A practical process method for precise integration of SiC_(f)/SiC composite(CMC)and a Ni-based superalloy(K403)was proposed in this study.It involves Nb coating pretreatment of the CMC via the chemical vapor depositio...A practical process method for precise integration of SiC_(f)/SiC composite(CMC)and a Ni-based superalloy(K403)was proposed in this study.It involves Nb coating pretreatment of the CMC via the chemical vapor deposition(CVD)at 1000℃and subsequent integral precision casting between the pretreated CMC and the K403 superalloy melt.The method solves the difficulty for the dissimilar material to be cast together,forming a robust bonding interface with an average shear strength of 94.8 MPa at room temperature.During the pretreatment process,the Nb reacted with the CMC,forming a reactive coating with the microstructure composed of NbC,Nb2C and Nb5Si3 phases.In the following integral casting,the Nb reactive coating effectively blocked detrimental graphitization reaction between the Ni element in the superalloy melt and the CMC,and mitigated the interface thermal stress generated by both the mismatch of thermal expansion coefficients and temperature difference,resulting in the increase of interfacial strength.The typical interfacial microstructure consists of the CMC,NbC,NbSi_(2)/NbC,SiC,NbSi_(2),Nb_(2)C,Nb_(5)Si_(3),Al_(4)C_(3),Nb_(2)Al/γ/γ'and MC(M=W,Mo,Ti).A formula for estimating the interfacial thermal stress of an integrated cast was derived.展开更多
Introduction Frequency-dependent dielectric response is one of the important properties of ferroelectrics,reflecting the polarization response to high-frequency electric fields.Polarizations are closely related to fer...Introduction Frequency-dependent dielectric response is one of the important properties of ferroelectrics,reflecting the polarization response to high-frequency electric fields.Polarizations are closely related to ferroelectric domain structures,such as single domain,which represents the region with homogeneous polarizations direction.Ferroelectrics usually possess complex domain structures with domain walls(DWs)separating adjacent homogeneously polarized domains.DWs have attracted much attention during the past two decades due to their properties and potential for device designing.The related issues include DW motion,nonvolatile memory,topological defects,enhanced susceptibility,enhanced quality factor,low dielectric loss,and others.(Ba0.8,Sr0.2)TiO3(BST0.8)is a ferroelectric usually with multi-domain structures.Previous work identified two typical types of domain walls(DWs),i.e.,90°DWs and 180°DWs.The enhancement of dielectric response in systems with 90°DWs is now well understood,and the behavior of dielectric response in multi-domain systems with 180°DWs remains unclear.Therefore,gaining insights into how 180°DWs affect the dielectric response can clarify the effects in multidomain systems.Methods We performed molecular dynamics simulations using the ALFE-H code with the first-principles-based effective Hamiltonian method to study the BST0.8 system.All the calculations were performed in the NPT ensemble using the Evans-Hoover thermostat,and periodic boundary condition(PBC)along all three directions.To simulate the substrate,a uniform biaxial strain was fixed to the 1.55%in-plane strain.To analyze the multi-domain with different DWs,the simulations started with a self-constructed initial multi-domain polarization configuration.Subsequent 50 ps MD simulation was performed under chosen strains for structural relaxation.In the initial configuration,the magnitude of non-zero components of soft mode on each site was set to 0.1Å,atomic occupations(alloying)were randomized,and unless otherwise specified,all other mode variables were set to zero.The trajectory of local mode averaged over the supercell during MD simulations was extracted to calculate the dielectric response.The 8 ns MD simulations were performed to obtain an autocorrelation function for any time t ranging from 0 to 1 ns by one step of 10 fs.The fast Fourier transformation(FFT)was performed to calculate the dielectric response.Then two uncoupled damped harmonic oscillators(DHOs)were used to fit the data of dielectric response.Results and discussion The dielectric response of single domain at 300 K with the different electric fields along[110]from 0 to 2 MV/cm was computed.The computational results can be well fitted with the model of two uncoupled DHOs.The real and imaginary parts of the predicted dielectric response at each chosen electric field both exhibit two peaks.As the electric field increases,the low-frequency mode with 300 GHz at zero field in the system gradually disappears,and a high-frequency mode of larger than 8 THz appears when electric field is larger than 1 MV/cm.The high frequencies modes of 3 THz at zero filed and 8 THz under 1 MV/cm shift towards higher frequencies as the electric field increases.In other words,the present simulations reveal that it is possible to manipulate the frequency of peaks in dielectric response via changing the magnitude of the external electric field.The dielectric responses of multi-domain with 90°DWs and 180°DWs are further analyzed.According to the experimental PFM results,the multi-domain structures are simulated and the dielectric response through MD simulations is calculated.The analysis of the dielectric response of single domain structure and multi-domain structures shows that the single domain structures exhibit high-frequency peaks at>300 GHz,whereas the multi-domain structures exhibit low-frequency peaks at 8 GHz and 120 GHz for 180°DWs system and at 10 GHz for 90°DWs system,revealing that there exists a low-frequency mode related to collective oscillation of DWs in multi-domain structures.In addition,the frequencies of peaks in multi-domain with DWs are in a gigahertz range,whereas the single domain structure exhibits peaks in a terahertz range.The contribution of DWs to the dielectric response primarily arises from the timescale of DWs motion,such as sliding or breathing,which differs significantly from the high-frequency vibrations of optical phonon modes.The vibrational frequency of DWs is much lower,with relaxation times in the order of nanoseconds,resulting in a response frequency in GHz range,which is far below the terahertz range of optical phonon modes.Therefore,DWs oscillations dominate the dielectric response at a low frequency.Moreover,multi-domain structure with 180°DWs exhibits a unique low frequency mode at 120 GHz,which is significantly different from single domain and 90°DWs system.In other words,multi-domain structures with 180°DWs and 90°DWs exhibit different dielectric responses.There exists a common low-frequency mode related to the oscillations of DWs in BST0.8.Conclusions It was possible to manipulate the frequency of peaks in dielectric response of single domain through changing the magnitude of the external electric field.Domain walls oscillations dominated the dielectric response in a low frequency gigahertz range,whereas the single domain structures exhibited resonant peaks in a terahertz range.Moreover,multi-domain structures with different domain walls in BST0.8 had different dielectric responses,but the both have a same low-frequency mode at 10 GHz related to the domain walls oscillations.The results of this study indicated the dielectric response behaviors of ferroelectrics induced in an external electric field and internal multi-domain configurations and provided the potential mechanisms and guidance for optimizing application performance.展开更多
