For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state elect...For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state electrolytes(Na-ion SSEs)are the critical parts and mostly determine the electrochemical performance of SIBs.Among the studied ones,inorganic Na-ion SSEs stand out for their good safety performance and high ionic conductivity.In this review,we outline the research progress of inorganic SSEs in SIBs based on the perspectives of crystal structure,performance optimization,synthesis methods,allsolid-state SIBs,interface modification and related characterization techniques.We hope to provide some ideas for the design of future high-performance Na-ion SSEs.展开更多
An inorganic-organic hybrid compound, [H_3NC_2H_4NH_2]VOPO_4 was synthesized by means of the hydrothermal method. It was crystallized in a monoclinic system, a space group P2_1/c, with the crystal cell parameters: a=0...An inorganic-organic hybrid compound, [H_3NC_2H_4NH_2]VOPO_4 was synthesized by means of the hydrothermal method. It was crystallized in a monoclinic system, a space group P2_1/c, with the crystal cell parameters: a=0.92285(11) nm, b=0.72994(9) nm, c=0.98495(11) nm, β=101.280(3)°, V=0.65067(13) nm^3, M_r=223.02 g/mol, D_c=2.277 g/cm^3, Z=4, R=0.0315, ωR=0.0865, GOF=1.085. The VO_5N octahedra chains are corner-linked by PO_4 tetrahedra; the VO_5N octahedra are all trans-linked with V—O bonds being alternately short and long. The monoprotonated ethylenediamine was intercalated between the layers with one end coordinating to V and the other end as an H-bond donor interacting with a terminal O atom of PO_4 from a neighboring sheet. The elementary analysis, infrared spectrum characters and thermal stability were also given.展开更多
A novel one-dimensional inorganic-organic hybrid gallophosphate compound, Ga（2,2＇-bipy）（HPO4）. （H2PO4）（denoted JGP-2） was synthesized hydrothermally with 2,2＇-bipyridine as a ligand and characterized by X-ra...A novel one-dimensional inorganic-organic hybrid gallophosphate compound, Ga（2,2＇-bipy）（HPO4）. （H2PO4）（denoted JGP-2） was synthesized hydrothermally with 2,2＇-bipyridine as a ligand and characterized by X-ray powder diffraction （XRD）, elemental analysis, inductively coupled plasma（ICP）, TGA analysis, solid-state ^31p NMR, and luminescence spectra and structurally determined by single-crystal X-ray diffraction analysis. JGP-2 crystallized in the triclinic system, space group P^-1（No.2）, with a=0.7818（1） nm, b=0.8611 （2） nm, c=1.0908（2） nm, V=0.6727（2） nm^3 and Z=2 with R1=0.0223. The structure of JGP-2 was built up by alternate arrangement of GaO4N2 octahedra, and HPO4（or H2PO4） tetrahedra to form an infinite one-dimensional corner-sharing-corner（CSC） chain. Through P sites, the CSC chains link with an unusual edge-sharing dimmer, Ga2F4（H2O）2, giving rise to a 4,10-membered ring net layered structure of JGP-7. On excitation at 254 nm, JGP-2 can emit strong blue light at ,λmax=388 rim. JGP-7 presents a strong fluorescence emission band centered at 394 nm（λex=340 nm）, the emission energy of JGP-7 is red-shifted comoared with that of JGP-2.展开更多
To make inorganic structure data more useful for further studies a five-point list of simple procedures to be followed by authors of crystal structure papers is proposed. 1. A crystal structure should be described wit...To make inorganic structure data more useful for further studies a five-point list of simple procedures to be followed by authors of crystal structure papers is proposed. 1. A crystal structure should be described with the space group corresponding to its true symmetry. 2. A new structure proposal should be tested, if it is realistic in principle. 3. A structure should be described with a space group in a setting given in the International Tables. 4. For a comparison with other structures the structure data should be standardized with the program STRUCTURE TIDY. 5. 揘ew?structure data should be checked in the databases, Chemical Abstracts or on-line internet resources, if they are really new. The list is supplemented with many explanations, commentaries, examples and references.展开更多
Wood-based panels containing urea-formaldehyde resin result in the long-term release of formaldehyde and threaten human health.In this study,inorganic aluminosilicate coatings prepared by combining metakaolin,silica f...Wood-based panels containing urea-formaldehyde resin result in the long-term release of formaldehyde and threaten human health.In this study,inorganic aluminosilicate coatings prepared by combining metakaolin,silica fume,NaOH,and H_(2)O were applied to the surfaces of wood-based panels to obstruct formaldehyde release.The Si/Al,Na/Al,and H_(2)O/Na_(2)O molar ratios of the coatings were regulated to investigate their effects on the structure and formaldehyde-resistant barrier properties of coatings.Results showed that the cracks in the coatings gradually disappeared and the formaldehyde resistance rates of the barrier increased as the Si/Al molar ratio was increased from 1.6 to 2.2.This value also increased as the Na/Al molar ratio was increased from 0.9 to 1.2 because of the improvement of the degree of polymerization.As the H_(2)O/Na_(2)O molar ratio was increased from 12 to 15,the thickness of the dry film decreased gradually and led to the reduction in the formaldehyde resistance rate.When the Si/Al,Na/Al,and H_(2)O/Na_(2)O molar ratios were 2.2,1.2,and 12,respectively,the inorganic aluminosilicate coating showed good performance as a formaldehyde-resistant barrier and its formaldehyde resistance rate could reach up to 83.2%.展开更多
The increasing anthropogenic emissions of greenhouse gases(GHG)is encouraging extensive research in CO_(2)utilisation.Dry reforming of methane(DRM)depicts a viable strategy to convert both CO_(2)and CH4into syngas,a w...The increasing anthropogenic emissions of greenhouse gases(GHG)is encouraging extensive research in CO_(2)utilisation.Dry reforming of methane(DRM)depicts a viable strategy to convert both CO_(2)and CH4into syngas,a worthwhile chemical intermediate.Among the different active phases for DRM,the use of nickel as catalyst is economically favourable,but typically deactivates due to sintering and carbon deposition.The stabilisation of Ni at different loadings in cerium zirconate inorganic complex structures is investigated in this work as strategy to develop robust Ni-based DRM catalysts.XRD and TPR-H2analyses confirmed the existence of different phases according to the Ni loading in these materials.Besides,superficial Ni is observed as well as the existence of a CeNiO_(3)perovskite structure.The catalytic activity was tested,proving that 10 wt.%Ni loading is the optimum which maximises conversion.This catalyst was also tested in long-term stability experiments at 600and 800℃in order to study the potential deactivation issues at two different temperatures.At 600℃,carbon formation is the main cause of catalytic deactivation,whereas a robust stability is shown at 800℃,observing no sintering of the active phase evidencing the success of this strategy rendering a new family of economically appealing CO_(2)and biogas mixtures upgrading catalysts.展开更多
