摘要：Designing and fabricating highly efficient photocatalysts for water splitting is a promising strategy to address energy and environmental *** sulfide(CdS)has received significant interest as a photocatalyst for visible‐light‐induced hydrogen(H2)***,the severe photocorrosion,high overpotential,rapid charge recombination,and sluggish surface reaction kinetics drastically hinder its practical application in water ***,uniform zinc cadmium sulfide(Zn_(0.5)Cd_(0.5)S)nanoparticles were anchored on ultrathin Ni(OH)_(2)nanosheets via a facile solution‐phase approach to form an intimate two‐dimensional(2D)/zero‐dimensional(0D)*** visible light irradiation,the 7%Ni(OH)_(2)/Zn_(0.5)Cd_(0.5)S composite exhibited the highest H2 production rate of 6.87 mmol·h^(–1)·g^(–1)with an apparent quantum yield of 16.8%at 420 nm,which is almost 43 times higher than that of pristine Zn_(0.5)Cd_(0.5)S and considerably higher than that of the Pt/Zn_(0.5)Cd_(0.5)S *** high photoactivity of the 2D/0D Ni(OH)_(2)/Zn_(0.5)Cd_(0.5)S heterojunction can be ascribed to its unique and robust structure,wherein the ultrathin Ni(OH)_(2)nanosheets not only provide an excellent platform for the incorporation of Zn_(0.5)Cd_(0.5)S nanoparticles but also serve as an effective cocatalyst to promote photoinduced electron transfer and offer more active sites for photocatalytic H_(2) *** work paves the way toward the development of versatile,low‐cost,and highly efficient 2D/0D heterojunction photocatalysts for solar energy conversion.

摘要：The high surface energy of nanomaterials endows them a metastable nature,which greatly limits their ***,in some cases,the degradation process derived from the poor stability of nanomaterials offers an unconventional approach to design and obtain functional ***,based on the poor stability of ZnSe-[DETA]0.5 hybrid nanobelts,we developed a new strategy to chemically graphitize and functionalize graphene oxide(GO).When ZnSe[DETA]0.5 hybrid nanobelts encountered a strong acid,they were attacked by H^+cations and could release highly reactive Se^2−anions into the reaction *** other common reductants(such as N2H4·H2O),these Se^2−anions exhibited an excellent ability to restore the structure of *** structural restoration of GO was greatly affected by the reaction time,the volume of HCl,and the mass ratio between GO and ZnSe[DETA]0.5 *** carefully controlling the reaction process and the post-processing process,we finally obtained several Se-based reduced GO(RGO)nanocomposites(such as ZnSe/Se-RGO,ZnSe-RGO,and Se-RGO)and various selenide/metal-RGO nanocomposites(such as Ag2Se-RGO,Cu2Se-RGO,and Pt-RGO).Although the original structure and composition of ZnSe[DETA]0.5 nanobelts are destroyed,the procedure presents an unconventional way to chemically graphitize and functionalize GO and thus provides a new material synthesis platform for nanocomposites.

摘要：Ionic liquids combined with supercriticalfluid technology hold great promise as working solvents for developing compact *** liquids,which are organic molten salts,typically have extremely low volatility and high functionality,but possess high viscos-ities,surface tensions and low diffusion coefficients,which can limit their ***_(2),on the other hand,especially in its supercritical state,is a green solvent that can be used advantageously when combined with the ionic liquid to provide viscosity and surface tension reduction and to promote mass *** solubility of CO_(2) in the ionic liquid is key to estimating the important physical properties that include partition coefficients,viscosities,densities,interfacial tensions,thermal conductivities and heat capacities needed in contactor *** this work,we examine a subset of available high pressure pure component ionic liquid PVT data and high pressure CO_(2)-ionic liquid solubility data and report new correlations for CO_(2)-ionic liquid systems with equations of state that have some industrial applications including:(1)general,(2)fuel desulfurization,(3)CO_(2) capture,and(4)chiral *** measurements of solubility data for the CO_(2) and 1-butyl-3-methylimidazolium octyl sulfate,[bmim][OcSO4]system are reported and *** the correlation of the CO_(2) ionic liquid phase behavior,the Peng-Robinson and the Sanchez-Lacombe equations of state were considered and are *** is shown that excellent correlation of CO_(2) solubility can be obtained with either equation and they share some common characteristics regarding inter-action *** the Sanchez-Lacombe equation,parameters that are derived from the supercritical region were found to be important for obtaining good correlation of the CO_(2)-ionic liquid solubility data.

摘要：Photocatalytic solar fuel generation is currently a hot topic because of its potential for solving the energy crisis owing to its low cost and zero-carbon ***,the rapid bulk recombination of photoexcited carrier pairs is a fundamental *** resolve this problem,we synthesized a dual cocatalysts system of cobalt phosphide(Co P)and molybdenum carbide(Mo_(2)C)embedded on strontium titanate(Sr TiO_(3))*** with those of pristine SrTiO_(3) and binary samples,the dual cocatalysts system(denoted SCM)showed a significant improvement in the hydrogen evolution and CO_(2) reduction ***,the structure of SCM effectively promoted spatial charge separation and enhanced the photocatalytic *** addition,the Schottky junction formed between the SrTiO_(3) and cocatalysts enabled the rapid transfer of photoexcited electrons from SrTiO_(3) to the cocatalysts,resulting in effective separation and prolonged photoexcited electron *** electron migration route between SrTiO_(3) and the cocatalysts was determined by in situ irradiation X-ray spectroscopy,and band structures of Sr TiO_(3) and the cocatalysts are proposed based on results obtained from UV-vis diffraction reflection spectroscopy and ultraviolet photoelectron spectroscopy *** the basis of our results,the dual cocatalysts unambiguously boosts charge separation and enhances photocatalytic *** summary,we have investigated the flux of photoexcited electrons in a dual cocatalysts system and provided a theoretical basis and ideas for subsequent research.

