Room-temperature phosphorescence(RTP)materials exhibiting long emission lifetimes have gained increasing attention owing to their potential applications in encryption,anti-counterfeiting,and sensing.However,most polym...Room-temperature phosphorescence(RTP)materials exhibiting long emission lifetimes have gained increasing attention owing to their potential applications in encryption,anti-counterfeiting,and sensing.However,most polymers exhibit a short RTP lifetime(<1 s)because of their unstable triplet excitons.Herein,a new strategy of polymer chain stabilized phosphorescence(PCSP),which yields a new kind of RTP polymers with an ultralong lifetime and a sensitive oxygen response,has been reported.The rigid polymer chains of poly(methyl mathacrylate)(PMMA)immobilize the emitter molecules through multiple interactions between them,giving rise to efficient RTP.Meanwhile,the loosely-packed amorphous polymer chains allow oxygen to diffuse inside,endowing the doped polymers with oxygen sensitivity.Flexible and transparent polymer films exhibited an impressive ultralong RTP lifetime of 2.57 s at room temperature in vacuum,which was among the best performance of PMMA.Intriguingly,their RTP was rapidly quenched in the presence of oxygen.Furthermore,RTP microparticles with a diameter of 1.63μm were synthesized using in situ dispersion polymerization technique.Finally,oxygen sensors for quick,visual,and quantitative oxygen detection were developed based on the RTP microparticles through phosphorescence lifetime and image analysis.With distinctive advantages such as an ultralong lifetime,oxygen sensitivity,ease of fabrication,and cost-effectiveness,PCSP opens a new avenue to sensitive materials for oxygen detection.展开更多
Room-temperature sodium-sulfur(RT Na-S)batteries have been regarded as promising energy storage technologies in grid-scale stationary energy storage systems due to their low cost,natural abundance,and high-energy dens...Room-temperature sodium-sulfur(RT Na-S)batteries have been regarded as promising energy storage technologies in grid-scale stationary energy storage systems due to their low cost,natural abundance,and high-energy density.However,the practical application of RT Na-S batteries is hindered by low reversible capacity and unsatisfying long-cycling performance arising from the severe shuttle effect and sluggish S redox kinetics.This review provides an overview of recent efforts for the optimization strategies of the electronic structure of catalysts via catalyst engineering to enhance the adsorption and catalytic activity toward soluble long-chain sodium polysulfides(NaPSs).Finally,the current challenges and prospects for further optimization strategies of catalysts,understanding catalysis and structural evolution mechanism,and achieving practical applications are highlighted to meet the commercial requirements of RT Na-S batteries.展开更多
Reducing the hot working temperature and high-temperature deformation resistance of titanium alloy to improve hot rolling and hot extrusion workability of products with thin walls and complex section shapes has always...Reducing the hot working temperature and high-temperature deformation resistance of titanium alloy to improve hot rolling and hot extrusion workability of products with thin walls and complex section shapes has always been an important topic in the field of titanium alloy processing.This paper proposed a strategy of adding Mo and Fe elements to simultaneously reduce the hot working temperature and high-temperature deformation resistance of Ti-6Al-4V alloy.The effects of Mo and Fe contents on the mi-crostructure,β transus temperature(Tp),and high-temperature flow stress(HFS)of Ti-6Al-4V-xMo-xFe(x=0-5)alloys were investigated.The results showed that adding Mo and Fe can substantially reduce the Tp and HFS of the alloy,and greatly improve its room-temperature strength.Compared with com-mercial Ti-6Al-4V samples,the T_(β) of Ti-6Al-4V-2Mo-2Fe and Ti-6Al-4V-3Mo-3Fe samples was decreased by 68-98 ℃,and the HFS at 800-900 ℃ was decreased by 37.8%-46.0%.Compared with hot-rolled Ti-6Al-4V samples,the room-temperature tensile strength of hot-rolled Ti-6Al-4V-2Mo-2Fe samples was increased by about 30%,while the elongation hardly decreased.The increased strength was mainly at-tributed to fine grain strengthening and solid solution strengthening.The hot workability and room-temperature strength of Ti-6Al-4V alloy can be significantly improved by adding 2-3 wt.%Mo and Fe simultaneously.展开更多
Stimulus-responsive room-temperature phosphorescence(RTP)materials have gained significant attention for their important optoelectronic application prospects.However,the fabrication strategy and underlying mechanism o...Stimulus-responsive room-temperature phosphorescence(RTP)materials have gained significant attention for their important optoelectronic application prospects.However,the fabrication strategy and underlying mechanism of stimulus-responsive RTP materials remain less explored.Herein,we present a reliable strategy for achieving pH-responsive RTP materials by integrating poly(vinyl alcohol)(PVA)with carboxylic acid or amino group functionalized terpyridine(Tpy)derivatives.The resulting Tpy derivativesbased RTP materials displayed reversible changes in emission color,intensity,and lifetime of both prompt and delayed emission.Notably,the RTP emission undergoes a significant diminish upon exposure to acid due to the protonation of Tpy units.Taking advantage of the decent RTP emission and pH-responsiveness of these RTP films,a spatial-time-resolved anti-counterfeiting application is demonstrated as a proof-ofconcept for largely enhancing the security level.This study not only provides new prospects for developing smart RTP materials but also promotes the advancement of optical anti-counterfeiting applications.展开更多