Nitric oxide(NO),which generally originates from vehicle exhaust and industrial flue gases,is one of the most serious air pollutants.In this case,the electrochemical NO reduction reaction(NORR)not only removes the atm...Nitric oxide(NO),which generally originates from vehicle exhaust and industrial flue gases,is one of the most serious air pollutants.In this case,the electrochemical NO reduction reaction(NORR)not only removes the atmospheric pollutant NO but also produces valuable ammonia(NH_(3)).Hence,through the synthesis and modification of Fe_(3)C nanocrystal cata-lysts,the as-obtained optimal sample of Fe_(3)C/C-900 was adopted as the NORR catalyst at ambient conditions.As a result,the Fe_(3)C/C-900 catalyst showed an NH_(3)Faraday efficiency of 76.5%and an NH_(3)yield rate of 177.5μmol·h^(-1)·cm^(-2)at the working potentials of-0.8 and-1.2 V versus reversible hydrogen electrode(vs.RHE),respectively.And it delivered a stable NORR activity during the electrolysis.Moreover,we attribute the high NORR properties of Fe_(3)C/C-900 to two aspects:one is the enhanced intrinsic activity of Fe_(3)C nanocrystals,including the lowering of the energy barrier of rate-limiting step(*NOH→*N)and the inhibition of hydrogen evolution;on the other hand,the favorable dispersion of active components,the effective adsorption of gaseous NO,and the release of liquid NH_(3)products facilitated by the porous carbon substrate.展开更多
Owing to outstanding hydrophilicity and ionic interaction,layered double hydroxides(LDHs)have emerged as a promising carrier for high performance catalysts.However,the synthesis of new specialized catalytic LDHs for d...Owing to outstanding hydrophilicity and ionic interaction,layered double hydroxides(LDHs)have emerged as a promising carrier for high performance catalysts.However,the synthesis of new specialized catalytic LDHs for degradation of antibiotics still faces some challenges.In this study,a CoFe_(2)O_(4)/MgAl-LDH composite catalyst was synthesized using a hydrothermal coprecipitation method.Comprehensive characterization reveals that the surface of MgAl-LDH is covered with nanometer CoFe_(2)O_(4) particles.The specific surface area of CoFe_(2)O_(4)/MgAl-LDH is 82.84 m^(2)·g^(-)1,which is 2.34 times that of CoFe_(2)O_(4).CoFe_(2)O_(4)/MgAl-LDH has a saturation magnetic strength of 22.24 A·m^(2)·kg^(-1) facilitating efficient solid-liquid separation.The composite catalyst was employed to activate peroxymonosulfate(PMS)for the efficient degradation of tetracycline hydrochloride(TCH).It is found that the catalytic performance of CoFe_(2)O_(4)/MgAl-LDH significantly exceeds that of CoFe_(2)O_(4).The maximum TCH removal reaches 98.2%under the optimal conditions([TCH]=25 mg/L,[PMS]=1.5 mmol/L,CoFe_(2)O_(4)/MgAl-LDH=0.20 g/L,pH 7,and T=25℃).Coexisting ions in the solution,such as SO_(4)^(2-),Cl-,H_(2)PO_(4)^(-),and CO_(3)^(2-),have a negligible effect on catalytic performance.Cyclic tests demonstrate that the catalytic performance of CoFe_(2)O_(4)/MgAl-LDH remains 67.2%after five cycles.Mechanism investigations suggest that O_(2)^(•-)and ^(1)O_(2) produced by CoFe_(2)O_(4)/MgAl-LDH play a critical role in the catalytic degradation.展开更多
Developing a low-cost stable and high-performance peroxymonosulfate(PMS)catalyst to degrade refractory organic pollutants is still an urgent problem.Herein,this study reported FeVO_(4)nanorods decorated sepiolite(FeVO...Developing a low-cost stable and high-performance peroxymonosulfate(PMS)catalyst to degrade refractory organic pollutants is still an urgent problem.Herein,this study reported FeVO_(4)nanorods decorated sepiolite(FeVO_(4)/sepiolite)through simple hydrothermal method as an adsorptive-catalyst for PMS activation to degrade tetracycline(TC).Benefiting from the introduction of sepiolite support,FeVO_(4)nanorods could be uniformly immobilized onto fibrous sepiolite surface.As a result,FeVO_(4)/sepiolite composite was endowed with excellent adsorption properties,rich surface hydroxyl groups,more reaction active sites,and the stable redox cycle of Fe^(3+)/Fe^(2+)and V5^(+)/V4^(+).Therefore,higher TC degradation efficiency(91.19%within 40 min)and larger reaction rate constant(0.1649 min^(-1))were obtained in FeVO_(4)/sepiolite/PMS system than in FeVO_(4)/PMS system.Besides,the composite presented good stability and reusability,and the effects of application parameters on TC degradation were investigated in detail.Through quenching experiment and electron paramagentic resonance(EPR)test,it was found that both radical and non-radical species participates in TC degradation,and ^(1)O_(2) were the main active species.The PMS activation mechanism was proposed,and the possible degradation pathway was also analyzed according to the high performance liquid chromatography-mass spectrometry(HPLC-MS)results.Overall,this work provides meaningful insights for designing natural mineral based PMS activators to effectively remediate antibiotic wastewater.展开更多
As cathode materials for alkali-ion batteries,sodium manganese oxides have been receiving considerable and continuous attention in recent decades.In this work,the structure and environment-dependent stability of NaMn_...As cathode materials for alkali-ion batteries,sodium manganese oxides have been receiving considerable and continuous attention in recent decades.In this work,the structure and environment-dependent stability of NaMn_(2)O_(4) surface were studied based on the first principles calculations.The surface stability diagram of NaMn_(2)O_(4) involving various different terminations of(100),(110)and(111)surfaces was constructed,and the stability of these different terminations could be compared as a function of chemical environment.It is found that the(100)-MnO and(111)-ONa terminations are two more stable terminations under the investigated chemical conditions.And the surface energies of(110)surfaces are negative under the investigated chemical potential,hence,(110)surfaces are unstable.The surface energy of NaMn_(2)O_(4) as a function of O chemical potential is also investigated under constant Na chemical potential.The structure relaxation indicates that the surface rumpling and surface reconstruction can affect the electronic structure of the surface,thereby reducing surface energy and stabilizing the surface.Furthermore,the Wulff shape of NaMn_(2)O_(4) was also constructed based on Gibbs-Wulff theorem.展开更多
Understanding the adsorption behavior of heavy metals and metalloids on clay minerals is essential for remediating heavy metal-contaminated soils.The adsorption of heavy metals and metalloids on illite(001)and sodium ...Understanding the adsorption behavior of heavy metals and metalloids on clay minerals is essential for remediating heavy metal-contaminated soils.The adsorption of heavy metals and metalloids on illite(001)and sodium montmorillonite(Na-MMT)(001)surfaces was investigated using first-principles calculations in this study,especially As atom and H_(3)AsO_(3) molecule.The adsorption energies of the As atom were−1.94 eV on the illite(001)and−0.56 eV on the Na-MMT(001),whereas,the adsorption energies of the H_(3)AsO_(3) molecule were−1.40 eV on illite(001)and−1.01 eV on Na-MMT(001).The above results indicate that the adsorption was more energetically favorable on illite(001).Additionally,compared to Na-MMT(001),there were more significant interactions between the atoms/molecules on the illite(001).After As atom and H_(3)AsO_(3) molecule adsorption,the electrons were transferred from mineral surface atoms to the adsorbates on both illite(001)and Na-MMT(001)surfaces.Moreover,the adsorption of As atom on illite(001)and Na-MMT(001)surfaces were more energy favorable compared to Hg,Cd,and Cr atoms.Overall,this work provides new insights into the adsorption behavior of As atoms and As molecules on illite and Na-MMT.The results indicate that illite rich soils are more prone to contamination by arsenic compared to soils primarily composed of Na-MMT minerals.展开更多
