In this work, we have investigated the mechanical properties of Cu/Ta, Ag/Cu and Ag/Nb multilayers with different heterogeneous interfaces. The results suggest that when individual layer thickness （h） is larger than...In this work, we have investigated the mechanical properties of Cu/Ta, Ag/Cu and Ag/Nb multilayers with different heterogeneous interfaces. The results suggest that when individual layer thickness （h） is larger than 5-10 nm, the hardness/strength of three different multilayer systems has the similar length scale effect with decreasing layer thickness, while when h ≤ 5 nm, the three multilayer systems show remarkably different plastic deformation behaviors. The strength curves exhibit the variation trends of unchanging, softening and increasing corresponding to Cu/Ta, Ag/Cu and Ag/Nb multilayers, respectively. The microstructure analysis shows that three kinds of multilayers have totally different interfacial structures, which lead to the different strengthening or softening mechanisms.展开更多
Photoelectrocatalytic(PEC)seawater splitting as a green and sustainable route to harvest hydrogen is attractive yet hampered by low activity of photoanodes and unexpected high selectivity to the corrosive and toxic ch...Photoelectrocatalytic(PEC)seawater splitting as a green and sustainable route to harvest hydrogen is attractive yet hampered by low activity of photoanodes and unexpected high selectivity to the corrosive and toxic chlorine.Especially,it is full of challenges to unveil the key factors influencing the selectivity of such complex PEC processes.Herein,by regulating the energy band and surface structure of the anatase TiO_(2) nanotube array photoanode via nitrogen-doping,the seawater PEC oxidation shifts from Cl^(-)oxidation reaction(ClOR)dominant on the TiO_(2) photoanode(61.6%)to oxygen evolution reaction(OER)dominant on the N-TiO_(2) photoanode(62.9%).Comprehensive investigations including operando photoelectrochemical FTIR and DFT calculations unveil that the asymmetric hydrogen-bonding water at the N-TiO_(2) electrode/electrolyte interface enriches under illumination,facilitating proton transfer and moderate adsorption strength of oxygen-intermediates,which lowers the energy barrier for the OER yet elevates the energy barrier for the ClOR,resulting to a promoted selectivity towards the OER.The work sheds light on the underlying mechanism of the PEC water oxidation processes,and highlights the crucial role of interfacial water on the PEC selectivity,which could be regulated by controlling the energy band and the surface structure of semiconductors.展开更多
Current research on the fabrication of rolled composite plates primarily focuses on processing and bonding mechanisms.Compared with hot-rolling technology,the electrically assisted rolling process has demonstrated exc...Current research on the fabrication of rolled composite plates primarily focuses on processing and bonding mechanisms.Compared with hot-rolling technology,the electrically assisted rolling process has demonstrated excellent performance in interfacial bonding effects.However,the influence of different current loading modes on the interfacial recombination process of composite panels varies significantly.In this study,low-frequency electrically assisted rolling was used in the first pass to pre-bond a composite plate at a low reduction rate of 15%.High-frequency electrically assisted rolling was used during the second pass,and Al/Mg alloy composite plates were obtained.The interfacial microstructure and mechanical properties of the composite plate were coordinated regulation by designing the rolling reduction rate.The results showed the interfacial morphology of the alternating distribution of the melt-diffusion layer,diffusion layer,and the formation of a new Al/Mg bonding interface.At the melt-diffusion interface,the irregular intermetallic compounds(IMCs)and the new Al/Mg bonding interface were alternately distributed,and the IMCs contained theα-Mg,Mg17Al12,and Mg2Al3 phases.In addition,an extremely high shear strength of 78.26 MPa was achieved.Adhesion of the Mg alloy matrix was observed on the fracture surface of the Al alloy side.The high shear strength was mainly attributed to the formation of a unique interfacial structure and the appearance of a melt-diffusion layer.Compared to the diffusion-reduction interface,the regular rectangular IMCs and the new Al/Mg bonding interface were alternately distributed,and the IMCs consisted of the Mg17Al12 and Mg2Al3 phases.The shear test results showed that the shear strength of the interface reached 68.69 MPa,and a regular distribution of the Mg alloy matrix with dimples and the Al alloy matrix with a necking zone was observed on the fracture surface of the Al side.Tensile strength test results revealed a maximum value of 316.86 MPa for the Al/Mg alloy composite plate.The tensile and interfacial bonding strengths can be synchronously enhanced by coordinating the regulation of the interfacial structure.This study proposes a new electrically assisted rolling technology that is useful for the fabrication of composite plates with excellent mechanical properties.展开更多
The employment of single atom catalysts(SACs)remarkably increases atomic utilization and catalytic efficiency in various electrochemical processes,especially when coupled with metal clusters/nanoparticles.However,the ...The employment of single atom catalysts(SACs)remarkably increases atomic utilization and catalytic efficiency in various electrochemical processes,especially when coupled with metal clusters/nanoparticles.However,the synergistic effects mainly focus on the energetics of key intermediates during the electrocatalysis,while the properties of electrode surface and electric-double-layer(EDL)structure are largely overlooked.Herein,we report the synthesis of Ru nanoparticles integrated with neighboring Ru single atoms on nitrogen doped carbon(Ru1,n/NC)as efficient catalysts toward hydrogen oxidation reaction(HOR)under alkaline electrolytes.Electrochemical data,in situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy,and density functional theory calculations reveal that the positively charged Ru single atoms could lead to the dynamically regulated proportion of strongly hydrogen-bonded interfacial water structure with O-down conformation and optimized connectivity of the hydrogen-bond network in the EDL region,which contribute to the accelerated diffusion of hydroxide ions to the electrified interfaces.Consequently,the obtained Ru1,n/NC catalyst displays remarkable HOR performance with the mass activity of 1.15 mAμgPGM^(-1) under alkaline electrolyte.This work demonstrates the promise of single atoms for interfacial water environment adjustment and mass transfer process modulation,providing new insights into rational design of highly-effective SAC-based electrocatalysts.展开更多