Quantitative oxygen detection,especially at low concentrations,holds significant importance in the realms of biology,complex environments,and chemical process engineering.Due to the high sensitivity and rapid response...Quantitative oxygen detection,especially at low concentrations,holds significant importance in the realms of biology,complex environments,and chemical process engineering.Due to the high sensitivity and rapid response of the triplet excitons of phosphorescence to oxygen,pure organic room-temperature phosphorescence(RTP)materials have garnered widespread attention in recent years for oxygen detection.However,simultaneously achieving ultralong phosphorescence at room temperature and quantitative oxygen detection from pure organic host-vip doped materials poses challenges.The d ensely packed materials may decrease non-radiative decay to increase the phosphorescence,but are unsuitable for oxygen diffusion in oxygen detection.Herein,the oxygen sensitivity of host-vip doped RTP materials using 4-bromo-N,N-bis(4-(tertbutyl)phenyl)aniline(TPABuBr)as the host and 6-bromo-2-butyl-1H-benzo[de]isoquinoline-1,3(2H)-dione(NIBr)as the vip was developed.The doped material exhibits fluorescence-phosphorescence dual-emission behavior at room temperature.The tert-butyl groups in TPABuBr facilitate appropriate intermolecular spacing in the crystal state,enhancing oxygen permeability.Therefore,oxygen penetration can quench the phosphorescence emission.The observed linear relationship between the phosphorescence intensity of the doped material and the oxygen volume fraction conforms to the Stern-Volmer equation,suggesting its potential for quantitative analysis of oxygen concentration.The calculated limit of detection is 0.015%(φ),enabling the analysis of oxygen with a volume fraction of less than 2.5%(φ).Moreover,the doped materials demonstrate rapid response and excellent photostability,indicating their potential utility as oxygen sensors.This study elucidates the design and characteristics of NIBr/TPABuBr doped materials,highlighting their potential application in oxygen concentration detection and offering insights for the design of oxygen sensors.展开更多
Photo-responsive room-temperature phosphorescent(RTP)materials have garnered significant interest due to the advantages of rapid response,spatiotemporal control,and contactless precision manipulation.However,the devel...Photo-responsive room-temperature phosphorescent(RTP)materials have garnered significant interest due to the advantages of rapid response,spatiotemporal control,and contactless precision manipulation.However,the development of such materials remains in its infancy,underscoring the importance of exploiting novel and efficient light-responsive RTP molecules.In this work,three phenothiazine derivatives of TPA-PTZ,TPA-2PTZ,and TPA-3PTZ were successfully synthesized via the Buchwald-Hartwig C—N coupling reaction.By embedding these molecules as RTP vips into polymethyl methacrylate(PMMA)matrix,photo-induced RTP properties were realized.Upon sustained UV irradiation,there was an enhancement of 19 times in the quantum yield to reach a value of 5.68%.Remarkably,these materials exhibit superior alongside robust light and thermal stability,maintaining high phosphorescence intensity even after prolonged UV exposure(irradiation for>200 s by a 365 nm UV lamp with the power of 500μW·cm-2)or at higher temperature up to 75℃.The outstanding properties of these photo-induced RTP materials make them promising candidates for applications in information encryption,anti-counterfeiting,and advanced optical materials.展开更多
La0.5Sm0.2Sr0.3MnO3/（Ag2O）x/2 （x = 0.00, 0.04, 0.08, 0.25, 0.30） samples were prepared by the solid-state reaction method, and their transport behaviors, transport mechanism, and magnetoresistance effect were stud...La0.5Sm0.2Sr0.3MnO3/（Ag2O）x/2 （x = 0.00, 0.04, 0.08, 0.25, 0.30） samples were prepared by the solid-state reaction method, and their transport behaviors, transport mechanism, and magnetoresistance effect were studied through the measurement and fitting of p-T curves. The results show that the element Ag takes part in reaction when the doping amount is small. Ag is mainly distributed at the grain boundary of the host material and is in metallic state when the doping amount is relatively large; then the system becomes a two-phase composite. A small amount of Ag doping can apparently increase grain-boundary magnetoresistance induced by the spin-dependent scattering. The resistivity of the sample doped with 30 mol% Ag is one order of magnitude smaller than that of low-doped samples, and its magnetoresistance in the magnetic field of 0.5 T and at 300 K is strengthened apparently reaching 9.4%, which is connected not only with the improvement of the grain-boundary structure of the host material but also with the decrease of material resistivity.展开更多
Near-equiaxed β grain was achieved in the near-α Ti60(Ti-5.7Al-4.0Sn-3.5Zr-0.4Mo-0.4Si-0.4Nb-1.0Ta-0.05C) titanium alloy via laser directed energy deposition(LDED). The microstructural evolution along the building d...Near-equiaxed β grain was achieved in the near-α Ti60(Ti-5.7Al-4.0Sn-3.5Zr-0.4Mo-0.4Si-0.4Nb-1.0Ta-0.05C) titanium alloy via laser directed energy deposition(LDED). The microstructural evolution along the building direction and the room-temperature tensile properties along the horizontal and vertical directions(building direction) were systematically studied through SEM and OM. EBSD and XRD were utilized to accurately demonstrate the texture of the α and β phases. The results showed that the α phase presented a low texture intensity, which was ascribed to the weak textured β grain with near-equiaxed morphology, since there are Burgers orientation relationships during the β →α transition. In addition, numerical simulation, combined with the CET curve of Ti60 alloy considering the effect of multi-composition,was utilized to elucidate the formation mechanism of the near-equiaxed β grains. Furthermore, according to the solidification theory, we proposed that the solidification temperature range ΔTfwas more accurate than the growth restriction factor Q in predicting the formation tendency of equiaxed β grain in different titanium alloys. Tensile results showed that the horizontal and vertical samples had similar strength,while the former exhibited larger elongation than the latter. The effect of the near-equiaxed β grain and the internal α phase on mechanical properties were revealed at last.展开更多
This work reports influence of two different electrolytes,carbonate ester and ether electrolytes,on the sulfur redox reactions in room-temperature Na-S batteries.Two sulfur cathodes with different S loading ratio and ...This work reports influence of two different electrolytes,carbonate ester and ether electrolytes,on the sulfur redox reactions in room-temperature Na-S batteries.Two sulfur cathodes with different S loading ratio and status are investigated.A sulfur-rich composite with most sulfur dispersed on the surface of a carbon host can realize a high loading ratio(72%S).In contrast,a confined sulfur sample can encapsulate S into the pores of the carbon host with a low loading ratio(44%S).In carbonate ester electrolyte,only the sulfur trapped in porous structures is active via‘solid-solid’behavior during cycling.The S cathode with high surface sulfur shows poor reversible capacity because of the severe side reactions between the surface polysulfides and the carbonate ester solvents.To improve the capacity of the sulfur-rich cathode,ether electrolyte with NaNO_(3) additive is explored to realize a‘solid-liquid’sulfur redox process and confine the shuttle effect of the dissolved polysulfides.As a result,the sulfur-rich cathode achieved high reversible capacity(483 mAh g^(−1)),corresponding to a specific energy of 362 Wh kg^(−1) after 200 cycles,shedding light on the use of ether electrolyte for high-loading sulfur cathode.展开更多
