Passive intermodulation（PIM） has gradually become a serious electromagnetic interference due to the development of high-power and high-sensitivity RF/microwave communication systems, especially large deployable mesh...Passive intermodulation（PIM） has gradually become a serious electromagnetic interference due to the development of high-power and high-sensitivity RF/microwave communication systems, especially large deployable mesh reflector antennas. This paper proposes a field-circuit coupling method to analyze the PIM level of mesh reflectors. With the existence of many metal–metal（MM） contacts in mesh reflectors, the contact nonlinearity becomes the main reason for PIM generation. To analyze these potential PIM sources, an equivalent circuit model including nonlinear components is constructed to model a single MM contact so that the transient current through the MM contact point induced by incident electromagnetic waves can be calculated. Taking the electric current as a new electromagnetic wave source, the far-field scattering can be obtained by the use of electromagnetic numerical methods or the communication link method. Finally, a comparison between simulation and experimental results is illustrated to verify the validity of the proposed method.展开更多
Two-dimensional(2D)materials have attracted a great deal of research interest because of their unique electrical,magnetic,optical,mechanical,and catalytic properties for various applications.To date,however,it is stil...Two-dimensional(2D)materials have attracted a great deal of research interest because of their unique electrical,magnetic,optical,mechanical,and catalytic properties for various applications.To date,however,it is still difficult to fabricate most functional oxides as 2D materials unless they have a layered structure.Herein,we report a one-step universal strategy for preparing versatile non-layered oxide nanosheets by directly annealing the mixture of metal nitrate and dimethyl imidazole(2-MI).The 2-MI plays the key role for 2D oxides since 2-MI owns a very low molten point and sublimation temperature,in which its molten liquid can coordinate with metal ions,forming a metal-organic framework,and easily puffing by its gas molecules.A total of 17 materials were prepared by this strategy,including non-layered metal oxide nanosheets as well as metal/metal oxide loaded nitrogen-doped carbon nanosheets.The as-prepared cobalt particle-loaded nitrogen-doped carbon nanosheets(Co@N/C)exhibit remarkable bifunctional oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)electrocatalytic activity and durability.Besides,the Zn-air battery utilizing a Co@N/C catalyst exhibits high power density of 174.3 mW·cm^(-2).This facile strategy opens up a new way for large-scale synthesis of 2D oxides that holds great potential to push 2D oxides for practical applications.展开更多
The complexes [Pt2L2（μ-dppm）]（ClO4）2 （1） and {[Pt2L2（μ-dppm）Li（CH3CN）2]（ClO4）3}n （2）, where HL is 6-[4-（diethoxyphosphorylmethyl）phenyl]-2,2′-bipyridinyl and dppm is bis（diphenylphosphino）methane,...The complexes [Pt2L2（μ-dppm）]（ClO4）2 （1） and {[Pt2L2（μ-dppm）Li（CH3CN）2]（ClO4）3}n （2）, where HL is 6-[4-（diethoxyphosphorylmethyl）phenyl]-2,2′-bipyridinyl and dppm is bis（diphenylphosphino）methane, have been synthesized and characterized. In complex 1 the platinum（Ⅱ） center adopts a distorted square planar coordination geometry. The polymer 2 exhibits a ＂stairstep＂ configuration with one-dimensional Pt（Ⅱ）N^N^CPO- Li（Ⅰ）-OPC^N^ NPt（Ⅱ） mixed-metal units which are linked through dppm. Both complexes have metal-metal interaction with Pt- Pt distances of 3.325（2） and 3.1432（9） A, respectively, and display strong metal-metal-to-ligand charge-transfer （MMLCT） triplet state emission. The density-functional-theory calculation was used to interpret the absorption spectra of the complexes.展开更多
We report here the synthesis and characterization of two new members of the M2 E 12 family of endohe-dral Zintl clusters,[Fe_(2)Sn_(4)Bi_(8)]^(3-)and[Cr_(2)Sb_(12)]^(3-),both of which contain open-shell metal dimers e...We report here the synthesis and characterization of two new members of the M2 E 12 family of endohe-dral Zintl clusters,[Fe_(2)Sn_(4)Bi_(8)]^(3-)and[Cr_(2)Sb_(12)]^(3-),both of which contain open-shell metal dimers encap-sulated inside a triple-decker cluster of main-group atoms.The 75-electron[Fe_(2)Sn_(4)Bi_(8)]^(3-)cluster has a D4h-symmetric structure,while[Cr_(2)Sb_(12)]^(3-),despite having the same 75-electron count,is strongly dis-torted to a geometry that resembles a CrSb_(8)crown capped by a CrSb_(4)unit.The structural differences between the two are driven by the increasing availability of 3d electron density in the earlier transi-tion metal,which leads,ultimately,to different electronic configurations in the two clusters.The trends precisely mirror those observed in the ME_(10)and ME_(12)families containing a single transition metal ion.展开更多
Organoplatinum（Ⅱ） compounds have received enormous attention over the past decades due to their square-planar geometry as well as intriguing photo-physical properties.Self-assembly has emerged as an excellent appro...Organoplatinum（Ⅱ） compounds have received enormous attention over the past decades due to their square-planar geometry as well as intriguing photo-physical properties.Self-assembly has emerged as an excellent approach to create well-ordered supramolecular architectures with tunable properties,which underpin the role of solvent-directed approach for the design of functional materials.In this minireview,the recent advances on supramolecular self-assembly of cyclometalated platinum（Ⅱ） complexes have been discussed.During the self-assembly process,non-covalent Pt-Pt and π-π interactions play crucial roles in controlling the structures and functions of the resulting assemblies.展开更多