FeO_(2)is proposed to be a kind of substance in the Earth’s lower mantle in recent years.In this pa-per,the equation of state,elastic properties and sound velocities are obtained based on the first principle calcula-...FeO_(2)is proposed to be a kind of substance in the Earth’s lower mantle in recent years.In this pa-per,the equation of state,elastic properties and sound velocities are obtained based on the first principle calcula-tions.By solving the Boltzmann transport equations,we investigated the lattice thermal con-ductivity of FeO_(2)under high pressure and high temperature.The calculated compressional and shear sound velocities of FeO_(2)agree with the data of preliminary reference Earth model.The lattice thermal conductivity of FeO_(2)at core-mantleboundary(~135 GPa,~3500 K)is 1.77 W/mK,and the total thermal conductivity is 135.10 W/mK.The influence of lattice thermal conductivity can be ignored above 3000 K.展开更多
The influence of electronic structure on the performance of catalysts for peroxymonosulfate(PMS)activation remains ambiguous.In this study,the 3d electron configuration of Fe(Ⅲ)in AgFeO_(2) was atomically regulated u...The influence of electronic structure on the performance of catalysts for peroxymonosulfate(PMS)activation remains ambiguous.In this study,the 3d electron configuration of Fe(Ⅲ)in AgFeO_(2) was atomically regulated using cobalt doping.The amount of PMS adsorbed and the catalytic performance were positively correlated with the total effective magnetic moment and the ratios of high-spin Fe(Ⅲ)and eg filling within the catalysts.These 3d electron regulations favor PMS adsorption and electron transfer owing to the lower PMS adsorption energy,increased electronic states near the Fermi level,and reduced dz^(2) orbital occupancy.Benefiting from fine tailoring of the electron configuration,the AgFe_(0.80)Co_(0.20)O_(2) catalyst exhibited outstanding catalytic PMS activation and favorable application potential,achieving efficient pharmaceutical wastewater treatment and more than 80%ofloxacin removal after 72 h of continuous-flow operation.Notably,this study offers a comprehensive understanding for the influence mechanism of electronic structure regulation on PMS activation,providing design guidance for the development of efficient heterogeneous Fenton-like catalytic systems.展开更多
Selective reduction of N_(2)O by CO under excess O_(2) was effectively catalyzed by Fe(0.9 wt%)-exchangedβzeolite(Fe0.9β)in the temperature range of 250–500°C.Kinetic experiments showed that the apparent activ...Selective reduction of N_(2)O by CO under excess O_(2) was effectively catalyzed by Fe(0.9 wt%)-exchangedβzeolite(Fe0.9β)in the temperature range of 250–500°C.Kinetic experiments showed that the apparent activation energy for N_(2)O reduction with CO was lower than that for the direct N_(2)O decomposition,and the rate of N_(2)O reduction with CO at 300℃ was 16 times higher than that for direct N_(2)O decomposition.Reaction order analyses showed that CO and N_(2)O were involved in the kinetically important step,while O_(2) was not involved in the important step.At 300℃,the rate of CO oxidation with 0.1%N_(2)O was two times higher than that of CO oxidation with 10%O_(2).This quantitatively demonstrates the preferential oxidation of CO by N_(2)O under excess O_(2) over Fe0.9β.Operando/in-situ diffuse reflectance ultraviolet-visible spectroscopy showed a redox-based catalytic cycle;α-Fe-O species are reduced by CO to give CO_(2) and reduced Fe species,which are then re-oxidized by N_(2)O to regenerate theα-Fe-O species.The initial rate for the regeneration ofα-Fe-O species under 0.1%N_(2)O was four times higher than that under 10%O_(2).This result shows quantitative evidence on the higher reactivity of N_(2)O than O_(2) for the regeneration ofα-Fe-O intermediates,providing a fundamental reason why the Fe0.9βcatalyst selectively promotes the CO+N_(2)O reaction under excess O_(2) rather than the undesired side reaction of CO+O_(2).The mechanistic model was verified by the results of in-situ Fe K-edge X-ray absorption spectroscopy.展开更多
The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstr...The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.展开更多
Precise regulation of atomic and electronic structures of two-dimensional tungsten disulfide(WS_(2))is significant for rational design of high-performance and low-cost catalyst for acetylene hydrogenation to ethylene(...Precise regulation of atomic and electronic structures of two-dimensional tungsten disulfide(WS_(2))is significant for rational design of high-performance and low-cost catalyst for acetylene hydrogenation to ethylene(AHE),yet remains a major challenge.Herein,we report that by substituting a W atom of WS_(2) with a series of transition metal atoms,sulfur vacancy-confined Cu in the WS_(2) basal plane(Cu@WS_(2)-Sv)is theoretically screened as a superior non-noble metal-based catalyst with higher activity,selectivity,and stability for the AHE than other candidates.The co-adsorption of C_(2)H_(2) and H_(2) and hydrogenation of C_(2)H_(3)^(*) to C_(2)H_(4)^(*) are revealed as the key steps establishing a volcano-like activity trend among the candidates,which present Cu@WS_(2)-Sv as the optimum catalyst combined with molecular dynamics and reaction kinetics analyses.The kinetically more favorable desorption of C_(2)H_(4) than the over hydrogenation path validates a higher selectivity toward C_(2)H_(4) over C_(2)H_(6).Furthermore,a machine-learning model reveals the significant effect of d-electron number and electronegativity of the metal heteroatoms in modulating the AHE activity.展开更多
Preferential oxidation of CO is an effective process to clean up CO in hydrogen for proton exchange membrane fuel cells(PEMFCs).Herein,we synthesis a highly efficient catalyst for preferential oxidation(PROX)of CO thr...Preferential oxidation of CO is an effective process to clean up CO in hydrogen for proton exchange membrane fuel cells(PEMFCs).Herein,we synthesis a highly efficient catalyst for preferential oxidation(PROX)of CO through the deposition of Ru/Ir nanojunctions on Fe_(2)O_(3) nanoparticles.The as-prepared catalyst shows 90%CO conversion at 80℃ within the working temperature of PEMFCs and the total CO conversion in the temperature range of 140℃ to 160℃under gas flow velocity of 36000 mL·g^(−1)h^(−1) while maintaining good stability for 24 h.Density functional theory calculations reveal that the substrate Fe_(2)O_(3) not only serves as a source of lattice oxygen atoms for the catalytic process but also acts as an electron acceptor from Ru/Ir,thereby regulating its valence state.This regulation is beneficial for the adsorption of reaction intermediates and reduces the activation energy of PROX.展开更多
TiO2/γ-Al2O3 supported In/Ag catalysts were prepared by impregnation method,and investigated for NO reduction with CO as the reducing agent under lean burn conditions.The microscopic structure and surface properties ...TiO2/γ-Al2O3 supported In/Ag catalysts were prepared by impregnation method,and investigated for NO reduction with CO as the reducing agent under lean burn conditions.The microscopic structure and surface properties of the catalysts were studied by N2 adsorption-desorption,X-ray diffraction,transmission electron microscopy,X-ray photoelectron spectroscopy,ultraviolet-visible spectroscopy,H2 temperature-programmed reduction and Fourier transform infrared spectroscopy.TiO2/γ-Al2O3 supported In/Ag is a good catalyst for the reduction of NO to N2.It displayed high dispersion,large amounts of surface active components and high NO adsorption capacity,which gave good catalytic performance and stability for the reduction of NO with CO under lean burn conditions.The silver species stabilized and improved the dispersion of the indium species.The introduction of TiO2 into the γ-Al2O3 support promoted NO adsorption and improved the dispersion of the indium species and silver species.展开更多
