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Luminescent mechanochromic materials are particularly appealing for the development of stimuli-responsive materials. Establishing the mechanism responsible for the mechanochromism is always an issue owing to the difficulty in characterizing the ground phase. Herein, the study of real crystalline polymorphs of a mechanochromic and thermochromic luminescent copper iodide cluster permits us to clearly establish the mechanism involved. The local disruption of the crystal packing induces changes in the cluster geometry and in particular the modification of the cuprophilic interactions, which consequently modify the emissive states. This study constitutes a step further toward the understanding of the mechanism involved in the mechanochromic luminescent properties of multimetallic coordination complexes.
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Lanthanum phosphate (LaPO4) nanorods dispersed in the non-aqueous solvent of ethylene glycol form a system exhibiting large intrinsic birefringence, high colloidal stability and the ability to self-organize into liquid crystalline phases. In order to probe the electro-optical response of these rod dispersions we study here the electric-field-induced birefringence, also called Kerr effect, for a concentrated isotropic liquid state with an in-plane a.c. sinusoidal electric field, in conditions of directly applied (electrodes in contact with the sample) or externally applied (electrodes outside the sample cell) fields. Performing an analysis of the electric polarizability of our rod-like particles in the framework of Maxwell-Wagner-O'Konski theory, we account quantitatively for the coupling between the induced steady-state birefringence and the electric field as a function of the voltage frequency for both sample geometries. The switching time of this non-aqueous transparent system has been measured, and combined with its high Kerr coefficients and its features of optically isotropic "off-state" and athermal phase behavior, this represents a promising proof-of-concept for the integration of anisotropic nanoparticle suspensions into a new generation of electro-optical devices.
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For the development of applications based on mechanochromic luminescent materials, a comprehensive study of the mechanism responsible for the emission changes is required. We report the study of a mechanochromic copper iodide cluster under hydrostatic pressure, which allows control of crystal packing via modification of the intermolecular interactions. In situ single-crystal powder X-ray diffraction analysis and emission measurements under pressure permit one to establish a direct correlation between the molecular structure and luminescence properties and, in particular, to demonstrate that cuprophilic interactions are responsible for the stimuli-responsive luminescence properties of such multinuclear coordination compounds.
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An original copper(I) iodide cluster of novel geometry obtained by using a diphosphine ligand is reported and is formulated [Cu6I6(PPh2(CH2)3PPh2)3] (1). Interestingly, this sort of "eared cubane" cluster based on the [Cu6I6] inorganic core can be viewed as a combination of the two known [Cu4I4] units, namely, the cubane and the open-chair isomeric geometries. The synthesis, structural and photophysical characterisations, as well as theoretical study of this copper iodide along with the derived cubane (3) and open-chair (2) [Cu4I4(PPh3)4] forms, were investigated. A new polymorph of the cubane [Cu4I4(PPh3)4] cluster is indeed presented (3). The structural differences of the clusters were analyzed by solid-state nuclear magnetic resonance spectroscopy. Luminescence properties of the three clusters were studied in detail as a function of the temperature showing reversible luminescence thermochromism for 1 with an intense orange emission at room temperature. This behavior presents different feature compared to the cubane cluster and completely contrasts with the open isomer, which is almost nonemissive at room temperature. Indeed, the thermochromism of 1 differs by a concomitant increase of the two emission bands by lowering the temperature, in contrast to an equilibrium phenomenon for 3. The luminescence properties of 2 are very different by exhibiting only one single band when cooled. To rationalize the different optical properties observed, density functional theory calculations were performed for the three clusters giving straightforward explanation for the different luminescence thermochromism observed, which is attributed to different contributions of the ligands to the molecular orbitals. Comparison of 3 with its [Cu4I4(PPh3)4] cubane polymorphs highlights the sensibility of the emission properties to the cuprophilic interactions.
