Circularly polarized luminescence(CPL)and two-photon absorption(TPA)materials have garnered considerable attentions due to their minimal energy loss and superior optical penetration[1,2].However,the current challenge ...Circularly polarized luminescence(CPL)and two-photon absorption(TPA)materials have garnered considerable attentions due to their minimal energy loss and superior optical penetration[1,2].However,the current challenge lies in the absence of well-developed strategies for designing materials that combine these two exceptional optical properties.展开更多
Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level st...Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level stemming from the doped rare earth ion or intrinsic defects to the electronic structure of the host,and therefore thermoluminescence measurement becomes a radical technology in studying trap depth,which is one of the significant parameters that determine the properties of persistent luminescence and photostimulated luminescence.However,the results of trap depth obtained by different thermoluminescence methods are quite different so that they are not comparable.Herein,we analyzed different thermoluminescence methods,selected and improved the traditional peak position method of T_(m)/500 to be E=(-0.94Inβ+30.09)kT_(m).Only the experimental heating rate(β)is needed additionally,but the accuracy is improved greatly in most cases.This convenient and accurate method will accelerate the discovery of novel rare earth-doped materials.展开更多
Persistent luminescence is a unique optical phenomenon that continues to emit light for minutes or even hours after the excitation stops,which can significantly enhance the sensitivity and signal-to-noise ratio of ima...Persistent luminescence is a unique optical phenomenon that continues to emit light for minutes or even hours after the excitation stops,which can significantly enhance the sensitivity and signal-to-noise ratio of imaging[1].Among numerous persistent luminescence materials,lanthanide-doped fluoride nanoparticles have shown tunable persistent luminescence across the UV-vis-NIR spectrum(200-1700 nm)under X-ray excitation and adjustable size,promising significant applications in deep-tissue imaging[2,3],security encryption,and data storage[4].In particular,those exhibiting NIR-II luminescence(1000-1700 nm)provide key advantages such as deeper tissue penetration,higher contrast,and minimal interference from biological autofluorescence.However,challenges such as low brightness and rapid signal decay,especially in the NIR-II region,limit their effectiveness in long-term monitoring,including tumor theranostics[5].Traditional approaches like size control and surface passivation yield only marginal improvements,underscoring the need for next-generation nanoparticles with superior NIR-II brightness.展开更多
The reaction of Mg^(2+)and 5-{1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl}terephthalic acid(H_(2)L)leads to two metal-organic frameworks,[Mg(L)(DMF)_(2)(H_(2)O)_(2)]_(2)·5DMF·2H_(2)O(1)with a 1D structure and...The reaction of Mg^(2+)and 5-{1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl}terephthalic acid(H_(2)L)leads to two metal-organic frameworks,[Mg(L)(DMF)_(2)(H_(2)O)_(2)]_(2)·5DMF·2H_(2)O(1)with a 1D structure and[Mg_(2)(L)_(2)(DMSO)_(3)(H_(2)O)](2)with a 2D(4,4)-net structure.Interestingly,the two compounds exhibit distinct luminescent responses to external mechanical stimuli.1 exhibited exceptional resistance mechanical chromic luminescence(RMCL),which can be attributed to the predominant hydrogen bonds and the presence of high-boiling-point solvent molecules within its structure.2 had a reversible MCL property,which can be attributed to the dominantπ-πweak interactions,coupled with the reversible destruction/restoration of its crystallinity under grinding/fumigation.CCDC:2410963,1;2410964,2.展开更多
Persistent Luminescence(PersL)materials,which use traps to store energy and emit photons over a long period,have found important applications in the fields of optical information storage,security labeling,and biologic...Persistent Luminescence(PersL)materials,which use traps to store energy and emit photons over a long period,have found important applications in the fields of optical information storage,security labeling,and biological imaging.The trap depth is a crucial factor determining the performance of these materials;however,achieving the desired trap depth with high precision remains a great challenge.Here,we provide double perovskite phosphors(Cs_(2)SnCl_(6)-Cs_(2)ZrCl_(6)-Cs_(2)HfCl_(6)series)with highly compatible crystal structures,enabling continuous and precise tuning of trap depth over an ultra-wide range of 0.11-1.25 eV.By incorporating W4+as the luminescent centers,these phosphors exhibit outstanding near-infrared(NIR)PersL performance at approximately 900 nm and a lasting emission duration exceeding 10 h.The underlying mechanism of PersL is elucidated,and the wide-range tunability of trap depth is attributed to the universal applicability of band-gap engineering in the entire material system.Furthermore,we demonstrate the practical application of these materials by designing a flexible detector plate for X-ray imaging.The detector plate exhibits a storage time of more than 1 week,a detection limit of 0.83μGyair·s^(-1)in the near-infrared region,and real-time and delay-time imaging resolutions of 14.2 lp·mm^(-1)and 2.5 lp·mm^(-1),respectively.These attributes demonstrate strong potential for X-ray luminescence extension imaging.展开更多
Given customizable crystal structure and intriguing optical properties,lanthanide titanium-oxygen clusters(LTOCs)with atomic-level accuracy have gained a lot of interest.In this study,we prepared[Ln_(9)Ti_(2)(μ4-O)(...Given customizable crystal structure and intriguing optical properties,lanthanide titanium-oxygen clusters(LTOCs)with atomic-level accuracy have gained a lot of interest.In this study,we prepared[Ln_(9)Ti_(2)(μ4-O)(μ3-OH)_(14)(acac)_(17)(CH_(3)O)_(2)(CH_(3)OH)_(3)](Ln=Tb_(x)Eu_(9−x)(x=0,4,6,7,8,9),Hacac=acetylacetone),Tb^(3+)and Eu^(3+)co-doped LTOCs,to modify the optical properties for the luminescence thermometer.In detail,the serial LTOCs display dual characteristic emission peaks of ^(5)D_(4)→^(7)F_(5) for Tb^(3+)and^(5)D_(0)→^(7)F_(2) for Eu^(3+)at 548 and 616 nm,respectively,under 330 nm excitation.Effective energy transfer(ET)between Tb^(3+)ions and Eu^(3+)ions was revealed in terms of both emission spectra and luminescence lifetime.The ^(5)D_(0)→^(7)F_(2) emission intensity of Eu^(3+)ions at 616 nm is maximally enhanced(by a factor of 11.2)with a change in the relative molar ratio of Tb^(3+)to Eu^(3+),along with a change in the ET efficiency of Tb^(3+)→Eu^(3+).In addition,the luminescent color changes from red,orange,yellow,to green.This precise control of the ET process between rare-earth ions allows{Tb_(6)Eu_(3)Ti_(2)}to reach a maximum relative sensitivity of 1.241 K^(−1) at 355 K,which is an enhancement of up to 4.6-fold with respect to the previously reported homonuclear emission,holding great potential in the optical thermometers.展开更多
