Solar-driven water splitting for photocatalytic hydrogen evolution is considered a highly promising and costeffective solution to achieve a stable renewable energy supply.However,the sluggish kinetics of electron-hole...Solar-driven water splitting for photocatalytic hydrogen evolution is considered a highly promising and costeffective solution to achieve a stable renewable energy supply.However,the sluggish kinetics of electron-hole pairs’separation poses challenges in attaining satisfactory hydrogen production efficiency.Herein,we synthesized the exceptional performance of highly crystalline C_(3)N_(5)(HC–C_(3)N_(5))nanosheet as a photocatalyst,demonstrating a remarkable hydrogen evolution rate of 3.01 mmol h^(-1)g^(-1),which surpasses that of bulk C_(3)N_(5)(B–C_(3)N_(5))by a factor of 3.27.Experimental and theoretical analyses reveal that HC-C_(3)N_(5)nanosheets exhibit intriguing macroscopic photoinduced color changes,effectively broadening the absorption spectrum and significantly enhancing the generation of excitons.Besides,the cyano groups in HC-C_(3)N_(5)efficiently captures and converts photoexcited electrons into bound states,thereby prolonging their lifetimes and effectively separating electrons and holes into catalytically active regions.This research provides valuable insights into the establishment of bound electronic states for developing efficient photocatalysts.展开更多
Photochromic materials with multicolor upconversion reversible modulations are attractive in optical switching devices.Herein,the fabricated YNbO_(4):Er^(3+)/Tm^(3+)/Yb^(3+) materials exhibit excellent photochromism a...Photochromic materials with multicolor upconversion reversible modulations are attractive in optical switching devices.Herein,the fabricated YNbO_(4):Er^(3+)/Tm^(3+)/Yb^(3+) materials exhibit excellent photochromism and multicolor upconversion properties from green,red to near infrared(NIR) emissions with increasing Yb concentrations.Reversible multiband upconversion modulations are achieved by alternating light(365 and 405 nm) or thermal stimuli.After 365 nm irradiation,the luminescence color changes from yellow to red,the luminescent photoswitching contrast reaches up to 86.21%(green),82.12%(red) and 77.38%(NIR) in the Y_(0.83)Er_(0.01)Tm_(0.01)NbO_(4):0.15 Yb sample.Besides,the upconversion emission intensity before and after photochromic reaction shows remarkable change in a wide temperature range of 298-718 K.These results indicate that the Er^(3+)/Tm^(3+)/Yb^(3+) tri-doped YNbO_(4) materials can be a good candidate in optical switching and data storage applications.展开更多
Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexi...Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexible cation(H_(2)imb)^(2+)((H_(2)imb)^(2+)=di-protonated 2,3-bis(imidazolin-2-yl)-2,3-dimethylbutane)has been developed.Electron-donating Cl−and(ZnCl4)2−are used to direct folding a flexible electron-deficient(H_(2)imb)^(2+)cation.Three complexes(H_(2)imb)(NO_(3))2(1),(H_(2)imb)Cl2·H_(2)O(2),and(H_(2)imb)ZnCl4(3)have been synthesized in which(H_(2)imb)^(2+)crystallize in an anti-conformation,88.8°-gauche,and 51.8°-gauche,respectively.In contrary to X-ray silent complex 1,X-ray induced photochromism has been achieved in both complex 2 and 3.An intermolecular charge-transfer mechanism has been elucidated and the anion directed folding of(H_(2)imb)^(2+)has been validated to be critical to yield colored long-lived charge-separated states.展开更多
A series of photochromic diarylethene derivatives containing different fluorophores was synthesized by the Sonogashira coupling reaction and characterized by 1H nuclear magnetic resonance (NMR), 13C NMR and mass spect...A series of photochromic diarylethene derivatives containing different fluorophores was synthesized by the Sonogashira coupling reaction and characterized by 1H nuclear magnetic resonance (NMR), 13C NMR and mass spectroscopy. Photochromic conversion of Cz-MS was observed and its structural change was confirmed by proton NMR. Switchable absorption and emission phenomena were observed for these molecules. These phenomena were attributed to the reversible photochromic fluorescence resonance energy transfer (pcFRET) process. The design of this novel photochromic system of Py-4MS enables information to be processed in a non-destructive manner. This overcomes the problem of the destructive nature of tracking photochromism using ultraviolet (UV)-vis spectroscopy.展开更多
Copper-cadmium halide doped photochromic glass coating on plate glass has been prepared by a sol-gel process. The sample shows reversible photochromic effect. The results of X-ray diffraction (XRD) and infrared (IR) s...Copper-cadmium halide doped photochromic glass coating on plate glass has been prepared by a sol-gel process. The sample shows reversible photochromic effect. The results of X-ray diffraction (XRD) and infrared (IR) spectrum investigations indicate that the photochromic phase of tile coating is CuBr_xCl_(1-x), solid solution, and that the structure network of the coating is connected with the bonds of Si-O-Si, Si-O-B and Si-O-Al.展开更多