Oxygen reduction reaction(ORR)is an electrochemical reaction in which dissolved oxygen in an electrolyte is reduced toOH−/H2Owhen receiving electrons.This reaction plays a crucial role in shaping the efficiency of bot...Oxygen reduction reaction(ORR)is an electrochemical reaction in which dissolved oxygen in an electrolyte is reduced toOH−/H2Owhen receiving electrons.This reaction plays a crucial role in shaping the efficiency of both metal-air batteries and fuel cells,and precious metals are the dominant catalysts carrying out the ORR in their cathodes.However,how to manipulate the electronic structure of precious metals as active sites to further promote ORR performance and maximize the utilization rate is still under development.Metal oxide serves as suitable and promising support that can strongly interact with precious metals for both activity and durability enhancement.Herein,we present recent research updates on strong precious metal-metal oxide interaction(SPMMOI)utilized in ORR.We start by introducing the background of ORR,the issues to be solved,and its practical applications followed by a thorough discussion of the reaction mechanism and comprehensive evaluation protocols of performance.We then provide a complete understanding of theworking principle of SPMMOI and highlight the related advances.Finally,we summarize the merits of the precious metal-metal oxide systemand propose the research direction aswell as some urgent problems to be addressed in the future.展开更多
In order to investigate the real-time cracking behavior of each component of a composite with strong interfacial bonding among lamellae, Ti-18 Nb(at.%) composite was prepared by spark plasma sintering(SPS), followed b...In order to investigate the real-time cracking behavior of each component of a composite with strong interfacial bonding among lamellae, Ti-18 Nb(at.%) composite was prepared by spark plasma sintering(SPS), followed by hot-rolling, annealing, and quenching. The microstructure and mechanical properties were characterized by scanning electron microscopy(SEM), energy dispersive spectroscopy(EDS), micro-region X-ray diffractometry(MRXRD), nanoindentation, and in-situ scanning electron microscopy tensile testing. The results show that the Ti-18 Nb consists of Ti-enriched, diffusion and Nb-enriched zones, and the sharp Nb gradient across different zones leads to inhomogeneous distribution of phase and mechanical properties. A remarkable finding is that the diffusion zones not only enable the cooperative deformation between the brittle Ti-enriched zones and the ductile Nb-enriched zones but also act as the crack-arresters to prevent the local cracks in the Ti-enriched zones from further propagating across the composite.展开更多
Comprehensive Summary The experimental investigation of rare-earth metal-metal bonds remains a challenge in the study of chemical bonds.Herein,we report the synthesis and characterization of a novel heteronuclear di-m...Comprehensive Summary The experimental investigation of rare-earth metal-metal bonds remains a challenge in the study of chemical bonds.Herein,we report the synthesis and characterization of a novel heteronuclear di-metallofullerene,ScY@C_(3v)(8)-C_(82),which contains a mixed rare-earth metal-metal bond.ScY@C_(3v)(8)-C_(82)was successfully synthesized by arc-discharging method and characterized by mass spectrometry,UV-vis-NIR spectroscopy and single-crystal X-ray diffraction crystallography,which unambiguously determined its molecular structure.Theoretical calculations were also performed to study the optimized positions of Sc-Y metallic dimer and the electronic configuration.The combined experimental and theoretical results confirmed that both Sc and Y atoms transfer two electrons to the C_(3v)(8)-C_(82)cage,i.e.,(ScY)4+@(C_(3v)(8)-C_(82))4-.In particular,a covalent Sc-Yσ2 bond,which has never been reported before,is proven to be formed inside C_(3v)(8)-C_(82)fullerene cage.This work presents a novel di-metallofullerene containing mixed rare-earth metal-metal bond and expands the understanding of metal-metal bonding of rare earth elements.展开更多
The unique components and architecture of Prussian blue analogous(PBAs) offer great potential for the construction of various functional nanostructures. Herein, we reported the preparation of a series of Mn–Fe oxides...The unique components and architecture of Prussian blue analogous(PBAs) offer great potential for the construction of various functional nanostructures. Herein, we reported the preparation of a series of Mn–Fe oxides-based hybrids using Mn–Fe PBA as a template and an organic carbon source by calcination.The study focuses on revealing the interaction between the microstructure and electrochemical performance of the products obtained at different calcination temperatures. Notably, the as-derived porous Fe–Fe0.33Mn0.67O/C nanocubes(i.e., M600) exhibited the best rate capability and cycle life compared with other samples(~890 m Ah/g at 0.1 A/g, 626.8 m Ah/g after 1000 cycles at 1.0 A/g with a 99% capacity retention). These can be attributed to the fact that the porous structure provides shorter Li+diffusion path and promotes the penetration of electrolyte. Besides, the N-doped C formed by the carbonization of organic ligands can buffer the volume change and prevent the aggregation of Fe_(0.33)Mn_(0.67)O nanoparticles during the discharge/charge cycles. Moreover, the presence of metallic Fe enhances the conductivity and the electrochemical activity, which accelerates the electrochemical reactions. Therefore, reasonable design of microstructure and compositions of functional nanocomposites is the key to obtain ideal electrochemical properties.展开更多