The enhancement of the intensity of red upconversion(UC)emission has significant implications for biological applications.In KZnF_(3):Yb^(3+),Er^(3+)which inherently produces high-purity red emission,the introduction ...The enhancement of the intensity of red upconversion(UC)emission has significant implications for biological applications.In KZnF_(3):Yb^(3+),Er^(3+)which inherently produces high-purity red emission,the introduction of Fe^(3+)markedly improves the UC intensity by a factor of 13.The mechanism behind the enhanced UC red luminescence is deduced to originate from the Yb^(3+)-Fe^(3+)dimer,as determined by first principle calculation and analysis of UC luminescence properties.The thermometry performance,based on splitting peaks of red emission,demonstrated enhanced temperature sensitivity at lower ranges.Exploring the photothermal properties,it was observed that temperature exhibited a linear correlation with pump power under a 980 nm laser,achieving levels up to 48℃.This temperature range is ideal for applications in mild photothermal therapy(MPTT).This work elucidates the material’s potential in advanced biological applications,merging optical thermometry and photothermics,indicating its multifunctional utility.展开更多
Broadband near-infrared(NIR)luminescent materials have shown great promise in applications such as optical communication,biomedicine,and optoelectronic devices.However,the current research is focused on phos⁃phors and...Broadband near-infrared(NIR)luminescent materials have shown great promise in applications such as optical communication,biomedicine,and optoelectronic devices.However,the current research is focused on phos⁃phors and glasses,and it is important to develop broadband NIR luminescent nanomaterials.Here,we report an erbi⁃um-sensitized core-shell nanocrystal design for broadband NIR emission.Based on the structural design with suitable dopings of Tm^(3+)and Ho^(3+),the broadband NIR emission covering 1.5-2.1μm region is achieved under 980 nm and 808 nm excitations.Moreover,the emission intensity is further enhanced by introducing Yb^(3+)and Nd^(3+)into the sam⁃ple,respectively,and the energy transfer processes between them are systematically discussed.Our results present a novel approach for developing broadband NIR luminescent materials and devices.展开更多
One Yb(Ⅲ)-based coordination polymer,{[Yb(H_(2)dhtp)1.5(H_(2)O)_(4)]·3H_(2)O}n(1)(H_(4)dhtp=2,5-dihydroxytere-phthalic acid),was fabricated and structurally characterized by single-crystal X-ray diffraction,IR,p...One Yb(Ⅲ)-based coordination polymer,{[Yb(H_(2)dhtp)1.5(H_(2)O)_(4)]·3H_(2)O}n(1)(H_(4)dhtp=2,5-dihydroxytere-phthalic acid),was fabricated and structurally characterized by single-crystal X-ray diffraction,IR,powder X-ray diffraction,X-ray diffraction,and elemental analysis.Complex 1 displays a 1D chain structure,and belongs to P1 group.The solid-state luminescent spectrum of 1 showed an emission band with the maximum at 508 nm(λex=408 nm).It exhibited the emission characteristic of the H_(4)dhtp ligand.The fluorescence of 1 in water displayed the stron-gest intensity.In detecting various metal ions,adding Zr^(4+)led to a blue shift in fluorescence,accompanied by an increase in intensity,whereas the presence of Fe^(3+)resulted in a decrease in luminescence.The changes observed in the IR spectrum indicate an interaction between Fe^(3+)/Zr^(4+)and complex 1,resulting in the variation of luminescence properties.展开更多
Four new coordination polymers,{[Cd(mbtx)(4OHphCOO)]NO_(3)}n(1),{[Zn(mbtx)(1,4-bdc)_(0.5)(H_(2)O)_(2)]·(1,4-bdc)_(0.5)·4H_(2)O}n(2),{[Cd2(mbtx)(5NO_(2)-bdc)_(2)(H_(2)O)_(3)]·4.5H_(2)O}n(3),and{[Zn(H_(2)...Four new coordination polymers,{[Cd(mbtx)(4OHphCOO)]NO_(3)}n(1),{[Zn(mbtx)(1,4-bdc)_(0.5)(H_(2)O)_(2)]·(1,4-bdc)_(0.5)·4H_(2)O}n(2),{[Cd2(mbtx)(5NO_(2)-bdc)_(2)(H_(2)O)_(3)]·4.5H_(2)O}n(3),and{[Zn(H_(2)O)6][Zn_(2)(mbtx)_(2)(btc)_(2)(H_(2)O)_(4)]·2H_(2)O}n(4)(mbtx=1,3-bis(4H-1,2,4-triazole)benzene,4OHphCOO-=p-hydroxybenzoate,1,4-bdc2-=1,4-benzenedicarboxylate,5NO_(2)-bdc2-=5-nitro-isophthalate,btc3-=1,3,5-benzenetricarboxylate),were synthesized under room temperature condition and characterized by single-crystal X-ray diffraction,elemental analyses,and powder X-ray diffraction.Single-crystal X-ray structural analysis shows that complexes 1 and 3 are 2D networks.In 1,the adjacent 2D networks are linked to a 3D network byπ-πstacking interaction.2 and 4 exhibit 1D chains,and the 1D chains are connected into a 3D network byπ-πstacking interaction and intermolecular hydrogen bond.Luminescence and thermogravimetric analysis of the four complexes were discussed.CCDC:2416406,1;2416407,2;2416408,3;2416409,4.展开更多
To develop efficient luminescence and optical thermometry materials for color display and non-contact temperature measurement,novel RE^(3+)(RE=Eu,Sm)doped self-activated Na_(2)LuMg_(2)V_(3)O_(12)phosphors were prepare...To develop efficient luminescence and optical thermometry materials for color display and non-contact temperature measurement,novel RE^(3+)(RE=Eu,Sm)doped self-activated Na_(2)LuMg_(2)V_(3)O_(12)phosphors were prepared by a typical solid-state reaction method.Their crystal structure,morphology,multi-color luminescence and temperature sensing properties were elaborately investigated.Under UV light excitation,an intense and broad green-yellow emission band from VO_(4)^(3-)group is observed in the Na_(2)LuMg_(2)V_(3)O_(12)matrix,indicating its potential application in solid state lighting.After the incorpo ration of Eu^(3+)and Sm^(3+)ions,efficient energy transfer(ET)from VO_(4)^(3-)group to Eu^(3+)/Sm^(3+)ions occurs and the emission color of the samples can be readily tuned among different color ranges.Besides,based on the change of luminescence intensity and lifetimes of VO_(4)^(3-)group in Na_(2)LuMg_(2)V_(3)O_(12):Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):Sm^(3+),the ET efficiency was analyzed and the mechanism is illustrated.Finally,large discrepancy between the thermal stability of VO_(4)^(3-)group and Eu^(3+)/Sm^(3+)ions is observed in the temperature-dependent emission spectra of Na_(2)LuMg_(2)V_(3)O_(12):Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):Sm^(3+).By taking advantage of the luminescence intensity ratio(LIR)between VO_(4)^(3-)group and Eu^(3+)/Sm^(3+)ions in Na_(2)LuMg_(2)V_(3)O_(12):0.01Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):0.07Sm^(3+),two new types of optical thermometry mediums were designed and their basic temperature sensing parameters were calculated.展开更多