The microstructure of the 18R-type long period stacking ordered （LPSO） phase in Mg 97 Y 2 Zn 1 alloy was investigated by the first principles calculation. The arrangement rule of Zn and Y atoms in the LPSO structure...The microstructure of the 18R-type long period stacking ordered （LPSO） phase in Mg 97 Y 2 Zn 1 alloy was investigated by the first principles calculation. The arrangement rule of Zn and Y atoms in the LPSO structure is determined theoretically. The calculation results reveal that the additive atoms are firstly located in the fault layers at the two ends of the 18R-type LPSO structure, and then extend to fault layers in the interior, which is in good agreement with the experimental observations. This feature also implies the microstructural relationship between 18R and other LPSO structures. The cohesive energy and the formation heat indicate the dependence of the stability of 18R LPSO structure on contents of Y and Zn atoms. The calculated electronic structures reveal the underlying mechanism of microstructure and the stability of 18R LPSO structure.展开更多
The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. Acco...The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.展开更多
Heterostructured BiOI@La（OH）3 nanorod photocatalysts were prepared by a facile chemical impregnation method.The enhanced visible light absorption and charge carrier separation can be simultaneously realized after th...Heterostructured BiOI@La（OH）3 nanorod photocatalysts were prepared by a facile chemical impregnation method.The enhanced visible light absorption and charge carrier separation can be simultaneously realized after the introduction of BiOI particles into La（OH）3 nanorods.The BiOI@La（OH）3 composites were applied for visible light photocatalytic oxidization of NO in air and exhibited an enhanced activity compared with BiOI and pure La（OH）3 nanorods.The results show that the energy levels between the La（OH）3 and BiOI phases matched well with each other,thus forming a heterojunctioned BiOI@La（OH）3 structure.This band structure matching could promote the separation and transfer of photoinduced electron-hole pairs at the interface,resulting in enhanced photocatalytic performance under visible light irradiation.The photocatalytic performance of BiOI@La（OH）3 is shown to be dependent on the mass ratio of BiOI to La（OH）3.The highest photocatalytic performance can be achieved when the mass ratio of BiOI to La（OH）3 is controlled at 1.5.A further increase of the mass ratio of BiOI weakened the redox abilities of the photogenerated charge carriers.A new photocatalytic mechanism for BiOI@La（OH）3 heterostructures is proposed,which is directly related to the efficient separation of photogenerated charge carriers by the heterojunction.Importantly,the as-prepared BiOI@La（OH）3 heterostructures exhibited a high photochemical stability after multiple reaction runs.Our findings demonstrate that BiOI is an effective component for the formation of a heterostructure with the properties of a wide bandgap semiconductor,which is of great importance for extending the light absorption and photocatalytic activity of wide bandgap semiconductors into visible light region.展开更多
The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy o...The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy of O2 on pyrrhotite surface is the largest, followed by that on marcasite surface and then pyrite surface. O2 molecules adsorbed on pyrite, marcasite and pyrrhotite surfaces are all dissociated. The oxygen atoms and surface atoms of pyrite, marcasite and pyrrhotite surfaces have different bonding structures. Due to more atoms on pyrrhotite and marcasite surfaces interaction with oxygen atoms, the adsorption energies of O2 on pyrrhotite and marcasite surfaces are larger than that on pyrite surface. Larger values of Mulliken populations for O？Fe bond of pyrrhotite surface result in relative larger adsorption energy compared with that on marcasite surface.展开更多
Ternary Ag/AgC l/BiO IO3 composite photocatalysts are prepared by a facile method. Enhanced visible-light absorption and charge carrier separation are achieved after the introduction of Ag/AgC l particles into BiO IO3...Ternary Ag/AgC l/BiO IO3 composite photocatalysts are prepared by a facile method. Enhanced visible-light absorption and charge carrier separation are achieved after the introduction of Ag/AgC l particles into BiO IO3 systems,as revealed by ultraviolet-visible diffuse-reflectance spectrometry,photocurrent response and electrochemical impedance spectroscopy. The Ag/AgC l/BiO IO3 composites are applied to the visible-light photocatalytic oxidization of NO in air and exhibit an enhanced activity for NO removal in comparison with Ag/AgC l and pure BiO IO3. A possible photocatalytic mechanism for Ag/AgC l/BiO IO3 is proposed,which is related to the surface plasmon resonance effects of Ag metal and the effective carrier separation ability of BiO IO3. This work provides insight into the design and preparation of BiO IO3-based materials with enhanced visible-light photocatalysis ability.展开更多
The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking f...The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking fault（CSF） energies of the binary Ni3Al alloys with different Al contents and the ternary Ni3Al intermetallic alloys with addition of alloying elements,such as Pd,Pt,Ti,Mo,Ta,W and Re.The results show that the energies of SISF and CSF increase significantly with increase of Al contents in Ni3Al.Addition of Pd and Pt occupying the Ni sublattices does not change the SISF and CSF energies of Ni3Al markedly in comparison with the Ni-23.75Al alloy.While addition of alloying elements,such as Ti,Mo,Ta,W and Re,occupying the Al sublattices dramatically increases the SISF and CSF energies of Ni3Al.The results suggest that the energies of SISF and CSF are dependent both on the Al contents and on the site occupancy of the ternary alloying element in Ni3Al intermetallic alloys.展开更多
基金the financial support from the Fundamental Research Funds for the Central Universities,China(No.FRF-GF-18-006A)。
文摘A practical process method for precise integration of SiC_(f)/SiC composite(CMC)and a Ni-based superalloy(K403)was proposed in this study.It involves Nb coating pretreatment of the CMC via the chemical vapor deposition(CVD)at 1000℃and subsequent integral precision casting between the pretreated CMC and the K403 superalloy melt.The method solves the difficulty for the dissimilar material to be cast together,forming a robust bonding interface with an average shear strength of 94.8 MPa at room temperature.During the pretreatment process,the Nb reacted with the CMC,forming a reactive coating with the microstructure composed of NbC,Nb2C and Nb5Si3 phases.In the following integral casting,the Nb reactive coating effectively blocked detrimental graphitization reaction between the Ni element in the superalloy melt and the CMC,and mitigated the interface thermal stress generated by both the mismatch of thermal expansion coefficients and temperature difference,resulting in the increase of interfacial strength.The typical interfacial microstructure consists of the CMC,NbC,NbSi_(2)/NbC,SiC,NbSi_(2),Nb_(2)C,Nb_(5)Si_(3),Al_(4)C_(3),Nb_(2)Al/γ/γ'and MC(M=W,Mo,Ti).A formula for estimating the interfacial thermal stress of an integrated cast was derived.