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Cobre/química , Iodetos/química , Compostos Organometálicos/síntese química , Fosfinas/química , Cristalografia por Raios X , Ligantes , Luminescência , Espectroscopia de Ressonância Magnética , Modelos Moleculares , Estrutura Molecular , Teoria Quântica , Temperatura , TermodinâmicaRESUMO
An in-depth study of mechanochromic and thermochromic luminescent copper iodide clusters exhibiting structural polymorphism is reported and gives new insights into the origin of the mechanochromic luminescence properties. The two different crystalline polymorphs exhibit distinct luminescence properties with one being green emissive and the other one being yellow emissive. Upon mechanical grinding, only one of the polymorphs exhibits great modification of its emission from green to yellow. Interestingly, the photophysical properties of the resulting partially amorphous crushed compound are closed to those of the other yellow polymorph. Comparative structural and optical analyses of the different phases including a solution of clusters permit us to establish a correlation between the Cu-Cu bond distances and the luminescence properties. In addition, the local structure of the [Cu4I4P4] cluster cores has been probed by (31)P and (65)Cu solid-state NMR analysis, which readily indicates that the grinding process modifies the phosphorus and copper atoms environments. The mechanochromic phenomenon is thus explained by the disruption of the crystal packing within intermolecular interactions inducing shortening of the Cu-Cu bond distances in the [Cu4I4] cluster core and eventually modification of the emissive state. These results definitely establish the role of cuprophilic interactions in the mechanochromism of copper iodide clusters. More generally, this study constitutes a step further into the understanding of the mechanism involved in the mechanochromic luminescent properties of metal-based compounds.
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We report emission spectrum measurements on single YxEu(1-x)VO4 nanoparticles. The inhomogeneous widths of the emission peaks are identical for single nanoparticles and for ensembles of nanoparticles, while being broader than those of the bulk material. This indicates that individual nanoparticles are identical in terms of the distribution of different local Eu3+ sites due to crystalline defects and confirms their usability as identical, single-particle oxidant biosensors. Moreover, we report a 465 nm solid-state laser based on sum-frequency mixing that provides a compact, efficient solution for direct Eu3+ excitation of these nanoparticles. Both these two aspects should broaden the scope of Eu-doped nanoparticle applications.
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We track single toxin receptors on the apical cell membrane of MDCK cells with Eu-doped oxide nanoparticles coupled to two toxins of the pore-forming toxin family: α-toxin of Clostridium septicum and ε-toxin of Clostridium perfringens. These nonblinking and photostable labels do not perturb the motion of the toxin receptors and yield long uninterrupted trajectories with mean localization precision of 30 nm for acquisition times of 51.3 ms. We were thus able to study the toxin-cell interaction at the single-molecule level. Toxins bind to receptors that are confined within zones of mean area 0.40 ± 0.05 µm(2). Assuming that the receptors move according to the Langevin equation of motion and using Bayesian inference, we determined mean diffusion coefficients of 0.16 ± 0.01 µm(2)/s for both toxin receptors. Moreover, application of this approach revealed a force field within the domain generated by a springlike confining potential. Both toxin receptors were found to experience forces characterized by a mean spring constant of 0.30 ± 0.03 pN/µm at 37°C. Furthermore, both toxin receptors showed similar distributions of diffusion coefficient, domain area, and spring constant. Control experiments before and after incubation with cholesterol oxidase and sphingomyelinase show that these two enzymes disrupt the confinement domains and lead to quasi-free motion of the toxin receptors. Our control data showing cholesterol and sphingomyelin dependence as well as independence of actin depolymerization and microtubule disruption lead us to attribute the confinement of both receptors to lipid rafts. These toxins require oligomerization to develop their toxic activity. The confined nature of the toxin receptors leads to a local enhancement of the toxin monomer concentration and may thus explain the virulence of this toxin family.
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Toxinas Bacterianas/química , Európio/química , Microdomínios da Membrana/química , Nanopartículas/química , Óxidos/química , Receptores de Superfície Celular/química , Actinas/metabolismo , Animais , Compostos Bicíclicos Heterocíclicos com Pontes/farmacologia , Linhagem Celular , Colesterol/metabolismo , Colesterol Oxidase/farmacologia , Cães , Microdomínios da Membrana/efeitos dos fármacos , Microtúbulos/efeitos dos fármacos , Microtúbulos/metabolismo , Movimento (Física) , Polimerização/efeitos dos fármacos , Proteínas Citotóxicas Formadoras de Poros/química , Estrutura Terciária de Proteína , Esfingomielina Fosfodiesterase/farmacologia , Esfingomielinas/metabolismo , Termodinâmica , Tiazolidinas/farmacologiaRESUMO
A copper iodide cluster bearing reactive silanol groups exhibits thermochromic luminescence properties sensitive to its chemical environment and is thus a suitable building block for the synthesis of optically active materials.
