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Fractal Description of the Solid/Liquid Interface of a Directionally Solidified Superalloy with Different Phosphorus Content
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作者 Liling SUN Lianke DONG Jinghua ZHANG Zhuangqi HU Institute of Metal Research,Academia Sinica,Shenyang,110015,China 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 1993年第6期441-444,共4页
The solid/liquid interface of a directionally solidified Ni-base superalloy with different phosphorus contents was quantitatively described by means of fractat method.When the solidification rate was fixed,the relatio... The solid/liquid interface of a directionally solidified Ni-base superalloy with different phosphorus contents was quantitatively described by means of fractat method.When the solidification rate was fixed,the relationship between the fractal dimensionality of the solid/liquid interface and the phos- phorus content of the test alloy was given.Combined the thermodynamics and fractal theory,the ef- fect mechanism of phosphorus content on fractal dimensionality of the solid/liquid interface was discussed. 展开更多
关键词 fractal description solid/liquid interface PHOSPHORUS SUPERALLOY
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Microstructure and Solid/Liquid Interface Evolutions of Directionally Solidified Fe-Al-Ta Eutectic Alloy 被引量:2
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作者 CUI Chunjuan WANG Songyuan +4 位作者 YANG Meng SU Haijun WEN Yagang WANG Pei REN Chiqiang 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2019年第3期656-661,共6页
A modified Bridgman directional solidification technique was used to prepare Fe-Al-Ta eutectic in situ composites at different growth rates ranging from 6 to 80 μm/s. The directionally solidified FeAl-Ta eutectic com... A modified Bridgman directional solidification technique was used to prepare Fe-Al-Ta eutectic in situ composites at different growth rates ranging from 6 to 80 μm/s. The directionally solidified FeAl-Ta eutectic composites are composed of two phases: Fe(Al,Ta) matrix phase, and Fe2 Ta(Al) Laves phase. Solidification microstructure is affected by solidification rate. Microstructure of the Fe-Al-Ta eutectic alloy grown at 6.0 μm/s is broken-lamellar eutectic. Eutectic colonies are formed with the increase of the solidification rate. Microstructures are mainly composed of the lamellar or fibrous eutectic at the center of the colony and coarse lamellar eutectic zone at the boundary. Meanwhile, the inter-lamellar spacing(or the inter-rod spacing) is decreased. The spacing adjustments are also observed in Fe-Al-Ta eutectic alloy. The solid/liquid interface evolves from planar interface to shallow cellular interface, then to deep cellular, and finally to shallow cellular planar with the increase of the solidification rate. 展开更多
关键词 directional solidIFICATION solidIFICATION rate EUTECTIC alloy solid/liquid interface
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Engineering large-scaled electrochromic semiconductor films as reproductive SERS substrates for operando investigation at the solid/liquid interfaces 被引量:2
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作者 Lingling Yang Jiuju Feng +4 位作者 Jia-Ning Wang Zhida Gao Jingwen Xu Ye Mei Yan-Yan Song 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第12期5169-5173,共5页
Although surface-enhanced Raman spectroscopy(SERS)has been applied for gathering fingerprint information,even in single molecule analysis,the decayed Raman signals in aqueous solutions largely obstruct the on-site ins... Although surface-enhanced Raman spectroscopy(SERS)has been applied for gathering fingerprint information,even in single molecule analysis,the decayed Raman signals in aqueous solutions largely obstruct the on-site insight reaction process.In this study,large-scaled semiconductor films with multi-walled(TiO_(2)/WO_(3)/TiO_(2))nanopore distribution are fabricated by combining electrochemical anodization and sputtering technique,and then employed as the SERS substrates for detection of molecules at the solid/liquid interfaces.Given the remarkably improved electrochromic property of the multi-walled film,such SERS substrates were endowed with tunable oxygen vacancy(VO)density and distribution via simply applying electrochemical bias voltage,which enabled one to achieve an enhanced charge transfer efficiency and thus a remarkably increased Raman signal even in solution.The VO-rich SERS substrate is highly repeatable,thus providing a reliable platform for in-situ monitoring of the target molecules or intermediates at the solid/liquid interfaces. 展开更多
关键词 Charge transfer ELECTROCHROMISM Oxygen vacancies SERS substrate solid liquid interface
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Lithium-Ion Dynamic Interface Engineering of Nano-Charged Composite Polymer Electrolytes for Solid-State Lithium-Metal Batteries