Carbon dots(CDs)-based composites have shown impressive performance in fields of information encryption and sensing,however,a great challenge is to simultaneously implement multi-mode luminescence and room-temperature...Carbon dots(CDs)-based composites have shown impressive performance in fields of information encryption and sensing,however,a great challenge is to simultaneously implement multi-mode luminescence and room-temperature phosphorescence(RTP)detection in single system due to the formidable synthesis.Herein,a multifunctional composite of Eu&CDs@p RHO has been designed by co-assembly strategy and prepared via a facile calcination and impregnation treatment.Eu&CDs@p RHO exhibits intense fluorescence(FL)and RTP coming from two individual luminous centers,Eu3+in the free pores and CDs in the interrupted structure of RHO zeolite.Unique four-mode color outputs including pink(Eu^(3+),ex.254 nm),light violet(CDs,ex.365 nm),blue(CDs,254 nm off),and green(CDs,365 nm off)could be realized,on the basis of it,a preliminary application of advanced information encoding has been demonstrated.Given the free pores of matrix and stable RTP in water of confined CDs,a visual RTP detection of Fe^(3+)ions is achieved with the detection limit as low as 9.8μmol/L.This work has opened up a new perspective for the strategic amalgamation of luminous vips with porous zeolite to construct the advanced functional materials.展开更多
Multifunctional semiconductors play an important role in developing advanced photoelectric technologies.In this work,based on an octahedral replacement strategy in chalcogenides,a new selenide semiconductor NaMn_(3)Ga...Multifunctional semiconductors play an important role in developing advanced photoelectric technologies.In this work,based on an octahedral replacement strategy in chalcogenides,a new selenide semiconductor NaMn_(3)Ga_(3)Se_(8)was rationally designed,and synthesized by the flux method.The compound crystallizes in the noncentrosymmetric(NCS)P_(6)space group,and is composed of unique prismatic[NaSe_(6)],octahedral[MnSe_(6)]and tetrahedral[GaSe_(4)]motifs,inheriting the stable three-dimensional framework built by the octahedral and tetrahedral units in the A^(Ⅰ)Mg_(3)^(Ⅱ)C_(3)^(Ⅲ)Q_(8)^(Ⅵ)family.NaMn_(3)Ga_(3)Se_(8)shows the largest known secondary nonlinear optical(NLO)response of~2.1×AgGaS_(2)(AGS)in the A^(Ⅰ)Mg_(3)^(Ⅱ)C_(3)^(Ⅲ)Q_(8)^(Ⅵ)family,and a high laser-induced damage threshold of~3.0×AGS.Meanwhile,the introduction of Mn2t with unpaired 3d electrons induces a strong red emission band(685–805 nm)under the excitation source of 496 nm,as well as a paramagnetic to antiferromagnetic(AFM)transition at 7.3 K.The results confirm that NaMn_(3)Ga_(3)Se_(8)possesses multifunctional features including significant NLO response,fluorescence emission and AFM properties,and illustrate that replacing octahedral units with approaching size and geometry(like[MgSe_(6)]and[MnSe_(6)])could be a feasible way to develop multifunctional chalcogenides.展开更多
Perovskites showcased potential promise for innovative circularly polarized luminescence (CPL)-active multi-channelinformation encryption, owing to the exceptional luminescence brightness. It was still a formidablecha...Perovskites showcased potential promise for innovative circularly polarized luminescence (CPL)-active multi-channelinformation encryption, owing to the exceptional luminescence brightness. It was still a formidablechallenge to fabricate CPL-active perovskites with significant luminescent asymmetry factor (glum) and full-colour-tailorableCPL properties. Indeed, compared to isotropic perovskites, anisotropic perovskite nanowires (NWs)were conducive to carrier separation and transport for polarization enhancement. Herein, three types of CsPb(Br/I)3 NWs with green, orange, red fluorescence (FL) were respectively synthesized and assembled into chiral NWfilms. The right-handed/left-handed chiral NW films constructed by 4+4 layers and 45° inter-angles exhibitshighly symmetric and mirror-like chiral signals. The strongest chiral intensity is more than 3000 medg. CPLsignals with wide colour gamut produce ranging from 480 nm to 800 nm, and tailorable CPL wavelengths aremanipulated by the emission wavelength of perovskite NWs. A giant CPL signal with a maximum glum of up to 10^(-1) is achieved. The polarization imaging of chiral NW films produces brilliant differential circularly polarizedstructural colours, making it more widely used in multilevel anti-counterfeiting systems. A significant break-throughlies in the development of advanced chiral perovskite materials with remarkable glum and tailorable CPLproperties, which sheds new light on optical anti-counterfeiting and intelligent information encryption.展开更多