Photoelectrochemical water oxidation reaction (PEC-WOR) as a sustainable route to produce H_(2)O_(2) is attractive but limited by low activity and poor product selectivity of photoanodes due to limited photogenerated ...Photoelectrochemical water oxidation reaction (PEC-WOR) as a sustainable route to produce H_(2)O_(2) is attractive but limited by low activity and poor product selectivity of photoanodes due to limited photogenerated charge efficiency and unfavorable thermodynamics. Herein, by crystal orientation engineering, the WO_(3) photoanode exposing (200) facets achieves both superior WOR activity (15.4 mA cm^(−2) at 1.76 VRHE) and high selectivity to H_(2)O_(2) (∼70%). Comprehensive experimental and theoretical investigations discover that the high PEC-WOR activity of WO_(3)-(200) is attributed to the rapid photogenerated charge separation/transfer both in bulk and at interfaces of WO_(3)-(200) facet, which reduces the charge transfer resistance. This, coupling with the unique defective hydrogen bonding network at the WO_(3)-(200)/electrolyte interface evidenced by operando PEC Fourier transform infrared spectroscopy, facilitating the outward-transfer of the WOR-produced H^(+), lowers the overall reaction barrier for the PEC-WOR. The superior selectivity of PEC-WOR to H_(2)O_(2) is ascribed to the unique defective hydrogen bonding network alleviated adsorption of ∗OH over the WO_(3)-(200) facet, which specially lowers the energy barrier of the 2-electron pathway, as compared to the 4-electron pathway. This work addresses the significant role of crystal orientation engineering on photoelectrocatalytic activity and selectivity, and sheds lights on the underlying PEC mechanism by understanding the water adsorption behaviors under illumination. The knowledge gained is expected to be extended to other photoeletrochemical reactions.展开更多
Al_(2)O_(3)-based eutectic ceramics are considered as promising candidates for ultra-high-temperature structural materials due to their exceptional thermal stability and mechanical properties.Nonetheless,several chall...Al_(2)O_(3)-based eutectic ceramics are considered as promising candidates for ultra-high-temperature structural materials due to their exceptional thermal stability and mechanical properties.Nonetheless,several challenges must be overcome before they can be widely used.This paper reviews in detail the tailoring of microstructure from the aspect of process parameters,the updated knowledge gained in microstructure(crystallographic orientation,high-resolution interfacial structures)and the latest means of optimizing eutectic microstructure(seed-induced method,introducing low-energy grain boundaries and high-entropy phase).Additionally,the paper explores future techniques for the fabrication of bulk ceramic materials and effective toughening approaches.This review highlights the achievements made especially in the last 15 years,current limitations in Al_(2)O_(3)-based eutectic ceramics,and offers comprehensive insights and strategic guidance for further mechanical breakthroughs.展开更多
FeSiAl-based soft magnetic composites(SMCs),prepared from insulated FeSiAl powders,are widely applied in electronic devices.However,it is still challenging to achieve high magnetic and mechanical properties simultaneo...FeSiAl-based soft magnetic composites(SMCs),prepared from insulated FeSiAl powders,are widely applied in electronic devices.However,it is still challenging to achieve high magnetic and mechanical properties simultaneously due to the undesirable insulation layer.Here,double Al_(2)O_(3) insulation layers are prepared for FeSiAl SMC.Atomic-scale characterizations reveal an in-situ epitaxial Al_(2)O_(3) layer at FeSiAl surface under the catalysis of NaAlO_(2),and an outer amorphous Al_(2)O_(3) layer by subsequent NaAlO2 hydrolysis.The above structure ensures effective insulation of FeSiAl powders and excellent magnetic properties of the FeSiAl/NaAlO2 SMC,with permeability of 101 and power loss of 128 mW/cm^(3)(50 mT,100 kHz)respectively.Moreover,in-situ Al_(2)O_(3)/amorphous Al_(2)O_(3) on FeSiAl matrix also leads to distinguished crush strength of 36.5 MPa for the core sample,which is ascribed to the enhanced adhesion at different interfaces as evidenced by similar local oxygen coordination and low strain distribution.This work provides a novel method to fabricate high-performance FeSiAl SMCs.展开更多
The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 part...The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 particles, but an orbital interaction through the mutual overlap of the d orbits does exist in the interfacial regions between Ni atoms and Zr 3+ ions.展开更多
Low-temperature lithium sulfur(Li-S)batteries have attracted increasing attention,but lithium polysulfide(LiPSs)clu stering and tardy ionic mobility have been challenging issues,which could be exacerbated under high s...Low-temperature lithium sulfur(Li-S)batteries have attracted increasing attention,but lithium polysulfide(LiPSs)clu stering and tardy ionic mobility have been challenging issues,which could be exacerbated under high sulfur loading and lean electrolyte.The distinct behaviors of sulfur cathode in lowtemperature Li-S batteries call for special regulations of the sulfur host to improve the electrochemical performances.Here,a three-dimensional Ti_(3)C_(2)micro-cage(TCC)with an interfacial structure modulated by rich curvatures has been fabricated to propel the sulfur electrochemistry at subzero temperatures.Spectroscopic/microscopic analyses and theoretical calculations elucidate that the precipitation of ultrafine Ti-metal particles on the in-situ generated Ti_(3)C_(2)nanoribbons could trigger the self-scrolling of Ti_(3)C_(2)nanoribbons into TCC.Moreover,in-situ ultraviolet-visible spectra collected at low temperature and theoretical calculations verified that the TCC regulated by rich curvatures have effectively alleviated the Li+dissociation barrier,reduced the energy barrier for charge transfer at the electrode-electrolyte interface,and restrained the clustering and shuttling of LiPSs,thus accelerating the electrochemical conversion kinetics of sulfur species at low temperatures.The performances of the carbon-free TCC-S cathode at low temperatures have been also compared from the aspects of cathode configuration and measurement condition,to demonstrate the potential of TCC.This work can not only provide new methodology for regulating the interfacial structure of MXene to enrich the materials library for low-temperature Li-S batteries,but also expand understanding about the role of interfacial structure of sulfur host in Li-S batteries.展开更多