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作者 Shanshan Lv Jingwen Wang +7 位作者 Yuanming Zhai Yu Chen Jiarui Yang Zhiwei Zhu Rui Peng Xuewei Fu Wei Yang Yu Wang 《Nano-Micro Letters》 2026年第2期288-305,共18页
Composite polymer electrolytes(CPEs)offer a promising solution for all-solid-state lithium-metal batteries(ASSLMBs).However,conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving... Composite polymer electrolytes(CPEs)offer a promising solution for all-solid-state lithium-metal batteries(ASSLMBs).However,conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving the overall performance of CPEs due to their difficulty in achieving robust electrochemical and mechanical interfaces simultaneously.Here,by regulating the surface charge characteristics of halloysite nanotube(HNT),we propose a concept of lithium-ion dynamic interface(Li^(+)-DI)engineering in nano-charged CPE(NCCPE).Results show that the surface charge characteristics of HNTs fundamentally change the Li^(+)-DI,and thereof the mechanical and ion-conduction behaviors of the NCCPEs.Particularly,the HNTs with positively charged surface(HNTs+)lead to a higher Li^(+)transference number(0.86)than that of HNTs-(0.73),but a lower toughness(102.13 MJ m^(-3)for HNTs+and 159.69 MJ m^(-3)for HNTs-).Meanwhile,a strong interface compatibilization effect by Li^(+)is observed for especially the HNTs+-involved Li^(+)-DI,which improves the toughness by 2000%compared with the control.Moreover,HNTs+are more effective to weaken the Li^(+)-solvation strength and facilitate the formation of Li F-rich solid-electrolyte interphase of Li metal compared to HNTs-.The resultant Li|NCCPE|LiFePO4cell delivers a capacity of 144.9 m Ah g^(-1)after 400 cycles at 0.5 C and a capacity retention of 78.6%.This study provides deep insights into understanding the roles of surface charges of nanofillers in regulating the mechanical and electrochemical interfaces in ASSLMBs. 展开更多
关键词 Charged nanofillers Nanocomposite polymer electrolyte Dynamic lithium ion interface solid ion-conductors solidstate lithium-metal battery
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Adsorption-modulated dynamical stability of nanobubbles at the solid–liquid interface
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作者 Guiyuan Huang Lili Lan +2 位作者 Binghai Wen Li Yang Yong Yang 《Chinese Physics B》 2025年第6期401-408,共8页
We study the effects of gas adsorption on the dynamics and stability of nanobubbles at the solid–liquid interface. The phase diagram and dynamic evolution of surface nanobubbles were analyzed under varying equilibriu... We study the effects of gas adsorption on the dynamics and stability of nanobubbles at the solid–liquid interface. The phase diagram and dynamic evolution of surface nanobubbles were analyzed under varying equilibrium adsorption constant.Four distinct dynamic behaviors appear in the phase diagram: shrinking to dissolution, expanding to bursting, shrinking to stability, and expanding to stability. Special boundary states are identified in phase diagram, where the continuous growth of nanobubbles can take place even under very weak gas–surface interaction or with very small initial bubble size. Surface adsorption plays a critical role in the stability, lifetime, radius, and contact angle of nanobubbles, thereby demonstrating that pinning is not a prerequisite for stabilization. Furthermore, stable equilibrium nanobubbles exhibit a characteristic range of footprint radius, a limited height, and a small contact angle, consistent with experimental observations. 展开更多
关键词 NANOBUBBLES solidliquid interface phase diagram gas adsorption
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Effect and mechanism of Ti−O solid solution layer on interfacial bonding strength of cold roll bonded titanium/stainless steel laminated composite plate
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作者 Zhi-yan YANG Xue-feng LIU +1 位作者 Hong-ting CHEN Xin MA 《Transactions of Nonferrous Metals Society of China》 2026年第1期171-182,共12页
Titanium plates with a Ti−O solid solution surface-hardened layer were cold roll-bonded with 304 stainless steel plates with high work hardening rates.The evolution and mechanisms affecting the interfacial bonding str... Titanium plates with a Ti−O solid solution surface-hardened layer were cold roll-bonded with 304 stainless steel plates with high work hardening rates.The evolution and mechanisms affecting the interfacial bonding strength in titanium/stainless steel laminated composites were investigated.Results indicate that the hardened layer reduces the interfacial bonding strength from over 261 MPa to less than 204 MPa.During the cold roll-bonding process,the hardened layer fractures,leading to the formation of multi-scale cracks that are difficult for the stainless steel to fill.This not only hinders the development of an interlocking interface but also leads to the presence of numerous microcracks and hardened blocks along the nearly straight interface,consequently weakening the interfacial bonding strength.In metals with high work hardening rates,the conventional approach of enhancing interface interlocking and improving interfacial bonding strength by using a surface-hardened layer becomes less effective. 展开更多