The reaction of 4-nitro-N'-(pyridin-2-ylmethylene)benzohydrazide(HL) with Ln(OAc)_(3)·4H_(2)O in MeOH makes it possible to synthesize mononuclear complexes [Ln(L)_(2)(OAc)(MeOH)]·2H_(2)O(Ln=Tb^(Ⅲ)(1),E...The reaction of 4-nitro-N'-(pyridin-2-ylmethylene)benzohydrazide(HL) with Ln(OAc)_(3)·4H_(2)O in MeOH makes it possible to synthesize mononuclear complexes [Ln(L)_(2)(OAc)(MeOH)]·2H_(2)O(Ln=Tb^(Ⅲ)(1),Eu^(Ⅲ)(2) and Gd^(Ⅲ)(3)) with chelate acetate and L^(-)anions.Compound 1 can be crystallized in reaction with molar ratio HL:Ln=1:1,2:1,3:1,and we successfully synthesized complex with three chelate L anions[Tb(L)_(3)]_(2)·2MeOH·H_(2)O(4) by interaction of TbCl_(3)·6H_(2)O with deprotonated HL(HL:Ln=3:1).Terbium(Ⅲ) compound 1 starts to decompose at~323 K and becomes stable up to 552 K according to the STA.Compound 1 shows slow magnetic relaxation with parameters Δ_(eff)/k_B=(6.75±0.02) K,τ_(0)=(1.71 × 10^(-6)±1 × 10^(-8)) s.Complexes 1 and 2 exhibit only fluorescence and phosphorescence of the L^(-).Ion-centered luminescence of the Tb^(3+)or Eu^(3+)ion is not observed.Using the tangent method at the high-energy edge of the phospho rescence spectrum of Gd^(3+),complex 3 T_(1) energy level of L^(-)is estimated to be 19700 cm^(-1).Reasons of luminescence quenching are discussed.Structures of 1 and 4 were determined by single crystal X-ray diffraction,and compounds 1-3 were characterized by powder X-ray diffraction(PXRD).展开更多
Ce^(3+),due to its broadband emission,has the potential to serve as a donor ion for energy transfer to achieve the possible efficient tunable multi-emission in materials.However,current related research primarily focu...Ce^(3+),due to its broadband emission,has the potential to serve as a donor ion for energy transfer to achieve the possible efficient tunable multi-emission in materials.However,current related research primarily focuses on photoluminescent(PL)phosphors,while studies on achieving tunable long persistent luminescence(LPL),particularly in glass materials,are insufficient.In this work,Ce-Tb codoped boroaluminate glass was synthesized using a high-temperature melting method under a reducing atmosphere.Under the influence of oxygen vacancy traps induced during the reduction of Ce^(4+)to Ce^(3+),glass samples exhibit an obvious LPL with a broadband center wavelength at 420 nm and a narrowband center wavelength at 547 nm,which correspond well to Ce^(3+)ions'd-f transitions and Tb^(3+)ions'f-f transitions,respectively.A reasonable Ce^(3+)doping amount achieves the optimal trap depth and concentration to enhance LPL intensity and duration.Additionally,it improves the PL intensity of Tb^(3+)by enhancing the energy transfer from Ce^(3+)to Tb^(3+),thereby enabling the glass to exhibit variable LPL colo rs ranging from blue to cyan.Finally,based on the PL and LPL characteristics of the samples,a dynamic encryption anticounterfeiting application is described.展开更多
In this work,rare earth ions(REs)including Yb^(3+)/Er^(3+),Yb^(3+)/Ho^(3+)and Yb^(3+)/Tm^(3+)co-doped manganese oxyfluoride glasses were fabricated using melt quenching method.By fully utilizing the upconversion lumin...In this work,rare earth ions(REs)including Yb^(3+)/Er^(3+),Yb^(3+)/Ho^(3+)and Yb^(3+)/Tm^(3+)co-doped manganese oxyfluoride glasses were fabricated using melt quenching method.By fully utilizing the upconversion luminescence(UCL)of REs and regulating energy transfer between the different energy levels of RE ions and the4T1level of Mn^(2+),the output of UCL was regulated and even pure-red light can be achieved.Moreover,owing to the selective partitioning caused by phase-separation network structure in the oxyfluoride glass,the UCL intensity of glasses annealed for 72 h is significantly enhanced 58 times compared to the rapidly quenched samples.展开更多
Symmetry breaking,a critical phenomenon in both natural and artificial systems,is pivotal in constructing chiral structures from achiral building units.This study focuses on the achiral molecule 8,8',8'',8...Symmetry breaking,a critical phenomenon in both natural and artificial systems,is pivotal in constructing chiral structures from achiral building units.This study focuses on the achiral molecule 8,8',8'',8'''-((pyrazine-2,3,5,6-tetrayltetrakis(benzene-4,1-iyl))tetrakis(oxy))tetrakis(octan-1-ol)(TPP-C8OH),an aggregation-induced emission(AIE)molecule,to explore its symmetry breaking behavior in supramolecular assembly.By analyzing TPP-C8OH in various solvents—both non-chiral and chiral—we find that chiral solvents significantly enhance the molecule's symmetry breaking and chiroptical properties.Specially,alcohol solvents,particularly dodecyl alcohol,facilitate the formation of helical structures with both left-handed(M)and right-handed(P)helices within single twisted nanoribbons.This observation contrasts with previously reported symmetry breaking phenomena in assembly systems.Chiral solvents induce assemblies with distinct helical orientations,resulting in notable circularly polarized luminescence(CPL)and circular dichroism(CD)signals.This study elucidates the impact of solvent choice on symmetry breaking and chiral assembly,offering insights into the design of advanced chiral materials with tailored self-assembly processes.展开更多
Recently circularly polarized luminescence(CPL)materials have attracted significant interest.Introducing reversible dynamic property to these materials has been a key focus in cutting-edge fields,such as in high-level...Recently circularly polarized luminescence(CPL)materials have attracted significant interest.Introducing reversible dynamic property to these materials has been a key focus in cutting-edge fields,such as in high-level information encryption.Here,we provided a novel and general strategy involving handednessselective filtration and ground-state chiral self-recovery(CSR)in double film system to address this issue.Based on this strategy,we achieved CPL switch through the reversible modulation of ground-state chirality including absorption and scattering circular dichroism(CD)signals over the full UV-visible wavelength range(365-700 nm)in a single azobenzene polymer(PAzo)film.More importantly,by flexibly changing the type of fluorescent films,it is convenient to achieve general excited-state CSR,that is reversible switching of full-color including ideal white(CIE coordinate(0.33,0.33)),as well as room-temperature phosphorescent CPL.All these CPL signals without almost any intensity decay after three cycles of onand-off switching.Experimental results indicated that the trans-cis isomerization and ordered rearrangement of azobenzene units in PAzo film were the fundamental reasons for realizing CPL switching.Finally,based on this system we achieved dynamic visual encryption and decryption process including multiple decryption methods.This study provides an effective method for constructing a universally applicable chiroptical switch in excited state.展开更多
基金supported by NSFC(22271282)the Self-deployment Project Research Program of Haixi Institutes,Chinese Academy of Sciences with the grant number of CXZX-2022-JQ04.