GeTe is an excellent mid-temperature thermoelectric material with high dimensionless figure of merit(ZT)values at temperatures over 600 K.Its near-room-temperature performance is less studied due to the intrinsic high...GeTe is an excellent mid-temperature thermoelectric material with high dimensionless figure of merit(ZT)values at temperatures over 600 K.Its near-room-temperature performance is less studied due to the intrinsic high carrier concentration.Here,we successfully enhance the Seebeck coefficient of GeTe from~30 to 220μV·K^(−1) at 300 K,which is achieved by AgInSe2 alloying and Bi doping.It is demonstrated that Bi doping helps to optimize the Seebeck coefficient without deteriorating the intrinsic electrical transport properties of the matrix.A high room-temperature power factor(PF)of~11μW·cm^(−1)·K^(−2) is achieved for a wide range of Bi-doped samples.The simultaneously introduced abundant point defects cause mass and strain fluctuations,which decrease the lattice thermal conductivity(κ_(L))to a low value of 0.6 W·m^(−1)·K^(−1) at 300 K.Due to the synergetic effects of Bi doping in AgInSe2-alloyed GeTe,a high room-temperature ZT value of 0.46 is obtained together with a high ZT value of 1.1 at 523 K.展开更多
Low-temperature assembly of MXene nanosheets into three-dimensional(3D) robust aerogels addresses the crucial stability concern of the nano-building blocks during the fabrication process,which is of key importance for...Low-temperature assembly of MXene nanosheets into three-dimensional(3D) robust aerogels addresses the crucial stability concern of the nano-building blocks during the fabrication process,which is of key importance for transforming the fascinating properties at the nanoscale into the macroscopic scale for practical applications.Herein,suitable cross-linking agents(amino-propyltriethoxysilane,Mn^(2+),Fe^(2+),Zn^(2+),and Co^(2+)) as interfacial mediators to engineer the interlayer interactions are reported to realize the graphene oxide(GO)-assisted assembly of Ti_(3)C_(2)T_(x) MXene aerogel at room temperature.This elaborate aerogel construction not only suppresses the oxidation degradation of Ti_(3)C_(2)T_(x) but also generates porous aerogels with a high Ti_(3)C_(2)T_(x) content(87 wt%) and robustness,thereby guaranteeing the functional accessibility of Ti_(3)C_(2)T_(x) nanosheets and operational reliability as integrated functional materials.In combination with a further sulfur modification,the Ti_(3)C_(2)T_(x) aerogel electrode shows promising electrochemical performances as the freestanding anode for sodium-ion storage.Even at an ultrahigh loading mass of 12.3 mg cm^(-2),a pronounced areal capacity of 1.26 mAh cm^(-2) at a current density of 0.1 A g^(-1) has been achieved,which is of practical significance.This work conceptually suggests a new way to exert the utmost surface functionalities of MXenes in 3D monolithic form and can be an inspiring scaffold to promote the application of MXenes in different areas.展开更多
Room-temperature phosphorescence（RTP） materials have attracted great attention due to their involvement of excited triplet states and comparatively long decay lifetimes.In this short review,recent progress on enhanc...Room-temperature phosphorescence（RTP） materials have attracted great attention due to their involvement of excited triplet states and comparatively long decay lifetimes.In this short review,recent progress on enhancement of RTP from purely organic materials is summarized.According to the mechanism of phosphorescence emission,two principles are discussed to construct efficient RTP materials：one is promoting intersystem crossing（ISC） efficiency by using aromatic carbonyl,heavyatom,or/and heterocycle/heteroatom containing compounds;the other is suppressing intramolecular motion and intermolecular collision which can quench excited triplet states,including embedding phosphors into polymers and packing them tightly in crystals.With aforementioned strategies,RTP from purely organic materials was achieved both in fluid and rigid media.展开更多
Carbon dots(CDs) with fluorescence(FL) and room-temperature phosphorescence(RTP) optical properties have attracted dramatically growing interest in anti-counterfeiting application. Herein, color-tunable and stable FL ...Carbon dots(CDs) with fluorescence(FL) and room-temperature phosphorescence(RTP) optical properties have attracted dramatically growing interest in anti-counterfeiting application. Herein, color-tunable and stable FL and ultralong RTP(to naked eyes ~14 s) are successfully achieved in CDs system. Encoding information and patterns fabricated by directly screen-printing method are invisible to eyes under natural light. Interestingly, clear and multicolor patterns with tunable FL and RTP emissions are identified under the 365 nm, 395 nm and 465 nm excitation and removal of them, indicating potential application of carbon dots with different FL and RTP outputs in the high-level photonic anti-counterfeiting field.展开更多
Synthesis and applications of three-dimensional(3 D)porous graphene frameworks(GFs)have attracted extensive interest owing to their intriguing advantages of high specific surface area,enriched porosity,excellent elect...Synthesis and applications of three-dimensional(3 D)porous graphene frameworks(GFs)have attracted extensive interest owing to their intriguing advantages of high specific surface area,enriched porosity,excellent electrical conductivity,exceptional compressibility and processability.However,it is still challenging for economically viable,fast and scalable assembly of 3 D GFs at room-temperature.Herein,we reported a one-step scalable strategy for fast self-assembly of graphene oxide into 3 D macroscopically porous GFs,with assistance of polyoxometalates(POM)as functional cross-linker and hydrazine hydrate as reductant at room-temperature.The resulting 3 D interconnected macroporous POM-GFs uniformly decorated with ultrasmall POM nanoclusters were directly processed into binder-/additive-free film compact electrodes(1.68 g cm^(-3))with highly aligned,layer-stacked structure and electrically conductivity(622 S m-1)for high-performance supercapacitors,showing an impressive gravimetric capacitance of205 F g-1,volumetric capacitance of 334 F cm^(-3) at 1 mV s^(-1),and remarkable cycling stability with capacitance retention of 83%after 10,000 cycles,outperforming the most reported GFs.Further,the solid-state supercapacitors offered excellent gravimetric capacitance of 157 F g-1 exceptionally volumetric capacitance of 115 F cm^(-3) at 2 mV s^(-1) based on single electrode,and volumetric energy density of2.6 mWh cm^(-3).Therefore,this work will open novel opportunities to room-temperature fast assembly of 3 D porous graphene architectures for high-energy-density supercapacitors.展开更多