文摘Introduction Frequency-dependent dielectric response is one of the important properties of ferroelectrics,reflecting the polarization response to high-frequency electric fields.Polarizations are closely related to ferroelectric domain structures,such as single domain,which represents the region with homogeneous polarizations direction.Ferroelectrics usually possess complex domain structures with domain walls(DWs)separating adjacent homogeneously polarized domains.DWs have attracted much attention during the past two decades due to their properties and potential for device designing.The related issues include DW motion,nonvolatile memory,topological defects,enhanced susceptibility,enhanced quality factor,low dielectric loss,and others.(Ba0.8,Sr0.2)TiO3(BST0.8)is a ferroelectric usually with multi-domain structures.Previous work identified two typical types of domain walls(DWs),i.e.,90°DWs and 180°DWs.The enhancement of dielectric response in systems with 90°DWs is now well understood,and the behavior of dielectric response in multi-domain systems with 180°DWs remains unclear.Therefore,gaining insights into how 180°DWs affect the dielectric response can clarify the effects in multidomain systems.Methods We performed molecular dynamics simulations using the ALFE-H code with the first-principles-based effective Hamiltonian method to study the BST0.8 system.All the calculations were performed in the NPT ensemble using the Evans-Hoover thermostat,and periodic boundary condition(PBC)along all three directions.To simulate the substrate,a uniform biaxial strain was fixed to the 1.55%in-plane strain.To analyze the multi-domain with different DWs,the simulations started with a self-constructed initial multi-domain polarization configuration.Subsequent 50 ps MD simulation was performed under chosen strains for structural relaxation.In the initial configuration,the magnitude of non-zero components of soft mode on each site was set to 0.1Å,atomic occupations(alloying)were randomized,and unless otherwise specified,all other mode variables were set to zero.The trajectory of local mode averaged over the supercell during MD simulations was extracted to calculate the dielectric response.The 8 ns MD simulations were performed to obtain an autocorrelation function for any time t ranging from 0 to 1 ns by one step of 10 fs.The fast Fourier transformation(FFT)was performed to calculate the dielectric response.Then two uncoupled damped harmonic oscillators(DHOs)were used to fit the data of dielectric response.Results and discussion The dielectric response of single domain at 300 K with the different electric fields along[110]from 0 to 2 MV/cm was computed.The computational results can be well fitted with the model of two uncoupled DHOs.The real and imaginary parts of the predicted dielectric response at each chosen electric field both exhibit two peaks.As the electric field increases,the low-frequency mode with 300 GHz at zero field in the system gradually disappears,and a high-frequency mode of larger than 8 THz appears when electric field is larger than 1 MV/cm.The high frequencies modes of 3 THz at zero filed and 8 THz under 1 MV/cm shift towards higher frequencies as the electric field increases.In other words,the present simulations reveal that it is possible to manipulate the frequency of peaks in dielectric response via changing the magnitude of the external electric field.The dielectric responses of multi-domain with 90°DWs and 180°DWs are further analyzed.According to the experimental PFM results,the multi-domain structures are simulated and the dielectric response through MD simulations is calculated.The analysis of the dielectric response of single domain structure and multi-domain structures shows that the single domain structures exhibit high-frequency peaks at>300 GHz,whereas the multi-domain structures exhibit low-frequency peaks at 8 GHz and 120 GHz for 180°DWs system and at 10 GHz for 90°DWs system,revealing that there exists a low-frequency mode related to collective oscillation of DWs in multi-domain structures.In addition,the frequencies of peaks in multi-domain with DWs are in a gigahertz range,whereas the single domain structure exhibits peaks in a terahertz range.The contribution of DWs to the dielectric response primarily arises from the timescale of DWs motion,such as sliding or breathing,which differs significantly from the high-frequency vibrations of optical phonon modes.The vibrational frequency of DWs is much lower,with relaxation times in the order of nanoseconds,resulting in a response frequency in GHz range,which is far below the terahertz range of optical phonon modes.Therefore,DWs oscillations dominate the dielectric response at a low frequency.Moreover,multi-domain structure with 180°DWs exhibits a unique low frequency mode at 120 GHz,which is significantly different from single domain and 90°DWs system.In other words,multi-domain structures with 180°DWs and 90°DWs exhibit different dielectric responses.There exists a common low-frequency mode related to the oscillations of DWs in BST0.8.Conclusions It was possible to manipulate the frequency of peaks in dielectric response of single domain through changing the magnitude of the external electric field.Domain walls oscillations dominated the dielectric response in a low frequency gigahertz range,whereas the single domain structures exhibited resonant peaks in a terahertz range.Moreover,multi-domain structures with different domain walls in BST0.8 had different dielectric responses,but the both have a same low-frequency mode at 10 GHz related to the domain walls oscillations.The results of this study indicated the dielectric response behaviors of ferroelectrics induced in an external electric field and internal multi-domain configurations and provided the potential mechanisms and guidance for optimizing application performance.
基金supported by the Guangxi Natural Science Fund for Distinguished Young Scholars(2024GXNSFFA010008)Shenzhen Science and Technology Program(JCYJ20230807112503008).
文摘Nitric oxide(NO),which generally originates from vehicle exhaust and industrial flue gases,is one of the most serious air pollutants.In this case,the electrochemical NO reduction reaction(NORR)not only removes the atmospheric pollutant NO but also produces valuable ammonia(NH_(3)).Hence,through the synthesis and modification of Fe_(3)C nanocrystal cata-lysts,the as-obtained optimal sample of Fe_(3)C/C-900 was adopted as the NORR catalyst at ambient conditions.As a result,the Fe_(3)C/C-900 catalyst showed an NH_(3)Faraday efficiency of 76.5%and an NH_(3)yield rate of 177.5μmol·h^(-1)·cm^(-2)at the working potentials of-0.8 and-1.2 V versus reversible hydrogen electrode(vs.RHE),respectively.And it delivered a stable NORR activity during the electrolysis.Moreover,we attribute the high NORR properties of Fe_(3)C/C-900 to two aspects:one is the enhanced intrinsic activity of Fe_(3)C nanocrystals,including the lowering of the energy barrier of rate-limiting step(*NOH→*N)and the inhibition of hydrogen evolution;on the other hand,the favorable dispersion of active components,the effective adsorption of gaseous NO,and the release of liquid NH_(3)products facilitated by the porous carbon substrate.