A novel process route using tape casting and stacking for fabricating porous scaffold of solid oxide fuel cells （SOFC） was demonstrated. The linear shrinkages of anode （Ni-YSZ, YSZ stands for 3% Y2O3 （mole fractio...A novel process route using tape casting and stacking for fabricating porous scaffold of solid oxide fuel cells （SOFC） was demonstrated. The linear shrinkages of anode （Ni-YSZ, YSZ stands for 3% Y2O3 （mole fraction） stabilized ZrO2 ） and cathode （LSM-YSZ, LSM stands for La0.8Sr0.2MnO3 ） were optimized to be uniform with that of electrolyte during sintering, by controlling the content of pore former. The micromorphology and interface microstructure of the cross-section of the porous scaffold were observed by optical microscope and scanning electron microscope, respectively. The element distribution and phase composition were analyzed by energy dispersive spectrometer and X-ray diffraction, respectively. The results showed that the porous scaffold with regular pore shape and high specific surface area was obtained after sintering at 1 350℃. The fabricated porous scaffold had defect free interracial structures due to the uniform shrinkage of anode, cathode and electrolyte layers. In addition, it was shown that diffusions of Zr, Ni and La caused a progressive boundary between YSZ, Ni-YSZ and LSM-YSZ layers. The interface between anode and electrolyte （Ni-YSZ/YSZ） was mainly composed of Ni, YSZ and a small amount of NiO, and the interface between cathode and electrolyte （LSM-YSZ/YSZ） was mainly composed of YSZ, LSM and a small amount of La2Zr2O7.展开更多
Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bon...Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bonding temperature of 1273K Ni reacts with SiC and forms various Ni silicides con- taining graphite baside SiC. Ni3Si without graphite was formed at Ni side.The interface structure of SiC/Ni joint was SiC/Ni2Si + C/Ni31 Si12 + G/Ni3 Si/Ni. At the interface between SiC and Ni- 25at%Cr alloy the Ni silicide was only Ni2Si at the same bonding temperature,and further(Cr, Ni)7 (Si, C)3 carbide was formed between Ni silicide + graphite zone and Ni - 25at%Cr alloy.The interface structure of SiC/Ni - 25at%Cr alloy was SiC/Ni2Si + C/(Cr, Ni)7 (Si, C)3+Ni(ss. Cr, Si)/Ni - 25at%Cr.展开更多
Interfacial structure greatly affects the mechanical properties of laminated plates.However,the critical material properties that impact the interfacial morphology,appearance,and associated bonding mechanism of explos...Interfacial structure greatly affects the mechanical properties of laminated plates.However,the critical material properties that impact the interfacial morphology,appearance,and associated bonding mechanism of explosive welded plates are still unknown.In this paper,the same base plate(AZ31B alloy)and different flyer metals(aluminum alloy,copper,and stainless steel)were used to investigate interfacial morphology and structure.SEM and TEM results showed that typical sine wave,wave-like,and half-wave-like interfaces were found at the bonding interfaces of Al/Mg,Cu/Mg and SS/Mg clad plates,respectively.The different interfacial morphologies were mainly due to the differences in hardness and yield strength between the flyer and base metals.The results of the microstructural distribution at the bonding interface indicated metallurgical bonding,instead of the commonly believed solid-state bonding,in the explosive welded clad plate.In addition,the shear strength of the bonding interface of the explosive welded Al/Mg,Cu/Mg and SS/Mg clad plates can reach up to 201.2 MPa,147.8 MPa,and 128.4 MPa,respectively.The proposed research provides the design basis for laminated composite metal plates fabrication by explosive welding technology.展开更多
It is a challenge to identify each phase in a multi-component polymer system and uniquely determine the interfacial properties between the different phases.Using atomic force microscopy nanomechanical mapping(AFM-NM)a...It is a challenge to identify each phase in a multi-component polymer system and uniquely determine the interfacial properties between the different phases.Using atomic force microscopy nanomechanical mapping(AFM-NM)and AFM-based infrared spectroscopy(AFM-IR),we identify each phase,visualize structural developments,and determine the interfacial properties in a blend of three polymers:high-density polyethylene(HDPE),polyamide(PA6)and poly(styrene-b-ethylene-co-butylene-b-styrene)(SEBS).Each phase can be identified from the Young’s modulus,along with the structural development within the phases before and after compatibilization.The interfacial widths between HDPE/PA6,HDPE/SEBS and SEBS/PA6 were determined independently in one measurement from a Young’s modulus map.The structural,mechanical property development and identity of the phases were determined by AFM-NM,while AFM-IR,providing complementary chemical information,identified interfacial reactions,showed the chemical affinity of a compatibilizer with the component phases,and mapped the distribution of the compatibilizer in the ternary polymer blends.The chemical,structural and interfacial information obtained by these measurements provide information that is essential for producing mechanically robust materials from incompatible mixtures of polymers.展开更多
The interfacial properties of steel-mushy Al-28Pb bonding plate with different interfacial structures, and the influence of ratio of Fe-Al compound at the interface on interfacial shear strength were investigated. The...The interfacial properties of steel-mushy Al-28Pb bonding plate with different interfacial structures, and the influence of ratio of Fe-Al compound at the interface on interfacial shear strength were investigated. The results show that there is a nonlinear relationship between the ratio of Fe-Al compound at the interface and the interfacial shear strength. When the ratio of Fe-Al compound at the interface is smaller than 71.4%, with the increase of the ratio of Fe-Al compound at the interface, the interfacial shear strength increases gradually; when the ratio of Fe-Al compound at the interface is larger than 71.4%, with the increase of the ratio of Fe-Al compound at the interface, the interfacial shear strength decreases continuously; when the ratio of Fe-Al compound at the interface is 71.4%, the largest interfacial shear strength 70.2MPa is obtained.展开更多
The hierarchical structure and interfacial morphology of injection-molded bars of polypropylene （PP） based blends and composites have been investigated in detail from the skin to the core. For preparation of injecti...The hierarchical structure and interfacial morphology of injection-molded bars of polypropylene （PP） based blends and composites have been investigated in detail from the skin to the core. For preparation of injection-molded bars with high-level orientation and good interfacial adhesion, a dynamic packing injection molding technology was applied to exert oscillatory shear on the melts during solidification stage. Depending on incorporated component, interfacial adhesion and processing conditions, various oriented structure and morphology could be obtained. First, we will elucidate the epitaxial behavior between PP and high-density polyethylene occurring in practical molded processing. Then, the shear-induced transcrystalline structure will be the main focus for PP/fiber composites. At last, various oriented clay structures have been ascertained unambiguously in PP/organoclay nanocomposites along the thickness of molded bars.展开更多