文摘Circularly polarized luminescence(CPL)and two-photon absorption(TPA)materials have garnered considerable attentions due to their minimal energy loss and superior optical penetration[1,2].However,the current challenge lies in the absence of well-developed strategies for designing materials that combine these two exceptional optical properties.
基金Project supported by the National Natural Science Foundation of China(52372134,12274023)the Fundamental Re search Funds for the Central Universities(FRF-EYIT-23-04)。
文摘Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level stemming from the doped rare earth ion or intrinsic defects to the electronic structure of the host,and therefore thermoluminescence measurement becomes a radical technology in studying trap depth,which is one of the significant parameters that determine the properties of persistent luminescence and photostimulated luminescence.However,the results of trap depth obtained by different thermoluminescence methods are quite different so that they are not comparable.Herein,we analyzed different thermoluminescence methods,selected and improved the traditional peak position method of T_(m)/500 to be E=(-0.94Inβ+30.09)kT_(m).Only the experimental heating rate(β)is needed additionally,but the accuracy is improved greatly in most cases.This convenient and accurate method will accelerate the discovery of novel rare earth-doped materials.
基金supported by the Major Research Plan of the National Natural Science Foundation of China(No.92361202)National Natural Science Foundation of China(No.12204481).
文摘Persistent luminescence is a unique optical phenomenon that continues to emit light for minutes or even hours after the excitation stops,which can significantly enhance the sensitivity and signal-to-noise ratio of imaging[1].Among numerous persistent luminescence materials,lanthanide-doped fluoride nanoparticles have shown tunable persistent luminescence across the UV-vis-NIR spectrum(200-1700 nm)under X-ray excitation and adjustable size,promising significant applications in deep-tissue imaging[2,3],security encryption,and data storage[4].In particular,those exhibiting NIR-II luminescence(1000-1700 nm)provide key advantages such as deeper tissue penetration,higher contrast,and minimal interference from biological autofluorescence.However,challenges such as low brightness and rapid signal decay,especially in the NIR-II region,limit their effectiveness in long-term monitoring,including tumor theranostics[5].Traditional approaches like size control and surface passivation yield only marginal improvements,underscoring the need for next-generation nanoparticles with superior NIR-II brightness.
文摘The reaction of Mg^(2+)and 5-{1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl}terephthalic acid(H_(2)L)leads to two metal-organic frameworks,[Mg(L)(DMF)_(2)(H_(2)O)_(2)]_(2)·5DMF·2H_(2)O(1)with a 1D structure and[Mg_(2)(L)_(2)(DMSO)_(3)(H_(2)O)](2)with a 2D(4,4)-net structure.Interestingly,the two compounds exhibit distinct luminescent responses to external mechanical stimuli.1 exhibited exceptional resistance mechanical chromic luminescence(RMCL),which can be attributed to the predominant hydrogen bonds and the presence of high-boiling-point solvent molecules within its structure.2 had a reversible MCL property,which can be attributed to the dominantπ-πweak interactions,coupled with the reversible destruction/restoration of its crystallinity under grinding/fumigation.CCDC:2410963,1;2410964,2.
基金supported by the National Natural Science Foundation of China(Nos.52172156,12474412)the Natural Science Foundation of Fujian Province(No.2023J06005)+2 种基金the Natural Science Foundation of Guangdong Province(No.2024A1515011197)the Fundamental Research Funds for the Central Universities(No.20720240057)The DFT calculations in this work was done with the assistance of the Intelligent Computing Center of Tan Kah Kee Innovation Laboratory(IKKEM).
文摘Persistent Luminescence(PersL)materials,which use traps to store energy and emit photons over a long period,have found important applications in the fields of optical information storage,security labeling,and biological imaging.The trap depth is a crucial factor determining the performance of these materials;however,achieving the desired trap depth with high precision remains a great challenge.Here,we provide double perovskite phosphors(Cs_(2)SnCl_(6)-Cs_(2)ZrCl_(6)-Cs_(2)HfCl_(6)series)with highly compatible crystal structures,enabling continuous and precise tuning of trap depth over an ultra-wide range of 0.11-1.25 eV.By incorporating W4+as the luminescent centers,these phosphors exhibit outstanding near-infrared(NIR)PersL performance at approximately 900 nm and a lasting emission duration exceeding 10 h.The underlying mechanism of PersL is elucidated,and the wide-range tunability of trap depth is attributed to the universal applicability of band-gap engineering in the entire material system.Furthermore,we demonstrate the practical application of these materials by designing a flexible detector plate for X-ray imaging.The detector plate exhibits a storage time of more than 1 week,a detection limit of 0.83μGyair·s^(-1)in the near-infrared region,and real-time and delay-time imaging resolutions of 14.2 lp·mm^(-1)and 2.5 lp·mm^(-1),respectively.These attributes demonstrate strong potential for X-ray luminescence extension imaging.
基金supported by the National Natural Science Foundation of China(Nos.12174151 and 12304448)the Specific Research Fund of the Innovation Platform for Academicians of Hainan Province(No.YSPTZX202208)+3 种基金Hainan Province Clinical Medical Center(No.QWYH_(2)022341)the Key Laboratory of New Energy and Rare Earth Resource Utilization of the State People’s Committee of China(No.NERE202206)the Department of Science and Technology of Jilin Province(No.20220101059JC)the Key Laboratory of the Ministry of Education for First Aid and Trauma Research(No.KLET-202218).