Pure organic room-temperature phosphorescence (RTP) materials have been attracting much attention recently. Herein, we report a facile approach combining heavy atom effect and external solvent stimuli to realize RTP. ...Pure organic room-temperature phosphorescence (RTP) materials have been attracting much attention recently. Herein, we report a facile approach combining heavy atom effect and external solvent stimuli to realize RTP. N-Allylquinolinium bromide under 365 nm UV exhibited intense green RTP emission with response upon adding chloroform. This interesting phenomenon endowed N-allylquinolinium bromide great potential as an anti-counterfeiting material.展开更多
Stabilizing triplet excited states is important for room temperature phosphorescence(RTP)materials to achieve multifunctional applications in humid environment.However,due to the lack of preparation strategies,the rea...Stabilizing triplet excited states is important for room temperature phosphorescence(RTP)materials to achieve multifunctional applications in humid environment.However,due to the lack of preparation strategies,the realization of RTP materials in water still faces challenges.Herein,a new design strategy was presented to achieve RTP in water by confining carbonized polymer dots(CPDs)in amino functional mesoporous silica(MSNs-NH_(2)).The as-prepared MSNs-CPDs aqueous dispersion exhibited blue afterglow,lasting more than 3 s to naked eyes.The triplet excited states were protected from non-radiative deactivation by the double-confinement effect including covalent bonding fixation and mesoporous structure confinement.The MSNs-CPDs inherited the structure of MSNs-NH_(2),so the stability of morphology and properties were superior to CPDs and even most of silica-based CPDs RTP materials.A water-related encryption technique demonstrated the promising application of MSNs-CPDs as smart materials in the field of information security.Besides,the possibility of potential application in ion detection was also explored.展开更多
Metal oxide semiconductors(MOS)-reduced graphene oxide(rGO)nanocomposites have attracted great attention for room-tempe rature gas sensing applications.The development of novel sensing materials is the key issue for t...Metal oxide semiconductors(MOS)-reduced graphene oxide(rGO)nanocomposites have attracted great attention for room-tempe rature gas sensing applications.The development of novel sensing materials is the key issue for the effective detection of ammoniagas at room temperature.In the present work,the novel reduced graphene oxide(rGO)-In2 O3 nanocubes hybrid materials have been prepared via a simple electrostatic self-assembly strategy.Characterization re sults exhibit that the intimate interfacial contact between In2 O3 nanocubes and the rGO sheets are achieved.Particularly,the as-prepared rGO/In2 O3 nanocomposites displayed high sensitivity,fast response and excellent selectivity towards ammonia(NH3)at room-temperature,which clearly uncovers the merit of structural design and rational integration with rGO sheets.The superior gas sensing performance of the rGO/In2 O3 nanocomposites can be attributed to the synergetic effects of rGO sheets and porous In2 O3 nanocubes.The reported synthesis offers a general approach to rGO/MOS-based semiconductor composites for room-temperature gas sensing applications.展开更多
Pure organic room-temperature phosphorescence(RTP)materials have attracted wide attention owing to their excellent luminescent properties and great potential in various applications.In this work,iminostilbene and its ...Pure organic room-temperature phosphorescence(RTP)materials have attracted wide attention owing to their excellent luminescent properties and great potential in various applications.In this work,iminostilbene and its analogues are applied to realize RTP emission by copolymerizing with acrylamide.It can be concluded that the growth of alkane chain in monomers can enhance the lifetime and photoluminescence quantum yield of RTP emission,and polymers with the larger conjugated structure of the monomer show a longer RTP emission wavelength.This work provides a series of new pure organic RTP materials and might provide new thoughts for designing more advanced and superior RTP materials.展开更多
Benzoin condensation promoted efficiently in three imidazolium based room tempera- ture ionic liquids [bmim]Br, [bmim]BF4 and [Bnmim]BF4 is reported for the first time. Benzoins were obtained in up to 91% yield within...Benzoin condensation promoted efficiently in three imidazolium based room tempera- ture ionic liquids [bmim]Br, [bmim]BF4 and [Bnmim]BF4 is reported for the first time. Benzoins were obtained in up to 91% yield within less than 30 min under mild conditions.展开更多
A novel green nanophosphor CaHPO4：Tb3＋ was synthesized via a room-temperatureco-precipitation route driven by ethanol solvent. X-ray powder diffraction （XRD）, scanningelectron microscopy （SEM） and photoluminesce...A novel green nanophosphor CaHPO4：Tb3＋ was synthesized via a room-temperatureco-precipitation route driven by ethanol solvent. X-ray powder diffraction （XRD）, scanningelectron microscopy （SEM） and photoluminescence spectroscopy （PL） techniques were utilizedto characterize the structure, morphology and fluorescence performance of the obtained powders.The results demonstrated that the prepared samples were well crystallized with triclinic phaseCaHPO4 structure and particle-like morphology. Photoluminescence measurements indicated thatCaHPOa：Tb3＋ had a strong absorption peak at 370 nm and exhibited characteristic emissions withseveral sharp peaks corresponding to the transitions 5D4-7FJ （jr = 6-3） of Tb3＋. Moreover, theluminescence optimum concentration for CaHPO4：Tb3＋ was determined to be 11 mol%, whichmight be a promising green-emitting ohosohor for display applications.展开更多
基金National Natural Science Foundation of China(No.22475241)Guangdong Basic and Applied Basic Research Foundation(Nos.2022A1515010826 and 2023A1515012696)the Fundamental Research Funds for the Central Universities(Nos.17lgjc03 and 18lgpy04).