TiO2 nanotube arrays were prepared by means of an electrochemical anodization technique in an organic electrolyte solution doped with polyvinyl pyrrolidone (PVP) and were subsequently modified with phosphomolybdic aci...TiO2 nanotube arrays were prepared by means of an electrochemical anodization technique in an organic electrolyte solution doped with polyvinyl pyrrolidone (PVP) and were subsequently modified with phosphomolybdic acid (PMoA) to obtain PMoA/TiO2 nanotube arrays. The microstructure and photochromic properties were investigated via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results indicated that the Keggin structure of PMoA and the nanotube structure of TiO2 were not destroyed, and there was a strong degree of interaction between PMoA and TiO2 at the biphasic interface with lattice interlacing during the compositing process. The XPS results further indicated that there was a change in the chemical microenvironment during the formation process of the composite, and a new charge transfer bridge was formed through the Mo-O-Ti bond. Under visible light irradiation, the colorless PMoA/TiO2 nanotube array quickly turned blue and exhibited a photochromic response together with reversible photochromism in the presence of H2O2. After visible light irradiation for 60s, the appearance of Mo^5+ species in the XPS spectra indicated a photoreduction process in accordance with a photoinduced electron transfer mechanism.展开更多
Aggregation-induced emission(AIE) active photochromic molecules have attracted growing attention for their versatile applications.Here we designed and synthesized five newly unsymmetrical photochromic diarylethene(DAE...Aggregation-induced emission(AIE) active photochromic molecules have attracted growing attention for their versatile applications.Here we designed and synthesized five newly unsymmetrical photochromic diarylethene(DAE) dyads(BTE1-5) by connecting tetraphenylethene(TPE) and aromatic substituent via bithienylethene(BTE) bridge.The chemical structures of those compounds were identified by ^1H NMR,^(13)C NMR and HRMS.The absorption and emission of these dyads were investigated by UV-vis and fluore scence spectroscopy,respectively.The results showed that all those compounds exhibited typically AIE or aggregation-induced emission enhancement(AIEE) characteristic.Particularly,when an aggregationcaused quenching(ACQ) fluorophore(triphenylamine) was grafted to the molecule,connecting with TPE via BTE-bridge,the ACQ phenomenon was dissipated and converted to an AIE luminophore,and those compounds exhibited photochromism upon irradiation with alternative UV and visible light.The solution or solid of those compounds showed distinctly fluorescence switching "ON" or "OFF" observation upon irradiation with alternative UV and visible light.It is interesting that BTE1 could be applied in recording and rewritable information storage,and the cyclization quantum yields could be affected by substituent significantly.展开更多
It has been challenging to achieve multi-photochromic systems without affecting the individual photoswitching properties of the constituent units. Herein, we present the design and synthesis of a new family of platinu...It has been challenging to achieve multi-photochromic systems without affecting the individual photoswitching properties of the constituent units. Herein, we present the design and synthesis of a new family of platinum-acetylide dendrimers containing up to twenty-one photochromic dithienylethene(DTE)units that exhibit both high photochromic efficiency and individual switching properties. Upon irradiation with ultraviolet(UV) and visible(vis) light, the resultant metallodendrimers display high conversion yield and good fatigue resistance. More interestingly, cyclization-cycloreversion kinetics revealed that the photochromic property of each DTE unit in these metallodendrimers is unaffected by its neighbor and the full ring-closure of up to twenty-one DTE units in one single dendrimer has been achieved.展开更多
The photochromic spiropyrans and spirooxazine having a succinimidyl ester or isothiocyanate pendant group can form covalent products with transaminated DNA. The absorption spectra and solid reflection spectra of modi...The photochromic spiropyrans and spirooxazine having a succinimidyl ester or isothiocyanate pendant group can form covalent products with transaminated DNA. The absorption spectra and solid reflection spectra of modified DNA with these photochromic spiro compounds were investigated.展开更多
Photochromic and photoluminescence materials show bright colors under different excitation conditions,and thus,these functional materials have been applied in many fields.Based on the photochromic and photoluminescenc...Photochromic and photoluminescence materials show bright colors under different excitation conditions,and thus,these functional materials have been applied in many fields.Based on the photochromic and photoluminescence theories,a block copolymer,which could be directly processed into nanofibers by electrospinning,was successfully prepared through atom transfer radical polymerization(ATRP).To synthesize the block copolymer,a vinyl monomer containing a spiropyran unit was employed to prepare the photochromic chain segment,and a polymethyl methacrylate(PMMA)chain segment was introduced to improve the processability of the block copolymer.Acting as the photoluminescence unit,the rare earth complex was linked to the side chain through coordination bonding between the rare earth ions and the ester groups of PMMA.When the photochromic and photoluminescence block copolymer was exposed to different wavelengths of ultraviolet(UV)light and visible(Vis)light,it could show white,red,green,yellow,and blue-purple.These results provide the potential of the as-prepared photochromic and photoluminescence block copolymer for application in fibers and fabrics.展开更多
A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts ...A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts of stable, non-radioactive labeled DNA and RNA hybridization probes. And it is supposed to be easily detected for its photochromic properties.展开更多