文摘Given customizable crystal structure and intriguing optical properties,lanthanide titanium-oxygen clusters(LTOCs)with atomic-level accuracy have gained a lot of interest.In this study,we prepared[Ln_(9)Ti_(2)(μ4-O)(μ3-OH)_(14)(acac)_(17)(CH_(3)O)_(2)(CH_(3)OH)_(3)](Ln=Tb_(x)Eu_(9−x)(x=0,4,6,7,8,9),Hacac=acetylacetone),Tb^(3+)and Eu^(3+)co-doped LTOCs,to modify the optical properties for the luminescence thermometer.In detail,the serial LTOCs display dual characteristic emission peaks of ^(5)D_(4)→^(7)F_(5) for Tb^(3+)and^(5)D_(0)→^(7)F_(2) for Eu^(3+)at 548 and 616 nm,respectively,under 330 nm excitation.Effective energy transfer(ET)between Tb^(3+)ions and Eu^(3+)ions was revealed in terms of both emission spectra and luminescence lifetime.The ^(5)D_(0)→^(7)F_(2) emission intensity of Eu^(3+)ions at 616 nm is maximally enhanced(by a factor of 11.2)with a change in the relative molar ratio of Tb^(3+)to Eu^(3+),along with a change in the ET efficiency of Tb^(3+)→Eu^(3+).In addition,the luminescent color changes from red,orange,yellow,to green.This precise control of the ET process between rare-earth ions allows{Tb_(6)Eu_(3)Ti_(2)}to reach a maximum relative sensitivity of 1.241 K^(−1) at 355 K,which is an enhancement of up to 4.6-fold with respect to the previously reported homonuclear emission,holding great potential in the optical thermometers.
基金supported by the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD),"Qinglan Project"Young and Middle-aged Academic Leaders Program of Jiangsu Province,and the National Natural Science Foundation of China(General Program).
文摘The enhancement of the intensity of red upconversion(UC)emission has significant implications for biological applications.In KZnF_(3):Yb^(3+),Er^(3+)which inherently produces high-purity red emission,the introduction of Fe^(3+)markedly improves the UC intensity by a factor of 13.The mechanism behind the enhanced UC red luminescence is deduced to originate from the Yb^(3+)-Fe^(3+)dimer,as determined by first principle calculation and analysis of UC luminescence properties.The thermometry performance,based on splitting peaks of red emission,demonstrated enhanced temperature sensitivity at lower ranges.Exploring the photothermal properties,it was observed that temperature exhibited a linear correlation with pump power under a 980 nm laser,achieving levels up to 48℃.This temperature range is ideal for applications in mild photothermal therapy(MPTT).This work elucidates the material’s potential in advanced biological applications,merging optical thermometry and photothermics,indicating its multifunctional utility.
文摘Broadband near-infrared(NIR)luminescent materials have shown great promise in applications such as optical communication,biomedicine,and optoelectronic devices.However,the current research is focused on phos⁃phors and glasses,and it is important to develop broadband NIR luminescent nanomaterials.Here,we report an erbi⁃um-sensitized core-shell nanocrystal design for broadband NIR emission.Based on the structural design with suitable dopings of Tm^(3+)and Ho^(3+),the broadband NIR emission covering 1.5-2.1μm region is achieved under 980 nm and 808 nm excitations.Moreover,the emission intensity is further enhanced by introducing Yb^(3+)and Nd^(3+)into the sam⁃ple,respectively,and the energy transfer processes between them are systematically discussed.Our results present a novel approach for developing broadband NIR luminescent materials and devices.
文摘One Yb(Ⅲ)-based coordination polymer,{[Yb(H_(2)dhtp)1.5(H_(2)O)_(4)]·3H_(2)O}n(1)(H_(4)dhtp=2,5-dihydroxytere-phthalic acid),was fabricated and structurally characterized by single-crystal X-ray diffraction,IR,powder X-ray diffraction,X-ray diffraction,and elemental analysis.Complex 1 displays a 1D chain structure,and belongs to P1 group.The solid-state luminescent spectrum of 1 showed an emission band with the maximum at 508 nm(λex=408 nm).It exhibited the emission characteristic of the H_(4)dhtp ligand.The fluorescence of 1 in water displayed the stron-gest intensity.In detecting various metal ions,adding Zr^(4+)led to a blue shift in fluorescence,accompanied by an increase in intensity,whereas the presence of Fe^(3+)resulted in a decrease in luminescence.The changes observed in the IR spectrum indicate an interaction between Fe^(3+)/Zr^(4+)and complex 1,resulting in the variation of luminescence properties.
文摘Four new coordination polymers,{[Cd(mbtx)(4OHphCOO)]NO_(3)}n(1),{[Zn(mbtx)(1,4-bdc)_(0.5)(H_(2)O)_(2)]·(1,4-bdc)_(0.5)·4H_(2)O}n(2),{[Cd2(mbtx)(5NO_(2)-bdc)_(2)(H_(2)O)_(3)]·4.5H_(2)O}n(3),and{[Zn(H_(2)O)6][Zn_(2)(mbtx)_(2)(btc)_(2)(H_(2)O)_(4)]·2H_(2)O}n(4)(mbtx=1,3-bis(4H-1,2,4-triazole)benzene,4OHphCOO-=p-hydroxybenzoate,1,4-bdc2-=1,4-benzenedicarboxylate,5NO_(2)-bdc2-=5-nitro-isophthalate,btc3-=1,3,5-benzenetricarboxylate),were synthesized under room temperature condition and characterized by single-crystal X-ray diffraction,elemental analyses,and powder X-ray diffraction.Single-crystal X-ray structural analysis shows that complexes 1 and 3 are 2D networks.In 1,the adjacent 2D networks are linked to a 3D network byπ-πstacking interaction.2 and 4 exhibit 1D chains,and the 1D chains are connected into a 3D network byπ-πstacking interaction and intermolecular hydrogen bond.Luminescence and thermogravimetric analysis of the four complexes were discussed.CCDC:2416406,1;2416407,2;2416408,3;2416409,4.
基金Project supported by Natural Science Foundation of Shandong Province(ZR2020KF017,ZR2020QE053,ZR2023QB261)the Natural Science Foundation of Anhui Province(2108085MB53)。
文摘To develop efficient luminescence and optical thermometry materials for color display and non-contact temperature measurement,novel RE^(3+)(RE=Eu,Sm)doped self-activated Na_(2)LuMg_(2)V_(3)O_(12)phosphors were prepared by a typical solid-state reaction method.Their crystal structure,morphology,multi-color luminescence and temperature sensing properties were elaborately investigated.Under UV light excitation,an intense and broad green-yellow emission band from VO_(4)^(3-)group is observed in the Na_(2)LuMg_(2)V_(3)O_(12)matrix,indicating its potential application in solid state lighting.After the incorpo ration of Eu^(3+)and Sm^(3+)ions,efficient energy transfer(ET)from VO_(4)^(3-)group to Eu^(3+)/Sm^(3+)ions occurs and the emission color of the samples can be readily tuned among different color ranges.Besides,based on the change of luminescence intensity and lifetimes of VO_(4)^(3-)group in Na_(2)LuMg_(2)V_(3)O_(12):Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):Sm^(3+),the ET efficiency was analyzed and the mechanism is illustrated.Finally,large discrepancy between the thermal stability of VO_(4)^(3-)group and Eu^(3+)/Sm^(3+)ions is observed in the temperature-dependent emission spectra of Na_(2)LuMg_(2)V_(3)O_(12):Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):Sm^(3+).By taking advantage of the luminescence intensity ratio(LIR)between VO_(4)^(3-)group and Eu^(3+)/Sm^(3+)ions in Na_(2)LuMg_(2)V_(3)O_(12):0.01Eu^(3+)and Na_(2)LuMg_(2)V_(3)O_(12):0.07Sm^(3+),two new types of optical thermometry mediums were designed and their basic temperature sensing parameters were calculated.