Ionothermal synthesis was used to prepare a novel amino acid containing hybrid zincophosphate monomer,[Zn（HPO4）（H2PO4）][C6H10N3O2]（denoted as ZnPO-CJ58）.The inorganic framework of [Zn（HPO4）（H2PO4）]·[C6H...Ionothermal synthesis was used to prepare a novel amino acid containing hybrid zincophosphate monomer,[Zn（HPO4）（H2PO4）][C6H10N3O2]（denoted as ZnPO-CJ58）.The inorganic framework of [Zn（HPO4）（H2PO4）]·[C6H10N3O2] consists of 4-membered rings formed by ZnO3OHis and PO2（OH）2 tetrahedra.The HPO4 and amino acid moieties hang on the Zn center.Such a framework is stabilized by extensive multipoint hydrogen bonds involving the phosphate units and histidine molecules to form a pseudo-3D supramolecular structure.It is noteworthy that ZnPO-CJ58 is the first zinc phosphate cluster with amino acid acting as the ligand.It exhibits photoluminescence excited at a wavelength of 220 nm.Interestingly,ZnPO-CJ58 can transform into a layered structure （C6H10N3O2）Zn2·（HPO4）（PO4）·H2O（ZnPO-CJ36） through further reacting with water or zinc acetate dihydrate in water at 85℃ for 1 h.This work will be helpful for the synthesis of crystalline inorganic-organic hybrid materials with biofunctional molecules.展开更多
A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in...A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in the future. Numerous olygophosphates, polyphosphates, double condensed phosphates and cyclophosphates with diverse formula, such as double tetra-, octa- and dodecaphosphates were obtained and described by us last years. The offered data are the outcomes of our scientific researches： of synthesis, analysis, and estimation of results in correlation with new achievements in inorganic polymer＇s chemistry. Many double condensed compounds, containing monovalent metals are obtained by us during systematic investigation of polycomponent systems, containing mono- and trivalent metals at temperature range 100-600 ~C. Synthesised condensed phosphates, in fact--inorganic polymers were examined in detail by chemical and thermogravimetric analysis, most compounds were examined by paper chromatography and the structures are determined by X-ray structural techniques/diffraction analysis. During our fundamental researches numerous new （about 70） unknown until now condensed phosphates have been obtained. Dependency of composition VS temperature and molar ratio, reliance of structure from duration of synthesis and radius of the ions are revealed.展开更多
Flexible aqueous zinc-air batteries with high energy density and safety have garnered significant attention.Gel polymer electrolytes have emerged as the preferred option over conventional liquid electrolytes due to th...Flexible aqueous zinc-air batteries with high energy density and safety have garnered significant attention.Gel polymer electrolytes have emerged as the preferred option over conventional liquid electrolytes due to their ability to prevent electrolyte leakage.In this study,a composite PANa-PVP-TiO_(2)(NH_(2))hydrogel with high alkaline resistance and ionic conductivity is designed,where the inorganic TiO_(2)(NH_(2))nanoparticles are evenly distributed and integrated into the organic dual network of polyacrylate sodium and polyvinyl pyrrolidone.The organic-inorganic hybrid structure enhances the absorption and retention capabilities for electrolyte solution,leading to impressive ionic conductivity of the gel polymer electrolyte throughout the operation of flexible aqueous zinc-air batteries.Additionally,the incorporation of TiO_(2)(NH_(2))nanoparticles and the dual network construction effectively strengthen the mechanical strength and flexibility of the gel polymer electrolyte,suppressing by-products and zinc dendrite formation.The enhancements lead to the extended cycling longevity of zinc symmetric batteries and excellent power density,as well as the prolonged cycle life of flexible aqueous zinc-air batteries.展开更多
Self-assembled inorganic halide perovskite superlattices(HPSLs)have attracted extensive attention for their well-ordered structure and unique collective photonic properties,which differ from those of individual nanocr...Self-assembled inorganic halide perovskite superlattices(HPSLs)have attracted extensive attention for their well-ordered structure and unique collective photonic properties,which differ from those of individual nanocrystals(NCs).However,the manipulation of ordered HPSLs with all-halogen and alloyed halogen components,as well as the regulation of their coherent spontaneous emission across the visible spectrum,remains underexplored.In this study,we employ a combination of anion-exchange reactions and a slow solvent evaporation strategy to self-assemble monodisperse,uniform all inorganic perovskite NCs into a series of well-defined,long-range ordered,and densely packed CsPbX3(X=Cl,Br,I,and mixed halide systems such as Cl/Br,Br/I,and Cl/Br/I)superlattices,achieving coherent photoluminescence(PL)emission across the entire visible spectrum(400–700 nm).Notably,the collective coherent emission of all HPSLs exhibits dynamic redshifts and accelerated collective radiative decay due to strong electronic coupling between NCs at cryogenic temperatures(7 K).This study not only systematically investigates all-halide compositional HPSLs but also paves the way for quantum light source applications across the visible spectrum.展开更多
Two new inorganic-organic hybrid polymers, Mn(QS)(H<sub>2</sub>O) (1) and Co(QS)(H<sub>2</sub>O)<sub>2</sub> (2) (H<sub>2</sub>QS=8-hydroxylquinoline-5-sulfonic acid), b...Two new inorganic-organic hybrid polymers, Mn(QS)(H<sub>2</sub>O) (1) and Co(QS)(H<sub>2</sub>O)<sub>2</sub> (2) (H<sub>2</sub>QS=8-hydroxylquinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.展开更多
In this study,polyacrylic acid(PAA)films were employed as a model system,and a series of PAA films with tunable water wettability was systematically prepared by varying molecular weight and curing temperature.Using at...In this study,polyacrylic acid(PAA)films were employed as a model system,and a series of PAA films with tunable water wettability was systematically prepared by varying molecular weight and curing temperature.Using attenuated total reflectance Fourier-transform infrared spectroscopy(ATR-FTIR),the molecular configurations of surface carboxyl groups(COOH),free carboxyl(COOH_(f))and hydrogen-bonded carboxyl(COOH_(HB),were directly correlated with the polar component of surface energy(γ^(s,p)).By decomposing theγ^(s,p)values of the PAA thin films as a sum of the contributions of COOH_(f)and COOH_(H B),the intrinsic polar component of surface energy of COOH_(H B)(γ_(H B)^(s,p*))was quantified for the first time as 8.34 mN/m,significantly lower than that of COOH_(f)(γ_(f)^(s,p*)=34 mN/m).This result highlights that hydrogen bonding markedly reduces theγ^(s,p),providing a rational explanation for the relatively large water contact angle observed on PAA thin films.Furthermore,it establishes a thermodynamic basis for estimating the fraction of surface COOH_(H B)groups(f H B)from wettability measurements.Further extension of the model to carboxyl-terminated self-assembled monolayers(COOH-SAMs)revealed that surface COOH density(ΣCOOH)critically regulates wetting behavior:whenΣCOOH ranges from 4.30 to 5.25 nm^(-2),COOH groups predominantly exist in a free state and facilitate effective hydration layers,thereby promoting superhydrophilicity.Overall,this study not only establishes a unified thermodynamic framework linking surface COOH configurations to macroscopic wettability,but also validates its universality by extending it to COOH-SAMs systems,thereby providing a unified theoretical framework for the controllable design of hydrophilicity in various COOH-functionalized surfaces.展开更多