关键词 titanium/stainless steel laminated composite plate Ti−O solid solution hardened layer interlocking interface formation mechanism interfacial bonding strength
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Temperature tailored robust solid electrolyte interface for improved high-areal-capacity prelithiated silicon-carbon anode
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作者 Yanyan Lu Xinrong Lv +3 位作者 Jiacheng Shao Cunman Zhang Liming Jin Junsheng Zheng 《Journal of Energy Chemistry》 2025年第10期76-88,共13页
Silicon is considered one of the most promising candidates for incorporation into carbon-based anodes in lithium-ion batteries(LIBs)due to its high specific capacity.However,the significant volume changes during charg... Silicon is considered one of the most promising candidates for incorporation into carbon-based anodes in lithium-ion batteries(LIBs)due to its high specific capacity.However,the significant volume changes during charge and discharge cycles lead to repeated reconstruction of the solid electrolyte interface(SEI)film and continuous loss of active lithium.Pre-lithiation method is regarded as a highly attractive approach for effectively compensating for active lithium loss during the charge and discharge cycles of LIBs.Constructing a stable SEI film is particularly crucial in the pre-lithiation process.In this study,we developed a direct contact pre-lithiation(DC-Pr)method to create a temperature-tailored robust SEI film interface on silicon-carbon(Si@C)electrodes.By investigating the morphology,structure,and composition of the SEI formed on Si@C electrodes at different pre-lithiation temperatures(50,25,0,and-25℃),we demonstrated that controlling the lithiation temperature to regulate the migration rate of lithium ions within the Si@C electrode yields a lithiated Si@C anode(25-Pr-Si@C)at 25℃ with a continuous,uniform SEI film(~3.65 nm)enriched with Li_(2)O-LiF,which exhibits synergistic effects.Importantly,the initial Coulombic efficiency(ICE)of 25-Pr-Si@C significantly improved from 85.4% in the unlithiated Si@C electrode(Blank-Si@C)to 106.1%.Additionally,the full cell configuration using a high areal loading of lithiated Si@C(~5.5 mA h cm^(-2))as the anode and NCM811 as the cathode(NCM811||25-Pr-Si@C)demonstrated superior cycling performance,maintaining 69.4% of capacity retention and achieving a Coulombic efficiency of over 99.7% after 150 cycles(0.5 C).Therefore,this simple and efficient experimental design provides a high-performance,controllable,and scalable pre-lithiation method for LIBs,paving the way for the commercialization of LIBs utilizing pre-lithiation techniques. 展开更多
关键词 Pre-lithiation Silicon-carbon solid electrolyte interface film Lithium-ion batteries
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Evolution of bonding interface in solid-liquid cast-rolling bonding of Cu/Al clad strip 被引量:14
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作者 Hua-gui HUANG Yi-kang DONG +1 位作者 Meng YAN Feng-shan DU 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2017年第5期1019-1025,共7页
Cu/Al clad strips are prepared using solid?liquid cast-rolling bonding(SLCRB)technique with a d160mm×150mm twin-roll experimental caster.The extent of interfacial reactions,composition of the reaction products,an... Cu/Al clad strips are prepared using solid?liquid cast-rolling bonding(SLCRB)technique with a d160mm×150mm twin-roll experimental caster.The extent of interfacial reactions,composition of the reaction products,and their micro-morphology evolution in the SLCRB process are investigated with scanning electron microscope(SEM),energy dispersive spectrometer(EDS),and X-ray diffraction(XRD).In the casting pool,initial aluminized coating is first generated on the copper strip surface,with the diffusion layer mainly consisting ofα(Al)+CuAl2and growing at high temperatures,with the maximum thickness of10μm.After sequent rolling below the kiss point,the diffusion layer is broken by severe elongation,which leads to an additional crack bond process with a fresh interface of virgin base metal.The average thickness is reduced from10to5μm.The reaction products,CuAl2,CuAl,and Cu9Al4,are dispersed along the rolling direction.Peeling and bending test results indicate that the fracture occurs in the aluminum substrate,and the morphology is a dimple pattern.No crack or separation is found at the bonding interface after90°-180°bending.The presented method provides an economical way to fabricate Cu/Al clad strip directly. 展开更多
关键词 Cu/Al clad strip solid.liquid cast-rolling bonding bonding interface reaction diffusion peeling test
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An APXPS endstation for gas–solid and liquid–solid interface studies at SSRF 被引量:4
