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Electrochemical oxidation of rhodamine B by PbO_2/Sb-SnO_2/TiO_2 nanotube arrays electrode

Chinese Journal of Catalysis 2019年第6期40卷 917-927页

作者： Jia Wu Kai Zhu Hao Xu Wei Yan Xi’an XD Switchgear Electric Co. Ltd.Xi’an 710049ShaanxiChina Department of Environmental Science and Engineering State Key Laboratory of Multiphase Flow in Power EngineeringXi’an Jiaotong UniversityXi’an 710049ShaanxiChina

A PbO2/Sb-SnO2/TiO2 nanotube array composite electrode was successfully synthesized and its electrochemical oxidation properties were ***-emission scanning electron microscopy(FE-SEM)and X-ray diffraction(XRD)results showed that the PbO2 coating was composed of anα-PbO2 inner layer and aβ-PbO2 outer *** life measurement indicated that the composite electrode had a lifetime of 815 *** B(RhB)was employed as a model pollutant to analyze the electrocatalytic activity of the *** effects of initial RhB concentration,current density,initial pH,temperature,and chloride ion concentration on the electrochemical oxidation were investigated in *** coupled plasma atomic emission spectroscopy(ICP-AES)results suggested that the concentration of leached Pb^2+in the electrolyte during the electrocatalytic oxidation process can be ***,the degradation mechanism during the electrocatalytic oxidation process was proposed based on the results of solid-phase micro-extraction-gas chromatography-mass spectrometry(SPME-GC-MS).The high electrocatalytic performance of the composite electrode makes it a promising anode for the treatment of organic pollutants in aqueous solution.

关键词： TiO2 nanotube array Electrochemical oxidation Rhodamine B Degradation mechanism

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Error Analysis of Liquid Holdup Measurement in Gas-Liquid Annular flow Through Circular Pipes Using High-Speed Camera Method

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Journal of Shanghai Jiaotong university(Science) 2018年第S1期23卷 34-40页

作者： LIU Li BAI Bofeng School of Nuclear Science and Engineering Shanghai Jiao Tong University State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University

Accurate measurement of gas-liquid phase fraction is essential for the proper modelling of the pressure drop, heat transfer coefficient, mass transfer rate and interfacial area in two-phase flows. In this paper, taking the issue of optical distortion into account, an analytical model was proposed to estimate and correct the liquid holdup in gas-liquid annular flow through a circular pipe using high-speed camera method. The error in the liquid holdup measurement generated from different refractive indices among transparent circular pipe, liquid film and air core was firstly theoretically analyzed based on the geometric optics. Experimental tests were then carried out to identify the difference as well as to validate the proposed model. Results indicated that the prediction of the liquid holdup has a good performance with the experimental data(i.e., mean relative error is 4.1%) and the measured liquid holdup is larger than the real one. It was found that the measured liquid holdup is larger than the real one. Generally, when the real liquid holdup gets smaller, the discrepancy between the measured liquid holdup by image and the real liquid holdup becomes more significant. Thus, after measuring the liquid holdup from the images, the value of the measured liquid holdup must be corrected by the present model in order to obtain the real liquid holdup.

关键词： gas-liquid annular flow liquid holdup optical refraction analytical correction

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Electrocatalytically Activating and Reducing N2Molecule by Tuning Activity of Local Hydrogen Radical

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Angewandte Chemie 2023年第20期135卷

作者： Yuanyuan Yang Cejun Hu Dr. Jieqiong Shan Chuanqi Cheng Prof. Lili Han Prof. Xinzhe Li Ruguang Wang Prof. Wei Xie Prof. Yao Zheng Prof. Tao Ling Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education Tianjin Key Laboratory of Composite and Functional Materials School of Materials Science and Engineering Tianjin University Tianjin 300072 China Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) Tianjin Key Lab of Molecular Recognition & Biosensing Renewable Energy Conversion and Storage Center College of Chemistry Nankai University Tianjin 300071 China School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou 350002 China State Key Laboratory of Multiphase Flow in Power Engineering School of Energy and Power Engineering Xi'an Jiaotong University Xi An Shi Xi'an 710049 China