Six new lanthanide complexes:[Ln(3,4-DEOBA)3(4,4'-DM-2,2'-bipy)]2·2C_(2)H_(5)OH,[Ln=Dy(1),Eu(2),Tb(3),Sm(4),Ho(5),Gd(6);3,4-DEOBA-=3,4-diethoxybenzoate,4,4'-DM-2,2'-bipy=4,4'-dimethyl-2,2'...Six new lanthanide complexes:[Ln(3,4-DEOBA)3(4,4'-DM-2,2'-bipy)]2·2C_(2)H_(5)OH,[Ln=Dy(1),Eu(2),Tb(3),Sm(4),Ho(5),Gd(6);3,4-DEOBA-=3,4-diethoxybenzoate,4,4'-DM-2,2'-bipy=4,4'-dimethyl-2,2'-bipyridine]were successfully synthesized by the volatilization of the solution at room temperature.The crystal structures of six complexes were determined by single-crystal X-ray diffraction technology.The results showed that the complexes all have a binuclear structure,and the structures contain free ethanol molecules.Moreover,the coordination number of the central metal of each structural unit is eight.Adjacent structural units interact with each other through hydrogen bonds and further expand to form 1D chain-like and 2D planar structures.After conducting a systematic study on the luminescence properties of complexes 1-4,their emission and excitation spectra were obtained.Experimental results indicated that the fluorescence lifetimes of complexes 2 and 3 were 0.807 and 0.845 ms,respectively.The emission spectral data of complexes 1-4 were imported into the CIE chromaticity coordinate system,and their corre sponding luminescent regions cover the yellow light,red light,green light,and orange-red light bands,respectively.Within the temperature range of 299.15-1300 K,the thermal decomposition processes of the six complexes were comprehensively analyzed by using TG-DSC/FTIR/MS technology.The hypothesis of the gradual loss of ligand groups during the decomposition process was verified by detecting the escaped gas,3D infrared spectroscopy,and ion fragment information detected by mass spectrometry.The specific decomposition path is as follows:firstly,free ethanol molecules and neutral ligands are removed,and finally,acidic ligands are released;the final product is the corresponding metal oxide.CCDC:2430420,1;2430422,2;2430419,3;2430424,4;2430421,5;2430423,6.展开更多
Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticle...Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticles were chlorinated by NaClO solution to get AgCl@SiO_(2)/CTS‑based chloramine nano‑hybrid materials,denoted as AgCl@SiO_(2)/CTS‑Cl.A transmission electron microscope was used to observe the morphology of the as‑prepared samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.At the same time,an X‑ray diffractometer and an infrared spectroscope were utilized to characterize their crystal and chemical structures.Besides,ζpotentials were measured to elucidate the surface modification of AgCl nanoparticles by—NH_(2),the antibacterial mechanism of AgCl@SiO_(2)/CTS‑Cl was investigated by scanning electron microscopy,and Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)were used as the to‑be‑tested strains to evaluate the antimicrobial activity of samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.Findings demonstrate that sample AgCl@SiO_(2)/CTS exhibits a chain‑like structure ascribed to the interaction between—NH_(2),and each AgCl@SiO_(2)/CTS hybrid nanoparticle contains several AgCl cores.In the meantime,sample AgCl@SiO_(2)/CTS‑Cl exhibits excellent antibacterial activity against E.coli and S.aureus,which is attributed to the synergistic antibacterial effect of Ag^(+)and Cl^(-).Sample AgCl@SiO_(2)/CTS‑Cl with a dosage of 640.00μg·mL^(-1) could completely kill the two kinds of tested bacteria in 12 h of incubation;it retains a high antibacterial efficiency even after 10 cycles of antibacterial tests.展开更多
NiMo-based catalysts show significant potential for the hydrogen evolution reaction(HER).Optimizing the electronic structure and enhancing mass transfer are two critical factors for improving catalytic performance,but...NiMo-based catalysts show significant potential for the hydrogen evolution reaction(HER).Optimizing the electronic structure and enhancing mass transfer are two critical factors for improving catalytic performance,but they remain significant challenges.Herein,we present a route for synthesizing two-dimensional(2D)porous Mo_(2)N-Ni heterojunction nanosheets with tuned Ni-Mo ratio for enhanced alkaline HER performance.A precursor can be easily synthesized by assembling polyoxometalate clusters(PMo_(12))with layered hydroxy oxides(Ni(OH)_(2)).It is found that the interaction between PMo_(12)and Ni(OH)_(2)can effectively protect the particles from significant agglomeration during pyrolysis,resulting in the formation of 2D porous sheets composed of small Mo_(2)N-Ni units.The transfer of electrons from Ni to Mo_(2)N results in the redistribution of electrons at the heterojunction,optimizing the adsorption and desorption of intermediates.Moreover,the 2D porous structure comprised of small particles enhances mass transfer,thereby reducing the impedance of the catalyst.Consequently,the catalyst with an optimized Mo/Ni ratio exhibits an overpotential of 19 mV at 10 mA cm^(-2),being comparable to that of commercial Pt/C catalyst.The anion exchange membrane(AEM)electrolyzer,consisting of optimized Mo_(2)N-Ni and NiFe-LDH,achieves a current density of 500 mA cm^(-2)at 1.80 V and can operate stably for 300 h.This assembly method offers an effective strategy for the large-scale preparation of efficient catalysts.展开更多