Two photochromic compounds with the pyrazolonering as the photochromic functional structure, 2(1phenyl3methyl4benzoformylpyrazolone5)thiosemicarbazone(PMBPTSC) and 2(1phenyl3methyl4benzoformylpyrazolone5)smethylthiose...Two photochromic compounds with the pyrazolonering as the photochromic functional structure, 2(1phenyl3methyl4benzoformylpyrazolone5)thiosemicarbazone(PMBPTSC) and 2(1phenyl3methyl4benzoformylpyrazolone5)smethylthiosemicarbazone(PMBPMTSC), were synthesized and characterized by elemental analysis, MS, IR spectra, NMR spectra. The crystal structure of the photocolored product of PMBPTSC was determined by single crystal XRD analysis. The results show that the photochromic phenomenon is due to the photoisomerization from enol form to keto form. Their photochromic properties were studied by powderUV reflectance spectra under the irradiation of 200—380 nm light. The firstorder rate constants of the photocoloring reaction were found to be 780×10 -3 s -1 for compound 1A and 103×10 -3 s -1 for compound 2A.展开更多
We report that the ultraviolet （UV） light induced photochromic behavior of layered organic-inorganic perovskite material of （C4H9NH3）2CuCl4, changed from yellow to brown after irradiation with UV light （10 mW/cm^...We report that the ultraviolet （UV） light induced photochromic behavior of layered organic-inorganic perovskite material of （C4H9NH3）2CuCl4, changed from yellow to brown after irradiation with UV light （10 mW/cm^2） and partially recovered through storage in the dark. （C4H9NH3）2CuCl4 exhibited two distinct absorption bands centered at 286 nm （band Ⅰ） and 384 nm （band Ⅱ）, which were attributed to the photo-induced exciton formed in 2D inorganic layers sandwiched by organic layers. The blue shift of band Ⅰ from 287 to 269 nm as well as the decrease of the intensity of band Ⅰ and band Ⅱ could be found when samples were irradiated under UV light for different length of time. The simultaneous weakening of the intensity of the N-H...Cl hydrogen bond as well as the vibration of the long Cu-Cl bond in the distorted CuCl6^4- octahedron could be detected from the Fourier transform infrared （FTIR） spectra, which resulted the change of charge distribution of the dissymmetric Cl-Cu...Cl bond and the resulting photochromic behavior.展开更多
Incorporation of photochromic compounds to the polymer through chemical bonding will result in an enhancement of photoactivity and stabilization of optical properties.Here,spiropyran(SP)was introduced into polyurethan...Incorporation of photochromic compounds to the polymer through chemical bonding will result in an enhancement of photoactivity and stabilization of optical properties.Here,spiropyran(SP)was introduced into polyurethane(PU)through semi-continuous emulsion copolymerization to get waterborne polyurethane dispersion(SPU).Studies on photochromic properties by UV-vis technique demonstrated the absorption intensity increased with the increasing of SP concentration and the colorless film turned to purple under UV irradiation.The kinetics for ring-opening and ring-closing reaction against SP were both first order,but the rate constants decreased with the increasing of SP concentration.The prepared SPU films showed reasonable photostability and photoreversibility according to the convenient test methods under UV-vis irradiation.Temperature dependence studies demonstrated that the photobleaching rate increased at higher temperatures with the same SP concentration.The chemical combination between SP and isocyanate(NCO)end group of polyurethane was confirmed through swelling experiments.Morphology studies were conducted by scanning electron microscope(SEM)micrographs and showed good compatibility between SP and PU.展开更多
The photochromic ring-opening reaction of spiropyran（SP） has been investigated by a realistic semiclassical dynamics simulation,accompanied by SA3-CASSCF（12 10）/MS-CASPT2 potential energy curves（PECs） of S0–S2....The photochromic ring-opening reaction of spiropyran（SP） has been investigated by a realistic semiclassical dynamics simulation,accompanied by SA3-CASSCF（12 10）/MS-CASPT2 potential energy curves（PECs） of S0–S2.The main simulation results show the dominate pathway corresponds to the ringopening process of trans-SP to form the most stable merocyanine（MC） product.These findings provide more important complementarity for interpreting experimental observations.展开更多
Transparent wood(TW)is a wood-based biomaterial with several advantages,such as high optical transmittance,low thermal conductivity,and tunable haze.TW is functionalized according to its transparency to broaden its ap...Transparent wood(TW)is a wood-based biomaterial with several advantages,such as high optical transmittance,low thermal conductivity,and tunable haze.TW is functionalized according to its transparency to broaden its applications in different fields.Several studies have examined wood functionalization in recent years;however,few studies have reported photochromic TW(PTW)for ultraviolet(UV)-shielding window applications.Herein,PTW was obtained by infiltrating the delignified wood template with photochromic silver bromide(AgBr)nanoparticles and a pre-polymerized methyl methacrylate(MMA)mixture solution.The obtained PTW can adjust the luminous flux on change in the color in the visible light region.The photochromic properties were examined,and the optical properties of the composites were characterized using UV-Vis spectrophotometry.Light transmittance of PTW was up to 86.5%at 800 nm before UV irradiation,and it decreased to 70.1%at 800 nm after UV irradiation,as the wood color changed from colorless to dark purple under UV irradiation.Thus,this work not only achieves high-value utilization of wood,but also produces a new material that can be used in varied fields,such as UV-shielding,energy saving,and smart building.展开更多