基金University Synergy Innovation Program of Anhui Province(GXXT-2022-083)Science and Technology Plan Project of Wuhu City,China(2023kx12)Anhui Provincial Department of Education New Era Education Project(2023xscx070)。
文摘Owing to outstanding hydrophilicity and ionic interaction,layered double hydroxides(LDHs)have emerged as a promising carrier for high performance catalysts.However,the synthesis of new specialized catalytic LDHs for degradation of antibiotics still faces some challenges.In this study,a CoFe_(2)O_(4)/MgAl-LDH composite catalyst was synthesized using a hydrothermal coprecipitation method.Comprehensive characterization reveals that the surface of MgAl-LDH is covered with nanometer CoFe_(2)O_(4) particles.The specific surface area of CoFe_(2)O_(4)/MgAl-LDH is 82.84 m^(2)·g^(-)1,which is 2.34 times that of CoFe_(2)O_(4).CoFe_(2)O_(4)/MgAl-LDH has a saturation magnetic strength of 22.24 A·m^(2)·kg^(-1) facilitating efficient solid-liquid separation.The composite catalyst was employed to activate peroxymonosulfate(PMS)for the efficient degradation of tetracycline hydrochloride(TCH).It is found that the catalytic performance of CoFe_(2)O_(4)/MgAl-LDH significantly exceeds that of CoFe_(2)O_(4).The maximum TCH removal reaches 98.2%under the optimal conditions([TCH]=25 mg/L,[PMS]=1.5 mmol/L,CoFe_(2)O_(4)/MgAl-LDH=0.20 g/L,pH 7,and T=25℃).Coexisting ions in the solution,such as SO_(4)^(2-),Cl-,H_(2)PO_(4)^(-),and CO_(3)^(2-),have a negligible effect on catalytic performance.Cyclic tests demonstrate that the catalytic performance of CoFe_(2)O_(4)/MgAl-LDH remains 67.2%after five cycles.Mechanism investigations suggest that O_(2)^(•-)and ^(1)O_(2) produced by CoFe_(2)O_(4)/MgAl-LDH play a critical role in the catalytic degradation.
基金Project(23-2-1-107-zyyd-jch)supported by the Qingdao Natural Science Foundation,ChinaProject(ZR2022QE236)supported by the Natural Science Foundation of Shandong Province Youth Project,China+2 种基金Project(SDCX-ZG-202400211,SDCX-ZG-202203052)supported by the Shandong Postdoctoral Science Foundation,ChinaProject(ZD2023K03)supported by the Engineering Research Center of Non-metallic Minerals of Zhejiang Province,ChinaProject(01020240806)supported by the Qingdao Postdoctoral Program for Applied Research,China。
文摘Developing a low-cost stable and high-performance peroxymonosulfate(PMS)catalyst to degrade refractory organic pollutants is still an urgent problem.Herein,this study reported FeVO_(4)nanorods decorated sepiolite(FeVO_(4)/sepiolite)through simple hydrothermal method as an adsorptive-catalyst for PMS activation to degrade tetracycline(TC).Benefiting from the introduction of sepiolite support,FeVO_(4)nanorods could be uniformly immobilized onto fibrous sepiolite surface.As a result,FeVO_(4)/sepiolite composite was endowed with excellent adsorption properties,rich surface hydroxyl groups,more reaction active sites,and the stable redox cycle of Fe^(3+)/Fe^(2+)and V5^(+)/V4^(+).Therefore,higher TC degradation efficiency(91.19%within 40 min)and larger reaction rate constant(0.1649 min^(-1))were obtained in FeVO_(4)/sepiolite/PMS system than in FeVO_(4)/PMS system.Besides,the composite presented good stability and reusability,and the effects of application parameters on TC degradation were investigated in detail.Through quenching experiment and electron paramagentic resonance(EPR)test,it was found that both radical and non-radical species participates in TC degradation,and ^(1)O_(2) were the main active species.The PMS activation mechanism was proposed,and the possible degradation pathway was also analyzed according to the high performance liquid chromatography-mass spectrometry(HPLC-MS)results.Overall,this work provides meaningful insights for designing natural mineral based PMS activators to effectively remediate antibiotic wastewater.
基金Project(BK20241969)supported by the Natural Science Foundation of Jiangsu Province,ChinaProject(51971249)supported by the National Natural Science Foundation of China。
文摘As cathode materials for alkali-ion batteries,sodium manganese oxides have been receiving considerable and continuous attention in recent decades.In this work,the structure and environment-dependent stability of NaMn_(2)O_(4) surface were studied based on the first principles calculations.The surface stability diagram of NaMn_(2)O_(4) involving various different terminations of(100),(110)and(111)surfaces was constructed,and the stability of these different terminations could be compared as a function of chemical environment.It is found that the(100)-MnO and(111)-ONa terminations are two more stable terminations under the investigated chemical conditions.And the surface energies of(110)surfaces are negative under the investigated chemical potential,hence,(110)surfaces are unstable.The surface energy of NaMn_(2)O_(4) as a function of O chemical potential is also investigated under constant Na chemical potential.The structure relaxation indicates that the surface rumpling and surface reconstruction can affect the electronic structure of the surface,thereby reducing surface energy and stabilizing the surface.Furthermore,the Wulff shape of NaMn_(2)O_(4) was also constructed based on Gibbs-Wulff theorem.
基金Project(22376221)supported by the National Natural Science Foundation of ChinaProject(2024JJ2074)supported by the Natural Science Foundation of Hunan Province,ChinaProject(2023QNRC001)supported by the Young Elite Scientists Sponsorship Program by CAST。
文摘Understanding the adsorption behavior of heavy metals and metalloids on clay minerals is essential for remediating heavy metal-contaminated soils.The adsorption of heavy metals and metalloids on illite(001)and sodium montmorillonite(Na-MMT)(001)surfaces was investigated using first-principles calculations in this study,especially As atom and H_(3)AsO_(3) molecule.The adsorption energies of the As atom were−1.94 eV on the illite(001)and−0.56 eV on the Na-MMT(001),whereas,the adsorption energies of the H_(3)AsO_(3) molecule were−1.40 eV on illite(001)and−1.01 eV on Na-MMT(001).The above results indicate that the adsorption was more energetically favorable on illite(001).Additionally,compared to Na-MMT(001),there were more significant interactions between the atoms/molecules on the illite(001).After As atom and H_(3)AsO_(3) molecule adsorption,the electrons were transferred from mineral surface atoms to the adsorbates on both illite(001)and Na-MMT(001)surfaces.Moreover,the adsorption of As atom on illite(001)and Na-MMT(001)surfaces were more energy favorable compared to Hg,Cd,and Cr atoms.Overall,this work provides new insights into the adsorption behavior of As atoms and As molecules on illite and Na-MMT.The results indicate that illite rich soils are more prone to contamination by arsenic compared to soils primarily composed of Na-MMT minerals.
