Two novel out-of-plane ordered quaternary borides M'_(4)VSiB_(2) (M'=Nb and Mo) have been synthesized. The out-of-plane ordered characteristic has been confirmed by the X-ray diffraction, the neutron powder di...Two novel out-of-plane ordered quaternary borides M'_(4)VSiB_(2) (M'=Nb and Mo) have been synthesized. The out-of-plane ordered characteristic has been confirmed by the X-ray diffraction, the neutron powder diffraction and the scanning transmission electron microscopy with high-angle angular dark field images. By adjusting the stoichiometric ratio of Mo and V, the 16l site preferentially occupied by relatively larger atom and 4c site by relatively smaller atom have been confirmed. The further first-principle calculation demonstrates the dynamical and thermodynamical stability of Mo_(4)VSiB_(2) o-T2 phase. This work confirms the transition metal occupation strategy of o-T2 phase and enriches the out-of-plane ordered laminated borides family.展开更多
In most Suzuki–Miyaura carbon-carbon cross-coupling reactions,the borabicyclo[3.3.1]nonane scaffold(9-BBN)only serves as an auxiliary facilitating the transmetalation step and thus is transformed into by-products.The...In most Suzuki–Miyaura carbon-carbon cross-coupling reactions,the borabicyclo[3.3.1]nonane scaffold(9-BBN)only serves as an auxiliary facilitating the transmetalation step and thus is transformed into by-products.There are rare examples where the 9-BBN derivatives serve as the potentially diverse C8 building blocks in cross-coupling reactions.Herein,we report a cobalt-catalyzed migratory carboncarbon cross-coupling reaction of the in situ formed 9-BBN ate complexes to afford diverse aryl-and alkyl-functionalized cyclooctenes.Preliminary mechanistic studies suggest the oxidation-induced cisbicyclo[3.3.0]oct-1-ylborane is the key intermediate in this migratory cross-coupling reaction,which promotes the development of other diverse migratory cross-coupling of borate complexes.展开更多
The prediction of new fluorooxoborates as ultraviolet(UV)/deep ultraviolet(DUV)opto-electronic functional materials from a largely unexplored chemical space is a challenging task.It has been suggested that the anionic...The prediction of new fluorooxoborates as ultraviolet(UV)/deep ultraviolet(DUV)opto-electronic functional materials from a largely unexplored chemical space is a challenging task.It has been suggested that the anionic frameworks formed by B–O and B–O–F units significantly determine the physical properties of fluorooxoborates.Therefore,the rational design of anionic frameworks could facilitate the materials discovery process.Herein,we propose that a candidate anionic framework can be efficiently derived from an existing one by slightly altering its oxygen content.Following this idea,we hypothesized the existence of a 1D[B_(3)O_(5)F]_(∞)chain from the wellknown 2D[B_(6)O_(9)F_(2_)]_(∞)layer.Accordingly,seven CaB_(3)O_(5)F structures with the expected anionic framework were successfully predicted.First-principles calculations show that all these structures have potential in the UV/DUV birefringent or nonlinear optical(NLO)material field,indicating that the 1D[B_(3)O_(5)F]_(∞)chain is indeed a promising anionic framework for achieving UV/DUV birefringent and NLO performance.展开更多
Transition metal borides(TMBs)are a new class of promising electrocatalysts for hydrogen generation by water splitting.However,the synthesis of robust all-in-one electrodes is challenging for practical applications.He...Transition metal borides(TMBs)are a new class of promising electrocatalysts for hydrogen generation by water splitting.However,the synthesis of robust all-in-one electrodes is challenging for practical applications.Herein,a facile solid-state boronization strategy is reported to synthesize a series of self-supported TMBs thin films(TMB-TFs)with large area and high catalytic activity.Among them,MoB thin film(MoB-TF)exhibits the highest activity toward electrocatalytic hydrogen evolution reaction(HER),displaying a low overpotential(η10=191 and 219 mV at 10 mA cm^(−2))and a small Tafel slope(60.25 and 61.91 mV dec^(−1))in 0.5M H_(2)SO_(4)and 1.0M KOH,respectively.Moreover,it outperforms the commercial Pt/C at the high current density region,demonstrating potential applications in industrially electrochemical water splitting.Theoretical study reveals that both surfaces terminated by TM and B atoms can serve as the active sites and the H*binding strength of TMBs is correlated with the p band center of B atoms.This work provides a new pathway for the potential application of TMBs in largescale hydrogen production.展开更多
Owing to the orbital hybridization between the transition metal and the B element and the electron-trapping effect of the B ele-ment,transition metal borides are considered very promising materials for energy catalysi...Owing to the orbital hybridization between the transition metal and the B element and the electron-trapping effect of the B ele-ment,transition metal borides are considered very promising materials for energy catalysis.In this work,an amorphous scaly high-entropy boride(HEB)with electron traps was designed and fabricated via a facile reduction method to improve the hydrogen storage properties of magnesium hydride(MgH_(2)).For dehydrogenation,the onset temperature of MgH_(2)+10wt%HEB was dropped to 187.4℃;be-sides,the composite exhibited superior isothermal kinetics and the activation energy of the composite was reduced from(212.78±3.93)to(65.04±2.81)kJ/mol.In addition,MgH_(2)+10wt%HEB could absorb hydrogen at 21.5℃,and 5.02wt%H_(2) was charged in 50 min at 75℃.For reversible hydrogen storage capacity tests,the composite maintained a retention rate of 97%with 6.47wt%hydrogen capacity after 30 cycles.Combining microstructure evidence with hydrogen storage performance,the catalytic mechanism was proposed.During ball milling,scaly high-entropy borides riveted a large number of heterogeneous active sites on the surface of MgH_(2).Driven by the cocktail effect as well as the orbital hybridization of metal borides,numerous active sites steadily enhanced the hydrogen storage reactions in MgH_(2).展开更多