Understanding the photoluminescence(PL)mechanism of metal nanoclusters from both molecular and supramolecular perspectives is crucial for developing highly emissive cluster-based nanomaterials.In this study,we synthes...Understanding the photoluminescence(PL)mechanism of metal nanoclusters from both molecular and supramolecular perspectives is crucial for developing highly emissive cluster-based nanomaterials.In this study,we synthesized two structurally similar Ag14 nanoclusters with different phosphine stabilizers,which demonstrated opposite PL behaviors in solution and crystalline states.The Ag14 nanocluster stabilized by P(Ph-OMe)_(3) ligands exhibited a higher PL intensity compared to the one stabilized by P(Ph-F)_(3) ligands,which was attributed to the stronger electron-donating ability of the P(Ph-OMe)_(3) ligand that improved ligand-to-metal charge transfer efficiency.In contrast,the P(Ph-F)_(3) stabilized Ag14 crystals displayed greater PL intensity than the Ag14 cluster crystal with a-OMe surface,which was due to stronger intermolecular interactions within the cluster lattice of the former that limited non-radiative energy loss and thus enhanced PL.Overall,this work aims to promote a comprehensive understanding of the fluorescence in cluster-based nanomaterials,which will be beneficial for their downstream applications.展开更多
WS2 nanotubes have been filled and intercalated by molten phase caesium iodide.The presence of caesium iodide inside the WS_(2) nanotubes has been determined using high-resolution transmission electron microscopy(HRTE...WS2 nanotubes have been filled and intercalated by molten phase caesium iodide.The presence of caesium iodide inside the WS_(2) nanotubes has been determined using high-resolution transmission electron microscopy(HRTEM)coupled with electron energy-loss spectroscopy(EELS)and energy-dispersive X-ray spectroscopy(EDS).Noticeably,a Moirépattern was observed due to the interference between encapsulated CsI and WS_(2) layers.The intercalation of CsI into the host concentric WS2 lattices resulted in an increase in the interplanar spacing.展开更多
The photocatalytic oxidation of methane(CH_(4)) to valuable chemicals like low alcohols(CH_(3)OH and C_(2)H_(5)OH) represents a significant technological advancement with implications for energy conversion and environ...The photocatalytic oxidation of methane(CH_(4)) to valuable chemicals like low alcohols(CH_(3)OH and C_(2)H_(5)OH) represents a significant technological advancement with implications for energy conversion and environmental purification.A major challenge in this field is the chemical inertness of methane and the strong oxidizing nature of photogenerated holes,which can lead to over-oxidation and reduced selectivity and efficiency.To address these issues,we have developed a sodium-doped zinc oxide(Na-ZnO) modified with cobalt oxide(CoO) catalyst.This catalyst has demonstrated excellent performance in converting methane to low alcohols,achieving a yield of 130 μmol g^(-1)h^(-1) and a selectivity of up to 96 %.The doping of Na in ZnO significantly enhances methane adsorption,while the surface-modified CoO effectively captures photogenerated holes,activates water molecules,and uses hydroxyl radicals to activate methane,thus controlling the dehydrogenation degree of methane and preventing the formation of over-oxidized products.This strategy has successfully improved the efficiency and selectivity of photocatalytic methane oxidation to low alcohols,offering a new perspective for the application of photocatalytic technology in energy and environmental fields.展开更多
Some active metal oxides(Al_(2)O_(3),TiO_(2),and Cr_(2)O_(3))were selected as dopants to the Al_(2)O_(3)-based ceramic shells for investment casting of K417G superalloy.The effects of dopant types and contents(0,2,5,a...Some active metal oxides(Al_(2)O_(3),TiO_(2),and Cr_(2)O_(3))were selected as dopants to the Al_(2)O_(3)-based ceramic shells for investment casting of K417G superalloy.The effects of dopant types and contents(0,2,5,and 8 wt.%)on the wettability and interfacial reaction between the alloy and shell were investigated by a sessile-drop experiment.The results show that increasing the Al_(2)O_(3) doping contents(0−8 wt.%)reduces the porosity(21.74%−10.08%)and roughness(3.22−1.34μm)of the shell surface.The increase in Cr_(2)O_(3) dopant content(2−8 wt.%)further exacerbates the interfacial reaction,leading to an increase in the thickness of the reaction layer(2.6−3.1μm)and a decrease in the wetting angle(93.9°−91.0°).The addition of Al_(2)O_(3) and TiO_(2) dopants leads to the formation of Al_(2)TiO_(5) composite oxides in the reaction products,which effectively inhibits the interfacial reaction.The increase in TiO_(2) dopant contents(0−8 wt.%)further promotes the formation of Al_(2)TiO_(5),which decreases the thickness of the interfacial reaction layer(3.9−1.2μm)and increases the wetting angle(95.0°−103.8°).The introduced dopants enhance the packing density of the shell surface,while simultaneously suppress the diffusion of active metal elements from the alloy matrix to the interface.展开更多
Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herei...Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herein,a simple MOF-assisted etching-pyrolysis strategy is proposed to fabricate an advanced Mott-Schottky(M–S)electrocatalyst composed of Co/CeO_(2)hetero-nanoparticles embedded within N-doped hollow carbon nanoboxes(H-Co/CeO_(2)@NCBs).Notably,the interfacial Co–O–Ce bond bridging productively facilitates the electron transfer and modulates the charge distribution of the active center,thereby contributing to the ORR/OER kinetics.As expected,the optimal M–S H-Co/CeO_(2)@NCBs catalyst exhibits promising bifunctional electrocatalytic activity with a small potential discrepancy of 0.65 V.Theoretical calculations reveal that the built-in electric field in the M–S heterojunction promotes electron transfer in oxygen electrocatalysis and the interfacial bridge-induced electron redistribution optimizes the adsorption/desorption of the oxygen intermediates,leading to reduced activation energy for the bifunctional ORR/OER reactions.Importantly,H-Co/CeO_(2)@NCBs-assembled Zn-air battery(ZAB)delivers high power density(179.8 mW cm^(−2))and long-term stability(400 h).Furthermore,the assembled flexible solid-state ZAB with H-Co/CeO_(2)@NCBs cathode also exhibits excellent charge–discharge reversibility and flexibility at various bending angles.This work provides a novel perspective on developing efficient and stable M–S bifunctional oxygen electrocatalysts.展开更多
基金supported by the National Natural Science Foundation of China(Nos.22175070,22293041)supported by the National Key Research and Development Program(Nos.2021YFB2500200,2021YFB2400300)+1 种基金the National Natural Science Foundation of China(No.52177214)China Fujian Energy Devices Science and Technology Innovation Laboratory Open Fund(No.21C-OP202211)。
文摘For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state electrolytes(Na-ion SSEs)are the critical parts and mostly determine the electrochemical performance of SIBs.Among the studied ones,inorganic Na-ion SSEs stand out for their good safety performance and high ionic conductivity.In this review,we outline the research progress of inorganic SSEs in SIBs based on the perspectives of crystal structure,performance optimization,synthesis methods,allsolid-state SIBs,interface modification and related characterization techniques.We hope to provide some ideas for the design of future high-performance Na-ion SSEs.