We have studied the dynamic and static processes occurring in disordered multiparticle colloidal Ag aggregates with natural structure and affecting their plasmonic absorption spectra under pico-and nanosecond pulsed l...We have studied the dynamic and static processes occurring in disordered multiparticle colloidal Ag aggregates with natural structure and affecting their plasmonic absorption spectra under pico-and nanosecond pulsed laser radiations, as well as the physical origin responsible for these processes. We have shown that depending on the duration of the laser pulse,the mechanisms of laser modification of such aggregates can be associated both with changes in the resonant properties of the particles due to their heating and melting(picosecond irradiation mode) and with the particle shifts in the resonant domains of the aggregates(nanosecond pulses) which depend on the wavelength, intensity, and polarization of the radiation.These mechanisms result in formation of a narrow dip in the plasmonic absorption spectrum of the aggregates near the laser radiation wavelength and affect the shape and position of the dip. The effect of polydispersity of nanoparticle aggregates on laser photochromic reaction has been studied.展开更多
In recent years,organic field-effect transistors（OFETs） with high performance and novel multifunctionalities have attracted considerable attention.Meanwhile,featured with reversible photoisomerization and the corres...In recent years,organic field-effect transistors（OFETs） with high performance and novel multifunctionalities have attracted considerable attention.Meanwhile,featured with reversible photoisomerization and the corresponding variation in color,chemical/physical properties,photochromic molecules have been applied in sensors,photo-switches and memories.Incorporation of photochromic molecules to blend in the device functional layers or to modify the interfaces of OFETs is common way to build photo-transistors.In this review,we focus on the recent advantages on the study of photoresponsive transistors involving one of three typical photochromic compounds spiropyran,diarylethene and azobenzene.Three main strategies are demonstrated in detail.Firstly,photochromic molecules are doped in active layers or combined with semiconductor structure thus forming photoreversible active layers.Secondly,the modification of dielectric layer/active layer interface is mainly carried out by bilayer dielectric.Thirdly,the photo-isomerization of self-assembled monolayer（SAM） on the electrode/active layer interface can reversibly modulate the work functions and charge injection barrier,result in bifunctional OFETs.All in all,the combination of photochromic molecules and OFETs is an efficient way for the fabrication of organic photoelectric devices.Photoresponsive transistors consisted of photochromic molecules are potential candidate for real applications in the future.展开更多
Both thermochromic and photochromic coating have attracted many attentions due to their widely applications,but the low stability is a big obstacle.Inspired by the lotus leaf,to endow the chromic coating with superhyd...Both thermochromic and photochromic coating have attracted many attentions due to their widely applications,but the low stability is a big obstacle.Inspired by the lotus leaf,to endow the chromic coating with superhydrophobicity is a possible solution.In this research,a dual response coating was prepared by adding photochromic and thermochromic particles simultaneously.The prepared sample demonstrated at least four-state color switching,which can be successfully used in tactile imaging,multi-color fabric,erasable record,and security labels.The superhydrophobicity was achieved by introducing vinyl-terminated polydimethylsiloxane,which not only offers low surface energy but also can cross-link with the particles to increase the adhesion.Thus,the prepared sample maintained superhydrophobicity after various kinds of destruction(such as sandpaper abrasion,corrosive liquid attack,ultrasonic treatment,UV irradiation,and high-speed drops/turbulent jets impact).Even though the superhydrophobicity can be destroyed by plasma etching,it can be recovered after 12 h at room temperature.展开更多
A novel reversible photochromic nanocomposite film based on a hybrid inorganic-organic matrix in which heteropolyacid H4SiW12O40 （SiWA） was entrapped in Si-O-Ti network was prepared. Structure, photochromic behavior...A novel reversible photochromic nanocomposite film based on a hybrid inorganic-organic matrix in which heteropolyacid H4SiW12O40 （SiWA） was entrapped in Si-O-Ti network was prepared. Structure, photochromic behaviors and mechanism of the film were investigated by means of infrared spectroscopy （IR）, ultraviolet-visible （UV-Vis） absorption spectra and electron spin resonance （ESR）. The results showed that heteropolyanion i.e. SiW12O^4- 40 （SiW12）, maintained a Keggin structure in the film and there was a strong interaction between anion SiW12 and cation R-NH^＋3 （R=link of hybrid composite）. The photochromic properties of the composite film originated from reversible charge transfer between the anions and cations. Under UV irradiation, the anion would be reduced via one-electron step with simultaneous oxidation of the cation, accompanied by a color change from colorless to blue. Bleaching could occur when the film was in contact with ambient air or 02 in the dark.展开更多
基金supported by the National Natural Science Foundation of China(No.22006057,21906072 and 21908115)Postgraduate Research&Practice Innovation Program of Jiangsu Province(China)(SJCX23_2197)Natural Science Foundation of Zhejiang Province of China(LY20E080014).