Metal–metal battery bears great potential for next-generation large-scale energy storage system because of its simple manufacture process and low production cost.However,the cross-over of metal cations from the catho...Metal–metal battery bears great potential for next-generation large-scale energy storage system because of its simple manufacture process and low production cost.However,the cross-over of metal cations from the cathode to the anode causes a loss in capacity and influences battery stability.Herein,a coating of poly(ionic liquid)(PIL)with poly(diallyldimethylammonium bis(trifluoromethanesulfonyl)imide)(PDADMA^(+)TFSI^(−))on a commercial polypropylene(PP)separator serves as an anion exchange membrane for a 3.3 V copper–lithium battery.The PIL has a positively charged polymer backbone that can block the migration of copper ions,thus improving Coulombic efficiency,long-term cycling stability and inhibiting self-discharge of the battery.It can also facilitate the conduction of anions through the membrane and reduce polarization,especially for fast charging/discharging.Bruce-Vincent method gives the transport number in the electrolyte to be 0.25 and 0.04 for PP separator without and with PIL coating,respectively.This suggests that the PIL layer reduces the contribution of the internal current due to cation transport.The use of PIL as a coating layer for commercial PP separator is a cost-effective way to improve overall electrochemical performance of copper–lithium batteries.Compared to PP and polyacrylic acid(PAA)/PP separators,the PIL/PP membrane raises the Coulombic efficiency to 99%and decreases the average discharge voltage drop to about 0.09 V when the current density is increased from 0.1 to 1 mA cm^(−2).展开更多
Development of total hip arthroplasty (THA) now spans more than 5 decades encompassing combinations of metal-on-metal (MOM), ceramic-on-metal (COM), metal-on-plastic (MOP), ceramic-on-plastic (COM), and ceramic-on-cer...Development of total hip arthroplasty (THA) now spans more than 5 decades encompassing combinations of metal-on-metal (MOM), ceramic-on-metal (COM), metal-on-plastic (MOP), ceramic-on-plastic (COM), and ceramic-on-ceramic (COC). In every arena of extensive technical development, there exists a data set that when viewed in isolation seemed of little import, but when assembled in-toto may produce a generational shift in perception. Our review focused on two such THA events. Firstly, COC retrieval studies (1999-2001) noted habitual wear patterns on heads and peripheral wear stripes, along with femoral-neck impingement, and ceramic surfaces stained gray by metal debris. These COC<span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">data indicated THA risks included, </span><span style="font-family:Verdana;">1</span><span style="font-family:Verdana;">) cup edge-loading (E/L) on heads producing </span><span style="font-family:Verdana;">“</span><span style="font-family:Verdana;">stripe wear</span><span style="font-family:Verdana;">”</span><span style="font-family:Verdana;">,</span><span style="font-family:Verdana;"> 2</span><span style="font-family:Verdana;">) component impingement releasing metal particles resulting in </span><span style="font-family:Verdana;">3</span><span style="font-family:Verdana;">) tissues contaminated by metal debris. A corresponding MOM impingement-debris mechanism was only perceived by Howie (2005) in a McKee-Farrar retrieval study. Our anticipation at LLUMC was that MOM retrievals would provide superior wear details to those seen on COC retrievals. We noted stripe wear in the polar zone of CoCr heads and basal stripes in the non-wear areas. The basal-polar stripe combinations were </span><span style="font-family:Verdana;">found in all MOM retrievals. Basal-polar stripe combinations followed cup-rim</span><span style="font-family:Verdana;"> profiles in our LLUMC simulations of prosthetic impingement. LPUH videos demonstrated the formation of stripe wear in functiona展开更多
A new compound formulated [Ag2(idc)](NO3)?H2O (H2idc = iminodiacetic acid) was synthesized under mild conditions and characterized by IR spectrum and single-crystal X-ray diffraction. The crystal crystallizes in the m...A new compound formulated [Ag2(idc)](NO3)?H2O (H2idc = iminodiacetic acid) was synthesized under mild conditions and characterized by IR spectrum and single-crystal X-ray diffraction. The crystal crystallizes in the monoclinic system, space group of P21/n with a = 5.5029(2), b = 11.1316(5), c = 15.5319 (1) ?, β = 96.038(3)o, V = 946.15(6) ?3, Z = 4, R = 0.0619 and wR = 0.1606. Its structure is a 2D polymer, whose repeat units consist of dinuclear silver cluster coordinated by two bridging iminodiacetic acids. In the complex, the Ag(I) ions adopt three coordinate fashions, and the Ag-Ag metal-metal contacts of 2.8418 ? are observed.展开更多