The first-principle calculations are performed to investigate the structural,mechanical and electronic properties of titanium borides （Ti2B,TiB and TiB2）.Those calculated lattice parameters are in good agreement wit...The first-principle calculations are performed to investigate the structural,mechanical and electronic properties of titanium borides （Ti2B,TiB and TiB2）.Those calculated lattice parameters are in good agreement with the experimental data and previous theoretical values.All these borides are found to be mechanically stable at ambient pressure.Compared with parent metal Ti （120 GPa）,the larger bulk modulus of these borides increase successively with the increase of the boron content in three borides,which may be due to direction bonding introduced by the boron atoms in the lattice and the strong covalent Ti-B bonds.Additionally,TiB can be regarded as a candidate of incompressible and hard material besides TiB2.Furthermore,the elastic anisotropy and Debye temperatures are also discussed by investigating the elastic constants and moduli.Electronic density of states and atomic Mulliken charges analysis show that chemical bonding in these titanium borides is a complex mixture of covalent,ionic,and metallic characters.展开更多
Two new nonmetal borates, [（C2H10N2）]2[B14O20（OH）6] 1 and [C8H22N4][B5O6（OH）4]2 2, have been synthesized under mild conditions and characterized by single-crystal X-ray diffraction, FTIR, elemental analysis and ...Two new nonmetal borates, [（C2H10N2）]2[B14O20（OH）6] 1 and [C8H22N4][B5O6（OH）4]2 2, have been synthesized under mild conditions and characterized by single-crystal X-ray diffraction, FTIR, elemental analysis and thermogravimetric analysis. Crystal data for compound 1： triclinic, space group P^-1, a = 8.4979（17）, b = 8.8498（18）, c = 10.065（2）A^°, α = 95.01（3）, β = 96.99（3）, γ = 116.82（3）°, V= 661.8（3）A^°^3, Z= 1, Mr = 697.63, Dc = 1.751 g/cm^3,μ = 0.163 mm^-1, F（000） = 356, the final R = 0.0372 and wR = 0.0968 （I 〉 2σ（I））; and those for compound 2： monoclinic, space group P21/c, a = 9.1867（18）, b= 14.118（3）, c = 10.334（2）A^°, β = 91.48（3）°, V = 1339.8（5）A^°^3, Z = 2, Mr = 610.46, Dc = 1.513 g/cm^3,μ = 0.135 mm^-1, F（000） = 632, the final R = 0.0350 and wR = 0.0912 （I 〉 2σ（I））. For both 1 and 2, the anionic units are interlinked via O-H…O hydrogen bonds to form a 3D supramolecular network, while the protonated cations are located in the free space of the inorganic borate framework and interact with the anions by electrostatic attraction and extensive N-H…O hydrogen bonds.展开更多
Two new isostructural multi-metal beryllium borates, m^3 Li Na4Be4B10O24F（M = Sr（1）, Cd（2））, have been synthesized by spontaneous crystallization. The structures were verified by single-crystal X-ray crystallogr...Two new isostructural multi-metal beryllium borates, m^3 Li Na4Be4B10O24F（M = Sr（1）, Cd（2））, have been synthesized by spontaneous crystallization. The structures were verified by single-crystal X-ray crystallography. The compounds crystallize in the trigonal space group R 3, with a = b = 9.4645（1） A, c = 38.842（8） A, V = 3013.2（6） A3, Z = 6, F（000） = 2568, Dc = 3.005 g/cm^3, Mr = 908.9, R = 0.0327, w R = 0.0678, μ = 8.160 mm-1 for Sr3 Li Na4Be4B10O24F and a = b = 9.3019（8） A, c = 37.782（7） A, V = 2831.12（9） A3, Z = 6, F（000） = 2748, Dc = 3.459 g/cm^3, Mr = 983.24, R = 0.0158, w R = 0.0455, μ = 3.586 mm-1 for Cd3 Li Na4Be4B10O24F. The structures are characterized by an infinite two-dimensional [Be8B16O40F2]∞ double layer bridged by [B12O24] groups like a sandwich structure, while the cations reside in tunnels along different directions. UV-vis-IR diffuse reflectance spectroscopy demonstrates that their cut-off edges are below 200 nm. Thermal analysis shows that they melt incongruently and their melting points are around 740-770 ℃.展开更多
Given increasing energy demands and environmental pollution,it is highly desirable to design new hydrogen evolution reaction(HER)catalysts.In this study,we have performed high throughput screening of transition-metal ...Given increasing energy demands and environmental pollution,it is highly desirable to design new hydrogen evolution reaction(HER)catalysts.In this study,we have performed high throughput screening of transition-metal borides(M2B)and Janus counterparts for appealing catalysts.The simulations showcase that the Pd_(2)B,PdPtB,PdIrB and PdAuB possess favorable HER performance with the different chemical nature and unique asymmetry structure.展开更多
Electrochemical water splitting is a feasible method for producing environmental benignity energy of hydrogen,while high price and low availability on the earth of noble electrocatalysts constrain their global-scale a...Electrochemical water splitting is a feasible method for producing environmental benignity energy of hydrogen,while high price and low availability on the earth of noble electrocatalysts constrain their global-scale application.Transition metal borides(TMBs)have displayed unique metalloid characteristic and outstanding performance for oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)in the last few decades.Herein,recent developments of the TMBs for HER and OER are summarized.Initially,the impact factors and relevant evaluation of electrocatalytic performance are described,that is,overpotential,Tafel slope and exchange current density,stability,faradaic efficiency,turnover frequency,mass and specific activities.Moreover,the optimization strategies of borides are emphasized,which principally include coupling with effective substrates,elemental doping,phase modification,interfacial engineering,and morphology control.Finally,in order to reach the goal of application,the remaining challenges and perspectives are given to point out a direction for enhancing the performance of borides.展开更多