基金supported by the National Natural Science Foundation of China(No.22288101)the 111 Project(No.B17020)。
文摘Carbon dots(CDs)-based composites have shown impressive performance in fields of information encryption and sensing,however,a great challenge is to simultaneously implement multi-mode luminescence and room-temperature phosphorescence(RTP)detection in single system due to the formidable synthesis.Herein,a multifunctional composite of Eu&CDs@p RHO has been designed by co-assembly strategy and prepared via a facile calcination and impregnation treatment.Eu&CDs@p RHO exhibits intense fluorescence(FL)and RTP coming from two individual luminous centers,Eu3+in the free pores and CDs in the interrupted structure of RHO zeolite.Unique four-mode color outputs including pink(Eu^(3+),ex.254 nm),light violet(CDs,ex.365 nm),blue(CDs,254 nm off),and green(CDs,365 nm off)could be realized,on the basis of it,a preliminary application of advanced information encoding has been demonstrated.Given the free pores of matrix and stable RTP in water of confined CDs,a visual RTP detection of Fe^(3+)ions is achieved with the detection limit as low as 9.8μmol/L.This work has opened up a new perspective for the strategic amalgamation of luminous vips with porous zeolite to construct the advanced functional materials.
基金supported by the Natural Science Foundation of the Xinjiang Uygur Autonomous Region(2024D01E30)the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB0880000)+1 种基金the Open Fund of the Anhui Key Laboratory of Photonic Materials and Devices(AHKL2024KF02)the National Natural Science Foundation of China(22475234,22335007,22193044 and 22361132544).
文摘Multifunctional semiconductors play an important role in developing advanced photoelectric technologies.In this work,based on an octahedral replacement strategy in chalcogenides,a new selenide semiconductor NaMn_(3)Ga_(3)Se_(8)was rationally designed,and synthesized by the flux method.The compound crystallizes in the noncentrosymmetric(NCS)P_(6)space group,and is composed of unique prismatic[NaSe_(6)],octahedral[MnSe_(6)]and tetrahedral[GaSe_(4)]motifs,inheriting the stable three-dimensional framework built by the octahedral and tetrahedral units in the A^(Ⅰ)Mg_(3)^(Ⅱ)C_(3)^(Ⅲ)Q_(8)^(Ⅵ)family.NaMn_(3)Ga_(3)Se_(8)shows the largest known secondary nonlinear optical(NLO)response of~2.1×AgGaS_(2)(AGS)in the A^(Ⅰ)Mg_(3)^(Ⅱ)C_(3)^(Ⅲ)Q_(8)^(Ⅵ)family,and a high laser-induced damage threshold of~3.0×AGS.Meanwhile,the introduction of Mn2t with unpaired 3d electrons induces a strong red emission band(685–805 nm)under the excitation source of 496 nm,as well as a paramagnetic to antiferromagnetic(AFM)transition at 7.3 K.The results confirm that NaMn_(3)Ga_(3)Se_(8)possesses multifunctional features including significant NLO response,fluorescence emission and AFM properties,and illustrate that replacing octahedral units with approaching size and geometry(like[MgSe_(6)]and[MnSe_(6)])could be a feasible way to develop multifunctional chalcogenides.
基金supported by the National Natural Science Foundation of China(22278184,22272065)the Natural Science Foundation of Jiangsu Province(BK20211530)+1 种基金the Fundamental Research Funds for the Central Universities(JUSRP622018,JUSRP202404022)the Key Research and Development Special Project of Yichun City,Jiangxi Province,China(2023ZDYFZX06).
文摘Perovskites showcased potential promise for innovative circularly polarized luminescence (CPL)-active multi-channelinformation encryption, owing to the exceptional luminescence brightness. It was still a formidablechallenge to fabricate CPL-active perovskites with significant luminescent asymmetry factor (glum) and full-colour-tailorableCPL properties. Indeed, compared to isotropic perovskites, anisotropic perovskite nanowires (NWs)were conducive to carrier separation and transport for polarization enhancement. Herein, three types of CsPb(Br/I)3 NWs with green, orange, red fluorescence (FL) were respectively synthesized and assembled into chiral NWfilms. The right-handed/left-handed chiral NW films constructed by 4+4 layers and 45° inter-angles exhibitshighly symmetric and mirror-like chiral signals. The strongest chiral intensity is more than 3000 medg. CPLsignals with wide colour gamut produce ranging from 480 nm to 800 nm, and tailorable CPL wavelengths aremanipulated by the emission wavelength of perovskite NWs. A giant CPL signal with a maximum glum of up to 10^(-1) is achieved. The polarization imaging of chiral NW films produces brilliant differential circularly polarizedstructural colours, making it more widely used in multilevel anti-counterfeiting systems. A significant break-throughlies in the development of advanced chiral perovskite materials with remarkable glum and tailorable CPLproperties, which sheds new light on optical anti-counterfeiting and intelligent information encryption.