The Earth’s sustainable development is threatened by the increasing atmospheric COlevel which can be attributed to the imbalance of COdue to the rapid consumption of fossil fuels caused by human activities and the sl...The Earth’s sustainable development is threatened by the increasing atmospheric COlevel which can be attributed to the imbalance of COdue to the rapid consumption of fossil fuels caused by human activities and the slow absorption and conversion of COby nature. One of the efficient methods for reconstructing the balance of COshould involve the rapid conversion of COinto fuels and chemicals.The hydrogenation of COwith gaseous hydrogen is currently considered to be the most commercially feasible synthetic route, however, the supply of safe and economical hydrogen sources poses a significant challenge to up-scaling application. Direct utilization of hydrogen from dissociation of water, the most abundant, cheap and clean hydrogen resource, for the reduction of COwould be one of the most promising approaches for COutilization. This paper provides an overview of the current advances in research on highly efficient reduction of COor NaHCO, a representative compound of CO, into formic acid/formate by in situ hydrogen from water dissociation with a metal/metal oxide redox cycle under mild hydrothermal conditions.展开更多
Binuclear transition metal carbonyl clusters serve as the simplest models in understand- ing metal-metal and ligand bonding that are important organometallic chemistry catalysis. Binuclear first row transition metal c...Binuclear transition metal carbonyl clusters serve as the simplest models in understand- ing metal-metal and ligand bonding that are important organometallic chemistry catalysis. Binuclear first row transition metal carbonyl ions are produced via a pulsed laser vaporiza- tion/supersonic expansion cluster ion source in the gas phase. These ions are studied by mass-selected infrared photodissociation spectroscopy in the carbonyl stretching frequency region. Density functional theory calculations have been performed on the geometric struc- tures and vibrational spectra of the carbonyl ions. Their geometric and electronic structures are determined by comparison of the experimental IR spectra with the simulated spectra. The structure and the metM-metal and metal-CO bonding of both saturated and unsaturated homonuclear as well as heteronuclear carbonyl cluster cations and anions are discussed.展开更多
Two host-guest systems have been constructed,by employing structurally similar terpyridine platinum(II)macrocycle and molecular tweezer as the synthetic receptors.The macrocycle/guest complex displays low-energy emiss...Two host-guest systems have been constructed,by employing structurally similar terpyridine platinum(II)macrocycle and molecular tweezer as the synthetic receptors.The macrocycle/guest complex displays low-energy emission signal,reinforced non-covalent binding affinity,and enhanced photosensitization capability than those of the molecular tweezer/guest one.The discrepancy between macrocyclic and acyclic preorganization modes originates from the different numbers of Pt(II)Pt(II)metal-metal bonds in host-guest complexation structures.展开更多
Co_(2)VO_(4) with Co tetrahedrons and octahedrons of transition metal oxides has achieved progress in electrocatalysts and batteries.However,high metal-metal interactions make it challenging to maintain high reactivit...Co_(2)VO_(4) with Co tetrahedrons and octahedrons of transition metal oxides has achieved progress in electrocatalysts and batteries.However,high metal-metal interactions make it challenging to maintain high reactivity as well as increase the conductivity and stability of supercapacitors.In this work,spinel-structured CoZn_(0.5)V_(1.5)O_(4) with a high specific surface area was synthesized through an ion-exchange process from the metal-organic frameworks of zinc-cobalt.Density functional theory calculations indicate that the replacement of transition metal by Zn can decrease the interaction between the transition metals,leading to a downshift in the π^(∗)-orbitals(V-O)and half-filled a_(1g) orbitals near the Fermi level,thus increasing the conductivity and stability of CoZn_(0.5)V_(1.5)O_(4).As a supercapacitor electrode,CoZn_(0.5)V_(1.5)O_(4) exhibits high cycling durability(99.4% capacitance retention after 18,000 cycles)and specific capacitance(1100mFcm^(-2) at 1mAcm^(-2)).This work provides the possibility of designing octahedral and tetrahedral sites in transition metal oxides to improve their electrochemical performance.展开更多
文摘Passive intermodulation（PIM） has gradually become a serious electromagnetic interference due to the development of high-power and high-sensitivity RF/microwave communication systems, especially large deployable mesh reflector antennas. This paper proposes a field-circuit coupling method to analyze the PIM level of mesh reflectors. With the existence of many metal–metal（MM） contacts in mesh reflectors, the contact nonlinearity becomes the main reason for PIM generation. To analyze these potential PIM sources, an equivalent circuit model including nonlinear components is constructed to model a single MM contact so that the transient current through the MM contact point induced by incident electromagnetic waves can be calculated. Taking the electric current as a new electromagnetic wave source, the far-field scattering can be obtained by the use of electromagnetic numerical methods or the communication link method. Finally, a comparison between simulation and experimental results is illustrated to verify the validity of the proposed method.