The energy level alignment of CuPc and FePc on single-layer graphene/Ni（111） （SLG/Ni） substrate was investigated by using ultraviolet and X-ray photoelectron spectroscopy （UPS and XPS）. The highest occupied mole...The energy level alignment of CuPc and FePc on single-layer graphene/Ni（111） （SLG/Ni） substrate was investigated by using ultraviolet and X-ray photoelectron spectroscopy （UPS and XPS）. The highest occupied molecular orbitals （HO- MOs） in a thick layer of CuPc and FePc lie at 1.04 eV and 0.90 eV, respectively, below the Fermi level of the SLG/Ni substrate. Weak adsorbate-substrate interaction leads to negligible interfacial dipole at the CuPc/SLG/Ni interface, while a large interracial dipole （0.20 eV） was observed in the case of FePc/SLG/Ni interface, due to strong adsorbate-substrate coupling. In addition, a new interfacial electronic feature was observed for the first time in the case of FePc on SLG/Ni substrate. This interfacial state can be attributed to a charge transfer from the SLG/Ni substrate to unoccupied orbitals of FePc.展开更多
The bonding of steel plate to aluminum liquid was conducted using rapid solidification. The influence of diffusion time on interfacial structure was studied. The results showed that under the condition of 750癈 for th...The bonding of steel plate to aluminum liquid was conducted using rapid solidification. The influence of diffusion time on interfacial structure was studied. The results showed that under the condition of 750癈 for the temperature of aluminum liquid and 200癈 for the preheat temperature of steel plate, when diffusion time was shorter than 4.3 s, there was only Fe-AI solid solution at the interface. When diffusion time was longer than 4.3 s, Fe-AI compound began to form at the interface. The relationships between diffusion time t and thickness of Fe-AI compound layer H are H=-9.72+2.62t-0.08t2 (4.3 s<t<15 s) and H=2.79+0.647t-0.033t2 (t>15 s).展开更多
Fe-AI compound at the interface of steel-mushy AI-20Sn bonding plate was studied quantitatively. The relationship between ratio of Fe-AI compound at interface and bonding parameters (such as preheat temperature of ste...Fe-AI compound at the interface of steel-mushy AI-20Sn bonding plate was studied quantitatively. The relationship between ratio of Fe-AI compound at interface and bonding parameters (such as preheat temperature of steel plate, solid fraction of AI-20Sn slurry and rolling speed) was established by artificial neural networks perfectly. The results show that when the bonding parameters are 505℃ for preheat temperature of steel plate, 34.3% for solid fraction of AI-20Sn slurry and 10 mm/s for rolling speed, the reasonable ratio of Fe-AI compound corresponding to the largest interfacial shear strength of bonding plate is obtained. Its value is 72%. This reasonable ratio of Fe-AI compound is a quantitative criterion of interfacial embrittlement, that is, when the ratio of Fe-AI compound at interface is larger than 72%, interfacial embrittlement will occur.展开更多
In this paper, the vacuum brazing of Si3N4 ceramic was carried out with Ti40Zr25Ni15Cu20 amorphous filler metal. The interfacial microstructure was investigated by scanning electron microscopy （ SEM ）, energy disper...In this paper, the vacuum brazing of Si3N4 ceramic was carried out with Ti40Zr25Ni15Cu20 amorphous filler metal. The interfacial microstructure was investigated by scanning electron microscopy （ SEM ）, energy dispersive spectroscopy （EDS） etc. According to the analysis, the interface reaction layer was mode up of TiN abut on the ceramic and the Ti-Si, Zr-Si compounds. The influence of brazing temperature and holding time on the joint strength was also studied. The results shows that the joint strength first increased and then decreased with the increasing of holding time and brazing temperature. The joint strength was significantly affected by the thickness of the reaction layer. Under the same experimental conditions, the joint brazed with amorphous filler metal exhibits much higher strength compared with the one brazed with crystalline filler metal with the same composition. To achieve higher joint strength at relatively low temperature, it is favorable to use the amorphous filler metal than the crystalline filler metal.展开更多
Partial transient liquid-phase bonding （PTLP bonding） of Si3N4 ceramic with Ti/Cu/Ti multi-interlayer is performed with changing the thickness of Ti foil. The influence of Ti foil thickness on interface structure an...Partial transient liquid-phase bonding （PTLP bonding） of Si3N4 ceramic with Ti/Cu/Ti multi-interlayer is performed with changing the thickness of Ti foil. The influence of Ti foil thickness on interface structure and joint strength was discussed. The joint interface structures are investigated by scanning electron microscope （SEM） and energy dispersion spectroscopy（EDS）. The results show that the maximum joint strength of 210 MPa is obtained at room temperature in the experiments. When joining temperature and time are not changed and the process of isothermal solidification is sufficient , interface structure, reaction layer thickness and isothermal solidification thickness change with the thickness of Ti foil.展开更多
基金financially supported by the PAPD(No.50831004)the Fundamental Research Funds for the Central Universities+3 种基金the Innovation Fund of Jiangsu Province(No.BY2013072-06)the Natural Science Foundation of Jiangsu Province(No.20141234)the National Natural Science Foundation of China(Nos.51171078 and 51371096)the State Key Program for Basic Research of China(No.2010CB631004)
文摘In this work, we have investigated the mechanical properties of Cu/Ta, Ag/Cu and Ag/Nb multilayers with different heterogeneous interfaces. The results suggest that when individual layer thickness （h） is larger than 5-10 nm, the hardness/strength of three different multilayer systems has the similar length scale effect with decreasing layer thickness, while when h ≤ 5 nm, the three multilayer systems show remarkably different plastic deformation behaviors. The strength curves exhibit the variation trends of unchanging, softening and increasing corresponding to Cu/Ta, Ag/Cu and Ag/Nb multilayers, respectively. The microstructure analysis shows that three kinds of multilayers have totally different interfacial structures, which lead to the different strengthening or softening mechanisms.