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作者 Jun Cai Qiao Dong +7 位作者 Yong Han Bao-Hua Mao Hui Zhang Patrik G.Karlsson John ?hlund Ren-Zhong Tai Yi Yu Zhi Liu 《Nuclear Science and Techniques》 SCIE CAS CSCD 2019年第5期103-112,共10页
In the past few decades, various surface analysis techniques find wide applications in studies of interfacial phenomena ranging from fundamental surface science,catalysis, environmental science and energy materials.Wi... In the past few decades, various surface analysis techniques find wide applications in studies of interfacial phenomena ranging from fundamental surface science,catalysis, environmental science and energy materials.With the help of bright synchrotron sources, many of these techniques have been further advanced into novel in-situ/operando tools at synchrotron user facilities, providing molecular level understanding of chemical/electrochemical processes in-situ at gas–solid and liquid–solid interfaces.Designing a proper endstation for a dedicated beamline is one of the challenges in utilizing these techniques efficiently for a variety of user's requests. Many factors,including pressure differential, geometry and energy of the photon source, sample and analyzer, need to be optimized for the system of interest. In this paper, we discuss the design and performance of a new endstation at beamline02 B at the Shanghai Synchrotron Radiation Facility for ambient pressure X-ray photoelectron spectroscopy studies.This system, equipped with the newly developed hightransmission HiPP-3 analyzer, is demonstrated to be capable of efficiently collecting photoelectrons up to 1500 eV from ultrahigh vacuum to ambient pressure of 20 mbar.The spectromicroscopy mode of HiPP-3 analyzer also enables detection of photoelectron spatial distribution with resolution of 2.8 ± 0.3 lm in one dimension. In addition,the designing strategies of systems that allow investigations in phenomena at gas–solid interface and liquid–solid interface will be highlighted through our discussion. 展开更多
关键词 AMBIENT pressure XPS SYNCHROTRON liquid- solid interface SPECTROMICROSCOPY
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In-situ observation of solid-liquid interface transition during directional solidification of Al-Zn alloy via X-ray imaging 被引量:3
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作者 Yuanhao Dong Sansan Shuai +4 位作者 Tianxiang Zheng Jiawei Cao Chaoyue Chen Jiang Wang Zhongming Ren 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2020年第4期113-123,共11页
The morphological instability of solid/liquid(S/L)interface during solidification will result in different patterns of microstructure.In this study,two dimension(2 D)and three dimension(3 D)in-situ observation of soli... The morphological instability of solid/liquid(S/L)interface during solidification will result in different patterns of microstructure.In this study,two dimension(2 D)and three dimension(3 D)in-situ observation of solid/liquid interfacial morphology transition in Al-Zn alloy during directional solidification were performed via X-ray imaging.Under a condition of increasing temperature gradient(G),the interface transition from dendritic pattern to cellular pattern,and then to planar growth with perturbation was captured.The effect of solidification parameter(the ratio of temperature gradient and growth velocity(v),G/v)on morphological instabilities was investigated and the experimental results were compared to classical"constitutional supercooling"theory.The results indicate that 2 D and 3 D evolution process of S/L interface morphology under the same thermal condition are different.It seems that the S/L interface in 2 D observation is easier to achieve planar growth than that in 3 D,implying higher S/L interface stability in 2 D thin plate samples.This can be explained as the restricted liquid flow under 2 D solidification which is beneficial to S/L interface stability.The in-situ observation in present study can provide coherent dataset for microstructural formation investigation and related model validation during solidification. 展开更多
关键词 AL-ZN ALLOY Directional solidIFICATION solid/liquid interface INSTABILITY IN-SITU observation X-ray imaging
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Targeting stability:Recent progress and perspectives on both anode and cathode interface of halide solid electrolytes
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作者 Nan Zhang Xing-Qi Chen +5 位作者 Xiaoting Lin Peng-Fei Wang Zong-Lin Liu Jie Shu Ping He Ting-Feng Yi 《Journal of Energy Chemistry》 2025年第10期497-517,共21页