基金supported by the National Key Research and Development Program of China(No.2022YFA1203500)the National Natural Science Foundation of China(Nos.51972124 and 51902115)the Opening Project of Hubei Key Laboratory of Biomass Fibers and Eco-Dyeing&Finishing(No.223009025).
文摘Two-dimensional(2D)materials have attracted a great deal of research interest because of their unique electrical,magnetic,optical,mechanical,and catalytic properties for various applications.To date,however,it is still difficult to fabricate most functional oxides as 2D materials unless they have a layered structure.Herein,we report a one-step universal strategy for preparing versatile non-layered oxide nanosheets by directly annealing the mixture of metal nitrate and dimethyl imidazole(2-MI).The 2-MI plays the key role for 2D oxides since 2-MI owns a very low molten point and sublimation temperature,in which its molten liquid can coordinate with metal ions,forming a metal-organic framework,and easily puffing by its gas molecules.A total of 17 materials were prepared by this strategy,including non-layered metal oxide nanosheets as well as metal/metal oxide loaded nitrogen-doped carbon nanosheets.The as-prepared cobalt particle-loaded nitrogen-doped carbon nanosheets(Co@N/C)exhibit remarkable bifunctional oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)electrocatalytic activity and durability.Besides,the Zn-air battery utilizing a Co@N/C catalyst exhibits high power density of 174.3 mW·cm^(-2).This facile strategy opens up a new way for large-scale synthesis of 2D oxides that holds great potential to push 2D oxides for practical applications.
文摘The complexes [Pt2L2（μ-dppm）]（ClO4）2 （1） and {[Pt2L2（μ-dppm）Li（CH3CN）2]（ClO4）3}n （2）, where HL is 6-[4-（diethoxyphosphorylmethyl）phenyl]-2,2′-bipyridinyl and dppm is bis（diphenylphosphino）methane, have been synthesized and characterized. In complex 1 the platinum（Ⅱ） center adopts a distorted square planar coordination geometry. The polymer 2 exhibits a ＂stairstep＂ configuration with one-dimensional Pt（Ⅱ）N^N^CPO- Li（Ⅰ）-OPC^N^ NPt（Ⅱ） mixed-metal units which are linked through dppm. Both complexes have metal-metal interaction with Pt- Pt distances of 3.325（2） and 3.1432（9） A, respectively, and display strong metal-metal-to-ligand charge-transfer （MMLCT） triplet state emission. The density-functional-theory calculation was used to interpret the absorption spectra of the complexes.
基金supported by the National Natural Science Foundation of China(Nos.92161102,21971118)the Natural Science Foundation of Tianjin City(Nos.21JCZXJC00140,20JCYBJC01560)the 111 Project(No.B18030)from Ministry of Education China
文摘We report here the synthesis and characterization of two new members of the M2 E 12 family of endohe-dral Zintl clusters,[Fe_(2)Sn_(4)Bi_(8)]^(3-)and[Cr_(2)Sb_(12)]^(3-),both of which contain open-shell metal dimers encap-sulated inside a triple-decker cluster of main-group atoms.The 75-electron[Fe_(2)Sn_(4)Bi_(8)]^(3-)cluster has a D4h-symmetric structure,while[Cr_(2)Sb_(12)]^(3-),despite having the same 75-electron count,is strongly dis-torted to a geometry that resembles a CrSb_(8)crown capped by a CrSb_(4)unit.The structural differences between the two are driven by the increasing availability of 3d electron density in the earlier transi-tion metal,which leads,ultimately,to different electronic configurations in the two clusters.The trends precisely mirror those observed in the ME_(10)and ME_(12)families containing a single transition metal ion.