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Titanium dioxide is a well known photocatalyst for reactions involving surface trapped photogenerated carriers. Noble metal photo-reduction may be used for the processing of silver/TiO(2) nanocomposite coatings that may exhibit interesting optical and electrical properties. We present here results of our investigations performed on an original system consisting of preformed colloidal TiO(2) nanoparticles homogeneously dispersed within a mesoporous silica host matrix. Light irradiation of samples immerged in an aqueous silver salt solution leads to the homogeneous deposition of silver islands in the vicinity of the TiO(2) particles and throughout the film thickness. The silver volume fraction is directly controlled by the irradiation dose up to a value of about 16 vol.%. Films exhibit tunable plasmonic properties that correspond to silver nanoparticles in interaction, and a percolation threshold is observed at 8-10 vol.%, leading to films with a conductivity of about 40 S cm(-1). The major interest of this method lies in the high silver reduction quantum efficiency (about 50%) and the possibility to modulate optical and electronic properties by light irradiation while the low temperature of processing permits the photolithographic deposition of metallic patterns on organic flexible substrates.
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Three copper(I) iodide clusters coordinated by different phosphine ligands formulated [Cu(4)I(4)(PPh(3))(4)] (1), [Cu(4)I(4)(Pcpent(3))(4)] (2), and [Cu(4)I(4)(PPh(2)Pr)(4)] (3) (PPh(3) = triphenylphosphine, Pcpent(3) = tricyclopentylphosphine, and PPh(2)Pr = diphenylpropylphosphine) have been synthesized and characterized by (1)H and (31)P NMR, elemental analysis and single crystal X-ray diffraction analysis. They crystallize in different space groups, namely, monoclinic P21/c, cubic Pa Ì 3, and tetragonal I Ì 42m for 1, 2, and 3, respectively. The photoluminescence properties of clusters 1 and 3 show reversible luminescence thermochromism with two highly intense emission bands whose intensities are temperature dependent. In accordance to Density Functional Theory (DFT) calculations, these two emission bands have been attributed to two different transitions, a cluster centered (CC) one and a mixed XMCT/XLCT one. Cluster 2 does not exhibit luminescence variation in temperature because of the lack of the latter transition. The absorption spectra of the three clusters have been also rationalized by time dependent DFT (TDDFT) calculations. A simplified model is suggested to represent the luminescence thermochromism attributed to the two different excited states in thermal equilibrium. In contrast with the pyridine derivatives, similar excitation profiles and low activation energy for these phosphine-based clusters reflect high coupling of the two emissive states. The effect of the Cu-Cu interactions on the emission properties of these clusters is also discussed. Especially, cluster 3 with long Cu-Cu contacts exhibits a controlled thermochromic luminescence which is to our knowledge, unknown for this family of copper iodide clusters. These phosphine-based clusters appear particularly interesting for the synthesis of original emissive materials.
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Structured luminescent thin films are investigated in the context of improved light extraction of phosphors for solid-state-lighting applications. Thin films composed of a sol-gel titania matrix doped with europium chelates are studied as a model system. These films, patterned with a square photonic lattice by soft nanoimprint lithography, are characterized by angle-resolved fluorescence. Modeling of this simple technique is shown to fit well the experimental data, revealing in great detail the guided modes of the film and their extraction parameters. An eightfold extraction enhancement factor of the film emission is measured. To further improve the extraction efficiency, we investigate the role of an additional low-index mesoporous silica underlayer through its influence on the guided modes of different polarizations and their interactions with the photonic crystal. Results obtained on model systems open the way towards the optimization of light-emitting devices, using a strategy of dielectric microstructure engineering using the sol-gel process.
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The mechanochromic and thermochromic luminescence properties of a molecular copper(I) iodide cluster formulated [Cu(4)I(4)(PPh(2)(CH(2)CH=CH(2)))(4)] are reported. Upon mechanical grinding in a mortar, its solid-state emission properties are drastically modified as well as its thermochromic behavior. This reversible phenomenon has been attributed to distortions in the crystal packing leading to modifications of the intermolecular interactions and thus of the [Cu(4)I(4)] cluster core geometry. Notably, modification of the Cu-Cu interactions seems to be involved in this phenomenon directly affecting the emissive properties of the cluster.