文摘Room-temperature phosphorescence(RTP)materials exhibiting long emission lifetimes have gained increasing attention owing to their potential applications in encryption,anti-counterfeiting,and sensing.However,most polymers exhibit a short RTP lifetime(<1 s)because of their unstable triplet excitons.Herein,a new strategy of polymer chain stabilized phosphorescence(PCSP),which yields a new kind of RTP polymers with an ultralong lifetime and a sensitive oxygen response,has been reported.The rigid polymer chains of poly(methyl mathacrylate)(PMMA)immobilize the emitter molecules through multiple interactions between them,giving rise to efficient RTP.Meanwhile,the loosely-packed amorphous polymer chains allow oxygen to diffuse inside,endowing the doped polymers with oxygen sensitivity.Flexible and transparent polymer films exhibited an impressive ultralong RTP lifetime of 2.57 s at room temperature in vacuum,which was among the best performance of PMMA.Intriguingly,their RTP was rapidly quenched in the presence of oxygen.Furthermore,RTP microparticles with a diameter of 1.63μm were synthesized using in situ dispersion polymerization technique.Finally,oxygen sensors for quick,visual,and quantitative oxygen detection were developed based on the RTP microparticles through phosphorescence lifetime and image analysis.With distinctive advantages such as an ultralong lifetime,oxygen sensitivity,ease of fabrication,and cost-effectiveness,PCSP opens a new avenue to sensitive materials for oxygen detection.
基金supported by the National Natural Science Foundation of China(No.22005201)the Young Scholars Science Foundation of Lanzhou Jiaotong University(No.2022023)the Fundamental Research Funds for the Central Universities,and the Youth Science and Technology Foundation of Gansu Province(Nos.22JR5RA541 and 22JR5RA374).
文摘Room-temperature sodium-sulfur(RT Na-S)batteries have been regarded as promising energy storage technologies in grid-scale stationary energy storage systems due to their low cost,natural abundance,and high-energy density.However,the practical application of RT Na-S batteries is hindered by low reversible capacity and unsatisfying long-cycling performance arising from the severe shuttle effect and sluggish S redox kinetics.This review provides an overview of recent efforts for the optimization strategies of the electronic structure of catalysts via catalyst engineering to enhance the adsorption and catalytic activity toward soluble long-chain sodium polysulfides(NaPSs).Finally,the current challenges and prospects for further optimization strategies of catalysts,understanding catalysis and structural evolution mechanism,and achieving practical applications are highlighted to meet the commercial requirements of RT Na-S batteries.
基金National Natural Science Foundation of China(No.52090041).
文摘Reducing the hot working temperature and high-temperature deformation resistance of titanium alloy to improve hot rolling and hot extrusion workability of products with thin walls and complex section shapes has always been an important topic in the field of titanium alloy processing.This paper proposed a strategy of adding Mo and Fe elements to simultaneously reduce the hot working temperature and high-temperature deformation resistance of Ti-6Al-4V alloy.The effects of Mo and Fe contents on the mi-crostructure,β transus temperature(Tp),and high-temperature flow stress(HFS)of Ti-6Al-4V-xMo-xFe(x=0-5)alloys were investigated.The results showed that adding Mo and Fe can substantially reduce the Tp and HFS of the alloy,and greatly improve its room-temperature strength.Compared with com-mercial Ti-6Al-4V samples,the T_(β) of Ti-6Al-4V-2Mo-2Fe and Ti-6Al-4V-3Mo-3Fe samples was decreased by 68-98 ℃,and the HFS at 800-900 ℃ was decreased by 37.8%-46.0%.Compared with hot-rolled Ti-6Al-4V samples,the room-temperature tensile strength of hot-rolled Ti-6Al-4V-2Mo-2Fe samples was increased by about 30%,while the elongation hardly decreased.The increased strength was mainly at-tributed to fine grain strengthening and solid solution strengthening.The hot workability and room-temperature strength of Ti-6Al-4V alloy can be significantly improved by adding 2-3 wt.%Mo and Fe simultaneously.
基金financially supported by the National Natural Science Foundation of China(No.22205249)Zhejiang Provincial Natural Science Foundation of China(No.LQ23B040002)+2 种基金the Sino-German Mobility Program(No.M-0424)Ningbo International Cooperation Project(No.2023H019)China Postdoctoral Science Foundation(Nos.2021TQ0341,2022M723252)。
文摘Stimulus-responsive room-temperature phosphorescence(RTP)materials have gained significant attention for their important optoelectronic application prospects.However,the fabrication strategy and underlying mechanism of stimulus-responsive RTP materials remain less explored.Herein,we present a reliable strategy for achieving pH-responsive RTP materials by integrating poly(vinyl alcohol)(PVA)with carboxylic acid or amino group functionalized terpyridine(Tpy)derivatives.The resulting Tpy derivativesbased RTP materials displayed reversible changes in emission color,intensity,and lifetime of both prompt and delayed emission.Notably,the RTP emission undergoes a significant diminish upon exposure to acid due to the protonation of Tpy units.Taking advantage of the decent RTP emission and pH-responsiveness of these RTP films,a spatial-time-resolved anti-counterfeiting application is demonstrated as a proof-ofconcept for largely enhancing the security level.This study not only provides new prospects for developing smart RTP materials but also promotes the advancement of optical anti-counterfeiting applications.
文摘Quantitative oxygen detection,especially at low concentrations,holds significant importance in the realms of biology,complex environments,and chemical process engineering.Due to the high sensitivity and rapid response of the triplet excitons of phosphorescence to oxygen,pure organic room-temperature phosphorescence(RTP)materials have garnered widespread attention in recent years for oxygen detection.However,simultaneously achieving ultralong phosphorescence at room temperature and quantitative oxygen detection from pure organic host-vip doped materials poses challenges.The d ensely packed materials may decrease non-radiative decay to increase the phosphorescence,but are unsuitable for oxygen diffusion in oxygen detection.Herein,the oxygen sensitivity of host-vip doped RTP materials using 4-bromo-N,N-bis(4-(tertbutyl)phenyl)aniline(TPABuBr)as the host and 6-bromo-2-butyl-1H-benzo[de]isoquinoline-1,3(2H)-dione(NIBr)as the vip was developed.The doped material exhibits fluorescence-phosphorescence dual-emission behavior at room temperature.The tert-butyl groups in TPABuBr facilitate appropriate intermolecular spacing in the crystal state,enhancing oxygen permeability.Therefore,oxygen penetration can quench the phosphorescence emission.The observed linear relationship between the phosphorescence intensity of the doped material and the oxygen volume fraction conforms to the Stern-Volmer equation,suggesting its potential for quantitative analysis of oxygen concentration.The calculated limit of detection is 0.015%(φ),enabling the analysis of oxygen with a volume fraction of less than 2.5%(φ).Moreover,the doped materials demonstrate rapid response and excellent photostability,indicating their potential utility as oxygen sensors.This study elucidates the design and characteristics of NIBr/TPABuBr doped materials,highlighting their potential application in oxygen concentration detection and offering insights for the design of oxygen sensors.