文摘Photoelectrocatalytic(PEC)seawater splitting as a green and sustainable route to harvest hydrogen is attractive yet hampered by low activity of photoanodes and unexpected high selectivity to the corrosive and toxic chlorine.Especially,it is full of challenges to unveil the key factors influencing the selectivity of such complex PEC processes.Herein,by regulating the energy band and surface structure of the anatase TiO_(2) nanotube array photoanode via nitrogen-doping,the seawater PEC oxidation shifts from Cl^(-)oxidation reaction(ClOR)dominant on the TiO_(2) photoanode(61.6%)to oxygen evolution reaction(OER)dominant on the N-TiO_(2) photoanode(62.9%).Comprehensive investigations including operando photoelectrochemical FTIR and DFT calculations unveil that the asymmetric hydrogen-bonding water at the N-TiO_(2) electrode/electrolyte interface enriches under illumination,facilitating proton transfer and moderate adsorption strength of oxygen-intermediates,which lowers the energy barrier for the OER yet elevates the energy barrier for the ClOR,resulting to a promoted selectivity towards the OER.The work sheds light on the underlying mechanism of the PEC water oxidation processes,and highlights the crucial role of interfacial water on the PEC selectivity,which could be regulated by controlling the energy band and the surface structure of semiconductors.
基金Supported by National Natural Science Foundation of China(Grant Nos.52075360,52275360,51805359).
文摘Current research on the fabrication of rolled composite plates primarily focuses on processing and bonding mechanisms.Compared with hot-rolling technology,the electrically assisted rolling process has demonstrated excellent performance in interfacial bonding effects.However,the influence of different current loading modes on the interfacial recombination process of composite panels varies significantly.In this study,low-frequency electrically assisted rolling was used in the first pass to pre-bond a composite plate at a low reduction rate of 15%.High-frequency electrically assisted rolling was used during the second pass,and Al/Mg alloy composite plates were obtained.The interfacial microstructure and mechanical properties of the composite plate were coordinated regulation by designing the rolling reduction rate.The results showed the interfacial morphology of the alternating distribution of the melt-diffusion layer,diffusion layer,and the formation of a new Al/Mg bonding interface.At the melt-diffusion interface,the irregular intermetallic compounds(IMCs)and the new Al/Mg bonding interface were alternately distributed,and the IMCs contained theα-Mg,Mg17Al12,and Mg2Al3 phases.In addition,an extremely high shear strength of 78.26 MPa was achieved.Adhesion of the Mg alloy matrix was observed on the fracture surface of the Al alloy side.The high shear strength was mainly attributed to the formation of a unique interfacial structure and the appearance of a melt-diffusion layer.Compared to the diffusion-reduction interface,the regular rectangular IMCs and the new Al/Mg bonding interface were alternately distributed,and the IMCs consisted of the Mg17Al12 and Mg2Al3 phases.The shear test results showed that the shear strength of the interface reached 68.69 MPa,and a regular distribution of the Mg alloy matrix with dimples and the Al alloy matrix with a necking zone was observed on the fracture surface of the Al side.Tensile strength test results revealed a maximum value of 316.86 MPa for the Al/Mg alloy composite plate.The tensile and interfacial bonding strengths can be synchronously enhanced by coordinating the regulation of the interfacial structure.This study proposes a new electrically assisted rolling technology that is useful for the fabrication of composite plates with excellent mechanical properties.
文摘The employment of single atom catalysts(SACs)remarkably increases atomic utilization and catalytic efficiency in various electrochemical processes,especially when coupled with metal clusters/nanoparticles.However,the synergistic effects mainly focus on the energetics of key intermediates during the electrocatalysis,while the properties of electrode surface and electric-double-layer(EDL)structure are largely overlooked.Herein,we report the synthesis of Ru nanoparticles integrated with neighboring Ru single atoms on nitrogen doped carbon(Ru1,n/NC)as efficient catalysts toward hydrogen oxidation reaction(HOR)under alkaline electrolytes.Electrochemical data,in situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy,and density functional theory calculations reveal that the positively charged Ru single atoms could lead to the dynamically regulated proportion of strongly hydrogen-bonded interfacial water structure with O-down conformation and optimized connectivity of the hydrogen-bond network in the EDL region,which contribute to the accelerated diffusion of hydroxide ions to the electrified interfaces.Consequently,the obtained Ru1,n/NC catalyst displays remarkable HOR performance with the mass activity of 1.15 mAμgPGM^(-1) under alkaline electrolyte.This work demonstrates the promise of single atoms for interfacial water environment adjustment and mass transfer process modulation,providing new insights into rational design of highly-effective SAC-based electrocatalysts.