基金Supported by the National Natural Science Foundation of China.
文摘An inorganic-organic hybrid compound, [H_3NC_2H_4NH_2]VOPO_4 was synthesized by means of the hydrothermal method. It was crystallized in a monoclinic system, a space group P2_1/c, with the crystal cell parameters: a=0.92285(11) nm, b=0.72994(9) nm, c=0.98495(11) nm, β=101.280(3)°, V=0.65067(13) nm^3, M_r=223.02 g/mol, D_c=2.277 g/cm^3, Z=4, R=0.0315, ωR=0.0865, GOF=1.085. The VO_5N octahedra chains are corner-linked by PO_4 tetrahedra; the VO_5N octahedra are all trans-linked with V—O bonds being alternately short and long. The monoprotonated ethylenediamine was intercalated between the layers with one end coordinating to V and the other end as an H-bond donor interacting with a terminal O atom of PO_4 from a neighboring sheet. The elementary analysis, infrared spectrum characters and thermal stability were also given.
基金Supported by the National Natural Science Foundation of China(Nos.20671025 and 20771030)China Postdoctoral Science Foundation Funded Project(No.65204)Heilongjiang Province Natural Science Foundation, China(No.B200603).
文摘A novel one-dimensional inorganic-organic hybrid gallophosphate compound, Ga（2,2＇-bipy）（HPO4）. （H2PO4）（denoted JGP-2） was synthesized hydrothermally with 2,2＇-bipyridine as a ligand and characterized by X-ray powder diffraction （XRD）, elemental analysis, inductively coupled plasma（ICP）, TGA analysis, solid-state ^31p NMR, and luminescence spectra and structurally determined by single-crystal X-ray diffraction analysis. JGP-2 crystallized in the triclinic system, space group P^-1（No.2）, with a=0.7818（1） nm, b=0.8611 （2） nm, c=1.0908（2） nm, V=0.6727（2） nm^3 and Z=2 with R1=0.0223. The structure of JGP-2 was built up by alternate arrangement of GaO4N2 octahedra, and HPO4（or H2PO4） tetrahedra to form an infinite one-dimensional corner-sharing-corner（CSC） chain. Through P sites, the CSC chains link with an unusual edge-sharing dimmer, Ga2F4（H2O）2, giving rise to a 4,10-membered ring net layered structure of JGP-7. On excitation at 254 nm, JGP-2 can emit strong blue light at ,λmax=388 rim. JGP-7 presents a strong fluorescence emission band centered at 394 nm（λex=340 nm）, the emission energy of JGP-7 is red-shifted comoared with that of JGP-2.
文摘To make inorganic structure data more useful for further studies a five-point list of simple procedures to be followed by authors of crystal structure papers is proposed. 1. A crystal structure should be described with the space group corresponding to its true symmetry. 2. A new structure proposal should be tested, if it is realistic in principle. 3. A structure should be described with a space group in a setting given in the International Tables. 4. For a comparison with other structures the structure data should be standardized with the program STRUCTURE TIDY. 5. 揘ew?structure data should be checked in the databases, Chemical Abstracts or on-line internet resources, if they are really new. The list is supplemented with many explanations, commentaries, examples and references.
基金financially supported by the National Key Research and Development Program of China(Nos.2016 YFC0700607,2017YFB0304305,and 2016YFC0700901)the Fundamental Research Funds for the Central Universities of China(No.FRF-TP-20-006A3).
文摘Wood-based panels containing urea-formaldehyde resin result in the long-term release of formaldehyde and threaten human health.In this study,inorganic aluminosilicate coatings prepared by combining metakaolin,silica fume,NaOH,and H_(2)O were applied to the surfaces of wood-based panels to obstruct formaldehyde release.The Si/Al,Na/Al,and H_(2)O/Na_(2)O molar ratios of the coatings were regulated to investigate their effects on the structure and formaldehyde-resistant barrier properties of coatings.Results showed that the cracks in the coatings gradually disappeared and the formaldehyde resistance rates of the barrier increased as the Si/Al molar ratio was increased from 1.6 to 2.2.This value also increased as the Na/Al molar ratio was increased from 0.9 to 1.2 because of the improvement of the degree of polymerization.As the H_(2)O/Na_(2)O molar ratio was increased from 12 to 15,the thickness of the dry film decreased gradually and led to the reduction in the formaldehyde resistance rate.When the Si/Al,Na/Al,and H_(2)O/Na_(2)O molar ratios were 2.2,1.2,and 12,respectively,the inorganic aluminosilicate coating showed good performance as a formaldehyde-resistant barrier and its formaldehyde resistance rate could reach up to 83.2%.
基金supported by grant PID2019-108502RJ-I00 and grant IJC2019-040560-I both funded by MCIN/AEI/10.13039/501100011033RYC2018-024387-I funded by MCIN/AEI/10.13039/501100011033 and by ESF Investing in your future。
文摘The increasing anthropogenic emissions of greenhouse gases(GHG)is encouraging extensive research in CO_(2)utilisation.Dry reforming of methane(DRM)depicts a viable strategy to convert both CO_(2)and CH4into syngas,a worthwhile chemical intermediate.Among the different active phases for DRM,the use of nickel as catalyst is economically favourable,but typically deactivates due to sintering and carbon deposition.The stabilisation of Ni at different loadings in cerium zirconate inorganic complex structures is investigated in this work as strategy to develop robust Ni-based DRM catalysts.XRD and TPR-H2analyses confirmed the existence of different phases according to the Ni loading in these materials.Besides,superficial Ni is observed as well as the existence of a CeNiO_(3)perovskite structure.The catalytic activity was tested,proving that 10 wt.%Ni loading is the optimum which maximises conversion.This catalyst was also tested in long-term stability experiments at 600and 800℃in order to study the potential deactivation issues at two different temperatures.At 600℃,carbon formation is the main cause of catalytic deactivation,whereas a robust stability is shown at 800℃,observing no sintering of the active phase evidencing the success of this strategy rendering a new family of economically appealing CO_(2)and biogas mixtures upgrading catalysts.