基金supported by the National Natural Science Foundation of China(No.12072044)the Natu-ral Science Foundation of Chongqing City(No.cstc2020jcyj-msxmX0616).
文摘FeO_(2)is proposed to be a kind of substance in the Earth’s lower mantle in recent years.In this pa-per,the equation of state,elastic properties and sound velocities are obtained based on the first principle calcula-tions.By solving the Boltzmann transport equations,we investigated the lattice thermal con-ductivity of FeO_(2)under high pressure and high temperature.The calculated compressional and shear sound velocities of FeO_(2)agree with the data of preliminary reference Earth model.The lattice thermal conductivity of FeO_(2)at core-mantleboundary(~135 GPa,~3500 K)is 1.77 W/mK,and the total thermal conductivity is 135.10 W/mK.The influence of lattice thermal conductivity can be ignored above 3000 K.
文摘The influence of electronic structure on the performance of catalysts for peroxymonosulfate(PMS)activation remains ambiguous.In this study,the 3d electron configuration of Fe(Ⅲ)in AgFeO_(2) was atomically regulated using cobalt doping.The amount of PMS adsorbed and the catalytic performance were positively correlated with the total effective magnetic moment and the ratios of high-spin Fe(Ⅲ)and eg filling within the catalysts.These 3d electron regulations favor PMS adsorption and electron transfer owing to the lower PMS adsorption energy,increased electronic states near the Fermi level,and reduced dz^(2) orbital occupancy.Benefiting from fine tailoring of the electron configuration,the AgFe_(0.80)Co_(0.20)O_(2) catalyst exhibited outstanding catalytic PMS activation and favorable application potential,achieving efficient pharmaceutical wastewater treatment and more than 80%ofloxacin removal after 72 h of continuous-flow operation.Notably,this study offers a comprehensive understanding for the influence mechanism of electronic structure regulation on PMS activation,providing design guidance for the development of efficient heterogeneous Fenton-like catalytic systems.
文摘Selective reduction of N_(2)O by CO under excess O_(2) was effectively catalyzed by Fe(0.9 wt%)-exchangedβzeolite(Fe0.9β)in the temperature range of 250–500°C.Kinetic experiments showed that the apparent activation energy for N_(2)O reduction with CO was lower than that for the direct N_(2)O decomposition,and the rate of N_(2)O reduction with CO at 300℃ was 16 times higher than that for direct N_(2)O decomposition.Reaction order analyses showed that CO and N_(2)O were involved in the kinetically important step,while O_(2) was not involved in the important step.At 300℃,the rate of CO oxidation with 0.1%N_(2)O was two times higher than that of CO oxidation with 10%O_(2).This quantitatively demonstrates the preferential oxidation of CO by N_(2)O under excess O_(2) over Fe0.9β.Operando/in-situ diffuse reflectance ultraviolet-visible spectroscopy showed a redox-based catalytic cycle;α-Fe-O species are reduced by CO to give CO_(2) and reduced Fe species,which are then re-oxidized by N_(2)O to regenerate theα-Fe-O species.The initial rate for the regeneration ofα-Fe-O species under 0.1%N_(2)O was four times higher than that under 10%O_(2).This result shows quantitative evidence on the higher reactivity of N_(2)O than O_(2) for the regeneration ofα-Fe-O intermediates,providing a fundamental reason why the Fe0.9βcatalyst selectively promotes the CO+N_(2)O reaction under excess O_(2) rather than the undesired side reaction of CO+O_(2).The mechanistic model was verified by the results of in-situ Fe K-edge X-ray absorption spectroscopy.
基金National Natural Science Foundation of China (No. 52274403)。
文摘The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.
文摘Precise regulation of atomic and electronic structures of two-dimensional tungsten disulfide(WS_(2))is significant for rational design of high-performance and low-cost catalyst for acetylene hydrogenation to ethylene(AHE),yet remains a major challenge.Herein,we report that by substituting a W atom of WS_(2) with a series of transition metal atoms,sulfur vacancy-confined Cu in the WS_(2) basal plane(Cu@WS_(2)-Sv)is theoretically screened as a superior non-noble metal-based catalyst with higher activity,selectivity,and stability for the AHE than other candidates.The co-adsorption of C_(2)H_(2) and H_(2) and hydrogenation of C_(2)H_(3)^(*) to C_(2)H_(4)^(*) are revealed as the key steps establishing a volcano-like activity trend among the candidates,which present Cu@WS_(2)-Sv as the optimum catalyst combined with molecular dynamics and reaction kinetics analyses.The kinetically more favorable desorption of C_(2)H_(4) than the over hydrogenation path validates a higher selectivity toward C_(2)H_(4) over C_(2)H_(6).Furthermore,a machine-learning model reveals the significant effect of d-electron number and electronegativity of the metal heteroatoms in modulating the AHE activity.
基金financially supported by the National Natural Science Foundation of China(No.22072140,No.22272155,and No.22102169)the National Key R&D Program of China(No.2021YFA1600202)。
文摘Preferential oxidation of CO is an effective process to clean up CO in hydrogen for proton exchange membrane fuel cells(PEMFCs).Herein,we synthesis a highly efficient catalyst for preferential oxidation(PROX)of CO through the deposition of Ru/Ir nanojunctions on Fe_(2)O_(3) nanoparticles.The as-prepared catalyst shows 90%CO conversion at 80℃ within the working temperature of PEMFCs and the total CO conversion in the temperature range of 140℃ to 160℃under gas flow velocity of 36000 mL·g^(−1)h^(−1) while maintaining good stability for 24 h.Density functional theory calculations reveal that the substrate Fe_(2)O_(3) not only serves as a source of lattice oxygen atoms for the catalytic process but also acts as an electron acceptor from Ru/Ir,thereby regulating its valence state.This regulation is beneficial for the adsorption of reaction intermediates and reduces the activation energy of PROX.