The development of efficient and cost-effective electrocatalysts toward anodic oxygen evolution reaction(OER) is crucial for the commercial application of electrochemical water splitting.As the most promising electroc...The development of efficient and cost-effective electrocatalysts toward anodic oxygen evolution reaction(OER) is crucial for the commercial application of electrochemical water splitting.As the most promising electrocatalysts,the OER performances of nickel-iron-based materials can be further improved by introducing metalloid elements to modify their electron structures.Herein,we developed an efficient hybrid electrocatalyst with nickel-iron boride(NiFeB) as core and amorphous nickel-iron borate(NiFeBi)as shell(NiFeB@NiFeBi) via a simple aqueous reduction.The obtained NiFeB@NiFeBi exhibits a small overpotential of 237 mV at 10 mA/cm^2 and Tafel slope of 57.65 mV/dec in 1.0 mol/L KOH,outperforming most of the documented precious-metal-free based electrocatalysts.Benefiting from the in situ formed amorphous NiFeBi layer,it shows excellent stability toward the oxygen evolution reaction(OER).These findings might provide a new way to design advanced precious-metal-free electrocatalysts for OER and the application of electrochemical water splitting.展开更多
The antiwear and friction-reducing performances of sodium borate, potassium borate and lanthanum chloride in water were evaluated on a four-ball friction tester. The topographies, element distribution and chemical cha...The antiwear and friction-reducing performances of sodium borate, potassium borate and lanthanum chloride in water were evaluated on a four-ball friction tester. The topographies, element distribution and chemical characteristics of the worn surfaces were investigated by scanning electron microscope （SEM）, energy dispersion of X-ray （EDX） and X-ray photoelectron spectroscope （XPS）. The results indicated that sodium borate, potassium borate and lanthanum chloride increased extreme pressure, antiwear and friction-reducing capacities of water to a certain extent, of which potassium borate was the best candidate. Combination of lanthanum chloride with sodium borate and po- tassium borate respectively further improved antiwear and friction-reducing capacities. Scratches of worn surfaces lubricated with water containing borates and lanthanum chloride were less severe than those lubricated with water containing borates alone. A tribochemical film mainly composed of oxides of lanthanum, boron and iron reduced friction and wear for water lubricant formulated with both borates and lanthanum chloride.展开更多
On the basis of the current theoretical understanding of boron-based hard superconductors under ambient conditions,numerous studies have been conducted with the aim of developing superconducting materials with favorab...On the basis of the current theoretical understanding of boron-based hard superconductors under ambient conditions,numerous studies have been conducted with the aim of developing superconducting materials with favorable mechanical properties using boron-rich compounds.In this paper,first-principles calculations reveal the existence of an unprecedented family of tetragonal pentaborides MB_(5)(M=Na,K,Rb,Ca,Sr,Ba,Sc,and Y),comprising B_(20)cages and centered metal atoms acting as stabilizers and electron donors to the boron sublattice.These compounds exhibit both superconductivity and high hardness,with the maximum superconducting transition temperature T_(c)of 18.6 K being achieved in RbB5 and the peak Vickers hardness Hv of 35.1 GPa being achieved in KB_(5)at 1 atm.The combination of these properties is particularly evident in KB_(5),RbB5,and BaB5,with Tc values of∼14.7,18.6,and 16.3 K and H_(v)values of∼35.1,32.4,and 33.8 GPa,respectively.The results presented here reveal that pentaborides can provide a framework for exploring and designing novel superconducting materials with favorable hardness at achievable pressures and even under ambient conditions.展开更多
Lithium−sulfur batteries are one of the most competitive high-energy batteries due to their high theoretical energy density of _(2)600 W·h·kg^(−1).However,their commercialization is limited by poor cycle sta...Lithium−sulfur batteries are one of the most competitive high-energy batteries due to their high theoretical energy density of _(2)600 W·h·kg^(−1).However,their commercialization is limited by poor cycle stability mainly due to the low intrinsic electrical conductivity of sulfur and its discharged products(Li_(2)S_(2)/Li_(2)S),the sluggish reaction kinetics of sulfur cathode,and the“shuttle effect”of soluble intermediate lithi-um polysulfides in ether-based electrolyte.To address these challenges,catalytic hosts have recently been introduced in sulfur cathodes to en-hance the conversion of soluble polysulfides to the final solid products and thus prevent the dissolution and loss of active-sulfur material.In this review,we summarize the recent progress on the use of metal phosphides and borides of different dimensions as the catalytic host of sulfur cathodes and demonstrate the catalytic conversion mechanism of sulfur cathodes with the help of metal phosphides and borides for high-en-ergy and long-life lithium-sulfur batteries.Finally,future outlooks are proposed on developing advanced catalytic host materials to improve battery performance.展开更多
This paper is devoted to the rare-earth borates described by the general formula RM3（BO3）4, M = Al, Fe, and Cr, that have non-centrosymmetric trigonal slructure of the natural mineral huntite. It give a brief review...This paper is devoted to the rare-earth borates described by the general formula RM3（BO3）4, M = Al, Fe, and Cr, that have non-centrosymmetric trigonal slructure of the natural mineral huntite. It give a brief review of a spectroscopic research on YbAI3（BO3）4 （YbAB）, on a large group of magnetic iron borates, and on NdCra（BO3）4.展开更多