基金supported by the National Natural Science Foundation of China(22478211,22179067)the Major Fundamental Research Program of Natural Science Foundation of Shandong Province(ZR2022ZD10).
文摘Photoelectrochemical water oxidation reaction (PEC-WOR) as a sustainable route to produce H_(2)O_(2) is attractive but limited by low activity and poor product selectivity of photoanodes due to limited photogenerated charge efficiency and unfavorable thermodynamics. Herein, by crystal orientation engineering, the WO_(3) photoanode exposing (200) facets achieves both superior WOR activity (15.4 mA cm^(−2) at 1.76 VRHE) and high selectivity to H_(2)O_(2) (∼70%). Comprehensive experimental and theoretical investigations discover that the high PEC-WOR activity of WO_(3)-(200) is attributed to the rapid photogenerated charge separation/transfer both in bulk and at interfaces of WO_(3)-(200) facet, which reduces the charge transfer resistance. This, coupling with the unique defective hydrogen bonding network at the WO_(3)-(200)/electrolyte interface evidenced by operando PEC Fourier transform infrared spectroscopy, facilitating the outward-transfer of the WOR-produced H^(+), lowers the overall reaction barrier for the PEC-WOR. The superior selectivity of PEC-WOR to H_(2)O_(2) is ascribed to the unique defective hydrogen bonding network alleviated adsorption of ∗OH over the WO_(3)-(200) facet, which specially lowers the energy barrier of the 2-electron pathway, as compared to the 4-electron pathway. This work addresses the significant role of crystal orientation engineering on photoelectrocatalytic activity and selectivity, and sheds lights on the underlying PEC mechanism by understanding the water adsorption behaviors under illumination. The knowledge gained is expected to be extended to other photoeletrochemical reactions.
基金financially supported by the National Natural Science Foundation of China(No.52171046)National Natural Science Foundation of China-key programme(No.52234010)the Fundamental Research Funds for the Central Universities and Shaanxi Provincial Key Science and Technology Innovation Team(No.2023-CX-TD-14).
文摘Al_(2)O_(3)-based eutectic ceramics are considered as promising candidates for ultra-high-temperature structural materials due to their exceptional thermal stability and mechanical properties.Nonetheless,several challenges must be overcome before they can be widely used.This paper reviews in detail the tailoring of microstructure from the aspect of process parameters,the updated knowledge gained in microstructure(crystallographic orientation,high-resolution interfacial structures)and the latest means of optimizing eutectic microstructure(seed-induced method,introducing low-energy grain boundaries and high-entropy phase).Additionally,the paper explores future techniques for the fabrication of bulk ceramic materials and effective toughening approaches.This review highlights the achievements made especially in the last 15 years,current limitations in Al_(2)O_(3)-based eutectic ceramics,and offers comprehensive insights and strategic guidance for further mechanical breakthroughs.
基金supported by the National Science Fund for Distinguished Young Scholars(No.52225312)National Natu-ral Science Foundation of China(Nos.52271173,52377022,and U23A20548)+1 种基金Key Research and Development Program of Zhejiang Province(No.2021C01193)Zhejiang Provincial Natural Science Foundation of China(No.LY23E010007).
文摘FeSiAl-based soft magnetic composites(SMCs),prepared from insulated FeSiAl powders,are widely applied in electronic devices.However,it is still challenging to achieve high magnetic and mechanical properties simultaneously due to the undesirable insulation layer.Here,double Al_(2)O_(3) insulation layers are prepared for FeSiAl SMC.Atomic-scale characterizations reveal an in-situ epitaxial Al_(2)O_(3) layer at FeSiAl surface under the catalysis of NaAlO_(2),and an outer amorphous Al_(2)O_(3) layer by subsequent NaAlO2 hydrolysis.The above structure ensures effective insulation of FeSiAl powders and excellent magnetic properties of the FeSiAl/NaAlO2 SMC,with permeability of 101 and power loss of 128 mW/cm^(3)(50 mT,100 kHz)respectively.Moreover,in-situ Al_(2)O_(3)/amorphous Al_(2)O_(3) on FeSiAl matrix also leads to distinguished crush strength of 36.5 MPa for the core sample,which is ascribed to the enhanced adhesion at different interfaces as evidenced by similar local oxygen coordination and low strain distribution.This work provides a novel method to fabricate high-performance FeSiAl SMCs.
文摘The interfacial interaction existing in the Ni ZrO 2 composite plating has been investigated. The experimental results show that no new phases were formed in the interfacial regions between matrix Ni and ZrO 2 particles, but an orbital interaction through the mutual overlap of the d orbits does exist in the interfacial regions between Ni atoms and Zr 3+ ions.
基金support from the National Natural Science Foundation of China for financial support(22175054)the Distinguished Project for Scientific Research in Universities of Anhui Province(2024AH020011)+2 种基金the Key Project for Cultivation of Outstanding Young Scholars in Universities of Anhui Province(YQZD2024015)the Key Project of Provincial Natural Science Research Foundation of Anhui Universities,China(No.2022AH050406)the Anhui Province Research Funding for Outstanding Young Talents in Colleges and Universities,China(No.gxyq2022021)。
文摘Low-temperature lithium sulfur(Li-S)batteries have attracted increasing attention,but lithium polysulfide(LiPSs)clu stering and tardy ionic mobility have been challenging issues,which could be exacerbated under high sulfur loading and lean electrolyte.The distinct behaviors of sulfur cathode in lowtemperature Li-S batteries call for special regulations of the sulfur host to improve the electrochemical performances.Here,a three-dimensional Ti_(3)C_(2)micro-cage(TCC)with an interfacial structure modulated by rich curvatures has been fabricated to propel the sulfur electrochemistry at subzero temperatures.Spectroscopic/microscopic analyses and theoretical calculations elucidate that the precipitation of ultrafine Ti-metal particles on the in-situ generated Ti_(3)C_(2)nanoribbons could trigger the self-scrolling of Ti_(3)C_(2)nanoribbons into TCC.Moreover,in-situ ultraviolet-visible spectra collected at low temperature and theoretical calculations verified that the TCC regulated by rich curvatures have effectively alleviated the Li+dissociation barrier,reduced the energy barrier for charge transfer at the electrode-electrolyte interface,and restrained the clustering and shuttling of LiPSs,thus accelerating the electrochemical conversion kinetics of sulfur species at low temperatures.The performances of the carbon-free TCC-S cathode at low temperatures have been also compared from the aspects of cathode configuration and measurement condition,to demonstrate the potential of TCC.This work can not only provide new methodology for regulating the interfacial structure of MXene to enrich the materials library for low-temperature Li-S batteries,but also expand understanding about the role of interfacial structure of sulfur host in Li-S batteries.