文摘Solar-driven water splitting for photocatalytic hydrogen evolution is considered a highly promising and costeffective solution to achieve a stable renewable energy supply.However,the sluggish kinetics of electron-hole pairs’separation poses challenges in attaining satisfactory hydrogen production efficiency.Herein,we synthesized the exceptional performance of highly crystalline C_(3)N_(5)(HC–C_(3)N_(5))nanosheet as a photocatalyst,demonstrating a remarkable hydrogen evolution rate of 3.01 mmol h^(-1)g^(-1),which surpasses that of bulk C_(3)N_(5)(B–C_(3)N_(5))by a factor of 3.27.Experimental and theoretical analyses reveal that HC-C_(3)N_(5)nanosheets exhibit intriguing macroscopic photoinduced color changes,effectively broadening the absorption spectrum and significantly enhancing the generation of excitons.Besides,the cyano groups in HC-C_(3)N_(5)efficiently captures and converts photoexcited electrons into bound states,thereby prolonging their lifetimes and effectively separating electrons and holes into catalytically active regions.This research provides valuable insights into the establishment of bound electronic states for developing efficient photocatalysts.
基金Project supported by the National Natural Science Foundation of China(52062042,51802164)the Natural Science Foundation of Inner Mongolia(2020MS05044)。
文摘Photochromic materials with multicolor upconversion reversible modulations are attractive in optical switching devices.Herein,the fabricated YNbO_(4):Er^(3+)/Tm^(3+)/Yb^(3+) materials exhibit excellent photochromism and multicolor upconversion properties from green,red to near infrared(NIR) emissions with increasing Yb concentrations.Reversible multiband upconversion modulations are achieved by alternating light(365 and 405 nm) or thermal stimuli.After 365 nm irradiation,the luminescence color changes from yellow to red,the luminescent photoswitching contrast reaches up to 86.21%(green),82.12%(red) and 77.38%(NIR) in the Y_(0.83)Er_(0.01)Tm_(0.01)NbO_(4):0.15 Yb sample.Besides,the upconversion emission intensity before and after photochromic reaction shows remarkable change in a wide temperature range of 298-718 K.These results indicate that the Er^(3+)/Tm^(3+)/Yb^(3+) tri-doped YNbO_(4) materials can be a good candidate in optical switching and data storage applications.
基金supported by National Natural Science Foundation of China(No.92261109)Natural Science Foundation of Fujian Province(No.2020J05080)+3 种基金Project Funded by China Postdoctoral Science Foundation(No.2023M733496)Natural Science Foundation of Xiamen(No.3502Z20206080)Fujian Science&Technology Innovation Laboratory for Optoelectronic Information of China(No.2021ZR110)Recruitment Program of Global Youth Experts,Youth Innovation Promotion Association CAS(No.2021302).
文摘Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexible cation(H_(2)imb)^(2+)((H_(2)imb)^(2+)=di-protonated 2,3-bis(imidazolin-2-yl)-2,3-dimethylbutane)has been developed.Electron-donating Cl−and(ZnCl4)2−are used to direct folding a flexible electron-deficient(H_(2)imb)^(2+)cation.Three complexes(H_(2)imb)(NO_(3))2(1),(H_(2)imb)Cl2·H_(2)O(2),and(H_(2)imb)ZnCl4(3)have been synthesized in which(H_(2)imb)^(2+)crystallize in an anti-conformation,88.8°-gauche,and 51.8°-gauche,respectively.In contrary to X-ray silent complex 1,X-ray induced photochromism has been achieved in both complex 2 and 3.An intermolecular charge-transfer mechanism has been elucidated and the anion directed folding of(H_(2)imb)^(2+)has been validated to be critical to yield colored long-lived charge-separated states.
基金Project supported by the National Natural Science Foundation of China (No. 20674070)the Natural Science Foundation of Zhejiang Province (No. R404109), China
文摘A series of photochromic diarylethene derivatives containing different fluorophores was synthesized by the Sonogashira coupling reaction and characterized by 1H nuclear magnetic resonance (NMR), 13C NMR and mass spectroscopy. Photochromic conversion of Cz-MS was observed and its structural change was confirmed by proton NMR. Switchable absorption and emission phenomena were observed for these molecules. These phenomena were attributed to the reversible photochromic fluorescence resonance energy transfer (pcFRET) process. The design of this novel photochromic system of Py-4MS enables information to be processed in a non-destructive manner. This overcomes the problem of the destructive nature of tracking photochromism using ultraviolet (UV)-vis spectroscopy.
文摘Copper-cadmium halide doped photochromic glass coating on plate glass has been prepared by a sol-gel process. The sample shows reversible photochromic effect. The results of X-ray diffraction (XRD) and infrared (IR) spectrum investigations indicate that the photochromic phase of tile coating is CuBr_xCl_(1-x), solid solution, and that the structure network of the coating is connected with the bonds of Si-O-Si, Si-O-B and Si-O-Al.