基金Supported by the National Natural Science Foundation of China(No.20080504)
文摘Ionothermal synthesis was used to prepare a novel amino acid containing hybrid zincophosphate monomer,[Zn（HPO4）（H2PO4）][C6H10N3O2]（denoted as ZnPO-CJ58）.The inorganic framework of [Zn（HPO4）（H2PO4）]·[C6H10N3O2] consists of 4-membered rings formed by ZnO3OHis and PO2（OH）2 tetrahedra.The HPO4 and amino acid moieties hang on the Zn center.Such a framework is stabilized by extensive multipoint hydrogen bonds involving the phosphate units and histidine molecules to form a pseudo-3D supramolecular structure.It is noteworthy that ZnPO-CJ58 is the first zinc phosphate cluster with amino acid acting as the ligand.It exhibits photoluminescence excited at a wavelength of 220 nm.Interestingly,ZnPO-CJ58 can transform into a layered structure （C6H10N3O2）Zn2·（HPO4）（PO4）·H2O（ZnPO-CJ36） through further reacting with water or zinc acetate dihydrate in water at 85℃ for 1 h.This work will be helpful for the synthesis of crystalline inorganic-organic hybrid materials with biofunctional molecules.
文摘A distinctive feature of phosphates is their special and significant ability to form inorganic polymeric compounds---condensed phosphates, which are destined to play a considerable role in our ＂high-tech＂ society in the future. Numerous olygophosphates, polyphosphates, double condensed phosphates and cyclophosphates with diverse formula, such as double tetra-, octa- and dodecaphosphates were obtained and described by us last years. The offered data are the outcomes of our scientific researches： of synthesis, analysis, and estimation of results in correlation with new achievements in inorganic polymer＇s chemistry. Many double condensed compounds, containing monovalent metals are obtained by us during systematic investigation of polycomponent systems, containing mono- and trivalent metals at temperature range 100-600 ~C. Synthesised condensed phosphates, in fact--inorganic polymers were examined in detail by chemical and thermogravimetric analysis, most compounds were examined by paper chromatography and the structures are determined by X-ray structural techniques/diffraction analysis. During our fundamental researches numerous new （about 70） unknown until now condensed phosphates have been obtained. Dependency of composition VS temperature and molar ratio, reliance of structure from duration of synthesis and radius of the ions are revealed.
基金supported by the National Natural Science Foundation of China(Grant Nos.51872147,22136003)the Project of Hubei Provincial Department of Education(Grant No.D20221202)+1 种基金the 111 Project(Grant No.D20015)the Hubei Provincial Natural Science Foundation of China(Grant Nos.2022CFA065,2022CFB820).
文摘Flexible aqueous zinc-air batteries with high energy density and safety have garnered significant attention.Gel polymer electrolytes have emerged as the preferred option over conventional liquid electrolytes due to their ability to prevent electrolyte leakage.In this study,a composite PANa-PVP-TiO_(2)(NH_(2))hydrogel with high alkaline resistance and ionic conductivity is designed,where the inorganic TiO_(2)(NH_(2))nanoparticles are evenly distributed and integrated into the organic dual network of polyacrylate sodium and polyvinyl pyrrolidone.The organic-inorganic hybrid structure enhances the absorption and retention capabilities for electrolyte solution,leading to impressive ionic conductivity of the gel polymer electrolyte throughout the operation of flexible aqueous zinc-air batteries.Additionally,the incorporation of TiO_(2)(NH_(2))nanoparticles and the dual network construction effectively strengthen the mechanical strength and flexibility of the gel polymer electrolyte,suppressing by-products and zinc dendrite formation.The enhancements lead to the extended cycling longevity of zinc symmetric batteries and excellent power density,as well as the prolonged cycle life of flexible aqueous zinc-air batteries.
基金financially supported by the National Natural Science Foundation of China(52072281)the Major Program of the National Natural Science Foundation of China(22293021)+1 种基金the Wuhan University of Technology Doctoral Research Initiation Fee(40120543)the Hubei Province's State-allocated Dual-class Research Platform Fee(40120623).
文摘Self-assembled inorganic halide perovskite superlattices(HPSLs)have attracted extensive attention for their well-ordered structure and unique collective photonic properties,which differ from those of individual nanocrystals(NCs).However,the manipulation of ordered HPSLs with all-halogen and alloyed halogen components,as well as the regulation of their coherent spontaneous emission across the visible spectrum,remains underexplored.In this study,we employ a combination of anion-exchange reactions and a slow solvent evaporation strategy to self-assemble monodisperse,uniform all inorganic perovskite NCs into a series of well-defined,long-range ordered,and densely packed CsPbX3(X=Cl,Br,I,and mixed halide systems such as Cl/Br,Br/I,and Cl/Br/I)superlattices,achieving coherent photoluminescence(PL)emission across the entire visible spectrum(400–700 nm).Notably,the collective coherent emission of all HPSLs exhibits dynamic redshifts and accelerated collective radiative decay due to strong electronic coupling between NCs at cryogenic temperatures(7 K).This study not only systematically investigates all-halide compositional HPSLs but also paves the way for quantum light source applications across the visible spectrum.
基金Supported by the State Basic Research Project (2006CB806100)Outstanding Young Scientist Foundation of the National Natural Science Foundation of China (20625102)+3 种基金the National Natural Science Foundation of China (Grant Nos. 20831D02, 20571030, 20531030, and 20371020)"111" Program of Ministry of Education of China and Bureau of Science & Technology of Jilin ProvinceJilin Province Hi-Tech Development Project (20090131)International Cooperation Project of Ministry of Science and Technology (2007DFA40830)
文摘Two new inorganic-organic hybrid polymers, Mn(QS)(H<sub>2</sub>O) (1) and Co(QS)(H<sub>2</sub>O)<sub>2</sub> (2) (H<sub>2</sub>QS=8-hydroxylquinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.
文摘In this study,polyacrylic acid(PAA)films were employed as a model system,and a series of PAA films with tunable water wettability was systematically prepared by varying molecular weight and curing temperature.Using attenuated total reflectance Fourier-transform infrared spectroscopy(ATR-FTIR),the molecular configurations of surface carboxyl groups(COOH),free carboxyl(COOH_(f))and hydrogen-bonded carboxyl(COOH_(HB),were directly correlated with the polar component of surface energy(γ^(s,p)).By decomposing theγ^(s,p)values of the PAA thin films as a sum of the contributions of COOH_(f)and COOH_(H B),the intrinsic polar component of surface energy of COOH_(H B)(γ_(H B)^(s,p*))was quantified for the first time as 8.34 mN/m,significantly lower than that of COOH_(f)(γ_(f)^(s,p*)=34 mN/m).This result highlights that hydrogen bonding markedly reduces theγ^(s,p),providing a rational explanation for the relatively large water contact angle observed on PAA thin films.Furthermore,it establishes a thermodynamic basis for estimating the fraction of surface COOH_(H B)groups(f H B)from wettability measurements.Further extension of the model to carboxyl-terminated self-assembled monolayers(COOH-SAMs)revealed that surface COOH density(ΣCOOH)critically regulates wetting behavior:whenΣCOOH ranges from 4.30 to 5.25 nm^(-2),COOH groups predominantly exist in a free state and facilitate effective hydration layers,thereby promoting superhydrophilicity.Overall,this study not only establishes a unified thermodynamic framework linking surface COOH configurations to macroscopic wettability,but also validates its universality by extending it to COOH-SAMs systems,thereby providing a unified theoretical framework for the controllable design of hydrophilicity in various COOH-functionalized surfaces.
