摘要：Heterostructured photocatalysts provide an effective way to achieve enhanced photocatalytic performances through efficient charge *** both wide-and narrow-band-gap photocatalysts have been widely investigated,the charge separation and transfer mechanism at the contacting interface of the two has not been fully ***,a novel SrTiO3/BiOI(STB)heterostructured photocatalyst was successfully fabricated by using a facile *** heterostructure in the photocatalyst extends the photoabsorption to the visible light range,and thus,high photocatalytic NO removal performance can be achieved under visible light irradiation.A combination of experimental and theoretical evidences indicated that the photogenerated electrons from the BiOI semiconductor can directly transfer to the SrTiO3 surface through a preformed electron delivery *** electron transfer was expected between the SrTiO3 and BiOI surfaces under light irradiation,and leads to efficient ROS generation and thus a high NO conversion ***,in situ diffused reflectance infrared Fourier transform spectroscopy revealed that STB can better inhibit the accumulation of the toxic intermediate NO2 and catalyze the NO oxidation more *** work presents a new insight into the mechanism of the interfacial charge separation in heterostructures and provides a simple strategy to promote the photocatalytic technology for efficient and safe air purification.

摘要：The design and preparation of suitable supports are of great importance for gold catalysts to attain excellent catalytic performance for alcohol *** this work,we found that ZnO-CuO mixed oxides supported gold catalysts showed much better catalytic activity for base-free aerobic oxidation of benzyl alcohol than Au/ZnO and Au/CuO catalysts,and among them Au/Zn0.7Cu0.3O displayed the best catalytic *** addition,the Au/Zn0.7Cu0.3O catalyst could selectively catalyze the aerobic oxidation of a wide range of alcohols to produce the corresponding carbonyl compounds with high yields under mild conditions without *** characterizations indicated that the outstanding catalytic performance of Au/Zn0.7Cu0.3O was correlated with the small size of Au nanoparticles(NPs),good low-temperature reducibility,high concentration of surface oxygen species,and collaborative interaction between Au NPs and mixed oxide.

摘要：In order to establish the constitutive relationship of high-ductility cementitious composites(HDCCs)under uniaxial tensile load and to guide the structural design of HDCCs,based on the analysis of the existing uniaxial tensile constitutive relationship and ideal elastoplastic linear strain-hardening model,a bilinear tensile constitutive equation of HDCCs was *** points of nominal initial cracking and nominal maximum stress were adopted as control points of the line segment,and the constitutive relationship of HDCCs was *** series of uniaxial tensile stress-strain curves of HDCCs were combined to perform an experimental application of the constitutive equation,along with an analysis of the key *** experimental results confirm the ability of the constitutive equation to overcome the problem of insufficient or excessive redundancy of existing models in terms of calculation bearing ***,the measured maximum stress value is larger than the nominal value,and the ratio between the two values ranges from 1.08 to ***,the tensile strain at the softening point obtained by fitting a straight line with the valley points of the strain-hardening stage curve is greater than or equal to the tensile strain at the measured maximum stress point and the ratio of the fitted values to the measured values ranges from 1.00 to 1.19.

摘要：Iron oxide supported Au nanomaterials are one of the most studied catalysts for low-temperature CO *** performance not only critically depends on the size of the supported Au nanoparticles(NPs)but also strongly on the chemical nature of the iron *** this study,Au NPs supported on iron oxide nanorods with different surface properties throughβ-FeOOH annealing,at varying temperatures,were synthesized,and applied in the CO *** characterizations of the interactions between Au NPs and iron oxides were obtained by X-ray diffraction,transmission electron microscopy(TEM),and X-ray photoelectron *** results indicate that the surface hydroxyl group on the Au/FeOOH catalyst,before calcination(Au/FeOOH-fresh),could facilitate the oxygen adsorption and dissociation on positively charged Au,thereby contributing to the low-temperature CO oxidation *** calcination at 200℃,under air exposure,the chemical state of the supported Au NP on varied iron oxides partly changed from metal cation to Au0,along with the disappearance of the surface OH ***/FeOOH with the highest Au0 content exhibits the highest activity in CO oxidation,among the as-synthesized ***,good durability in CO oxidation was achieved over the Au/FeOOH catalyst for 12 h without observable *** addition,the advanced identical-location TEM method was applied to the gas phase reaction to probe the structure evolution of the Au/iron oxide series of the catalysts and support structure.A Au NP size-dependent Ostwald ripening process mediated by the transport of Au(CO)x mobile species under certain reaction conditions is proposed,which offers a new insight into the validity of the structure-performance relationship.