文摘A novel process route using tape casting and stacking for fabricating porous scaffold of solid oxide fuel cells （SOFC） was demonstrated. The linear shrinkages of anode （Ni-YSZ, YSZ stands for 3% Y2O3 （mole fraction） stabilized ZrO2 ） and cathode （LSM-YSZ, LSM stands for La0.8Sr0.2MnO3 ） were optimized to be uniform with that of electrolyte during sintering, by controlling the content of pore former. The micromorphology and interface microstructure of the cross-section of the porous scaffold were observed by optical microscope and scanning electron microscope, respectively. The element distribution and phase composition were analyzed by energy dispersive spectrometer and X-ray diffraction, respectively. The results showed that the porous scaffold with regular pore shape and high specific surface area was obtained after sintering at 1 350℃. The fabricated porous scaffold had defect free interracial structures due to the uniform shrinkage of anode, cathode and electrolyte layers. In addition, it was shown that diffusions of Zr, Ni and La caused a progressive boundary between YSZ, Ni-YSZ and LSM-YSZ layers. The interface between anode and electrolyte （Ni-YSZ/YSZ） was mainly composed of Ni, YSZ and a small amount of NiO, and the interface between cathode and electrolyte （LSM-YSZ/YSZ） was mainly composed of YSZ, LSM and a small amount of La2Zr2O7.
文摘Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bonding temperature of 1273K Ni reacts with SiC and forms various Ni silicides con- taining graphite baside SiC. Ni3Si without graphite was formed at Ni side.The interface structure of SiC/Ni joint was SiC/Ni2Si + C/Ni31 Si12 + G/Ni3 Si/Ni. At the interface between SiC and Ni- 25at%Cr alloy the Ni silicide was only Ni2Si at the same bonding temperature,and further(Cr, Ni)7 (Si, C)3 carbide was formed between Ni silicide + graphite zone and Ni - 25at%Cr alloy.The interface structure of SiC/Ni - 25at%Cr alloy was SiC/Ni2Si + C/(Cr, Ni)7 (Si, C)3+Ni(ss. Cr, Si)/Ni - 25at%Cr.
基金Supported by National Natural Science Foundation of China(Grant Nos.51805359,51904206,51375328)Major program of national natural science foundation of China(U1710254),China Postdoctoral Science Foundation(Grant No.2018M631772)+2 种基金Shanxi Provincial Natural Science Foundation of China(Grant No.201901D211015)Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi Province(STIP)(Grant No.2019L0333)Central Special Fund for Guiding Local Science and Technology Development(YDZX20191400002149).
文摘Interfacial structure greatly affects the mechanical properties of laminated plates.However,the critical material properties that impact the interfacial morphology,appearance,and associated bonding mechanism of explosive welded plates are still unknown.In this paper,the same base plate(AZ31B alloy)and different flyer metals(aluminum alloy,copper,and stainless steel)were used to investigate interfacial morphology and structure.SEM and TEM results showed that typical sine wave,wave-like,and half-wave-like interfaces were found at the bonding interfaces of Al/Mg,Cu/Mg and SS/Mg clad plates,respectively.The different interfacial morphologies were mainly due to the differences in hardness and yield strength between the flyer and base metals.The results of the microstructural distribution at the bonding interface indicated metallurgical bonding,instead of the commonly believed solid-state bonding,in the explosive welded clad plate.In addition,the shear strength of the bonding interface of the explosive welded Al/Mg,Cu/Mg and SS/Mg clad plates can reach up to 201.2 MPa,147.8 MPa,and 128.4 MPa,respectively.The proposed research provides the design basis for laminated composite metal plates fabrication by explosive welding technology.
基金by the National Natural Science Foundation of China(No.51673016)the Beijing Advanced Innovation Center for Soft matter Science and Engineering.
文摘It is a challenge to identify each phase in a multi-component polymer system and uniquely determine the interfacial properties between the different phases.Using atomic force microscopy nanomechanical mapping(AFM-NM)and AFM-based infrared spectroscopy(AFM-IR),we identify each phase,visualize structural developments,and determine the interfacial properties in a blend of three polymers:high-density polyethylene(HDPE),polyamide(PA6)and poly(styrene-b-ethylene-co-butylene-b-styrene)(SEBS).Each phase can be identified from the Young’s modulus,along with the structural development within the phases before and after compatibilization.The interfacial widths between HDPE/PA6,HDPE/SEBS and SEBS/PA6 were determined independently in one measurement from a Young’s modulus map.The structural,mechanical property development and identity of the phases were determined by AFM-NM,while AFM-IR,providing complementary chemical information,identified interfacial reactions,showed the chemical affinity of a compatibilizer with the component phases,and mapped the distribution of the compatibilizer in the ternary polymer blends.The chemical,structural and interfacial information obtained by these measurements provide information that is essential for producing mechanically robust materials from incompatible mixtures of polymers.