基金supported by the National Natural Science Foundation of China (No.61774073)Open Project of State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University (No. 2016-25)Science and Technology Development Program of Jilin province (No. 20170101086JC)
文摘TiO2 nanotube arrays were prepared by means of an electrochemical anodization technique in an organic electrolyte solution doped with polyvinyl pyrrolidone (PVP) and were subsequently modified with phosphomolybdic acid (PMoA) to obtain PMoA/TiO2 nanotube arrays. The microstructure and photochromic properties were investigated via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results indicated that the Keggin structure of PMoA and the nanotube structure of TiO2 were not destroyed, and there was a strong degree of interaction between PMoA and TiO2 at the biphasic interface with lattice interlacing during the compositing process. The XPS results further indicated that there was a change in the chemical microenvironment during the formation process of the composite, and a new charge transfer bridge was formed through the Mo-O-Ti bond. Under visible light irradiation, the colorless PMoA/TiO2 nanotube array quickly turned blue and exhibited a photochromic response together with reversible photochromism in the presence of H2O2. After visible light irradiation for 60s, the appearance of Mo^5+ species in the XPS spectra indicated a photoreduction process in accordance with a photoinduced electron transfer mechanism.
基金financially supported by the National Natural Science Foundation of China(Nos.21878136,21372194 and 21773103)。
文摘Aggregation-induced emission(AIE) active photochromic molecules have attracted growing attention for their versatile applications.Here we designed and synthesized five newly unsymmetrical photochromic diarylethene(DAE) dyads(BTE1-5) by connecting tetraphenylethene(TPE) and aromatic substituent via bithienylethene(BTE) bridge.The chemical structures of those compounds were identified by ^1H NMR,^(13)C NMR and HRMS.The absorption and emission of these dyads were investigated by UV-vis and fluore scence spectroscopy,respectively.The results showed that all those compounds exhibited typically AIE or aggregation-induced emission enhancement(AIEE) characteristic.Particularly,when an aggregationcaused quenching(ACQ) fluorophore(triphenylamine) was grafted to the molecule,connecting with TPE via BTE-bridge,the ACQ phenomenon was dissipated and converted to an AIE luminophore,and those compounds exhibited photochromism upon irradiation with alternative UV and visible light.The solution or solid of those compounds showed distinctly fluorescence switching "ON" or "OFF" observation upon irradiation with alternative UV and visible light.It is interesting that BTE1 could be applied in recording and rewritable information storage,and the cyclization quantum yields could be affected by substituent significantly.
基金supported by the National Natural Science Foundation of China (Nos. 11674101, 21873030, 91850202,and 21871092)the Fundamental Research Funds for the Central Universities。
文摘It has been challenging to achieve multi-photochromic systems without affecting the individual photoswitching properties of the constituent units. Herein, we present the design and synthesis of a new family of platinum-acetylide dendrimers containing up to twenty-one photochromic dithienylethene(DTE)units that exhibit both high photochromic efficiency and individual switching properties. Upon irradiation with ultraviolet(UV) and visible(vis) light, the resultant metallodendrimers display high conversion yield and good fatigue resistance. More interestingly, cyclization-cycloreversion kinetics revealed that the photochromic property of each DTE unit in these metallodendrimers is unaffected by its neighbor and the full ring-closure of up to twenty-one DTE units in one single dendrimer has been achieved.
基金supported by the National Natural Science Foundation of China(No.29872015,29832030)
文摘The photochromic spiropyrans and spirooxazine having a succinimidyl ester or isothiocyanate pendant group can form covalent products with transaminated DNA. The absorption spectra and solid reflection spectra of modified DNA with these photochromic spiro compounds were investigated.
基金Application Fundamental and Advanced Technology Research Proposal Project of Tianjin,China(No.18JCZDJC38300)。
文摘Photochromic and photoluminescence materials show bright colors under different excitation conditions,and thus,these functional materials have been applied in many fields.Based on the photochromic and photoluminescence theories,a block copolymer,which could be directly processed into nanofibers by electrospinning,was successfully prepared through atom transfer radical polymerization(ATRP).To synthesize the block copolymer,a vinyl monomer containing a spiropyran unit was employed to prepare the photochromic chain segment,and a polymethyl methacrylate(PMMA)chain segment was introduced to improve the processability of the block copolymer.Acting as the photoluminescence unit,the rare earth complex was linked to the side chain through coordination bonding between the rare earth ions and the ester groups of PMMA.When the photochromic and photoluminescence block copolymer was exposed to different wavelengths of ultraviolet(UV)light and visible(Vis)light,it could show white,red,green,yellow,and blue-purple.These results provide the potential of the as-prepared photochromic and photoluminescence block copolymer for application in fibers and fabrics.
基金the National Natural Science Foundation of China for financial support.(Grant Nos.20072018 and 20372039).
文摘A series of photo active azido analogues have been synthesized and their photochromic properties have also been investigated by UV-Vis spectrum. It will be used for the rapid and reliable preparation of large amounts of stable, non-radioactive labeled DNA and RNA hybridization probes. And it is supposed to be easily detected for its photochromic properties.