Decarbonizing N 2 conversion is particularly challenging, but essential for sustainable development of industry and agriculture. Herein, we achieve electrocatalytic activation/reduction of N 2 on X/Fe−N−C (X=Pd, Ir and Pt) dual-atom catalysts under ambient condition. We provide solid experimental evidence that local hydrogen radical (H*) generated on the X site of the X/Fe−N−C catalysts can participate in the activation/reduction of N 2 adsorbed on the Fe site. More importantly, we reveal that the reactivity of X/Fe−N−C catalysts for N 2 activation/reduction can be well adjusted by the activity of H* generated on the X site, i.e., the interaction between the X−H bond. Specifically, X/Fe−N−C catalyst with the weakest X−H bonding exhibits the highest H* activity, which is beneficial to the subsequent cleavage of X−H bond for N 2 hydrogenation. With the most active H*, the Pd/Fe dual-atom site promotes the turnover frequency of N 2 reduction by up to 10 times compared with the pristine Fe site.

关键词： Carbon Materials Electrocatalysis Metal-Free Catalysts Nitrogen Reduction Reaction

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Tailoring Second Coordination Sphere for Tunable Solid–Liquid Interfacial Charge Transfer toward Enhanced Photoelectrochemical H2Production

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Angewandte Chemie 2024年第22期136卷

作者： Dr. Yangguang Hu Dr. Wu Zhou Dr. Wanbing Gong Prof. Chao Gao Prof. Shaohua Shen Prof. Tingting Kong Prof. Yujie Xiong Anhui Engineering Research Center of Carbon Neutrality The Key Laboratory of Functional Molecular Solids Ministry of Education College of Chemistry and Materials Science Anhui Normal University 241002 Wuhu Anhui China Hefei National Laboratory for Physical Sciences at the Microscale School of Chemistry and Materials Science University of Science and Technology of China 230026 Hefei Anhui China These authors equally contributed to this work International Research Centre for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University 710049 Xi'an Shaanxi China

The recombination of photogenerated charge carriers severely limits the performance of photoelectrochemical (PEC) H 2 production. Here, we demonstrate that this limitation can be overcome by optimizing the charge transfer dynamics at the solid–liquid interface via molecular catalyst design. Specifically, the surface of a p-Si photocathode is modulated using molecular catalysts with different metal atoms and organic ligands to improve H 2 production performance. Co(pda-SO 3 H) 2 is identified as an efficient and durable catalyst for H 2 production through the rational design of metal centers and first/second coordination spheres. The modulation with Co(pda-SO 3 H) 2 , which contains an electron-withdrawing −SO 3 H group in the second coordination sphere, elevates the flat-band potential of the polished p-Si photocathode and nanoporous p-Si photocathode by 81 mV and 124 mV, respectively, leading to the maximized energy band bending and the minimized interfacial carrier transport resistance. Consequently, both the two photocathodes achieve the Faradaic efficiency of more than 95 % for H 2 production, which is well maintained during 18 h and 21 h reaction, respectively. This work highlights that the band-edge engineering by molecular catalysts could be an important design consideration for semiconductor–catalyst hybrids toward PEC H 2 production.

关键词： PEC H2 production molecular catalyst coordination sphere surface modulation charge transfer

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Enhanced efficiency in Concentrated Parabolic Solar Collector(CPSC) with a porous absorber tube filled with metal nanoparticle suspension

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Green Energy & Environment 2018年第2期3卷 129-137页

作者： Mohammad Hatami Jiafeng Geng Dengwei Jing Mechanical Engineering Department Esfarayen University of Technology (EUT) International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power EngineeringXi'an Jiaotong University

