage of electron capture or transfer and induce molecule oxygen into active oxygen species to react with chlorobenzene molecules, resulting in a preferential catalytic oxidation capacity. Amongst, reduced La0.5Sr0.5MnO3±δ catalyst displays superior chlorobenzene destruction efficiency with 90% of which converted as low as 236 °C, which also exhibited a stable performance in long-time operation. However, the OVs would be refilled by water H2O molecules resulting in a weaker water resistance for OVs anchored catalyst. In summary, the annihilation of OVs is the most important factor for catalyst deactivation. The research offers a new avenue to construct interfacial oxygen species in perovskite oxides during the chlorobenzene deep oxidation process. © 2022, The Authors. All rights reserved.

关键词： Catalytic oxidation

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High-Ni Low-Co High-Capacity Li-Rich Cathode Materials Via Adjusting Li2mno3 Content and Li/Ni Mixing Structures

SSRN

引用

SSRN 2023年

作者： Wu, Zhen Zou, Kunyang Dai, Xin Zhang, Yu-Han Zhang, Xudong Wang, Hao Hou, Zhufeng Ma, Lijing Liu, Yan Chen, Yuanzhen Guo, Shengwu Liu, Yongning State Key Laboratory for Mechanical Behavior of Materials Xi’an Jiaotong University Xi’an710049 China Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao266101 China Center for High Performance Computing Network Information Center Xi’an Jiaotong University Xi’an710049 China Hefei Advanced Computing Center Operation Management Corp Ltd Hefei230088 China State Key Laboratory of Structural Chemistry Fujian Institute of Research the Structure of Matter Chinese Academy of Sciences Fuzhou350002 China International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Xi’an710049 China

Li-rich layered oxides (LLOs) are considered as the promising cathode materials for next-generation high energy density lithium-ion batteries (LIBs). However, severe voltage fade and capacity decay hinder their commercial applications. Increasing the Ni content in LLOs effectively improves the stability and discharge voltage, but shows reduced capacities, typically © 2023, The Authors. All rights reserved.

关键词： Lithium compounds

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fEffect of alkali and alkaline metals on gas formation behavior and kinetics during pyrolysis of pine wood

引用

Fuel 2021年 290卷

作者： Li, Jinhu Burra, Kiran G. Wang, Zhiwei Liu, Xuan Gupta, Ashwani K. The Combustion Laboratory Department of Mechanical Engineering University of Maryland College ParkMD20742 United States Faculty of Engineering China University of Geosciences WuhanHubei430074 China College of Environmental Engineering Henan University of Technology Zhengzhou450001 China State Key Laboratory of Multiphase Flow in Power Engineering School of Energy and Power Engineering Xi'an Jiaotong University Xi'an710049 China

This study examines the acid and alkaline treatment of pine wood to help understand the effect of alkali and alkaline earth metals (AAEMs) content on the pyrolysis behavior at different temperatures. Acid and alkali pretreatment of pine wood were conducted to modify AAEMs content by ion-exchanging method. Thermal kinetic behavior of the pretreated samples was first conducted by a thermogravimetric analyzer (TGA) at different heating rates that provided activation energies of pyrolysis. Gas formation behavior of the samples for different extents of conversion was carried out in a fixed-bed reactor at two different temperatures of 823 K and 1073 K. Evolutionary behavior of the gas components during pyrolysis, including flow rate, and yield and their energy content were measured and compared. Results showed that the values of activation energies increased with the extent of conversion for all the pretreated samples examined. The effect of AAEMs on pyrolysis behavior of biomass varied with the extent of conversion. The presence of AAEMs in biomass decreased the decomposition energy at low conversion while it greatly improved under high conversion. Besides, alkali treated sample with higher AAEM content enhanced the gas and char yield while it reduced the bio-oil production at low temperature with low conversion. However, at high temperature the opposite trend was observed. Presence of AAEMs was favorable for the generation of H2, CO, CO2 and CnHm at low temperature, while it showed an inhibition effect on CO and CnHm yield and syngas energy at high temperature. The catalytic mechanism of AAEMs on the pyrolysis behavior at different temperatures was discussed based on activation energy and gaseous formation. Results revealed decomposition of carboxylate at low temperature and formation of stable biomass-Na (BM-Na) structure at high temperature that led to the variation of activation energy and changed gaseous products yield and syngas energy. Acid washing pretreatment wa

关键词： Activation energy

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Electrochemical evolution of a metal oxyhydroxide surface on two-dimensional layered metal phosphorus trisulfides enables the oxidation of amine to nitrile

引用

Carbon Energy 2025年第03期 138-152页

作者： Binglan Wu Karim Harrath Marshet Getaye Sendeku Tofik Ahmed Shifa Yuxin Huang Jing Tai Fekadu Tsegaye Dajan Kassa Belay Ibrahim Xueying Zhan Zhenxing Wang Elisa Moretti Ying Yang Fengmei Wang Alberto Vomiero State Key Laboratory of Chemical Resource Engineering College of Chemistry Beijing University of Chemical Technology CAS Key Laboratory of Nanosystem and Hierarchical Fabrication National Center for Nanoscience and Technology (NCNST) Shaanxi Provincial Key Laboratory of Electroanalytical Chemistry Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education College of Chemistry & Materials Science Northwest University State Key Laboratory of Multiphase Flow in Power Engineering International Research Center for Renewable Energy Xi'an Jiaotong University Fundamental Science Center of Rare Earths Ganjiang Innovation Academy Chinese Academy of Science Ocean Hydrogen Energy R&D Center Research Institute of Tsinghua University in Shenzhen Department of Molecular Sciences and Nanosystems Ca' Foscari University of Venice Testing and Analysis Center Institute of Chemistry Chinese Academy of Sciences Department of Engineering Sciences and Mathematics Division of Materials Science Lule? University of Technology

Selective oxidation of amines to imines through electrocatalysis is an attractive and efficient way for the chemical industry to produce nitrile compounds,but it is limited by the difficulty of designing efficient catalysts and lack of understanding the mechanism of ***,we demonstrate a novel strategy by generation of oxyhydroxide layers on two-dimensional iron-doped layered nickel phosphorus trisulfides(Ni1-xFexPS3) during the oxidation of benzylamine（BA）.In-depth structural and surface chemical characterizations during the electrocatalytic process combined with theoretical calculations reveal that Ni（1-x）FexPS3undergoes surface reconstruction under alkaline conditions to form the metal oxyhydroxide/phosphorus trichalcogenide(NiFeOOH/Ni1-xFexPS3) ***,the generated heterointerface facilitates BA oxidation with a low onset potential of 1.39 V and Faradaic efficiency of 53% for benzonitrile（BN） *** calculations further indicate that the as-formed NiFeOOH/Ni1-xFexPS3heterostructure could offer optimum free energy for BA adsorption and BN desorption,resulting in promising BN synthesis.

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