基金Supported by the National Natural Science Foundation of China
文摘Two photochromic compounds with the pyrazolonering as the photochromic functional structure, 2(1phenyl3methyl4benzoformylpyrazolone5)thiosemicarbazone(PMBPTSC) and 2(1phenyl3methyl4benzoformylpyrazolone5)smethylthiosemicarbazone(PMBPMTSC), were synthesized and characterized by elemental analysis, MS, IR spectra, NMR spectra. The crystal structure of the photocolored product of PMBPTSC was determined by single crystal XRD analysis. The results show that the photochromic phenomenon is due to the photoisomerization from enol form to keto form. Their photochromic properties were studied by powderUV reflectance spectra under the irradiation of 200—380 nm light. The firstorder rate constants of the photocoloring reaction were found to be 780×10 -3 s -1 for compound 1A and 103×10 -3 s -1 for compound 2A.
基金supported by the National Natural Science Foundation of China (Nos. 50318001, 50433020, 50503021 and 50520150165)the Developing Program of Changjiang Scholar and Innovation Team from Ministry of Education of China (No. IRT0651)
文摘We report that the ultraviolet （UV） light induced photochromic behavior of layered organic-inorganic perovskite material of （C4H9NH3）2CuCl4, changed from yellow to brown after irradiation with UV light （10 mW/cm^2） and partially recovered through storage in the dark. （C4H9NH3）2CuCl4 exhibited two distinct absorption bands centered at 286 nm （band Ⅰ） and 384 nm （band Ⅱ）, which were attributed to the photo-induced exciton formed in 2D inorganic layers sandwiched by organic layers. The blue shift of band Ⅰ from 287 to 269 nm as well as the decrease of the intensity of band Ⅰ and band Ⅱ could be found when samples were irradiated under UV light for different length of time. The simultaneous weakening of the intensity of the N-H...Cl hydrogen bond as well as the vibration of the long Cu-Cl bond in the distorted CuCl6^4- octahedron could be detected from the Fourier transform infrared （FTIR） spectra, which resulted the change of charge distribution of the dissymmetric Cl-Cu...Cl bond and the resulting photochromic behavior.
基金Construction of High-Level Teachers of Beijing Institute of Fashion Technology,China(No.BIFT201808)。
文摘Incorporation of photochromic compounds to the polymer through chemical bonding will result in an enhancement of photoactivity and stabilization of optical properties.Here,spiropyran(SP)was introduced into polyurethane(PU)through semi-continuous emulsion copolymerization to get waterborne polyurethane dispersion(SPU).Studies on photochromic properties by UV-vis technique demonstrated the absorption intensity increased with the increasing of SP concentration and the colorless film turned to purple under UV irradiation.The kinetics for ring-opening and ring-closing reaction against SP were both first order,but the rate constants decreased with the increasing of SP concentration.The prepared SPU films showed reasonable photostability and photoreversibility according to the convenient test methods under UV-vis irradiation.Temperature dependence studies demonstrated that the photobleaching rate increased at higher temperatures with the same SP concentration.The chemical combination between SP and isocyanate(NCO)end group of polyurethane was confirmed through swelling experiments.Morphology studies were conducted by scanning electron microscope(SEM)micrographs and showed good compatibility between SP and PU.
基金supported by the National Natural Science Foundation of China (Nos. 21003100 and 21073242)Natural Science Basic Research Plan in Shaanxi Province of China (No. 2011JQ2013)Special Fund of Education Department of Shaanxi Province (No. 12JK0619)
文摘The photochromic ring-opening reaction of spiropyran（SP） has been investigated by a realistic semiclassical dynamics simulation,accompanied by SA3-CASSCF（12 10）/MS-CASPT2 potential energy curves（PECs） of S0–S2.The main simulation results show the dominate pathway corresponds to the ringopening process of trans-SP to form the most stable merocyanine（MC） product.These findings provide more important complementarity for interpreting experimental observations.
基金This work was supported by the Basic Research Project of Natural Science in Shaanxi Province(2019JM-485)National College Students'Innovation and Entrepreneurship Training Program(S202010708007).
文摘Transparent wood(TW)is a wood-based biomaterial with several advantages,such as high optical transmittance,low thermal conductivity,and tunable haze.TW is functionalized according to its transparency to broaden its applications in different fields.Several studies have examined wood functionalization in recent years;however,few studies have reported photochromic TW(PTW)for ultraviolet(UV)-shielding window applications.Herein,PTW was obtained by infiltrating the delignified wood template with photochromic silver bromide(AgBr)nanoparticles and a pre-polymerized methyl methacrylate(MMA)mixture solution.The obtained PTW can adjust the luminous flux on change in the color in the visible light region.The photochromic properties were examined,and the optical properties of the composites were characterized using UV-Vis spectrophotometry.Light transmittance of PTW was up to 86.5%at 800 nm before UV irradiation,and it decreased to 70.1%at 800 nm after UV irradiation,as the wood color changed from colorless to dark purple under UV irradiation.Thus,this work not only achieves high-value utilization of wood,but also produces a new material that can be used in varied fields,such as UV-shielding,energy saving,and smart building.