基金supported by the National Natural Science Foundation of China(No.21274139)the Fundamental Research Funds for the Central Universities(Nos.WK3450000001,WK2060200012)
文摘Organoplatinum（Ⅱ） compounds have received enormous attention over the past decades due to their square-planar geometry as well as intriguing photo-physical properties.Self-assembly has emerged as an excellent approach to create well-ordered supramolecular architectures with tunable properties,which underpin the role of solvent-directed approach for the design of functional materials.In this minireview,the recent advances on supramolecular self-assembly of cyclometalated platinum（Ⅱ） complexes have been discussed.During the self-assembly process,non-covalent Pt-Pt and π-π interactions play crucial roles in controlling the structures and functions of the resulting assemblies.
文摘Oxygen reduction reaction(ORR)is an electrochemical reaction in which dissolved oxygen in an electrolyte is reduced toOH−/H2Owhen receiving electrons.This reaction plays a crucial role in shaping the efficiency of both metal-air batteries and fuel cells,and precious metals are the dominant catalysts carrying out the ORR in their cathodes.However,how to manipulate the electronic structure of precious metals as active sites to further promote ORR performance and maximize the utilization rate is still under development.Metal oxide serves as suitable and promising support that can strongly interact with precious metals for both activity and durability enhancement.Herein,we present recent research updates on strong precious metal-metal oxide interaction(SPMMOI)utilized in ORR.We start by introducing the background of ORR,the issues to be solved,and its practical applications followed by a thorough discussion of the reaction mechanism and comprehensive evaluation protocols of performance.We then provide a complete understanding of theworking principle of SPMMOI and highlight the related advances.Finally,we summarize the merits of the precious metal-metal oxide systemand propose the research direction aswell as some urgent problems to be addressed in the future.
基金Project(51625404)supported by the National Natural Science Foundation for Distinguished Young Scholar of ChinaProjects(51604104,51504295)supported by the National Natural Science Foundation of China
文摘In order to investigate the real-time cracking behavior of each component of a composite with strong interfacial bonding among lamellae, Ti-18 Nb(at.%) composite was prepared by spark plasma sintering(SPS), followed by hot-rolling, annealing, and quenching. The microstructure and mechanical properties were characterized by scanning electron microscopy(SEM), energy dispersive spectroscopy(EDS), micro-region X-ray diffractometry(MRXRD), nanoindentation, and in-situ scanning electron microscopy tensile testing. The results show that the Ti-18 Nb consists of Ti-enriched, diffusion and Nb-enriched zones, and the sharp Nb gradient across different zones leads to inhomogeneous distribution of phase and mechanical properties. A remarkable finding is that the diffusion zones not only enable the cooperative deformation between the brittle Ti-enriched zones and the ductile Nb-enriched zones but also act as the crack-arresters to prevent the local cracks in the Ti-enriched zones from further propagating across the composite.
基金the National Science Foundation China(NSFC No.52172051)the NSF of Jiangsu Province(BK20200041)+2 种基金the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)A.R.-F.and J.M.P.thank the Spanish Ministry of Science(grant PID2020-112762GB-I00 funded by MCIN/AEl/10.13039/501100011033)the Generalitat de Catalunya(grant 2021 SGR 00110)and the URV for support.
文摘Comprehensive Summary The experimental investigation of rare-earth metal-metal bonds remains a challenge in the study of chemical bonds.Herein,we report the synthesis and characterization of a novel heteronuclear di-metallofullerene,ScY@C_(3v)(8)-C_(82),which contains a mixed rare-earth metal-metal bond.ScY@C_(3v)(8)-C_(82)was successfully synthesized by arc-discharging method and characterized by mass spectrometry,UV-vis-NIR spectroscopy and single-crystal X-ray diffraction crystallography,which unambiguously determined its molecular structure.Theoretical calculations were also performed to study the optimized positions of Sc-Y metallic dimer and the electronic configuration.The combined experimental and theoretical results confirmed that both Sc and Y atoms transfer two electrons to the C_(3v)(8)-C_(82)cage,i.e.,(ScY)4+@(C_(3v)(8)-C_(82))4-.In particular,a covalent Sc-Yσ2 bond,which has never been reported before,is proven to be formed inside C_(3v)(8)-C_(82)fullerene cage.This work presents a novel di-metallofullerene containing mixed rare-earth metal-metal bond and expands the understanding of metal-metal bonding of rare earth elements.