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Cobre/química , Iodetos/química , Medições Luminescentes , Fenômenos Mecânicos , Temperatura , Modelos Moleculares , Conformação Molecular , Fosfinas/químicaRESUMO
When placed in the vicinity of metal nanoparticles, fluorophore molecules can have their fluorescence intensity enhanced. In order to engineer highly fluorescent thin films, surface plasmon enhancement fluorescence was studied on macroscopic systems composed of gold nanoparticles deposited on a substrate and coated by a dye-containing polymer film. We developed a simple method based on surface silanization to get a good dispersion of up to 100 nm gold nanoparticles on a substrate. While controlling the nanoparticle size and the fluorophore concentration, we measured the fluorescence enhancement factors of systems doped with dyes possessing different quantum yields. We evidenced experimentally that a fluorescence enhancement factor of 4 could be reached for a low-quantum yield dye and that the fluorophore quantum yield affects significantly the enhancement factor. We then discussed how our experimental results agree with previously developed models.
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The influence of some previously reported critical parameters (aging of the silica sol, humidity, % of trivalent precursor) controlling the nature and the degree of organization of mesophases is studied in detail for CTAB-templated silica and organosilicate films prepared by rapid evaporation techniques. It is shown that all of these parameters directly influence the silica-condensation kinetics. Concerning films with the 2D-hexagonal structure belonging to the CTAB-water phase diagram, the mesophase is mainly stabilized by interactions between cylindrical micelles, and the reactivity of the silica sol does not drastically modify the extent of the order in films. In contrast, the formation of a rigid silica network just after the micellar organization appears to be crucial to prepare well-organized films with the 3D-hexagonal or the cubic transient structure. In the latter case, the size and reactivity of silica clusters have to be controlled to obtain rapid gelation in the deposited sol.
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This corrects the article DOI: 10.1038/nnano.2017.111.
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Rare-earth phosphors exhibit unique luminescence polarization features originating from the anisotropic symmetry of the emitter ion's chemical environment. However, to take advantage of this peculiar property, it is necessary to control and measure the ensemble orientation of the host particles with a high degree of precision. Here, we show a methodology to obtain the photoluminescence polarization of Eu-doped LaPO4 nanorods assembled in an electrically modulated liquid-crystalline phase. We measure Eu3+ emission spectra for the three main optical configurations (σ, π and α, depending on the direction of observation and the polarization axes) and use them as a reference for the nanorod orientation analysis. Based on the fact that flowing nanorods tend to orient along the shear strain profile, we use this orientation analysis to measure the local shear rate in a flowing liquid. The potential of this approach is then demonstrated through tomographic imaging of the shear rate distribution in a microfluidic system.
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We used lanthanide-ion doped oxide nanoparticles, Y(0.6)Eu(0.4)VO(4), as donors in fluorescent resonance energy transfer (FRET) experiments. The choice of these nanoparticles allows us to combine the advantages of the lanthanide-ion emission, in particular the long lifetime and the large Stokes shift between absorption and emission, with the detectability of the nanoparticles at the single-particle level. Using cyanine 5 (Cy5) organic molecules as acceptors, we demonstrated FRET down to the single-nanoparticle level. We showed that, due to the long donor lifetime, unambiguous and precise FRET measurements can be performed in solution even in the presence of large free acceptor concentrations. Highly efficient energy transfer was obtained for a large number of acceptor molecules per donor nanoparticle. We determined FRET efficiencies as a function of Cy5 concentration which are in good agreement with a multiple acceptor-multiple donor calculation. On the basis of the donor emission recovery due to acceptor photobleaching, we demonstrated energy transfer from single-nanoparticle donors in fluorescence microscopy experiments.
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Transferência Ressonante de Energia de Fluorescência/instrumentação , Transferência Ressonante de Energia de Fluorescência/métodos , Elementos da Série dos Lantanídeos/química , Nanopartículas/química , Nanotecnologia/métodos , Óxidos/química , Carbocianinas/farmacologia , Simulação por Computador , Luz , Microscopia de Fluorescência , Modelos Químicos , Modelos Estatísticos , Espectrometria de Fluorescência , Espectrofotometria , Temperatura , Fatores de TempoRESUMO
Nanorods of the photomagnetic coordination network Mo(CN)8Cu2 coated with polyvinylpyrrolidone were prepared and exhibit an enhanced effect upon irradiation when compared to the bulk.
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The 3D-hexagonal mesoporous films are used as templates to grow uniform silver nanoparticles. The grafting of hydrophobic groups at the pore surface, significantly slows down the silver ion diffusion, anchoring small silver clusters in micropores and leading to organized domains of silver particles in mesopores with a narrow size distribution.