Easy machining into sharp lending edge, nose tip and complex shape components plays a pivotal role in the application of ultrahigh temperature ceramics in hypersonic vehicles, wherein low and controllable hardness is ...Easy machining into sharp lending edge, nose tip and complex shape components plays a pivotal role in the application of ultrahigh temperature ceramics in hypersonic vehicles, wherein low and controllable hardness is a necessary parameter to ensure the easy machinability. However, the mechanism that driving the hardness of metal hexaborides is not clear. Here, using a combination of the empirical hardness model for polycrystalline materials and density functional theory investigation, the hardness dependence on shear anisotropic factors of high temperature metal hexaborides has been established. It has come to light that through controlling the shear anisotropic factors the hardness of polycrystalline metal hexaborides can be tailored from soft and ductile to extremely hard and brittle, which is underpinned by the degree of chemical bonding anisotropy, i.e., the difference of B-B bond within the B;octahedron and that connecting the B;octahedra.展开更多
In recent years,transition metal borides(TMBs)have attracted much attention because they are considered as potential superhard materials and have more abundant crystal structures compared with traditional superhard ma...In recent years,transition metal borides(TMBs)have attracted much attention because they are considered as potential superhard materials and have more abundant crystal structures compared with traditional superhard materials.So far,however,no superhard materials have been found in TMBs.A large number of structures and potential new properties in TMBs are induced by the various hybridization ways of boron atoms and the high valence electrons of transition metals,which provide many possibilities for its application.And most TMBs have layered structures,which make TMBs have the potential to be a two-dimensional(2D)material.The 2D materials have novel properties,but the research on 2D TMBs is still nearly blank.In this paper,the research progress of TMBs is summarized involving structure,mechanical properties,and multifunctional properties.The strong covalent bonds of boron atoms in TMBs can form one-dimensional,twodimensional,and three-dimensional substructures,and the multiple electron transfer between transition metal and boron leads to a variety of chemical bonds in TMBs,which are the keys to obtain high hardness and multifunctional properties of TMBs.Further research on the multifunctional properties of TMBs,such as superconductors,catalysts,and high hardness ferromagnetic materials,is of great significance to the discovery of new multifunctional hard materials.展开更多
The morphology and growth mechanism of borides in Ti 48Al+(0.2%～0.8%)B (mole fraction) alloys were investigated. The results show that TiB 2 phase are all flakes with width <0.5 μm and aspect ratio >100 in all...The morphology and growth mechanism of borides in Ti 48Al+(0.2%～0.8%)B (mole fraction) alloys were investigated. The results show that TiB 2 phase are all flakes with width <0.5 μm and aspect ratio >100 in alloys containing 0.2% and 0.5%B, respectively, but there are a few hexagonal blocky borides with habit planes of (0001) and {1010} type besides flakes in the alloy containing 0.8%B. Flake borides are the products of irregular eutectic reactions growing coupled with matrix and blocky borides are primary TiB 2 phases growing unconstrained in melt.展开更多
Mixtures of W and B13C2 powders were mechanically milled and subsequently annealed at 900-1200℃.It is found that amorphous W-B-C alloy formed as the mixtures were milled for 20.80 h.After annealing the 80 h-milled mi...Mixtures of W and B13C2 powders were mechanically milled and subsequently annealed at 900-1200℃.It is found that amorphous W-B-C alloy formed as the mixtures were milled for 20.80 h.After annealing the 80 h-milled mixtures at 900-950℃,solid solutions of C and/or B in tungsten[W（B,C）],C in tungsten boride[W2B（C）or WB（C）]formed by the crystallization of amorphous W-B-C.The formation temperature of W2B（C）and WB（C）is lower than that of W2B and WB reported previously.As the 80 h-milled mixtures were annealed at 1200℃,W reacted with amorphous W-B-C completely to form WB and W2B5 or W2B5 instead of the solid solutions of C in tungsten borides,which is determined by the mole ratio of W to B13C2.The formation mechanisms of the W2B（C）and WB（C）solid solutions as well as phase transition rules of the mixtures at annealing temperature and mole ratio were also investigated using first-principle calculation.展开更多
1 Introduction Lithium and its compounds as national strategic resources are extensively used in national defense,industrial and agricultural production.As we know,the salt lakes in the western of China are famous for...1 Introduction Lithium and its compounds as national strategic resources are extensively used in national defense,industrial and agricultural production.As we know,the salt lakes in the western of China are famous for its high展开更多
基金supported by the National Youth Talent Support Program(No.QNBJ-2022-03)the National Natu-ral Science Foundation of China(No.52371180)the Fundamental Research Funds for the Central Universities(Nos.N2209005 and N2309001).
文摘Two novel out-of-plane ordered quaternary borides M'_(4)VSiB_(2) (M'=Nb and Mo) have been synthesized. The out-of-plane ordered characteristic has been confirmed by the X-ray diffraction, the neutron powder diffraction and the scanning transmission electron microscopy with high-angle angular dark field images. By adjusting the stoichiometric ratio of Mo and V, the 16l site preferentially occupied by relatively larger atom and 4c site by relatively smaller atom have been confirmed. The further first-principle calculation demonstrates the dynamical and thermodynamical stability of Mo_(4)VSiB_(2) o-T2 phase. This work confirms the transition metal occupation strategy of o-T2 phase and enriches the out-of-plane ordered laminated borides family.