文摘Six new lanthanide complexes:[Ln(3,4-DEOBA)3(4,4'-DM-2,2'-bipy)]2·2C_(2)H_(5)OH,[Ln=Dy(1),Eu(2),Tb(3),Sm(4),Ho(5),Gd(6);3,4-DEOBA-=3,4-diethoxybenzoate,4,4'-DM-2,2'-bipy=4,4'-dimethyl-2,2'-bipyridine]were successfully synthesized by the volatilization of the solution at room temperature.The crystal structures of six complexes were determined by single-crystal X-ray diffraction technology.The results showed that the complexes all have a binuclear structure,and the structures contain free ethanol molecules.Moreover,the coordination number of the central metal of each structural unit is eight.Adjacent structural units interact with each other through hydrogen bonds and further expand to form 1D chain-like and 2D planar structures.After conducting a systematic study on the luminescence properties of complexes 1-4,their emission and excitation spectra were obtained.Experimental results indicated that the fluorescence lifetimes of complexes 2 and 3 were 0.807 and 0.845 ms,respectively.The emission spectral data of complexes 1-4 were imported into the CIE chromaticity coordinate system,and their corre sponding luminescent regions cover the yellow light,red light,green light,and orange-red light bands,respectively.Within the temperature range of 299.15-1300 K,the thermal decomposition processes of the six complexes were comprehensively analyzed by using TG-DSC/FTIR/MS technology.The hypothesis of the gradual loss of ligand groups during the decomposition process was verified by detecting the escaped gas,3D infrared spectroscopy,and ion fragment information detected by mass spectrometry.The specific decomposition path is as follows:firstly,free ethanol molecules and neutral ligands are removed,and finally,acidic ligands are released;the final product is the corresponding metal oxide.CCDC:2430420,1;2430422,2;2430419,3;2430424,4;2430421,5;2430423,6.
文摘Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticles were chlorinated by NaClO solution to get AgCl@SiO_(2)/CTS‑based chloramine nano‑hybrid materials,denoted as AgCl@SiO_(2)/CTS‑Cl.A transmission electron microscope was used to observe the morphology of the as‑prepared samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.At the same time,an X‑ray diffractometer and an infrared spectroscope were utilized to characterize their crystal and chemical structures.Besides,ζpotentials were measured to elucidate the surface modification of AgCl nanoparticles by—NH_(2),the antibacterial mechanism of AgCl@SiO_(2)/CTS‑Cl was investigated by scanning electron microscopy,and Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)were used as the to‑be‑tested strains to evaluate the antimicrobial activity of samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.Findings demonstrate that sample AgCl@SiO_(2)/CTS exhibits a chain‑like structure ascribed to the interaction between—NH_(2),and each AgCl@SiO_(2)/CTS hybrid nanoparticle contains several AgCl cores.In the meantime,sample AgCl@SiO_(2)/CTS‑Cl exhibits excellent antibacterial activity against E.coli and S.aureus,which is attributed to the synergistic antibacterial effect of Ag^(+)and Cl^(-).Sample AgCl@SiO_(2)/CTS‑Cl with a dosage of 640.00μg·mL^(-1) could completely kill the two kinds of tested bacteria in 12 h of incubation;it retains a high antibacterial efficiency even after 10 cycles of antibacterial tests.
基金supported by the National Key R&D Program of China(2022YFA1503002,2022YFA1503003)the National Natural Science Foundation of China(22271081)+2 种基金the Natural Science Foundation of Heilongjiang Province(PL2024B017)the Postdoctoral Science Foundation of Heilongjiang Province(LBH-Z22240)the Heilongjiang University Excellent Youth Foundation。
文摘NiMo-based catalysts show significant potential for the hydrogen evolution reaction(HER).Optimizing the electronic structure and enhancing mass transfer are two critical factors for improving catalytic performance,but they remain significant challenges.Herein,we present a route for synthesizing two-dimensional(2D)porous Mo_(2)N-Ni heterojunction nanosheets with tuned Ni-Mo ratio for enhanced alkaline HER performance.A precursor can be easily synthesized by assembling polyoxometalate clusters(PMo_(12))with layered hydroxy oxides(Ni(OH)_(2)).It is found that the interaction between PMo_(12)and Ni(OH)_(2)can effectively protect the particles from significant agglomeration during pyrolysis,resulting in the formation of 2D porous sheets composed of small Mo_(2)N-Ni units.The transfer of electrons from Ni to Mo_(2)N results in the redistribution of electrons at the heterojunction,optimizing the adsorption and desorption of intermediates.Moreover,the 2D porous structure comprised of small particles enhances mass transfer,thereby reducing the impedance of the catalyst.Consequently,the catalyst with an optimized Mo/Ni ratio exhibits an overpotential of 19 mV at 10 mA cm^(-2),being comparable to that of commercial Pt/C catalyst.The anion exchange membrane(AEM)electrolyzer,consisting of optimized Mo_(2)N-Ni and NiFe-LDH,achieves a current density of 500 mA cm^(-2)at 1.80 V and can operate stably for 300 h.This assembly method offers an effective strategy for the large-scale preparation of efficient catalysts.
基金support of the National Natural Science Foundation of China(NSFC,Nos.22371003,22101001,and 22471001)the Ministry of Education,Natural Science Foundation of Anhui Province(No.2408085Y006)+1 种基金the University Synergy Innovation Program of Anhui Province(No.GXXT-2020-053)the Scientific Research Program of Universities in Anhui Province(No.2022AH030009).
文摘Understanding the photoluminescence(PL)mechanism of metal nanoclusters from both molecular and supramolecular perspectives is crucial for developing highly emissive cluster-based nanomaterials.In this study,we synthesized two structurally similar Ag14 nanoclusters with different phosphine stabilizers,which demonstrated opposite PL behaviors in solution and crystalline states.The Ag14 nanocluster stabilized by P(Ph-OMe)_(3) ligands exhibited a higher PL intensity compared to the one stabilized by P(Ph-F)_(3) ligands,which was attributed to the stronger electron-donating ability of the P(Ph-OMe)_(3) ligand that improved ligand-to-metal charge transfer efficiency.In contrast,the P(Ph-F)_(3) stabilized Ag14 crystals displayed greater PL intensity than the Ag14 cluster crystal with a-OMe surface,which was due to stronger intermolecular interactions within the cluster lattice of the former that limited non-radiative energy loss and thus enhanced PL.Overall,this work aims to promote a comprehensive understanding of the fluorescence in cluster-based nanomaterials,which will be beneficial for their downstream applications.