基金supported by the National Science & Technology Pillar Program(2012BAF03B02)National Natural Science Foundation of China(21101085,U1162203)+3 种基金Natural Science Foundation of Liaoning Province(2015020196)Doctoral Fund of Shandong Province(BS2015HZ003)Fushun Science & Technology Program(FSKJHT 201423)Liaoning Excellent Talents Program in University(LJQ2012031)~~
文摘TiO2/γ-Al2O3 supported In/Ag catalysts were prepared by impregnation method,and investigated for NO reduction with CO as the reducing agent under lean burn conditions.The microscopic structure and surface properties of the catalysts were studied by N2 adsorption-desorption,X-ray diffraction,transmission electron microscopy,X-ray photoelectron spectroscopy,ultraviolet-visible spectroscopy,H2 temperature-programmed reduction and Fourier transform infrared spectroscopy.TiO2/γ-Al2O3 supported In/Ag is a good catalyst for the reduction of NO to N2.It displayed high dispersion,large amounts of surface active components and high NO adsorption capacity,which gave good catalytic performance and stability for the reduction of NO with CO under lean burn conditions.The silver species stabilized and improved the dispersion of the indium species.The introduction of TiO2 into the γ-Al2O3 support promoted NO adsorption and improved the dispersion of the indium species and silver species.
基金Projects(50861002,51071053)supported by the National Natural Science Foundation of ChinaProject(0991051)supported by NaturalScience Foundation of Guangxi Province,China+1 种基金Project(KF0803)supported by Open Project of Key Laboratory of Materials Design and Preparation Technology of Hunan Province,ChinaProject(X071117)supported by Scientific Research Foundation of Guangxi University,China
文摘The microstructure of the 18R-type long period stacking ordered （LPSO） phase in Mg 97 Y 2 Zn 1 alloy was investigated by the first principles calculation. The arrangement rule of Zn and Y atoms in the LPSO structure is determined theoretically. The calculation results reveal that the additive atoms are firstly located in the fault layers at the two ends of the 18R-type LPSO structure, and then extend to fault layers in the interior, which is in good agreement with the experimental observations. This feature also implies the microstructural relationship between 18R and other LPSO structures. The cohesive energy and the formation heat indicate the dependence of the stability of 18R LPSO structure on contents of Y and Zn atoms. The calculated electronic structures reveal the underlying mechanism of microstructure and the stability of 18R LPSO structure.
文摘The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.
基金supported by the National Key Research and Development Project (2016YFC0204702)the National Natural Science Foundation of China (51478070, 21501016, 51108487)+2 种基金the Innovative Research Team of Chongqing (CXTDG201602014)the Natural Science Foundation of Chongqing (cstc2016jcyjA0481)Youth Innovation Promotion Association of Chinese Academy of Sciences (2015316)~~
文摘Heterostructured BiOI@La（OH）3 nanorod photocatalysts were prepared by a facile chemical impregnation method.The enhanced visible light absorption and charge carrier separation can be simultaneously realized after the introduction of BiOI particles into La（OH）3 nanorods.The BiOI@La（OH）3 composites were applied for visible light photocatalytic oxidization of NO in air and exhibited an enhanced activity compared with BiOI and pure La（OH）3 nanorods.The results show that the energy levels between the La（OH）3 and BiOI phases matched well with each other,thus forming a heterojunctioned BiOI@La（OH）3 structure.This band structure matching could promote the separation and transfer of photoinduced electron-hole pairs at the interface,resulting in enhanced photocatalytic performance under visible light irradiation.The photocatalytic performance of BiOI@La（OH）3 is shown to be dependent on the mass ratio of BiOI to La（OH）3.The highest photocatalytic performance can be achieved when the mass ratio of BiOI to La（OH）3 is controlled at 1.5.A further increase of the mass ratio of BiOI weakened the redox abilities of the photogenerated charge carriers.A new photocatalytic mechanism for BiOI@La（OH）3 heterostructures is proposed,which is directly related to the efficient separation of photogenerated charge carriers by the heterojunction.Importantly,the as-prepared BiOI@La（OH）3 heterostructures exhibited a high photochemical stability after multiple reaction runs.Our findings demonstrate that BiOI is an effective component for the formation of a heterostructure with the properties of a wide bandgap semiconductor,which is of great importance for extending the light absorption and photocatalytic activity of wide bandgap semiconductors into visible light region.
基金Project supported by the High Level Innovation Team and Outstanding Scholar Program in Guangxi Colleges(the second batch),ChinaProjects(51304054+1 种基金51364002)supported by the National Natural Science Foundation of ChinaProject supported by the Open Foundation of Guangxi Colleges and University Key Laboratory of Minerals Engineering in Guangxi University,China
文摘The interaction of O2 with pyrite, marcasite and pyrrhotite surfaces was studied using first-principle calculations to obtain the oxidization mechanisms of these minerals. The results show that the adsorption energy of O2 on pyrrhotite surface is the largest, followed by that on marcasite surface and then pyrite surface. O2 molecules adsorbed on pyrite, marcasite and pyrrhotite surfaces are all dissociated. The oxygen atoms and surface atoms of pyrite, marcasite and pyrrhotite surfaces have different bonding structures. Due to more atoms on pyrrhotite and marcasite surfaces interaction with oxygen atoms, the adsorption energies of O2 on pyrrhotite and marcasite surfaces are larger than that on pyrite surface. Larger values of Mulliken populations for O？Fe bond of pyrrhotite surface result in relative larger adsorption energy compared with that on marcasite surface.
基金supported by the National Natural Science Foundation of China(5147807051108487)the Science and Technology Project from Chongqing Education Commission(KJ1400617)~~
文摘Ternary Ag/AgC l/BiO IO3 composite photocatalysts are prepared by a facile method. Enhanced visible-light absorption and charge carrier separation are achieved after the introduction of Ag/AgC l particles into BiO IO3 systems,as revealed by ultraviolet-visible diffuse-reflectance spectrometry,photocurrent response and electrochemical impedance spectroscopy. The Ag/AgC l/BiO IO3 composites are applied to the visible-light photocatalytic oxidization of NO in air and exhibit an enhanced activity for NO removal in comparison with Ag/AgC l and pure BiO IO3. A possible photocatalytic mechanism for Ag/AgC l/BiO IO3 is proposed,which is related to the surface plasmon resonance effects of Ag metal and the effective carrier separation ability of BiO IO3. This work provides insight into the design and preparation of BiO IO3-based materials with enhanced visible-light photocatalysis ability.
基金Project(50871065) supported by the National Natural Science Foundation of ChinaProjects(08DJ1400402,09JC1407200,10DZ2290904) supported by the Science and Technology Committee of Shanghai Municipality,China
文摘The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking fault（CSF） energies of the binary Ni3Al alloys with different Al contents and the ternary Ni3Al intermetallic alloys with addition of alloying elements,such as Pd,Pt,Ti,Mo,Ta,W and Re.The results show that the energies of SISF and CSF increase significantly with increase of Al contents in Ni3Al.Addition of Pd and Pt occupying the Ni sublattices does not change the SISF and CSF energies of Ni3Al markedly in comparison with the Ni-23.75Al alloy.While addition of alloying elements,such as Ti,Mo,Ta,W and Re,occupying the Al sublattices dramatically increases the SISF and CSF energies of Ni3Al.The results suggest that the energies of SISF and CSF are dependent both on the Al contents and on the site occupancy of the ternary alloying element in Ni3Al intermetallic alloys.