基金supported by the National Natural Science Foundation of China(No.22171046)the Hundred-Talent Project of Fujian(No.50021113)Fuzhou University(No.0480-00489503)。
文摘In most Suzuki–Miyaura carbon-carbon cross-coupling reactions,the borabicyclo[3.3.1]nonane scaffold(9-BBN)only serves as an auxiliary facilitating the transmetalation step and thus is transformed into by-products.There are rare examples where the 9-BBN derivatives serve as the potentially diverse C8 building blocks in cross-coupling reactions.Herein,we report a cobalt-catalyzed migratory carboncarbon cross-coupling reaction of the in situ formed 9-BBN ate complexes to afford diverse aryl-and alkyl-functionalized cyclooctenes.Preliminary mechanistic studies suggest the oxidation-induced cisbicyclo[3.3.0]oct-1-ylborane is the key intermediate in this migratory cross-coupling reaction,which promotes the development of other diverse migratory cross-coupling of borate complexes.
基金supported by the National Natural Science Foundation of China(Grant No.52403305)the Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB0880000)+1 种基金Tianchi Talent Program of Xinjiang Uygur Autonomous Region(Grant No.2024000068)Postdoctoral Fellow-ship Program(Grade C)(Grant No.GZC20232959)。
文摘The prediction of new fluorooxoborates as ultraviolet(UV)/deep ultraviolet(DUV)opto-electronic functional materials from a largely unexplored chemical space is a challenging task.It has been suggested that the anionic frameworks formed by B–O and B–O–F units significantly determine the physical properties of fluorooxoborates.Therefore,the rational design of anionic frameworks could facilitate the materials discovery process.Herein,we propose that a candidate anionic framework can be efficiently derived from an existing one by slightly altering its oxygen content.Following this idea,we hypothesized the existence of a 1D[B_(3)O_(5)F]_(∞)chain from the wellknown 2D[B_(6)O_(9)F_(2_)]_(∞)layer.Accordingly,seven CaB_(3)O_(5)F structures with the expected anionic framework were successfully predicted.First-principles calculations show that all these structures have potential in the UV/DUV birefringent or nonlinear optical(NLO)material field,indicating that the 1D[B_(3)O_(5)F]_(∞)chain is indeed a promising anionic framework for achieving UV/DUV birefringent and NLO performance.
基金National Natural Science Foundation of China,Grant/Award Number:52172058Outstanding Youth Fund of Natural Science Foundation of Inner Mongolia Autonomous Region,Grant/Award Number:2023JQ15+4 种基金Fundamental Research Funds for the Inner Mongolia Normal University,Grant/Award Numbers:2022JBBJ010,2022JBTD008Major Project Cultivation Fund for the Inner Mongolia Normal University,Grant/Award Number:2020ZD01Funds for Reform and Development of Local Universities Supported by The Central Government(Cultivation of First-Class Disciplines in Physics)Postdoctoral Fellowship Program of CPSF,Grant/Award Number:GZB20240101China Postdoctoral Science Foundation,Grant/Award Number:2024M750304.
文摘Transition metal borides(TMBs)are a new class of promising electrocatalysts for hydrogen generation by water splitting.However,the synthesis of robust all-in-one electrodes is challenging for practical applications.Herein,a facile solid-state boronization strategy is reported to synthesize a series of self-supported TMBs thin films(TMB-TFs)with large area and high catalytic activity.Among them,MoB thin film(MoB-TF)exhibits the highest activity toward electrocatalytic hydrogen evolution reaction(HER),displaying a low overpotential(η10=191 and 219 mV at 10 mA cm^(−2))and a small Tafel slope(60.25 and 61.91 mV dec^(−1))in 0.5M H_(2)SO_(4)and 1.0M KOH,respectively.Moreover,it outperforms the commercial Pt/C at the high current density region,demonstrating potential applications in industrially electrochemical water splitting.Theoretical study reveals that both surfaces terminated by TM and B atoms can serve as the active sites and the H*binding strength of TMBs is correlated with the p band center of B atoms.This work provides a new pathway for the potential application of TMBs in largescale hydrogen production.
基金supported by the National Natural Science Foundation of China(No.22179054)the Jiangsu Province Innovation Support Project,China(No.BZ2023010)+1 种基金the Project of Jiangsu University High-Tech Ship Collaborative Innovation Center(No.1174871801-11)the Ministry of Science and Technology of the People’s Republic of China(No.G2023014022L).
文摘Owing to the orbital hybridization between the transition metal and the B element and the electron-trapping effect of the B ele-ment,transition metal borides are considered very promising materials for energy catalysis.In this work,an amorphous scaly high-entropy boride(HEB)with electron traps was designed and fabricated via a facile reduction method to improve the hydrogen storage properties of magnesium hydride(MgH_(2)).For dehydrogenation,the onset temperature of MgH_(2)+10wt%HEB was dropped to 187.4℃;be-sides,the composite exhibited superior isothermal kinetics and the activation energy of the composite was reduced from(212.78±3.93)to(65.04±2.81)kJ/mol.In addition,MgH_(2)+10wt%HEB could absorb hydrogen at 21.5℃,and 5.02wt%H_(2) was charged in 50 min at 75℃.For reversible hydrogen storage capacity tests,the composite maintained a retention rate of 97%with 6.47wt%hydrogen capacity after 30 cycles.Combining microstructure evidence with hydrogen storage performance,the catalytic mechanism was proposed.During ball milling,scaly high-entropy borides riveted a large number of heterogeneous active sites on the surface of MgH_(2).Driven by the cocktail effect as well as the orbital hybridization of metal borides,numerous active sites steadily enhanced the hydrogen storage reactions in MgH_(2).