基金Project funded by the Russian Foundation for Basic Research,the Government of the Krasnoyarsk Territory and Krasnoyarsk Regional Fund of Science(Grant 18-42-243023)the RF Ministry of Science and Higher Education+1 种基金the State Contract with Siberian Federal University for Scientific Researchthe grant of the President of Russian Federation(agreement 075-15-2019-676)。
文摘We have studied the dynamic and static processes occurring in disordered multiparticle colloidal Ag aggregates with natural structure and affecting their plasmonic absorption spectra under pico-and nanosecond pulsed laser radiations, as well as the physical origin responsible for these processes. We have shown that depending on the duration of the laser pulse,the mechanisms of laser modification of such aggregates can be associated both with changes in the resonant properties of the particles due to their heating and melting(picosecond irradiation mode) and with the particle shifts in the resonant domains of the aggregates(nanosecond pulses) which depend on the wavelength, intensity, and polarization of the radiation.These mechanisms result in formation of a narrow dip in the plasmonic absorption spectrum of the aggregates near the laser radiation wavelength and affect the shape and position of the dip. The effect of polydispersity of nanoparticle aggregates on laser photochromic reaction has been studied.
基金supported financially by the National Natural Science Foundation of China(Nos.21302212 and 21522209)the "Strategic Priority Research Program"(No.XDB12010100)
文摘In recent years,organic field-effect transistors（OFETs） with high performance and novel multifunctionalities have attracted considerable attention.Meanwhile,featured with reversible photoisomerization and the corresponding variation in color,chemical/physical properties,photochromic molecules have been applied in sensors,photo-switches and memories.Incorporation of photochromic molecules to blend in the device functional layers or to modify the interfaces of OFETs is common way to build photo-transistors.In this review,we focus on the recent advantages on the study of photoresponsive transistors involving one of three typical photochromic compounds spiropyran,diarylethene and azobenzene.Three main strategies are demonstrated in detail.Firstly,photochromic molecules are doped in active layers or combined with semiconductor structure thus forming photoreversible active layers.Secondly,the modification of dielectric layer/active layer interface is mainly carried out by bilayer dielectric.Thirdly,the photo-isomerization of self-assembled monolayer（SAM） on the electrode/active layer interface can reversibly modulate the work functions and charge injection barrier,result in bifunctional OFETs.All in all,the combination of photochromic molecules and OFETs is an efficient way for the fabrication of organic photoelectric devices.Photoresponsive transistors consisted of photochromic molecules are potential candidate for real applications in the future.
基金supported by the National Nature Science Foundation of China(51977079,51607067)the Central Guid-ance on Local Science and Technology Development Fund of Hebei Province(226Z1204G)+2 种基金the Top Young Innovative Talents of Colleges and universities of Higher Learning Institutions of Hebei(BJ2021095)Youth Elite Scientists Sponsorship Program by the Chinese Society for Electrical Engineering(CSEE-YESS-2017002)the Funda-mental Research Funds for the Central Universities(2020MS115,2017MS149).
文摘Both thermochromic and photochromic coating have attracted many attentions due to their widely applications,but the low stability is a big obstacle.Inspired by the lotus leaf,to endow the chromic coating with superhydrophobicity is a possible solution.In this research,a dual response coating was prepared by adding photochromic and thermochromic particles simultaneously.The prepared sample demonstrated at least four-state color switching,which can be successfully used in tactile imaging,multi-color fabric,erasable record,and security labels.The superhydrophobicity was achieved by introducing vinyl-terminated polydimethylsiloxane,which not only offers low surface energy but also can cross-link with the particles to increase the adhesion.Thus,the prepared sample maintained superhydrophobicity after various kinds of destruction(such as sandpaper abrasion,corrosive liquid attack,ultrasonic treatment,UV irradiation,and high-speed drops/turbulent jets impact).Even though the superhydrophobicity can be destroyed by plasma etching,it can be recovered after 12 h at room temperature.
文摘A novel reversible photochromic nanocomposite film based on a hybrid inorganic-organic matrix in which heteropolyacid H4SiW12O40 （SiWA） was entrapped in Si-O-Ti network was prepared. Structure, photochromic behaviors and mechanism of the film were investigated by means of infrared spectroscopy （IR）, ultraviolet-visible （UV-Vis） absorption spectra and electron spin resonance （ESR）. The results showed that heteropolyanion i.e. SiW12O^4- 40 （SiW12）, maintained a Keggin structure in the film and there was a strong interaction between anion SiW12 and cation R-NH^＋3 （R=link of hybrid composite）. The photochromic properties of the composite film originated from reversible charge transfer between the anions and cations. Under UV irradiation, the anion would be reduced via one-electron step with simultaneous oxidation of the cation, accompanied by a color change from colorless to blue. Bleaching could occur when the film was in contact with ambient air or 02 in the dark.
