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41.
The influence of Stokes shift in optosensing was discussed. Then, the current status of large Stokes shift-based optosensing was reviewed here. 相似文献
42.
This work was aimed at understanding the structure of SiO2–MO2 (M = Ti, Zr, Hf) and SiO2–HfO2–MO2 (M = Ti, Zr) materials, used as mixed oxide glass hosts for Er3+ ions in the fabrication of optical planar waveguides by sol-gel processing. This structural study was performed by Waveguide
Raman Spectroscopy (WRS), complemented with X-ray diffraction (XRD). The admixture of TiO2 to HfO2, SiO2–HfO2 and HfO2–ZrO2 compositions was found to cause precipitation of nanocrystals of tetragonal HfO2 or ZrO2, or the formation of hafnia-titania mixed crystals, depending on the HfO2/TiO2 molar ratio. 相似文献
43.
F?rster resonance energy transfer (FRET), which involves the nonradiative transfer of excitation energy from an excited donor fluorophore to a proximal ground-state acceptor fluorophore, is a well-characterized photophysical tool. It is very sensitive to nanometer-scale changes in donor-acceptor separation distance and their relative dipole orientations. It has found a wide range of applications in analytical chemistry, protein conformation studies, and biological assays. Luminescent semiconductor nanocrystals (quantum dots, QDs) are inorganic fluorophores with unique optical and spectroscopic properties that could enhance FRET as an analytical tool, due to broad excitation spectra and tunable narrow and symmetric photoemission. Recently, there have been several FRET investigations using luminescent QDs that focused on addressing basic fundamental questions, as well as developing targeted applications with potential use in biology, including sensor design and protein conformation studies. Herein, we provide a critical review of those developments. We discuss some of the basic aspects of FRET applied to QDs as both donors and acceptors, and highlight some of the advantages offered (and limitations encountered) by QDs as energy donors and acceptors compared to conventional dyes. We also review the recent developments made in using QD bioreceptor conjugates to design FRET-based assays. 相似文献
44.
Shuhui Yu Kui Yao Francis Eng Hock Tay 《Journal of Sol-Gel Science and Technology》2007,42(3):357-364
The preferential formation of a pyrochlore structure is a knotty problem in the preparation of Pb(Zn1/3Nb2/3)O3 (PZN)-based thin film materials and its presence is significantly detrimental to the dielectric and piezoelectric properties.
In this study, 40 mol% of PZN was replaced with Pb(Mg1/3Nb2/3)O3 (PMN) for obtaining a perovskite composition around a morphotropic phase boundary (MPB), (1−x)(0.6PZN-0.4PMN)-xPT ((1−x)PZMN-xPT, PT: PbTiO3) where x = 0.23. The thin films with this composition were prepared with a polyethylene glycol (PEG) modi-fied sol-gel method on LaAlO3 substrates. The microstructural evolution of the films on heat treatment was examined with X-ray diffraction. With the aid
of PEG, the formation of the pyrochlore phase was suppressed and the perovskite phase formed directly from the amorphous gel
film. The multilayer films with a thickness around 0.25 μm showed a single perovskite phase without any detectable pyrochlore
structure. Microscopic images showed uniform grain size of a few tens of nanometers. The role of the polymer dramatically
promoting the perovskite phase was investigated with the aid of X-ray photoelectron spectroscopy and thermal analysis. The
dielectric constant of the obtained film was 4160 at 1 kHz. The film demonstrated typical ferroelectric hysteresis loops and
exhibited excellent piezoelectric performance. 相似文献
45.