文摘Photo-responsive room-temperature phosphorescent(RTP)materials have garnered significant interest due to the advantages of rapid response,spatiotemporal control,and contactless precision manipulation.However,the development of such materials remains in its infancy,underscoring the importance of exploiting novel and efficient light-responsive RTP molecules.In this work,three phenothiazine derivatives of TPA-PTZ,TPA-2PTZ,and TPA-3PTZ were successfully synthesized via the Buchwald-Hartwig C—N coupling reaction.By embedding these molecules as RTP vips into polymethyl methacrylate(PMMA)matrix,photo-induced RTP properties were realized.Upon sustained UV irradiation,there was an enhancement of 19 times in the quantum yield to reach a value of 5.68%.Remarkably,these materials exhibit superior alongside robust light and thermal stability,maintaining high phosphorescence intensity even after prolonged UV exposure(irradiation for>200 s by a 365 nm UV lamp with the power of 500μW·cm-2)or at higher temperature up to 75℃.The outstanding properties of these photo-induced RTP materials make them promising candidates for applications in information encryption,anti-counterfeiting,and advanced optical materials.
基金supported by the Key Program of the National Natural Science Foundation of China (No. 19934003)the Grand Program of Natural Science Research of Anhui Education Department (No. ZD2007003-1)the Natural Science Research Program of Universities and Colleges of Anhui Province, China (Nos. KJ2008A19ZC, KJ2009B281Z, and KJ2009A053Z)
文摘La0.5Sm0.2Sr0.3MnO3/（Ag2O）x/2 （x = 0.00, 0.04, 0.08, 0.25, 0.30） samples were prepared by the solid-state reaction method, and their transport behaviors, transport mechanism, and magnetoresistance effect were studied through the measurement and fitting of p-T curves. The results show that the element Ag takes part in reaction when the doping amount is small. Ag is mainly distributed at the grain boundary of the host material and is in metallic state when the doping amount is relatively large; then the system becomes a two-phase composite. A small amount of Ag doping can apparently increase grain-boundary magnetoresistance induced by the spin-dependent scattering. The resistivity of the sample doped with 30 mol% Ag is one order of magnitude smaller than that of low-doped samples, and its magnetoresistance in the magnetic field of 0.5 T and at 300 K is strengthened apparently reaching 9.4%, which is connected not only with the improvement of the grain-boundary structure of the host material but also with the decrease of material resistivity.
基金supported by the National Key Technologies R&D Program (Nos. 2016YFB1100102, 2018YFB1106003).
文摘Near-equiaxed β grain was achieved in the near-α Ti60(Ti-5.7Al-4.0Sn-3.5Zr-0.4Mo-0.4Si-0.4Nb-1.0Ta-0.05C) titanium alloy via laser directed energy deposition(LDED). The microstructural evolution along the building direction and the room-temperature tensile properties along the horizontal and vertical directions(building direction) were systematically studied through SEM and OM. EBSD and XRD were utilized to accurately demonstrate the texture of the α and β phases. The results showed that the α phase presented a low texture intensity, which was ascribed to the weak textured β grain with near-equiaxed morphology, since there are Burgers orientation relationships during the β →α transition. In addition, numerical simulation, combined with the CET curve of Ti60 alloy considering the effect of multi-composition,was utilized to elucidate the formation mechanism of the near-equiaxed β grains. Furthermore, according to the solidification theory, we proposed that the solidification temperature range ΔTfwas more accurate than the growth restriction factor Q in predicting the formation tendency of equiaxed β grain in different titanium alloys. Tensile results showed that the horizontal and vertical samples had similar strength,while the former exhibited larger elongation than the latter. The effect of the near-equiaxed β grain and the internal α phase on mechanical properties were revealed at last.
基金This research was supported by the Australian Research Council(ARC)(DE170100928,DP170101467)an Australian Renewable Energy Agency(ARENA)Project(G00849).The authors acknowledge the use of the facilities at the UOW Electron Microscopy Center(LE0882813 and LE0237478)and Dr.Tania Silver for critical reading of the manuscript.
文摘This work reports influence of two different electrolytes,carbonate ester and ether electrolytes,on the sulfur redox reactions in room-temperature Na-S batteries.Two sulfur cathodes with different S loading ratio and status are investigated.A sulfur-rich composite with most sulfur dispersed on the surface of a carbon host can realize a high loading ratio(72%S).In contrast,a confined sulfur sample can encapsulate S into the pores of the carbon host with a low loading ratio(44%S).In carbonate ester electrolyte,only the sulfur trapped in porous structures is active via‘solid-solid’behavior during cycling.The S cathode with high surface sulfur shows poor reversible capacity because of the severe side reactions between the surface polysulfides and the carbonate ester solvents.To improve the capacity of the sulfur-rich cathode,ether electrolyte with NaNO_(3) additive is explored to realize a‘solid-liquid’sulfur redox process and confine the shuttle effect of the dissolved polysulfides.As a result,the sulfur-rich cathode achieved high reversible capacity(483 mAh g^(−1)),corresponding to a specific energy of 362 Wh kg^(−1) after 200 cycles,shedding light on the use of ether electrolyte for high-loading sulfur cathode.