Halide solid-state electrolytes(SSEs)have become a new research focus for all-solid-state batteries because of their significant safety advantages,high ionic conductivity,high-voltage stability,and good ductility.None... Halide solid-state electrolytes(SSEs)have become a new research focus for all-solid-state batteries because of their significant safety advantages,high ionic conductivity,high-voltage stability,and good ductility.Nonetheless,stability issues are a key barrier to their practical application.In past reports,the analysis of halide electrolyte stability and its enhancement methods lacked relevance,which limited the design and optimization of halide solid electrolytes.This review focus on stability issues from a chemical,electrochemical,and interfacial point of view,with particular emphasis on the interaction of halide SSEs with anode and cathode interfaces.By focusing on innovative strategies to address the stability issue,this paper aims to further deepen the understanding and development of halide all-solid-state batteries by proposing to focus research efforts on improving their stability in order to address their inherent challenges and match higher voltage cathodes,paving the way for their wider application in the next generation of energy storage technologies. 展开更多
关键词 Halide solid electrolytes Ion transport mechanism Chemical stability Electrochemical stability interface stability
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Interface compatibility between sulfide solid electrolytes and Ni-rich oxide cathode materials:Factors,modification,perspectives
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作者 Tianwen Yang Haijuan Pei +3 位作者 Haijian Lv Shijie Lu Qi Liu Daobin Mu 《Journal of Energy Chemistry》 2025年第2期233-262,I0006,共31页
All-solid-state batteries(ASSBs)assembled with sulfide solid electrolytes(SSEs)and nickel(Ni)-rich oxide cathode materials are expected to achieve high energy density and safety,representing potential candidates for t... All-solid-state batteries(ASSBs)assembled with sulfide solid electrolytes(SSEs)and nickel(Ni)-rich oxide cathode materials are expected to achieve high energy density and safety,representing potential candidates for the next-generation energy storage systems.However,interfacial issues between SSEs and Nirich oxide cathode materials,attributed to space charge layer,interfacial side reactions,and mechanical contact failure,significantly restrict the performances of ASSBs.The interface degradation is closely related to the components of the composite cathode and the process of electrode fabrication.Focusing on the influencing factors of interface compatibility between SSEs and Ni-rich oxide cathode,this article systematically discusses how cathode active materials(CAMs),electrolytes,conductive additives,binders,and electrode fabrication impact the interface compatibility.In addition,the strategies for the compatibility modification are reviewed.Furthermore,the challenges and prospects of intensive research on the degradation and modification of the SSE/Ni-rich cathode material interface are discussed.This review is intended to inspire the development of high-energy-density and high-safety all-solid-state batteries. 展开更多
关键词 Sulfide solid electrolyte Ni-rich oxide cathode interface compatibility Influencing factors All-solid-state batteries
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Maternal stress and the early embryonic microenvironment:investigating long‑term cortisol effects on bovine oviductal epithelial cells using air–liquid interface culture
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作者 Fiona Wahl Jianchao Huo +2 位作者 Shuaizhi Du Jennifer Schoen Shuai Chen 《Journal of Animal Science and Biotechnology》 2025年第1期153-166,共14页
The oviduct epithelium is the initial maternal contact site for embryos after fertilization,offering the microenviron-ment before implantation.This early gestation period is particularly sensitive to stress,which can ... The oviduct epithelium is the initial maternal contact site for embryos after fertilization,offering the microenviron-ment before implantation.This early gestation period is particularly sensitive to stress,which can cause reduced fertil-ity and reproductive disorders in mammals.Nevertheless,the local impact of elevated stress hormones on the ovi-duct epithelium has received limited attention to date,except for a few reports on polyovulatory species like mice and pigs.In this study,we focused on the effects of chronic maternal stress on cattle,given its association with infertil-ity issues in this monoovulatory species.Bovine oviduct epithelial cells(BOEC)differentiated at the air–liquid interface(ALI)were stimulated with 250 nmol/L cortisol for 1 or 3 weeks.Subsequently,they were assessed for morphology,bioelectrical properties,and gene expression related to oviduct function,glucocorticoid pathway,cortisol metabo-lism,inflammation,and apoptosis.Results revealed adverse effects of cortisol on epithelium structure,featured by deciliation,vacuole formation,and multilayering.Additionally,cortisol exposure led to an increase in transepithelial potential difference,downregulated mRNA expression of the major glucocorticoid receptor(NR3C1),upregulated the expression of cortisol-responsive genes(FKBP5,TSC22D3),and significant downregulation of oviductal glycopro-tein 1(OVGP1)and steroid receptors PGR and ESR1.The systematic comparison to a similar experiment previously performed by us in porcine oviduct epithelial cells,indicated that bovine cultures were more susceptible to elevated cortisol levels than porcine.The distinct responses between both species are likely linked to their divergence in the cortisol-induced expression changes of HSD11B2,an enzyme controlling the cellular capacity to metabolise cortisol.These findings provide insights into the species-specific reactions and reproductive consequences triggered by maternal stress. 展开更多