In this study, effects of different nanoparticles and porosity of absorber tube on the performance of a Concentrating Parabolic Solar Collector(CPSC) were investigated. A section of porous-filled absorber tube was modeled as a semi-circular cavity under the solar radiation which is filled by nanofluids and the governing equations were solved by FlexPDE numerical software. The effect of four physical parameters, nanoparticles type, nanoparticles volume fraction(φ), Darcy number(Da) and Rayleigh number(Ra), on the Nusselt number(Nu) was discussed. It turns out that Cu nanoparticle is the most suitable one for such solar collectors, compared to the commonly used Fe_3O_4, Al_2O_3, TiO_*** the increased addition of Cu nanoparticles all the parameters φ, Da and Ra shows a significant increase against the Nu, indicates the enhanced heat transfer in such cases. As a result, low concentration of Cu nanoparticle suspension combined with porous matrix was supposed to be beneficial for the performance enhancement of concentrating parabolic solar collector.

关键词： Concentrating parabolic solar collector Porous absorber tube Nanofluid Nusselt number Finite Element Method

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Information Preservation Optimization Method Based on the Advection Upstream Splitting Method in Supersonic Rarefied flow Simulation

SSRN

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SSRN 2022年

作者： Xu, Xiao Ma, Xinjian Zhang, Jun Shen, Yan Zhang, Junyan School of Mechatronics and Power Engineering Jiangsu University of Science and Technology Zhangjiagang215600 China Shanghai Space Propulsion Technology Research Institute Shanghai201109 China Key Laboratory of Unsteady Aerodynamics and Flow Control Ministry of Industry and Information Technology Nanjing University of Aeronautics and Astronautics Nanjing210016 China China Academy of Aerospace Aerodynamics Beijing100074 China

An information preservation (IP) optimization approach for supersonic flow simulation is proposed in this paper. According to the conversion of the variables integrated in half-space and the analogical analysis, a similarity relationship between the integrated variables in the governing equations of the preserved information and macroscopic variables in Navier-Stokes equations is obtained. The computational approach of the flux for the correlation terms is reconstructed using the Advection Upstream Splitting Method (AUSM) scheme, giving the IP method windward characteristics. Additionally, the pressure boundary treatment is modified to improve the stability and accuracy of the IP method in the simulation of rarefied supersonic flow driven by high pressure. The particle number threshold method is proposed to solve the "carbuncle point" problem caused by insufficient local collisions. The IP optimization method combines the advantages of the AUSM scheme and the low statistical scatter method;thus, it can accurately and effectively investigate real-time variation characteristics of rarefied supersonic flow. This method simulates the supersonic microscale jet flow and hypersonic macroscale nozzle flow. The results indicate that the real-time statistical accuracy of the IP optimization method is much better than the direct simulation Monte Carlo method, whereas the correctness and accuracy of this method are satisfactory. Therefore, the proposed method provides an efficient algorithm for the variation mechanism and unsteady flow-characteristic research on rarefied supersonic flow on different scales. © 2022, The Authors. All rights reserved.

关键词： Supersonic flow

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Spin-to-orbital angular momentum conversion in non-Hermitian photonic graphene

arXiv

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arXiv 2025年

作者： Zhang, Zhaoyang Kokhanchik, Pavel Liu, Zhenzhi Shen, Yutong Liu, Fu Liu, Maochang Zhang, Yanpeng Xiao, Min Malpuech, Guillaume Solnyshkov, Dmitry Key Laboratory for Physical Electronics and Devices 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 National Laboratory of Solid State Microstructures School of Physics Nanjing University Nanjing210093 China Paris75231 France

Optical beams with orbital angular momentum (OAM) have numerous potential applications, but the means used for their generation often lack crucial on-demand control. In this work, we present a mechanism of converting spin angular momentum (SAM) to OAM in a non-structured beam. The conversion occurs through spin-orbit coupling in a reconfigurable photonic honeycomb lattice with staggering implemented by electromagnetically-induced transparency in an atomic vapor cell. The spin-orbit coupling allows to outcouple the OAM signal from a particular band in a given valley determined by the chirality of light or the lattice staggering, providing a non-zero Berry curvature for generating OAM. The dependence of the output OAM on the chirality of the input beam is the first control knob. The staggering works as a second control knob, flipping the sign of OAM for the fixed chirality. The demonstrated conversion between SAM and OAM is important for optical communications. Our results can be extended to other implementations of paraxial photonic graphene. Copyright © 2025, The Authors. All rights reserved.