基金supported by the National Natural Science Foundation of China (NSFC, Nos. 21901222, U1904215 and 21671170)Lvyangjinfeng Talent Program of Yangzhou+2 种基金the Top-notch Academic Programs Project of Jiangsu Higher Education Institutions(TAPP)Program for Young Changjiang Scholars of the Ministry of Education,China (No. Q2018270)Natural Science Foundation of Jiangsu Province (No. BK20200044)。
文摘The unique components and architecture of Prussian blue analogous(PBAs) offer great potential for the construction of various functional nanostructures. Herein, we reported the preparation of a series of Mn–Fe oxides-based hybrids using Mn–Fe PBA as a template and an organic carbon source by calcination.The study focuses on revealing the interaction between the microstructure and electrochemical performance of the products obtained at different calcination temperatures. Notably, the as-derived porous Fe–Fe0.33Mn0.67O/C nanocubes(i.e., M600) exhibited the best rate capability and cycle life compared with other samples(~890 m Ah/g at 0.1 A/g, 626.8 m Ah/g after 1000 cycles at 1.0 A/g with a 99% capacity retention). These can be attributed to the fact that the porous structure provides shorter Li+diffusion path and promotes the penetration of electrolyte. Besides, the N-doped C formed by the carbonization of organic ligands can buffer the volume change and prevent the aggregation of Fe_(0.33)Mn_(0.67)O nanoparticles during the discharge/charge cycles. Moreover, the presence of metallic Fe enhances the conductivity and the electrochemical activity, which accelerates the electrochemical reactions. Therefore, reasonable design of microstructure and compositions of functional nanocomposites is the key to obtain ideal electrochemical properties.
基金supported by grant from the Research Grants Council(City U 11305220)of the Hong Kong Special Administrative Region,China
文摘Metal–metal battery bears great potential for next-generation large-scale energy storage system because of its simple manufacture process and low production cost.However,the cross-over of metal cations from the cathode to the anode causes a loss in capacity and influences battery stability.Herein,a coating of poly(ionic liquid)(PIL)with poly(diallyldimethylammonium bis(trifluoromethanesulfonyl)imide)(PDADMA^(+)TFSI^(−))on a commercial polypropylene(PP)separator serves as an anion exchange membrane for a 3.3 V copper–lithium battery.The PIL has a positively charged polymer backbone that can block the migration of copper ions,thus improving Coulombic efficiency,long-term cycling stability and inhibiting self-discharge of the battery.It can also facilitate the conduction of anions through the membrane and reduce polarization,especially for fast charging/discharging.Bruce-Vincent method gives the transport number in the electrolyte to be 0.25 and 0.04 for PP separator without and with PIL coating,respectively.This suggests that the PIL layer reduces the contribution of the internal current due to cation transport.The use of PIL as a coating layer for commercial PP separator is a cost-effective way to improve overall electrochemical performance of copper–lithium batteries.Compared to PP and polyacrylic acid(PAA)/PP separators,the PIL/PP membrane raises the Coulombic efficiency to 99%and decreases the average discharge voltage drop to about 0.09 V when the current density is increased from 0.1 to 1 mA cm^(−2).
文摘Development of total hip arthroplasty (THA) now spans more than 5 decades encompassing combinations of metal-on-metal (MOM), ceramic-on-metal (COM), metal-on-plastic (MOP), ceramic-on-plastic (COM), and ceramic-on-ceramic (COC). In every arena of extensive technical development, there exists a data set that when viewed in isolation seemed of little import, but when assembled in-toto may produce a generational shift in perception. Our review focused on two such THA events. Firstly, COC retrieval studies (1999-2001) noted habitual wear patterns on heads and peripheral wear stripes, along with femoral-neck impingement, and ceramic surfaces stained gray by metal debris. These COC<span style="font-family:Verdana;"> </span><span style="font-family:Verdana;">data indicated THA risks included, </span><span style="font-family:Verdana;">1</span><span style="font-family:Verdana;">) cup edge-loading (E/L) on heads producing </span><span style="font-family:Verdana;">“</span><span style="font-family:Verdana;">stripe wear</span><span style="font-family:Verdana;">”</span><span style="font-family:Verdana;">,</span><span style="font-family:Verdana;"> 2</span><span style="font-family:Verdana;">) component impingement releasing metal particles resulting in </span><span style="font-family:Verdana;">3</span><span style="font-family:Verdana;">) tissues contaminated by metal debris. A corresponding MOM impingement-debris mechanism was only perceived by Howie (2005) in a McKee-Farrar retrieval study. Our anticipation at LLUMC was that MOM retrievals would provide superior wear details to those seen on COC retrievals. We noted stripe wear in the polar zone of CoCr heads and basal stripes in the non-wear areas. The basal-polar stripe combinations were </span><span style="font-family:Verdana;">found in all MOM retrievals. Basal-polar stripe combinations followed cup-rim</span><span style="font-family:Verdana;"> profiles in our LLUMC simulations of prosthetic impingement. LPUH videos demonstrated the formation of stripe wear in functiona
基金This work was supported by the National Natural Science Foundation of China (90206040, 20325106, 20333070), Natural Science Foundation of Fujian Province and the Key Project of the Chinese Academy of Sciences (B982003)
文摘A new compound formulated [Ag2(idc)](NO3)?H2O (H2idc = iminodiacetic acid) was synthesized under mild conditions and characterized by IR spectrum and single-crystal X-ray diffraction. The crystal crystallizes in the monoclinic system, space group of P21/n with a = 5.5029(2), b = 11.1316(5), c = 15.5319 (1) ?, β = 96.038(3)o, V = 946.15(6) ?3, Z = 4, R = 0.0619 and wR = 0.1606. Its structure is a 2D polymer, whose repeat units consist of dinuclear silver cluster coordinated by two bridging iminodiacetic acids. In the complex, the Ag(I) ions adopt three coordinate fashions, and the Ag-Ag metal-metal contacts of 2.8418 ? are observed.