基金Project(2010JK404) supported by the Education Committee Natural Science Foundation of Shaanxi Province,ChinaProjects(ZK0918,ZK0915) supported by the Baoji University of Arts and Sciences Key Research,China
文摘The first-principle calculations are performed to investigate the structural,mechanical and electronic properties of titanium borides （Ti2B,TiB and TiB2）.Those calculated lattice parameters are in good agreement with the experimental data and previous theoretical values.All these borides are found to be mechanically stable at ambient pressure.Compared with parent metal Ti （120 GPa）,the larger bulk modulus of these borides increase successively with the increase of the boron content in three borides,which may be due to direction bonding introduced by the boron atoms in the lattice and the strong covalent Ti-B bonds.Additionally,TiB can be regarded as a candidate of incompressible and hard material besides TiB2.Furthermore,the elastic anisotropy and Debye temperatures are also discussed by investigating the elastic constants and moduli.Electronic density of states and atomic Mulliken charges analysis show that chemical bonding in these titanium borides is a complex mixture of covalent,ionic,and metallic characters.
基金supported by the Natural Science Foundation of Ningbo City (2007A610022) K. C. Wong Magna Fund in Ningbo University
文摘Two new nonmetal borates, [（C2H10N2）]2[B14O20（OH）6] 1 and [C8H22N4][B5O6（OH）4]2 2, have been synthesized under mild conditions and characterized by single-crystal X-ray diffraction, FTIR, elemental analysis and thermogravimetric analysis. Crystal data for compound 1： triclinic, space group P^-1, a = 8.4979（17）, b = 8.8498（18）, c = 10.065（2）A^°, α = 95.01（3）, β = 96.99（3）, γ = 116.82（3）°, V= 661.8（3）A^°^3, Z= 1, Mr = 697.63, Dc = 1.751 g/cm^3,μ = 0.163 mm^-1, F（000） = 356, the final R = 0.0372 and wR = 0.0968 （I 〉 2σ（I））; and those for compound 2： monoclinic, space group P21/c, a = 9.1867（18）, b= 14.118（3）, c = 10.334（2）A^°, β = 91.48（3）°, V = 1339.8（5）A^°^3, Z = 2, Mr = 610.46, Dc = 1.513 g/cm^3,μ = 0.135 mm^-1, F（000） = 632, the final R = 0.0350 and wR = 0.0912 （I 〉 2σ（I））. For both 1 and 2, the anionic units are interlinked via O-H…O hydrogen bonds to form a 3D supramolecular network, while the protonated cations are located in the free space of the inorganic borate framework and interact with the anions by electrostatic attraction and extensive N-H…O hydrogen bonds.
基金supported by the National Natural Science Foundation of China(No.50972149,61138004,51402316)the National Instrumentation Program(No.2012YQ120048)
文摘Two new isostructural multi-metal beryllium borates, m^3 Li Na4Be4B10O24F（M = Sr（1）, Cd（2））, have been synthesized by spontaneous crystallization. The structures were verified by single-crystal X-ray crystallography. The compounds crystallize in the trigonal space group R 3, with a = b = 9.4645（1） A, c = 38.842（8） A, V = 3013.2（6） A3, Z = 6, F（000） = 2568, Dc = 3.005 g/cm^3, Mr = 908.9, R = 0.0327, w R = 0.0678, μ = 8.160 mm-1 for Sr3 Li Na4Be4B10O24F and a = b = 9.3019（8） A, c = 37.782（7） A, V = 2831.12（9） A3, Z = 6, F（000） = 2748, Dc = 3.459 g/cm^3, Mr = 983.24, R = 0.0158, w R = 0.0455, μ = 3.586 mm-1 for Cd3 Li Na4Be4B10O24F. The structures are characterized by an infinite two-dimensional [Be8B16O40F2]∞ double layer bridged by [B12O24] groups like a sandwich structure, while the cations reside in tunnels along different directions. UV-vis-IR diffuse reflectance spectroscopy demonstrates that their cut-off edges are below 200 nm. Thermal analysis shows that they melt incongruently and their melting points are around 740-770 ℃.
基金financially supported by the National Natural Science Foundation of China(Nos.52122308 and 51973200)the Project of China Postdoctoral Science Foundation(No.2022M712909)the National Supercomputing Center in Zhengzhou。
文摘Given increasing energy demands and environmental pollution,it is highly desirable to design new hydrogen evolution reaction(HER)catalysts.In this study,we have performed high throughput screening of transition-metal borides(M2B)and Janus counterparts for appealing catalysts.The simulations showcase that the Pd_(2)B,PdPtB,PdIrB and PdAuB possess favorable HER performance with the different chemical nature and unique asymmetry structure.
基金supported by the National Natural Science Foundation of China(52025013,51622102)Ministry of Science and Technology of China MOST(2018YFB1502101)+1 种基金the 111 Project(B12015)the Fundamental Research Funds for the Central Universities.