关键词： Angular momentum

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Erratum to “Study on droplet wettability of low surface tension working fluid based on special-shaped microstructure surface” [Colloids Surf. C: Environ. Asp. 1 (2023) 100001]

Colloids and Surfaces C: Environmental Aspects

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Colloids and Surfaces C: Environmental Aspects 2024年 2卷

作者： Chao Dang Xiaowei Wang Hao Li Liaofei Yin Mengjie Song School of Mechanical Electronic and Control Engineering Beijing Jiaotong University Beijing 100044 China Beijing Key Laboratory of Microscale Flow and Phase Change Heat Transfer Beijing 100044 China Department of Energy and Power Engineering School of Mechanical Engineering Beijing Institute of Technology Beijing 100081 China

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Instantaneous liquid and gas leakage flow during plunger lifting process in vertical wells 11

Instantaneous liquid and gas leakage flow during plunger lif...

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11th North American Conference on multiphase Technology

作者： Zhao, K. Bai, B. State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University China

Plunger lift is an economical artificial lift method to solve the liquid loading problem in gas wells. Because of the inevitable annular gap between plunger and tube wall, the liquid above plunger may leak downward and the gas may slip upward during lifting process. How to quantitatively describe the gas-liquid counter-current flow sealing property is still challenging to optimize the plunger lift method. In this paper, the liquid leakage and gas slippage were observed experimentally. The transient physical models for gas and liquid leakage were proposed and verified. © 11th North American Conference on multiphase Technology. All rights reserved.

关键词： Liquids

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Photothermal Synergistic Effect Induces Bimetallic Cooperation to Modulate Product Selectivity of CO2Reduction on Different CeO2Crystal Facets

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Angewandte Chemie 2024年第46期136卷

作者： Yuqi Ren Yitao Si Mingyue Du Changjun You Chunyang Zhang Yuan-Hao Zhu Prof. Zhenkun Sun Prof. Kai Huang Prof. Maochang Liu Prof. Lunbo Duan Prof. Naixu Li School of Chemistry and Chemical Engineering Southeast University No.2 Dongnandaxue Road Nanjing 211189 Jiangsu P.R. 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 Xi'an Shaanxi 710049 P.R. China Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education School of Energy and Environment No.2 Dongnandaxue Road Nanjing 210096 Jiangsu P.R. China

Product selectivity of solar-driven CO 2 reduction and H 2 O oxidation reactions has been successfully controlled by tuning the spatial distance between Pt/Au bimetallic active sites on different crystal facets of CeO 2 catalysts. The replacement depth of Ce atoms by monatomic Pt determines the distance between bimetallic sites, while Au clusters are deposited on the surface. This space configuration creates a favourable microenvironment for the migration of active hydrogen species (*H). The *H is generated via the activation of H 2 O on monatomic Pt sites and migrate towards Au clusters with a strong capacity for CO 2 adsorption. Under concentrated solar irradiation, selectivity of the (100) facet towards CO is 100 %, and the selectivity of the (110) and (111) facets towards CH 4 is 33.5 % and 97.6 %, respectively. Notably, the CH 4 yield on the (111) facet is as high as 369.4 μmol/g/h, and the solar-to-chemical energy efficiency of 0.23 % is 33.8 times higher than that under non-concentrated solar irradiation. The impacts of high-density flux photon and thermal effects on carriers and *H migration at the microscale are comprehensively discussed. This study provides a new avenue for tuning the spatial distance between active sites to achieve optimal product selectivity.

关键词： Photothermal catalysis CO2 reduction Product selectivity Bimetallic active sites Spatial distance

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