基金the financial support of the National Natural Science Foundation of China (Nos. 21277091 and 51472159)the State Key Program of National Natural Science Foundation of China (No. 21436007)+1 种基金the Key Basic Research Projects of Science and Technology Commission of Shanghai (No. 14JC1403100)the Chenxing-SMG Young Scholar Project of Shanghai Jiao Tong University
文摘The Earth’s sustainable development is threatened by the increasing atmospheric COlevel which can be attributed to the imbalance of COdue to the rapid consumption of fossil fuels caused by human activities and the slow absorption and conversion of COby nature. One of the efficient methods for reconstructing the balance of COshould involve the rapid conversion of COinto fuels and chemicals.The hydrogenation of COwith gaseous hydrogen is currently considered to be the most commercially feasible synthetic route, however, the supply of safe and economical hydrogen sources poses a significant challenge to up-scaling application. Direct utilization of hydrogen from dissociation of water, the most abundant, cheap and clean hydrogen resource, for the reduction of COwould be one of the most promising approaches for COutilization. This paper provides an overview of the current advances in research on highly efficient reduction of COor NaHCO, a representative compound of CO, into formic acid/formate by in situ hydrogen from water dissociation with a metal/metal oxide redox cycle under mild hydrothermal conditions.
基金supported by the National Natural Science Foundation of China(No.21688102,No.21573047and No.21273045)
文摘Binuclear transition metal carbonyl clusters serve as the simplest models in understand- ing metal-metal and ligand bonding that are important organometallic chemistry catalysis. Binuclear first row transition metal carbonyl ions are produced via a pulsed laser vaporiza- tion/supersonic expansion cluster ion source in the gas phase. These ions are studied by mass-selected infrared photodissociation spectroscopy in the carbonyl stretching frequency region. Density functional theory calculations have been performed on the geometric struc- tures and vibrational spectra of the carbonyl ions. Their geometric and electronic structures are determined by comparison of the experimental IR spectra with the simulated spectra. The structure and the metM-metal and metal-CO bonding of both saturated and unsaturated homonuclear as well as heteronuclear carbonyl cluster cations and anions are discussed.
基金supported by the National Natural Science Foundation of China(Nos.21674106 and 21871245)CAS Youth Innovation Promotion Association(No.2015365)the Fundamental Research Funds for the Central Universities(No.WK3450000004)
文摘Two host-guest systems have been constructed,by employing structurally similar terpyridine platinum(II)macrocycle and molecular tweezer as the synthetic receptors.The macrocycle/guest complex displays low-energy emission signal,reinforced non-covalent binding affinity,and enhanced photosensitization capability than those of the molecular tweezer/guest one.The discrepancy between macrocyclic and acyclic preorganization modes originates from the different numbers of Pt(II)Pt(II)metal-metal bonds in host-guest complexation structures.
基金supported by the National Natural Science Foundation of China(51872204,52072261 and 22011540379)the National Key Research and Development Program of China(2017YFA0204600)+1 种基金Shanghai Social Development Science and Technology Project(20dz1201800)Shanghai Sailing Program(21YF1430900).
文摘Co_(2)VO_(4) with Co tetrahedrons and octahedrons of transition metal oxides has achieved progress in electrocatalysts and batteries.However,high metal-metal interactions make it challenging to maintain high reactivity as well as increase the conductivity and stability of supercapacitors.In this work,spinel-structured CoZn_(0.5)V_(1.5)O_(4) with a high specific surface area was synthesized through an ion-exchange process from the metal-organic frameworks of zinc-cobalt.Density functional theory calculations indicate that the replacement of transition metal by Zn can decrease the interaction between the transition metals,leading to a downshift in the π^(∗)-orbitals(V-O)and half-filled a_(1g) orbitals near the Fermi level,thus increasing the conductivity and stability of CoZn_(0.5)V_(1.5)O_(4).As a supercapacitor electrode,CoZn_(0.5)V_(1.5)O_(4) exhibits high cycling durability(99.4% capacitance retention after 18,000 cycles)and specific capacitance(1100mFcm^(-2) at 1mAcm^(-2)).This work provides the possibility of designing octahedral and tetrahedral sites in transition metal oxides to improve their electrochemical performance.