基金This work was supported by the Israel Science Foundation,European Research Council(ERC)grant(No.INTIF 226639)H.Perlman Foundation and the Cherna Moskowitz Center for Nano and Bio-Nano imaging.We thank Dr.Rita Rosentsveig for the supply of WS_(2)inorganic nanotubes.G.T.acknowledges support through FP7 European Community Marie Curie European Reintegration Grant(ERG)(No.PERG04-GA-2008-239303)+1 种基金B.B.a contract from Ministry of Science and Innovation(Ministerio de Ciencia e Innovación,MICINN)Spain.S.Y.H was supported by a Samsung Corporation fellowship(2005-2009)B.G.D.is a Royal Society-Wolfson Research Merit Award recipient and is also supported by an Engineering and Physical Sciences Research Council of the UK(EPSRC)Platform Grant(No.EPSRC EP/E000614/1).
文摘WS2 nanotubes have been filled and intercalated by molten phase caesium iodide.The presence of caesium iodide inside the WS_(2) nanotubes has been determined using high-resolution transmission electron microscopy(HRTEM)coupled with electron energy-loss spectroscopy(EELS)and energy-dispersive X-ray spectroscopy(EDS).Noticeably,a Moirépattern was observed due to the interference between encapsulated CsI and WS_(2) layers.The intercalation of CsI into the host concentric WS2 lattices resulted in an increase in the interplanar spacing.
基金support from the Zhejiang Provincial Natural Science Foundation of China (No.LQ24B030011)the Ningbo Natural Science Foundation (No.2023J181)+4 种基金the Open Research Fund of Key Laboratory of Functional Inorganic Materials Chemistry of the Ministry of Education (Heilongjiang University)the Start-up Funding offered by Ningbo University of Technology to J.D.LiNational Natural Science Foundation of China (No.U24A2071)Postdoctoral Research Start-up Fund (No.2111224002)Harbin Normal University Talent Plan (No.1305124213) to Y.D.Liu。
文摘The photocatalytic oxidation of methane(CH_(4)) to valuable chemicals like low alcohols(CH_(3)OH and C_(2)H_(5)OH) represents a significant technological advancement with implications for energy conversion and environmental purification.A major challenge in this field is the chemical inertness of methane and the strong oxidizing nature of photogenerated holes,which can lead to over-oxidation and reduced selectivity and efficiency.To address these issues,we have developed a sodium-doped zinc oxide(Na-ZnO) modified with cobalt oxide(CoO) catalyst.This catalyst has demonstrated excellent performance in converting methane to low alcohols,achieving a yield of 130 μmol g^(-1)h^(-1) and a selectivity of up to 96 %.The doping of Na in ZnO significantly enhances methane adsorption,while the surface-modified CoO effectively captures photogenerated holes,activates water molecules,and uses hydroxyl radicals to activate methane,thus controlling the dehydrogenation degree of methane and preventing the formation of over-oxidized products.This strategy has successfully improved the efficiency and selectivity of photocatalytic methane oxidation to low alcohols,offering a new perspective for the application of photocatalytic technology in energy and environmental fields.
基金supported by the National Natural Science Foundation of China (No. 52374292)China Baowu Low Carbon Metallurgy Innovation Foundation, China (No. BWLCF202309)the Natural Science Foundation of Changsha City, China (No. KQ2208271)。
文摘Some active metal oxides(Al_(2)O_(3),TiO_(2),and Cr_(2)O_(3))were selected as dopants to the Al_(2)O_(3)-based ceramic shells for investment casting of K417G superalloy.The effects of dopant types and contents(0,2,5,and 8 wt.%)on the wettability and interfacial reaction between the alloy and shell were investigated by a sessile-drop experiment.The results show that increasing the Al_(2)O_(3) doping contents(0−8 wt.%)reduces the porosity(21.74%−10.08%)and roughness(3.22−1.34μm)of the shell surface.The increase in Cr_(2)O_(3) dopant content(2−8 wt.%)further exacerbates the interfacial reaction,leading to an increase in the thickness of the reaction layer(2.6−3.1μm)and a decrease in the wetting angle(93.9°−91.0°).The addition of Al_(2)O_(3) and TiO_(2) dopants leads to the formation of Al_(2)TiO_(5) composite oxides in the reaction products,which effectively inhibits the interfacial reaction.The increase in TiO_(2) dopant contents(0−8 wt.%)further promotes the formation of Al_(2)TiO_(5),which decreases the thickness of the interfacial reaction layer(3.9−1.2μm)and increases the wetting angle(95.0°−103.8°).The introduced dopants enhance the packing density of the shell surface,while simultaneously suppress the diffusion of active metal elements from the alloy matrix to the interface.
基金supported by the National Natural Science Foundation of China(U24A20550,52273264 and 52470073)the Key Project of the Heilongjiang Provincial Natural Science Foundation(ZD2024B001)Outstanding Youth Fund of Heilongjiang Province(JQ2022E005).
文摘Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herein,a simple MOF-assisted etching-pyrolysis strategy is proposed to fabricate an advanced Mott-Schottky(M–S)electrocatalyst composed of Co/CeO_(2)hetero-nanoparticles embedded within N-doped hollow carbon nanoboxes(H-Co/CeO_(2)@NCBs).Notably,the interfacial Co–O–Ce bond bridging productively facilitates the electron transfer and modulates the charge distribution of the active center,thereby contributing to the ORR/OER kinetics.As expected,the optimal M–S H-Co/CeO_(2)@NCBs catalyst exhibits promising bifunctional electrocatalytic activity with a small potential discrepancy of 0.65 V.Theoretical calculations reveal that the built-in electric field in the M–S heterojunction promotes electron transfer in oxygen electrocatalysis and the interfacial bridge-induced electron redistribution optimizes the adsorption/desorption of the oxygen intermediates,leading to reduced activation energy for the bifunctional ORR/OER reactions.Importantly,H-Co/CeO_(2)@NCBs-assembled Zn-air battery(ZAB)delivers high power density(179.8 mW cm^(−2))and long-term stability(400 h).Furthermore,the assembled flexible solid-state ZAB with H-Co/CeO_(2)@NCBs cathode also exhibits excellent charge–discharge reversibility and flexibility at various bending angles.This work provides a novel perspective on developing efficient and stable M–S bifunctional oxygen electrocatalysts.