关键词 Air–liquid interface BOVINE CORTISOL Early embryonic microenvironment Epithelial cells Maternal stress OVIDUCT
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Recent Progress in Metallurgical Bonding Mechanisms at the Liquid/Solid Interface of Dissimilar Metals Investigated via in situ X-ray Imaging Technologies 被引量:6
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作者 Zongye Ding Naifang Zhang +3 位作者 Liao Yu Wenquan Lu Jianguo Li Qiaodan Hu 《Acta Metallurgica Sinica(English Letters)》 SCIE EI CAS CSCD 2021年第2期145-168,共24页
The liquid/solid(L/S)interface of dissimilar metals is critical to the microstructure,mechanical strength,and structural integrity of interconnects in many important applications such as electronics,automotive,aeronau... The liquid/solid(L/S)interface of dissimilar metals is critical to the microstructure,mechanical strength,and structural integrity of interconnects in many important applications such as electronics,automotive,aeronautics,and astronautics,and therefore has drawn increasing research interests.To design preferential microstructure and optimize mechanical properties of the interconnects,it is crucial to understand the formation and growth mechanisms of diversified structures at the L/S interface during interconnecting.In situ synchrotron radiation or tube-generated X-ray radiography and tomography technologies make it possible to observe the evolution of the L/S interface directly and therefore have greatly propelled the research in this field.Here,we review the recent progress in understanding the L/S interface behaviors using advanced in situ X-ray imaging techniques with a particular focus on the following two issues:(1)interface behaviors in the solder joints for microelectronic packaging including the intermetallic compounds(IMCs)during refl ow,Sn dendrites,and IMCs during solidification and refl ow porosities and(2)growth characteristics and morphological transition of IMCs in the interconnect of dissimilar metals at high temperature.Furthermore,the main achievements and future research perspectives in terms of metallurgical bonding mechanisms under complex conditions with improved X-ray sources and detectors are remarked and discussed. 展开更多
关键词 liquid/solid interface Metallurgical bonding Dissimilar interconnects In situ X-ray imaging solidIFICATION Microelectronic packaging
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Simulation of the Influence of Pulsed Magnetic Field on the Superalloy Melt with the Solid-Liquid Interface in Directional Solidification 被引量:5
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作者 Kuiliang Zhang Yingju Li Yuansheng Yang 《Acta Metallurgica Sinica(English Letters)》 SCIE EI CAS CSCD 2020年第10期1442-1454,共13页
The effect of the pulsed magnetic field on the grain refinement of superalloy K4169 has been studied in directional solidification.In the presence of the solid-liquid interface condition,the distributions of the elect... The effect of the pulsed magnetic field on the grain refinement of superalloy K4169 has been studied in directional solidification.In the presence of the solid-liquid interface condition,the distributions of the electromagnetic force,flow field,temperature field,and Joule heat in front of the solid-liquid interface in directional solidification with the pulsed magnetic field are simulated.The calculation results show that the largest electromagnetic force in the melt appears near the solid-liquid interface,and the electromagnetic force is distributed in a gradient.There are intensive electromagnetic vibrations in front of the solid-liquid interface.The forced melt convection is mainly concentrated in front of the solid-liquid interface,accompanied by a larger flow velocity.The simulation results indicate that the grain refinement is attributed to that the electromagnetic vibration and forced convection increase the nucleation rate and the probability of dendrite fragments survival,for making dendrite easily fragmented,homogenizing the melt temperature,and increasing the undercooling in front of the solid-liquid interface. 展开更多
关键词 Pulsed magnetic field solidliquid interface SIMULATION Electromagnetic force Melt convection Superalloy
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Three-fold optimization of Pt/ionomer interface by ionic liquid-modified MOF-808 in cathode of proton exchange membrane fuel cells