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：Catalytic hydrogenation is a vital industrial means to produce value-added fuels and fine chemicals,however, requiring highly efficient catalysts, especially the nonprecious ones. To date, the majority of high-performance industrial hydrogenation catalysts are made of precious metals-based materials, and any given catalyst could only be used to catalyze one or few specific reactions. Herein, we exemplify a crystal phase engineering approach to empower Ni nanoparticles(NPs) with superb intrinsic catalytic activities toward a wide spectrum of hydrogenation reactions. A facile pyrolysis approach is used to directly convert a Ni-imidazole MOF precursor into hexagonal close-packed(hcp)-phased Ni NPs on carbon support. The as-synthesized hcp-phased Ni NPs exhibit unprecedented hydrogenation catalytic activities in pure water towards nitro-, aldehyde-, ketone-, alkene-and N heterocyclic-compounds, outperforming the face-centered cubic(fcc)-Ni counterpart and the reported transition metalsbased catalysts. The density functional theory calculations unveil that the presence of hcp-Ni boosts the intrinsic catalytic hydrogenation activity by coherently enhancing the substrate adsorption strength and lowering the reaction barrier energy of the rate-determining step. We anticipate that the crystal phase engineering design approach unveiled in this work would be adoptable to other types of reactions.

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：Single-atom catalysts(SACs)have been widely used in heterogeneous catalysis owing to the maximum utilization of metal-active sites with controlled structures and well-defined *** tailored coordination with nitrogen atom,the metal-nitrogen(M-N)-based SACs have demonstrated interesting physical,optical and electronic properties and have become intense in photocatalysis and electrocatalysis in the past *** substantial efforts in constructing various M–N-based SACs,the principles for modulating the intrinsic photocatalytic and electrocatalytic performance of their active sites and catalytic mechanism have not been sufficiently ***,the present review intends to shed some light on recent research made in studying the correlation between intrinsic electronic structure,catalytic mechanism,single-metal atom(SMA)confinement and their photocatalytic and electrocatalytic activities(conversion,selectivity,stability and etc).Based on the analysis of fundamentals of M–N-based SACs,theoretical calculations and experimental investigations,including synthetic methods and characterization techniques,are both included to provide an integral understanding of the underlying mechanisms behind improved coordination structure and observed ***,the challenges and perspectives for constructing highly active M–N based photocatalysis and electrocatalysis SACs are *** particular,extensive technical and mechanism aspects are thoroughly discussed,summarized and analyzed for promoting further advancement of M-N-based SACs in photocatalysis and electrocatalysis.

摘要：Silicon(Si)is a promising anode material for next-generation Li-ion *** nanometer-sized Si could alleviate the pulverization caused by large volume changes during deep ***,compression between agglomerated Si particles causes Si cracking and electrode *** this,we engineered a mechanical cushioning space between Si particles via elastic hollow graphene shells(GSs)to flexibly buffer volume changes and maintain the stability of the electrode *** stress generated from the Si volume expansion during lithiation was mechanically buffered and gently released by compression of the hollow space of the *** this Si/GS composite electrode,GS also reduced the local agglomeration of Si particles and effectively improved the overall *** these advantages,the designed Si/GS electrode showed an enhanced cycling performance with more than 1200 mA h g^(-1) at 0.8 A g^(-1) and an excellent rate capability of 1025 mA h g^(-1) at 4 A g^(-1) after 200 cycles.

摘要：The new properties of engineered nanoparti- cles drive the need for new knowledge on the safety, fate, behavior and biologic effects of these particles on organisms and ecosystems. Titanium dioxide nanoparticles have been used extensively for a wide range of applica- tions, e.g, self-cleaning surface coatings, solar cells, water treatment agents, topical sunscreens. Within this scenario increased environmental exposure can be expected but data on the ecotoxicological evaluation ofnanoparticles are still scarce. The main purpose of this work was the evaluation of effects of TiO2 nanoparticles in several organisms, covering different trophic levels, using a battery of aquatic assays. Using fish as a vertebrate model organism tissue histological and ultrastructural observations and the stress enzyme activity were also studied. TiO2 nanoparticles （Aeroxide~ P25）, two phase composition ofanatase （65%） and rutile （35%） with an average particle size value of 27.64-11 nm were used. Results on the ECs0 for the tested aquatic organisms showed toxicity for the bacteria, the algae and the crustacean, being the algae the most sensitive tested organism. The aquatic plant Lemna minor showed no effect on growth. The fish Carassius auratus showed no effect on a 21 day survival test, though at a biochemical level the cytosolic Glutathione-S-Transferase total activity, in intestines, showed a general significant decrease （p〈0.05） after 14 days of exposure for all tested concentrations. The presence of TiO2 nanoparticles aggregates were observed in the intestine lumen but their internalization by intestine cells could not be confirmed.