文摘Electrochemical water splitting is a feasible method for producing environmental benignity energy of hydrogen,while high price and low availability on the earth of noble electrocatalysts constrain their global-scale application.Transition metal borides(TMBs)have displayed unique metalloid characteristic and outstanding performance for oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)in the last few decades.Herein,recent developments of the TMBs for HER and OER are summarized.Initially,the impact factors and relevant evaluation of electrocatalytic performance are described,that is,overpotential,Tafel slope and exchange current density,stability,faradaic efficiency,turnover frequency,mass and specific activities.Moreover,the optimization strategies of borides are emphasized,which principally include coupling with effective substrates,elemental doping,phase modification,interfacial engineering,and morphology control.Finally,in order to reach the goal of application,the remaining challenges and perspectives are given to point out a direction for enhancing the performance of borides.
基金financially supported by the National Natural Science Foundation of China(No.21972107)the National Natural Science Foundation of Jiangsu Province(No.BK20191186)the Large-Scale Instrument and Equipment Sharing Foundation of Wuhan University。
文摘The development of efficient and cost-effective electrocatalysts toward anodic oxygen evolution reaction(OER) is crucial for the commercial application of electrochemical water splitting.As the most promising electrocatalysts,the OER performances of nickel-iron-based materials can be further improved by introducing metalloid elements to modify their electron structures.Herein,we developed an efficient hybrid electrocatalyst with nickel-iron boride(NiFeB) as core and amorphous nickel-iron borate(NiFeBi)as shell(NiFeB@NiFeBi) via a simple aqueous reduction.The obtained NiFeB@NiFeBi exhibits a small overpotential of 237 mV at 10 mA/cm^2 and Tafel slope of 57.65 mV/dec in 1.0 mol/L KOH,outperforming most of the documented precious-metal-free based electrocatalysts.Benefiting from the in situ formed amorphous NiFeBi layer,it shows excellent stability toward the oxygen evolution reaction(OER).These findings might provide a new way to design advanced precious-metal-free electrocatalysts for OER and the application of electrochemical water splitting.
基金the National Natural Science Foundation of China (50275147)Program for New Century Excellent Talents in Chinese University (NCET-04-1002)Program for Innovative Groups in Chongqing’s Higher Schools
文摘The antiwear and friction-reducing performances of sodium borate, potassium borate and lanthanum chloride in water were evaluated on a four-ball friction tester. The topographies, element distribution and chemical characteristics of the worn surfaces were investigated by scanning electron microscope （SEM）, energy dispersion of X-ray （EDX） and X-ray photoelectron spectroscope （XPS）. The results indicated that sodium borate, potassium borate and lanthanum chloride increased extreme pressure, antiwear and friction-reducing capacities of water to a certain extent, of which potassium borate was the best candidate. Combination of lanthanum chloride with sodium borate and po- tassium borate respectively further improved antiwear and friction-reducing capacities. Scratches of worn surfaces lubricated with water containing borates and lanthanum chloride were less severe than those lubricated with water containing borates alone. A tribochemical film mainly composed of oxides of lanthanum, boron and iron reduced friction and wear for water lubricant formulated with both borates and lanthanum chloride.
基金supported by the National Natural Science Foundation of China(Grant Nos.12104127 and 22131006)the Doctoral Starting Up Foundation of Hebei Normal University for Nationalities(Grant No.DR2020001)+1 种基金the Clean Energy(Carbon Peaking and Carbon Neutrality)Industry Research Institute of Chengde(Grant No.202205B090)the Natural Science Foundation of Shandong Province(Grant No.ZR2020QA060)。
文摘On the basis of the current theoretical understanding of boron-based hard superconductors under ambient conditions,numerous studies have been conducted with the aim of developing superconducting materials with favorable mechanical properties using boron-rich compounds.In this paper,first-principles calculations reveal the existence of an unprecedented family of tetragonal pentaborides MB_(5)(M=Na,K,Rb,Ca,Sr,Ba,Sc,and Y),comprising B_(20)cages and centered metal atoms acting as stabilizers and electron donors to the boron sublattice.These compounds exhibit both superconductivity and high hardness,with the maximum superconducting transition temperature T_(c)of 18.6 K being achieved in RbB5 and the peak Vickers hardness Hv of 35.1 GPa being achieved in KB_(5)at 1 atm.The combination of these properties is particularly evident in KB_(5),RbB5,and BaB5,with Tc values of∼14.7,18.6,and 16.3 K and H_(v)values of∼35.1,32.4,and 33.8 GPa,respectively.The results presented here reveal that pentaborides can provide a framework for exploring and designing novel superconducting materials with favorable hardness at achievable pressures and even under ambient conditions.
基金financially supported by the National Natural Science Foundation of China (Nos. 51725401, 51904030, and 21935006)
文摘Lithium−sulfur batteries are one of the most competitive high-energy batteries due to their high theoretical energy density of _(2)600 W·h·kg^(−1).However,their commercialization is limited by poor cycle stability mainly due to the low intrinsic electrical conductivity of sulfur and its discharged products(Li_(2)S_(2)/Li_(2)S),the sluggish reaction kinetics of sulfur cathode,and the“shuttle effect”of soluble intermediate lithi-um polysulfides in ether-based electrolyte.To address these challenges,catalytic hosts have recently been introduced in sulfur cathodes to en-hance the conversion of soluble polysulfides to the final solid products and thus prevent the dissolution and loss of active-sulfur material.In this review,we summarize the recent progress on the use of metal phosphides and borides of different dimensions as the catalytic host of sulfur cathodes and demonstrate the catalytic conversion mechanism of sulfur cathodes with the help of metal phosphides and borides for high-en-ergy and long-life lithium-sulfur batteries.Finally,future outlooks are proposed on developing advanced catalytic host materials to improve battery performance.