基金supported by the Russian Science Foundation (2273-10199)。
文摘The reaction of 4-nitro-N'-(pyridin-2-ylmethylene)benzohydrazide(HL) with Ln(OAc)_(3)·4H_(2)O in MeOH makes it possible to synthesize mononuclear complexes [Ln(L)_(2)(OAc)(MeOH)]·2H_(2)O(Ln=Tb^(Ⅲ)(1),Eu^(Ⅲ)(2) and Gd^(Ⅲ)(3)) with chelate acetate and L^(-)anions.Compound 1 can be crystallized in reaction with molar ratio HL:Ln=1:1,2:1,3:1,and we successfully synthesized complex with three chelate L anions[Tb(L)_(3)]_(2)·2MeOH·H_(2)O(4) by interaction of TbCl_(3)·6H_(2)O with deprotonated HL(HL:Ln=3:1).Terbium(Ⅲ) compound 1 starts to decompose at~323 K and becomes stable up to 552 K according to the STA.Compound 1 shows slow magnetic relaxation with parameters Δ_(eff)/k_B=(6.75±0.02) K,τ_(0)=(1.71 × 10^(-6)±1 × 10^(-8)) s.Complexes 1 and 2 exhibit only fluorescence and phosphorescence of the L^(-).Ion-centered luminescence of the Tb^(3+)or Eu^(3+)ion is not observed.Using the tangent method at the high-energy edge of the phospho rescence spectrum of Gd^(3+),complex 3 T_(1) energy level of L^(-)is estimated to be 19700 cm^(-1).Reasons of luminescence quenching are discussed.Structures of 1 and 4 were determined by single crystal X-ray diffraction,and compounds 1-3 were characterized by powder X-ray diffraction(PXRD).
基金Project supported by the Department of Science and Technology of Zhejiang Province,China(2024C01192)。
文摘Ce^(3+),due to its broadband emission,has the potential to serve as a donor ion for energy transfer to achieve the possible efficient tunable multi-emission in materials.However,current related research primarily focuses on photoluminescent(PL)phosphors,while studies on achieving tunable long persistent luminescence(LPL),particularly in glass materials,are insufficient.In this work,Ce-Tb codoped boroaluminate glass was synthesized using a high-temperature melting method under a reducing atmosphere.Under the influence of oxygen vacancy traps induced during the reduction of Ce^(4+)to Ce^(3+),glass samples exhibit an obvious LPL with a broadband center wavelength at 420 nm and a narrowband center wavelength at 547 nm,which correspond well to Ce^(3+)ions'd-f transitions and Tb^(3+)ions'f-f transitions,respectively.A reasonable Ce^(3+)doping amount achieves the optimal trap depth and concentration to enhance LPL intensity and duration.Additionally,it improves the PL intensity of Tb^(3+)by enhancing the energy transfer from Ce^(3+)to Tb^(3+),thereby enabling the glass to exhibit variable LPL colo rs ranging from blue to cyan.Finally,based on the PL and LPL characteristics of the samples,a dynamic encryption anticounterfeiting application is described.
基金Project supported by National Natural Science Foundation of China(62305244,62374112,62105078)Shandong Province Natural Science Foundation(ZR2021QE060,ZR2021QF009)+1 种基金Young Elite Scientists Sponsorship Program by China Association for Science and Technology(2022QNRC001)Youth Science and Technology Innovation Team of Shandong Province Institution of Higher Learning(2022KJ258)。
文摘In this work,rare earth ions(REs)including Yb^(3+)/Er^(3+),Yb^(3+)/Ho^(3+)and Yb^(3+)/Tm^(3+)co-doped manganese oxyfluoride glasses were fabricated using melt quenching method.By fully utilizing the upconversion luminescence(UCL)of REs and regulating energy transfer between the different energy levels of RE ions and the4T1level of Mn^(2+),the output of UCL was regulated and even pure-red light can be achieved.Moreover,owing to the selective partitioning caused by phase-separation network structure in the oxyfluoride glass,the UCL intensity of glasses annealed for 72 h is significantly enhanced 58 times compared to the rapidly quenched samples.
基金support from the National Natural Science Foundation of China(Nos.22471198,22101208)the Fundamental Research Funds for the Central Universities.
文摘Symmetry breaking,a critical phenomenon in both natural and artificial systems,is pivotal in constructing chiral structures from achiral building units.This study focuses on the achiral molecule 8,8',8'',8'''-((pyrazine-2,3,5,6-tetrayltetrakis(benzene-4,1-iyl))tetrakis(oxy))tetrakis(octan-1-ol)(TPP-C8OH),an aggregation-induced emission(AIE)molecule,to explore its symmetry breaking behavior in supramolecular assembly.By analyzing TPP-C8OH in various solvents—both non-chiral and chiral—we find that chiral solvents significantly enhance the molecule's symmetry breaking and chiroptical properties.Specially,alcohol solvents,particularly dodecyl alcohol,facilitate the formation of helical structures with both left-handed(M)and right-handed(P)helices within single twisted nanoribbons.This observation contrasts with previously reported symmetry breaking phenomena in assembly systems.Chiral solvents induce assemblies with distinct helical orientations,resulting in notable circularly polarized luminescence(CPL)and circular dichroism(CD)signals.This study elucidates the impact of solvent choice on symmetry breaking and chiral assembly,offering insights into the design of advanced chiral materials with tailored self-assembly processes.
基金the financial support from the National Natural Science Foundation of China(Nos.22301206,92356305 and 22301208)Natural Science Foundation of Anhui Province(No.2308085J15)+5 种基金Natural Science Foundation of Anhui Provincial Higher Education Institutions(No.2023AH010012)China Post-doctoral Science Foundation(No.2022M722312)the Key Laboratory of Polymeric Material Design and Synthesis for Biomedical Functionthe Priority Academic Program Development(PAPD)of Jiangsu Higher Education InstitutionsJiangsu Funding Program for Excellent Postdoctoral Talentthe Program of Innovative Research Team of Soochow University。
文摘Recently circularly polarized luminescence(CPL)materials have attracted significant interest.Introducing reversible dynamic property to these materials has been a key focus in cutting-edge fields,such as in high-level information encryption.Here,we provided a novel and general strategy involving handednessselective filtration and ground-state chiral self-recovery(CSR)in double film system to address this issue.Based on this strategy,we achieved CPL switch through the reversible modulation of ground-state chirality including absorption and scattering circular dichroism(CD)signals over the full UV-visible wavelength range(365-700 nm)in a single azobenzene polymer(PAzo)film.More importantly,by flexibly changing the type of fluorescent films,it is convenient to achieve general excited-state CSR,that is reversible switching of full-color including ideal white(CIE coordinate(0.33,0.33)),as well as room-temperature phosphorescent CPL.All these CPL signals without almost any intensity decay after three cycles of onand-off switching.Experimental results indicated that the trans-cis isomerization and ordered rearrangement of azobenzene units in PAzo film were the fundamental reasons for realizing CPL switching.Finally,based on this system we achieved dynamic visual encryption and decryption process including multiple decryption methods.This study provides an effective method for constructing a universally applicable chiroptical switch in excited state.