基金financially supported by the Singapore MOE AcRF Tier 2(Nos.2018-T2-1-010)Singapore A*STAR project(A19D9a0096 and SC25/21-102419)+3 种基金Singapore MOE Tier 1 RG128/21.Q.Zhu and A.Suwardi acknowledge Agency for Science,Technology and Research(A*STAR)Singapore Career Development Fund(CDF)(No.C210112022)the Sustainable Hybrid Lighting System for Controlled Environment Agriculture Program(No.A19D9a0096)support from S&T Program of Hebei(No.206Z4403G)。
文摘GeTe is an excellent mid-temperature thermoelectric material with high dimensionless figure of merit(ZT)values at temperatures over 600 K.Its near-room-temperature performance is less studied due to the intrinsic high carrier concentration.Here,we successfully enhance the Seebeck coefficient of GeTe from~30 to 220μV·K^(−1) at 300 K,which is achieved by AgInSe2 alloying and Bi doping.It is demonstrated that Bi doping helps to optimize the Seebeck coefficient without deteriorating the intrinsic electrical transport properties of the matrix.A high room-temperature power factor(PF)of~11μW·cm^(−1)·K^(−2) is achieved for a wide range of Bi-doped samples.The simultaneously introduced abundant point defects cause mass and strain fluctuations,which decrease the lattice thermal conductivity(κ_(L))to a low value of 0.6 W·m^(−1)·K^(−1) at 300 K.Due to the synergetic effects of Bi doping in AgInSe2-alloyed GeTe,a high room-temperature ZT value of 0.46 is obtained together with a high ZT value of 1.1 at 523 K.
基金This work was supported by the National Natural Science Foundation of China(52071137,51977071,51802040,and 21802020)the Science and Technology Innovation Program of Hunan Province(2021RC3066 and 2021RC3067)+1 种基金the Natural Science Foundation of Hunan Province(2020JJ3004 and 2020JJ4192)N.Zhang and X.Xie also acknowledge the financial support of the Fundamental Research Funds for the Central Universities.
文摘Low-temperature assembly of MXene nanosheets into three-dimensional(3D) robust aerogels addresses the crucial stability concern of the nano-building blocks during the fabrication process,which is of key importance for transforming the fascinating properties at the nanoscale into the macroscopic scale for practical applications.Herein,suitable cross-linking agents(amino-propyltriethoxysilane,Mn^(2+),Fe^(2+),Zn^(2+),and Co^(2+)) as interfacial mediators to engineer the interlayer interactions are reported to realize the graphene oxide(GO)-assisted assembly of Ti_(3)C_(2)T_(x) MXene aerogel at room temperature.This elaborate aerogel construction not only suppresses the oxidation degradation of Ti_(3)C_(2)T_(x) but also generates porous aerogels with a high Ti_(3)C_(2)T_(x) content(87 wt%) and robustness,thereby guaranteeing the functional accessibility of Ti_(3)C_(2)T_(x) nanosheets and operational reliability as integrated functional materials.In combination with a further sulfur modification,the Ti_(3)C_(2)T_(x) aerogel electrode shows promising electrochemical performances as the freestanding anode for sodium-ion storage.Even at an ultrahigh loading mass of 12.3 mg cm^(-2),a pronounced areal capacity of 1.26 mAh cm^(-2) at a current density of 0.1 A g^(-1) has been achieved,which is of practical significance.This work conceptually suggests a new way to exert the utmost surface functionalities of MXenes in 3D monolithic form and can be an inspiring scaffold to promote the application of MXenes in different areas.
基金the financial support from The National Basic Research Program of China(No.2014CB643802)Ministry of Science and Technology(No.2016YFB0401001)the State Key Laboratory of Advanced Technologies for Comprehensive Utilization of Platinum Metals
文摘Room-temperature phosphorescence（RTP） materials have attracted great attention due to their involvement of excited triplet states and comparatively long decay lifetimes.In this short review,recent progress on enhancement of RTP from purely organic materials is summarized.According to the mechanism of phosphorescence emission,two principles are discussed to construct efficient RTP materials：one is promoting intersystem crossing（ISC） efficiency by using aromatic carbonyl,heavyatom,or/and heterocycle/heteroatom containing compounds;the other is suppressing intramolecular motion and intermolecular collision which can quench excited triplet states,including embedding phosphors into polymers and packing them tightly in crystals.With aforementioned strategies,RTP from purely organic materials was achieved both in fluid and rigid media.
基金supported by the Natural Science Foundation of Hubei Province for Distinguished Young Scholars (No. 2019CFA056)the Fundamental Research Funds for the Central Universities and Wuhan University and the Fundamental Research Funds for the Central Universities (No. 2042021kf0226)。
文摘Carbon dots(CDs) with fluorescence(FL) and room-temperature phosphorescence(RTP) optical properties have attracted dramatically growing interest in anti-counterfeiting application. Herein, color-tunable and stable FL and ultralong RTP(to naked eyes ~14 s) are successfully achieved in CDs system. Encoding information and patterns fabricated by directly screen-printing method are invisible to eyes under natural light. Interestingly, clear and multicolor patterns with tunable FL and RTP emissions are identified under the 365 nm, 395 nm and 465 nm excitation and removal of them, indicating potential application of carbon dots with different FL and RTP outputs in the high-level photonic anti-counterfeiting field.
基金financially supported by the National Key R@D Program of China(Grants 2016YFB0100100,2016YFA0200200)the National Natural Science Foundation of China(Grant Nos.51872283,22075279,21805273,22005297,22005298)+7 种基金the Liao Ning Revitalization Talents Program(Grant XLYC1807153)the Natural Science Foundation of Liaoning ProvinceJoint Research Fund Liaoning-Shenyang National Laboratory for Materials Science(Grant 20180510038)Dalian Innovation Support Plan for High Level Talents(2019RT09)the Dalian National Laboratory For Clean Energy(DNL),CASDNL Cooperation Fund,CAS(DNL180310,DNL180308,DNL201912,and DNL201915)DICP(DICP ZZBS201708,DICP ZZBS201802,DICP I2020032)the China Postdoctoral Science Foundation(2019M661141,2020M680995)。
文摘Synthesis and applications of three-dimensional(3 D)porous graphene frameworks(GFs)have attracted extensive interest owing to their intriguing advantages of high specific surface area,enriched porosity,excellent electrical conductivity,exceptional compressibility and processability.However,it is still challenging for economically viable,fast and scalable assembly of 3 D GFs at room-temperature.Herein,we reported a one-step scalable strategy for fast self-assembly of graphene oxide into 3 D macroscopically porous GFs,with assistance of polyoxometalates(POM)as functional cross-linker and hydrazine hydrate as reductant at room-temperature.The resulting 3 D interconnected macroporous POM-GFs uniformly decorated with ultrasmall POM nanoclusters were directly processed into binder-/additive-free film compact electrodes(1.68 g cm^(-3))with highly aligned,layer-stacked structure and electrically conductivity(622 S m-1)for high-performance supercapacitors,showing an impressive gravimetric capacitance of205 F g-1,volumetric capacitance of 334 F cm^(-3) at 1 mV s^(-1),and remarkable cycling stability with capacitance retention of 83%after 10,000 cycles,outperforming the most reported GFs.Further,the solid-state supercapacitors offered excellent gravimetric capacitance of 157 F g-1 exceptionally volumetric capacitance of 115 F cm^(-3) at 2 mV s^(-1) based on single electrode,and volumetric energy density of2.6 mWh cm^(-3).Therefore,this work will open novel opportunities to room-temperature fast assembly of 3 D porous graphene architectures for high-energy-density supercapacitors.