基金supported in part by the Russian Foundation for Basic Research (07-02-01185)the Russian Academy of Sciences under thgrams for Basic Research
文摘This paper is devoted to the rare-earth borates described by the general formula RM3（BO3）4, M = Al, Fe, and Cr, that have non-centrosymmetric trigonal slructure of the natural mineral huntite. It give a brief review of a spectroscopic research on YbAI3（BO3）4 （YbAB）, on a large group of magnetic iron borates, and on NdCra（BO3）4.
基金pupported by the National Natural Science Foundation of China under Grant Nos. U1435206 and 51672064Beijing Municipal Science & Technology Commission under Grant Nos. Z151100003315012 and D16110000241600
文摘Easy machining into sharp lending edge, nose tip and complex shape components plays a pivotal role in the application of ultrahigh temperature ceramics in hypersonic vehicles, wherein low and controllable hardness is a necessary parameter to ensure the easy machinability. However, the mechanism that driving the hardness of metal hexaborides is not clear. Here, using a combination of the empirical hardness model for polycrystalline materials and density functional theory investigation, the hardness dependence on shear anisotropic factors of high temperature metal hexaborides has been established. It has come to light that through controlling the shear anisotropic factors the hardness of polycrystalline metal hexaborides can be tailored from soft and ductile to extremely hard and brittle, which is underpinned by the degree of chemical bonding anisotropy, i.e., the difference of B-B bond within the B;octahedron and that connecting the B;octahedra.
基金supported by the National Key Research and Development Program of China(Grant Nos.2016YFA0401503 and 2018YFA0305700)the National Natural Science Foundation of China(Grant No.11575288)+1 种基金the Strategic Priority Research Program and Key Research Program of Frontier Sciences of the Chinese Academy of Sciences(Grant Nos.XDB33000000,XDB25000000,and QYZDBSSW-SLH013)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(Grant No.Y202003)。
文摘In recent years,transition metal borides(TMBs)have attracted much attention because they are considered as potential superhard materials and have more abundant crystal structures compared with traditional superhard materials.So far,however,no superhard materials have been found in TMBs.A large number of structures and potential new properties in TMBs are induced by the various hybridization ways of boron atoms and the high valence electrons of transition metals,which provide many possibilities for its application.And most TMBs have layered structures,which make TMBs have the potential to be a two-dimensional(2D)material.The 2D materials have novel properties,but the research on 2D TMBs is still nearly blank.In this paper,the research progress of TMBs is summarized involving structure,mechanical properties,and multifunctional properties.The strong covalent bonds of boron atoms in TMBs can form one-dimensional,twodimensional,and three-dimensional substructures,and the multiple electron transfer between transition metal and boron leads to a variety of chemical bonds in TMBs,which are the keys to obtain high hardness and multifunctional properties of TMBs.Further research on the multifunctional properties of TMBs,such as superconductors,catalysts,and high hardness ferromagnetic materials,is of great significance to the discovery of new multifunctional hard materials.
文摘The morphology and growth mechanism of borides in Ti 48Al+(0.2%～0.8%)B (mole fraction) alloys were investigated. The results show that TiB 2 phase are all flakes with width <0.5 μm and aspect ratio >100 in alloys containing 0.2% and 0.5%B, respectively, but there are a few hexagonal blocky borides with habit planes of (0001) and {1010} type besides flakes in the alloy containing 0.8%B. Flake borides are the products of irregular eutectic reactions growing coupled with matrix and blocky borides are primary TiB 2 phases growing unconstrained in melt.
基金supported by the National Natural Science Foundation of China(Grant Nos.11274135,11074093,61205038)the Specialized Research Fund for the Doctoral Program of Higher Education(Grant No.20130061130011)+2 种基金the Ph.D Programs Foundation of Ministry of Education of China(Grant No.20120061120011)the Science and Technology Development Project of Jilin Province,China(Grant No.20170101142JC)supported by High Performance Computing Center of Jilin University,China
文摘Mixtures of W and B13C2 powders were mechanically milled and subsequently annealed at 900-1200℃.It is found that amorphous W-B-C alloy formed as the mixtures were milled for 20.80 h.After annealing the 80 h-milled mixtures at 900-950℃,solid solutions of C and/or B in tungsten[W（B,C）],C in tungsten boride[W2B（C）or WB（C）]formed by the crystallization of amorphous W-B-C.The formation temperature of W2B（C）and WB（C）is lower than that of W2B and WB reported previously.As the 80 h-milled mixtures were annealed at 1200℃,W reacted with amorphous W-B-C completely to form WB and W2B5 or W2B5 instead of the solid solutions of C in tungsten borides,which is determined by the mole ratio of W to B13C2.The formation mechanisms of the W2B（C）and WB（C）solid solutions as well as phase transition rules of the mixtures at annealing temperature and mole ratio were also investigated using first-principle calculation.
基金Financial supports from the NNSFCs (Grants 21276194 and 21306136)the Specialized Research Fund for the Doctoral Program of Chinese Higher Education (Grant 20101208110003)the Opening Funds of Tianjin Key Laboratory of Marine Resources and Chemistry for Tianjin University of Science and Technology (Grant 201206)
文摘1 Introduction Lithium and its compounds as national strategic resources are extensively used in national defense,industrial and agricultural production.As we know,the salt lakes in the western of China are famous for its high