摘要：The effects of TiB_(2) and Zr on the microstructure,aging response and mechanical properties of hot-extruded Al-Zn-Mg-Cu based materials were investigated and compared by multi-scale microstructure characterization *** results showed that proper addition of TiB_(2) particles could refine grain size during solidification,promote dynamic recrystallization during extrusion,and inhibit grain growth during solution ***,Zr addition had minor influence on the grain refinement during solidification,but could effectively suppress recrystallization and grain growth compared with the Zr-free ***,the TiB_(2) addition could simultaneously enhance the aging kinetics and peak-aged hardness of the ***,Zr addition could also improve the peak-aged hardness with minor effect on the aging kinetics of the ***,the quench sensitivity,elastic modulus and tensile properties of the materials were compared and ***,the relationship between the microstructure and mechanical properties,and the strengthening mechanisms were discussed in detail.

摘要：Variable stiffness composite laminates(VSCLs)are promising in aerospace engineering due to their designable material properties through changing fiber angles and stacking *** to control the thermal postbuckling and nonlinear panel flutter motions of VSCLs,a full-order numerical model is developed based on the linear quadratic regulator(LQR)algorithm in control theory,the classical laminate plate theory(CLPT)considering von Kármán geometrical nonlinearity,and the first-order Piston *** critical buckling temperature and the critical aerodynamic pressure of VSCLs are parametrically *** location and shape of piezoelectric actuators for optimal control of the dynamic responses of VSCLs are determined through comparing the norms of feedback control gain(NFCG).Numerical simulations show that the temperature field has a great effect on aeroelastic tailoring of VSCLs;the curvilinear fiber path of VSCLs can significantly affect the optimal location and shape of piezoelectric actuator for flutter suppression;the unstable panel flutter and the thermal postbuckling deflection can be suppressed effectively through optimal design of piezoelectric patches.

摘要：共晶高熵合金因其所展现出的特殊物理/化学性能而受到材料界的广泛关注.然而,除了FCC+B2系外,其他大部分所报道的共晶高熵合金系均呈现为固有脆性,这使得它们逐渐失去了工业应用的竞争优势.本工作提出了一种新的协同改善脆性CoCrNi_(2)(V_(3)B_(2)Si)_(0.2)共晶高熵合金强韧性的球化+再结晶工艺.基于该工艺,CoCrNi_(2)(V_(3)B_(2)Si)_(0.2)共晶高熵合金获得了一种精心设计的球状M3B2镶嵌在细小FCC晶界处的微观结构,使其抗拉强度、屈服强度和延伸率从923 MPa/620 MPa/1.3%提高到1326-1530 MPa/990-1330 MPa/8.4%-13.9%,提高了43.7%-65.8%/59.7%-114.5%/546%-9.69%.强塑化机制主要归因于球化和再结晶微观结构提供了更多的界面阻碍位错移动和促进了更加均匀的应力分布.该工作为协同改善脆性共晶高熵合金强韧性以满足工程安全性需求提供了新的思路.

摘要：To realize a sustainable hydrogen energy infrastructure,techniques to produce hydrogen gas without involving fossil fuels are *** has been proposed in last century that producing hydrogen gas by splitting water could be a sustainable way because of plenty of water in this planet.

摘要：To optimize the electronic structure of photocatalyst,a facile one‐step approach is developed for the simultaneous realization of Zn‐doping and surface oxygen vacancies(SOVs)formation on SnO_(2).The Zn‐doped SnO_(2)with abundant SOVs exhibits efficient and stable performance for photocatalytic degradation of toluene under both low and high relative *** and theoretical calculations results show that the synergistic effects of Zn‐doping and SOVs on SnO_(2)can considerably boost the charge transfer and separation *** the in situ DRIFTS and theoretical calculations methods,it is revealed that the benzene ring of toluene is opened at benzoic acid on the SnO_(2)surface and selectively at benzaldehyde on the Zn‐doped SnO_(2)*** implies that Zn‐doped SnO_(2)photocatalysts shorten the pathway of toluene degradation,and toxic intermediates can be significantly *** work could provide a promising and sustainable route for safe and efficient removal of aromatic VOCs with photocatalytic technology.

摘要：Regulating the selectivity of catalysts in selective hydrogenation reactions at the atomic level is highly desirable but remains a grand challenge. Here we report a simple and practical strategy to synthesize a monolithic single-atom catalyst(SAC) with isolated Pd atoms supported on bulk nitrogen-doped carbon foams(Pd-SAs/CNF). Moreover, we demonstrate that the single-atom Pd sites with unique electronic structure endow Pd-SAs/CNF with an isolated site effect, leading to excellent activity and selectivity in 4-nitrophenylacetylene semi-hydrogenation reaction. In addition, benefiting from the great integrity and excellent mechanical strength, monolithic Pd-SAs/CNF catalyst is easy to separate from the reaction system for conducting the subsequent recycling. The cyclic test demonstrates the excellent reusability and stability of monolithic Pd-SAs/CNF *** discovery of isolated site effect provides a new approach to design highly selective catalysts. And the development of monolithic SACs provides new opportunities to advance the practical applications of single-atom catalysts.