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作者 Huangli Yan Chengwen Yu +2 位作者 Xianming Zhang Meihua Tang Shengli Chen 《Chinese Journal of Catalysis》 2025年第8期84-94,共11页
The large-scale commercialization of proton exchange membrane fuel cells(PEMFCs)has been hindered by the high demand of platinum(Pt)in the cathode due to the sluggish kinetics of the oxygen reduction reaction.Reducing... The large-scale commercialization of proton exchange membrane fuel cells(PEMFCs)has been hindered by the high demand of platinum(Pt)in the cathode due to the sluggish kinetics of the oxygen reduction reaction.Reducing the amount of Pt would worsen the problems caused by the adsorption of perfluorinated sulfonic acid(PFSA)ionomers to Pt via the side chains,namely,blocking the active sites of Pt and inducing densely packed layers of fluorocarbon backbones on Pt surface to obstruct local O_(2)transport at the Pt/PFSA interfaces.This work aims at optimizing the Pt/ionomer interface to mitigate the sulfonate adsorption and in the meantime to reduce the local O_(2)transport resistance(R_(local)),by using a porous composite of 1-butyl-3-methylimidazolium hydrogen sulfate ionic liquid(IL)modified MOF-808(BMImHSO_(4)@MOF-808)as additive in cathodic catalyst layer(CCL).Through detailed physical,spectroscopic and electrochemical characterizations,we demonstrate a three-fold optimization mechanism of Pt/ionomer interface structure by BMImHSO_(4)@MOF-808:the unsaturated metal sites in MOF-808 effectively inhibit the sulfonate adsorption on Pt through coordination with the sulfonates of PFSA,thereby improving catalyst utilization;the pores in MOF-808 establish efficient transport channels for gaseous oxygen,significantly reducing R_(local);the IL modification layers facilitate the formation of continuous proton transport networks,increasing proton conductivity.The incorporation of BMImHSO_(4)@MOF-808 in a low-Pt CCL(0.1 mg_(Pt)cm^(-2))yields a peak power density of 1.9 W cm^(-2)for PEMFC under H_(2)-O_(2)condition,and ca.20%increase of power density under H_(2)-air condition as compared with conventional CCL,indicating the prospect of IL-MOF composites as an efficient additive to enhance the performance of PEMFCs. 展开更多
关键词 Proton exchange membrane fuel cells Pt/ionomer interface Local oxygen transport MOF-808 Ionic liquid Sulfonate adsorption
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Understanding fundamentals of electrochemical reactions with tender X-rays:A new lab-based operando X-ray photoelectron spectroscopy method for probing liquid/solid and gas/solid interfaces across a variety of electrochemical systems 被引量:1
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作者 Chiyan Liu Qiao Dong +5 位作者 Yong Han Yijing Zang Hui Zhang Xiaoming Xie Yi Yu Zhi Liu 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第11期2858-2870,共13页
Electrocatalysis is key to improving energy efficiency,reducing carbon emissions,and providing a sustainable way of meeting global energy needs.Therefore,elucidating electrochemical reaction mechanisms at the electrol... Electrocatalysis is key to improving energy efficiency,reducing carbon emissions,and providing a sustainable way of meeting global energy needs.Therefore,elucidating electrochemical reaction mechanisms at the electrolyte/electrode interfaces is essential for developing advanced renewable energy technologies.However,the direct probing of real-time interfacial changes,i.e.,the surface intermediates,chemical environment,and electronic structure,under operating conditions is challenging and necessitates the use of in situ methods.Herein,we present a new lab-based instrument commissioned to perform in situ chemical analysis at liquid/solid interfaces using ambient pressure X-ray photoelectron spectroscopy(APXPS).This setup takes advantage of a chromium source of tender X-rays and is designed to study liquid/solid interfaces by the“dip and pull”method.Each of the main components was carefully described,and the results of performance tests are presented.Using a three-electrode setup,the system can probe the intermediate species and potential shifts across the liquid electrolyte/solid electrode interface.In addition,we demonstrate how this system allows the study of interfacial changes at gas/solid interfaces using a case study:a sodium–oxygen model battery.However,the use of APXPS in electrochemical studies is still in the early stages,so we summarize the current challenges and some developmental frontiers.Despite the challenges,we expect that joint efforts to improve instruments and the electrochemical setup will enable us to obtain a better understanding of the composition–reactivity relationship at electrochemical interfaces under realistic reaction conditions. 展开更多
关键词 Tender X-rays Ambient pressure X-ray photoelectron spectroscopy ELECTROCATALYSIS liquid/solid interface Gas/solid interface