基金the financial support from the Instrument Developing Project of the Chinese Academy of Sciences (No. YJKYYQ20170009)the National Natural Science Foundation of China(NSFC Nos. 21722603 and 21871083)the Innovation Program of Shanghai Municipal Education Commission
文摘Pure organic room-temperature phosphorescence (RTP) materials have been attracting much attention recently. Herein, we report a facile approach combining heavy atom effect and external solvent stimuli to realize RTP. N-Allylquinolinium bromide under 365 nm UV exhibited intense green RTP emission with response upon adding chloroform. This interesting phenomenon endowed N-allylquinolinium bromide great potential as an anti-counterfeiting material.
基金financially supported by the National Natural Science Foundation of China (NSFC, No. 22035001)
文摘Stabilizing triplet excited states is important for room temperature phosphorescence(RTP)materials to achieve multifunctional applications in humid environment.However,due to the lack of preparation strategies,the realization of RTP materials in water still faces challenges.Herein,a new design strategy was presented to achieve RTP in water by confining carbonized polymer dots(CPDs)in amino functional mesoporous silica(MSNs-NH_(2)).The as-prepared MSNs-CPDs aqueous dispersion exhibited blue afterglow,lasting more than 3 s to naked eyes.The triplet excited states were protected from non-radiative deactivation by the double-confinement effect including covalent bonding fixation and mesoporous structure confinement.The MSNs-CPDs inherited the structure of MSNs-NH_(2),so the stability of morphology and properties were superior to CPDs and even most of silica-based CPDs RTP materials.A water-related encryption technique demonstrated the promising application of MSNs-CPDs as smart materials in the field of information security.Besides,the possibility of potential application in ion detection was also explored.
基金supported by the National Natural Science Foundation of China(No.61102006)Natural Science Foundation of Shandong Province,China(Nos.ZR2015EM019 and ZR2014EL006)。
文摘Metal oxide semiconductors(MOS)-reduced graphene oxide(rGO)nanocomposites have attracted great attention for room-tempe rature gas sensing applications.The development of novel sensing materials is the key issue for the effective detection of ammoniagas at room temperature.In the present work,the novel reduced graphene oxide(rGO)-In2 O3 nanocubes hybrid materials have been prepared via a simple electrostatic self-assembly strategy.Characterization re sults exhibit that the intimate interfacial contact between In2 O3 nanocubes and the rGO sheets are achieved.Particularly,the as-prepared rGO/In2 O3 nanocomposites displayed high sensitivity,fast response and excellent selectivity towards ammonia(NH3)at room-temperature,which clearly uncovers the merit of structural design and rational integration with rGO sheets.The superior gas sensing performance of the rGO/In2 O3 nanocomposites can be attributed to the synergetic effects of rGO sheets and porous In2 O3 nanocubes.The reported synthesis offers a general approach to rGO/MOS-based semiconductor composites for room-temperature gas sensing applications.
基金the financial support from the National Natural Science Foundation of China (Nos. 21788102, 22125803, 22020102006 and 21871083)Program of Shanghai Academic/Technology Research Leader (No. 20XD1421300)+2 种基金‘Shu Guang’ Project supported by Shanghai Municipal Education Commission and Shanghai Education Development Foundation (No. 19SG26)the Innovation Program of Shanghai Municipal Education Commission (No. 2017–01–07–00–02-E00010)the Fundamental Research Funds for the Central Universities.
文摘Pure organic room-temperature phosphorescence(RTP)materials have attracted wide attention owing to their excellent luminescent properties and great potential in various applications.In this work,iminostilbene and its analogues are applied to realize RTP emission by copolymerizing with acrylamide.It can be concluded that the growth of alkane chain in monomers can enhance the lifetime and photoluminescence quantum yield of RTP emission,and polymers with the larger conjugated structure of the monomer show a longer RTP emission wavelength.This work provides a series of new pure organic RTP materials and might provide new thoughts for designing more advanced and superior RTP materials.
基金We thank the financial support from the National Natural Science Foundation of China.(No.20172038)
文摘Benzoin condensation promoted efficiently in three imidazolium based room tempera- ture ionic liquids [bmim]Br, [bmim]BF4 and [Bnmim]BF4 is reported for the first time. Benzoins were obtained in up to 91% yield within less than 30 min under mild conditions.
基金supported by the National Natural Science Foundation of China(21663021)China Postdoctoral Science Foundation(2015M571977)+1 种基金the Natural Science Foundation of Jiangxi Province(20161BAB213058)the Natural Science Key Project of Jiangxi Province(2017ACB20040)
文摘A novel green nanophosphor CaHPO4：Tb3＋ was synthesized via a room-temperatureco-precipitation route driven by ethanol solvent. X-ray powder diffraction （XRD）, scanningelectron microscopy （SEM） and photoluminescence spectroscopy （PL） techniques were utilizedto characterize the structure, morphology and fluorescence performance of the obtained powders.The results demonstrated that the prepared samples were well crystallized with triclinic phaseCaHPO4 structure and particle-like morphology. Photoluminescence measurements indicated thatCaHPOa：Tb3＋ had a strong absorption peak at 370 nm and exhibited characteristic emissions withseveral sharp peaks corresponding to the transitions 5D4-7FJ （jr = 6-3） of Tb3＋. Moreover, theluminescence optimum concentration for CaHPO4：Tb3＋ was determined to be 11 mol%, whichmight be a promising green-emitting ohosohor for display applications.