文摘The interfacial properties of steel-mushy Al-28Pb bonding plate with different interfacial structures, and the influence of ratio of Fe-Al compound at the interface on interfacial shear strength were investigated. The results show that there is a nonlinear relationship between the ratio of Fe-Al compound at the interface and the interfacial shear strength. When the ratio of Fe-Al compound at the interface is smaller than 71.4%, with the increase of the ratio of Fe-Al compound at the interface, the interfacial shear strength increases gradually; when the ratio of Fe-Al compound at the interface is larger than 71.4%, with the increase of the ratio of Fe-Al compound at the interface, the interfacial shear strength decreases continuously; when the ratio of Fe-Al compound at the interface is 71.4%, the largest interfacial shear strength 70.2MPa is obtained.
基金This work was supported by the National Natural Science Foundation of China (Nos. 20404008, 50533050, 50373030 and 20490220). This work is subsidized by the Special Funds for Major State Basic Research Projects of China (No. 2003CB615600) by Ministry of Education of China as a key project (No. 104154).
文摘The hierarchical structure and interfacial morphology of injection-molded bars of polypropylene （PP） based blends and composites have been investigated in detail from the skin to the core. For preparation of injection-molded bars with high-level orientation and good interfacial adhesion, a dynamic packing injection molding technology was applied to exert oscillatory shear on the melts during solidification stage. Depending on incorporated component, interfacial adhesion and processing conditions, various oriented structure and morphology could be obtained. First, we will elucidate the epitaxial behavior between PP and high-density polyethylene occurring in practical molded processing. Then, the shear-induced transcrystalline structure will be the main focus for PP/fiber composites. At last, various oriented clay structures have been ascertained unambiguously in PP/organoclay nanocomposites along the thickness of molded bars.
基金Project supported by the National Natural Science Foundation of China(Grant No.61106131)the Natural Science Foundation of Zhejiang Province,China(Grant No.Y6110072)+1 种基金the Talents Project of Science and Technology Department of Qianjiang City,China(Grant No.2012R10075)the Postdoctoral Science Foundation of China(Grant No.2012M521119)
文摘The energy level alignment of CuPc and FePc on single-layer graphene/Ni（111） （SLG/Ni） substrate was investigated by using ultraviolet and X-ray photoelectron spectroscopy （UPS and XPS）. The highest occupied molecular orbitals （HO- MOs） in a thick layer of CuPc and FePc lie at 1.04 eV and 0.90 eV, respectively, below the Fermi level of the SLG/Ni substrate. Weak adsorbate-substrate interaction leads to negligible interfacial dipole at the CuPc/SLG/Ni interface, while a large interracial dipole （0.20 eV） was observed in the case of FePc/SLG/Ni interface, due to strong adsorbate-substrate coupling. In addition, a new interfacial electronic feature was observed for the first time in the case of FePc on SLG/Ni substrate. This interfacial state can be attributed to a charge transfer from the SLG/Ni substrate to unoccupied orbitals of FePc.
基金This project is supported by the Advanced Technical Committee of China, No.715-009-060.
文摘The bonding of steel plate to aluminum liquid was conducted using rapid solidification. The influence of diffusion time on interfacial structure was studied. The results showed that under the condition of 750癈 for the temperature of aluminum liquid and 200癈 for the preheat temperature of steel plate, when diffusion time was shorter than 4.3 s, there was only Fe-AI solid solution at the interface. When diffusion time was longer than 4.3 s, Fe-AI compound began to form at the interface. The relationships between diffusion time t and thickness of Fe-AI compound layer H are H=-9.72+2.62t-0.08t2 (4.3 s<t<15 s) and H=2.79+0.647t-0.033t2 (t>15 s).
基金This project was supported by the National Natural Science Foundation of China(No.50274047)Beijing Jiaotong Univer sity Foundation.
文摘Fe-AI compound at the interface of steel-mushy AI-20Sn bonding plate was studied quantitatively. The relationship between ratio of Fe-AI compound at interface and bonding parameters (such as preheat temperature of steel plate, solid fraction of AI-20Sn slurry and rolling speed) was established by artificial neural networks perfectly. The results show that when the bonding parameters are 505℃ for preheat temperature of steel plate, 34.3% for solid fraction of AI-20Sn slurry and 10 mm/s for rolling speed, the reasonable ratio of Fe-AI compound corresponding to the largest interfacial shear strength of bonding plate is obtained. Its value is 72%. This reasonable ratio of Fe-AI compound is a quantitative criterion of interfacial embrittlement, that is, when the ratio of Fe-AI compound at interface is larger than 72%, interfacial embrittlement will occur.
基金Funded by National Natural Science Foundation of China （No. 50875117）.
文摘In this paper, the vacuum brazing of Si3N4 ceramic was carried out with Ti40Zr25Ni15Cu20 amorphous filler metal. The interfacial microstructure was investigated by scanning electron microscopy （ SEM ）, energy dispersive spectroscopy （EDS） etc. According to the analysis, the interface reaction layer was mode up of TiN abut on the ceramic and the Ti-Si, Zr-Si compounds. The influence of brazing temperature and holding time on the joint strength was also studied. The results shows that the joint strength first increased and then decreased with the increasing of holding time and brazing temperature. The joint strength was significantly affected by the thickness of the reaction layer. Under the same experimental conditions, the joint brazed with amorphous filler metal exhibits much higher strength compared with the one brazed with crystalline filler metal with the same composition. To achieve higher joint strength at relatively low temperature, it is favorable to use the amorphous filler metal than the crystalline filler metal.
文摘Partial transient liquid-phase bonding （PTLP bonding） of Si3N4 ceramic with Ti/Cu/Ti multi-interlayer is performed with changing the thickness of Ti foil. The influence of Ti foil thickness on interface structure and joint strength was discussed. The joint interface structures are investigated by scanning electron microscope （SEM） and energy dispersion spectroscopy（EDS）. The results show that the maximum joint strength of 210 MPa is obtained at room temperature in the experiments. When joining temperature and time are not changed and the process of isothermal solidification is sufficient , interface structure, reaction layer thickness and isothermal solidification thickness change with the thickness of Ti foil.