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Treatment of discontinuous interface in liquid-solid forming with extended finite element method 被引量:1
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作者 周计明 齐乐华 《中国有色金属学会会刊:英文版》 CSCD 2010年第S3期911-915,共5页
Extended finite element method(XFEM) is proposed to simulate the discontinuous interface in the liquid-solid forming process.The discontinuous interface is an important phenomenon happening in the liquid-solid forming... Extended finite element method(XFEM) is proposed to simulate the discontinuous interface in the liquid-solid forming process.The discontinuous interface is an important phenomenon happening in the liquid-solid forming processes and it is difficult to be simulated accurately with conventional finite element method(CFEM) because it involves solid phase and liquid phase simultaneously.XFEM is becoming more and more popular with the need of solving the discontinuous problem happening in engineering field.The implementation method of XFEM is proposed on Abaqus code by using UEL(user element) with the flowchart.The key is to modify the element stiffness in the proposed method by using UEL on the platform of Abaqus code.In contrast to XFEM used in the simulation of solidification,the geometrical and physical properties of elements were modified at the same time in our method that is beneficial to getting smooth interface transition and precise analysis results.The analysis is simplified significantly with XFEM. 展开更多
关键词 EXTENDED FINITE ELEMENT method solid metal with liquid phase numerical simulation
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Mathematical Modelling of Particle Movement Ahead of the Solid-liquid Interface in Continuous Casting 被引量:4
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作者 HongLEI YongliJIN +1 位作者 MiaoyongZHU JichengHE 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2002年第5期403-406,共4页
Whether the particle will be trapped by the solid-liquid interface or not is dependent on its moving behavior ahead of the interface, so a mathematical model has been developed to investigate the movement of the parti... Whether the particle will be trapped by the solid-liquid interface or not is dependent on its moving behavior ahead of the interface, so a mathematical model has been developed to investigate the movement of the particle ahead of the solid-liquid interface. Based on the theory for the boundary layer, the fluid velocity field near the solid-liquid interface was obtained, and the trajectories of particles were calculated by the equations of motion for particles. In this model, the drag force, the added mass force, the buoyance force, the gravitational force, the Saffman force and the Basset history force are considered. The results show that the behavior of the particle ahead of the solid-liquid interface is affected by the physical property of the particle and fluid flow. And in the continuous casting process, if it moves in the stream directed upward or downward near vertical solid-liquid interface or in the horizontal flow under the solid-liquid interface, the particle with the diameter from 5 um to 60um can reach the solid-liquid interface. But if it moves in horizontal flow above the solid-liquid interface, only the particle with the diameter from 5 um to 10 um can reach the solid-liquid interface. 展开更多
关键词 Continuous casting. Particle Fluid flow solid-liquid interface Mathematical model
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Atomic-level characterization of liquid/solid interface 被引量:1
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作者 Jiani Hong Ying Jiang 《Chinese Physics B》 SCIE EI CAS CSCD 2020年第11期25-36,共12页
The detailed understanding of various underlying processes at liquid/solid interfaces requires the development of interface-sensitive and high-resolution experimental techniques with atomic precision.In this perspecti... The detailed understanding of various underlying processes at liquid/solid interfaces requires the development of interface-sensitive and high-resolution experimental techniques with atomic precision.In this perspective,we review the recent advances in studying the liquid/solid interfaces at atomic level by electrochemical scanning tunneling microscope(EC-STM),non-contact atomic force microscopy(NC-AFM),and surface-sensitive vibrational spectroscopies.Different from the ultrahigh vacuum and cryogenic experiments,these techniques are all operated in situ under ambient condition,making the measurements close to the native state of the liquid/solid interface.In the end,we present some perspectives on emerging techniques,which can defeat the limitation of existing imaging and spectroscopic methods in the characterization of liquid/solid interfaces. 展开更多
关键词 liquid/solid interface atomic scale scanning tunneling microscope(STM) atomic force microscopy(AFM)
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