Ruslan P. Liferovich 《Journal of solid state chemistry》2004,177(6):2188-2197
Ternary lanthanide scandates (Ln=La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, and Ho) have been synthesized at ambient pressure. Their structure has been investigated at room temperature by Rietveld analysis of powder X-ray diffraction data. The Ln-scandates are orthorhombic perovskites, adopting space group Pbnm (? 62), a≈b≈√2ap, c≈2ap, Z=4. Heavy lanthanides (Er-Lu), and Y do not form perovskites at ambient conditions. Compositionally driven phase transitions were not observed. The unit-cell parameters decrease with increasing ScO6 octahedron rotation and atomic number of the Ln cation. In common with lanthanide orthoferrites, the uniform structural evolution is interrupted at the middle-heavy part of the lanthanide sequence. This is probably due to an interplay between: (i) enlargement of the ScO6 octahedra relative to BO6 in other perovskites (e.g., FeO6 in GdFeO3); (ii) reduction in size of the first coordination sphere of Ln3+ coincident with the lanthanide contraction; (iii) coincident expansion of the second coordination sphere due to screening effects of OI1 on OI2, and entry of Sc to the lanthanide coordination sphere; (iv) complex mixing between oxygen and lanthanide lanthanide f- and scandium d-orbitals. In the series studied, Ln3+ are in eight-fold coordination (tetragonal antiprism), and are considerably displaced from the center of the LnO8 polyhedron along [001]. Evolution of the crystallochemical characteristics through the Ln orthoscandate series is complex due to both the antipathetic distortions of A- and B-site coordination polyhedra and interaction of the orbitals of oxygen, Ln and Sc. Empirically obtained limits of Goldschmidt and observed viiito tolerance factors for ternary LnBO3 compounds adopting the Pbnm structure are 0.795 and 0.841, respectively. 相似文献
46.
New phases which arise from partial substitution of Ti4+ by Cr3+ and Li+ of the compound La2/3TiO3 have been obtained, giving rise to the series La1.33LixCrxTi2−xO6 (x=0.66, 0.55 and 0.44). These phases adopt a perovskite-type structure as deduced from their structural characterization. Rietveld's analyses of neutron diffraction data show that it is orthorhombic (S.G. Pbnm) with ordered domains. Conductivity has been examined by complex impedance spectroscopy and it increases with increasing lithium and chromium content. These materials behave as mixed conductors with low activation energies. Magnetic susceptibility variation with temperature shows antiferromagnetic interactions at the lowest temperatures. 相似文献
47.
Ayae Sugawara Akira Oichi Hiroko Suzuki Yuzo Shigesato Toshihiro Kogure Takashi Kato 《Journal of polymer science. Part A, Polymer chemistry》2006,44(17):5153-5160
Assembled structures of calcium carbonate (CaCO3) nanocrystals have been examined for polymer/CaCO3 thin-film composites synthesized through a self-organization process inspired by biomineralization. For the crystallization of CaCO3, a thin-film matrix of chitosan has been used as a polymeric substrate. When the matrix is immersed into a supersaturated aqueous solution of CaCO3 containing 1.4 × 10−3 wt % poly(aspartate) (PAsp), thin-film crystals of CaCO3 are formed spontaneously. Three kinds of disklike films have been observed under a polarizing optical microscope. Electron diffraction analyses of each film have revealed that one is aragonite, displaying radial orientation of the c axes, and the others are vaterite, exhibiting different orientations. Detailed observation by scanning electron microscopy has clarified that these films are assemblies of crystalline particles 10–20 nm in size. The thin-film composites have been obtained over a PAsp concentration range of 4.4 × 10−4 to 1.0 × 10−2 wt %. Vaterite formation becomes dominant when the concentration of PAsp is increased. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5153–5160, 2006 相似文献
48.
Single phase perovskite-based rare earth cobaltates (Ln1−xSrxCoO3−δ) (Ln=La3+, Pr3+, Nd3+, Sm3+, Gd3+, Dy3+, Y3+, Ho3+, Er3+, Tm3+ and Yb3+; 0.67?x?0.9) have been synthesized at 1100°C under 1 atmosphere of oxygen. X-ray diffraction of phases containing the larger rare earth ions La3+, Pr3+ and Nd3+ reveals simple cubic structures; however electron diffraction shows orientational twinning of a local, tetragonal (I4/mmm; ap×ap×2ap) superstructure phase. Orientational twinning is also present for Ln1−xSrxCoO3−δ compounds containing rare earth ions smaller than Nd3+. These compounds show a modulated intermediate parent with a tetragonal superstructure (I4/mmm; 2ap×2ap×4ap). Thermogravimetric measurements have determined the overall oxygen content, and these phases show mixed valence (3+/4+) cobalt oxidation states with up to 50% Co(IV). X-ray diffraction data and Rietveld techniques have been used to refine the structures of each of these tetragonal superstructure phases (Ln=Sm3+-Yb3+). Coupled Ln/Sr and oxygen/vacancy ordering and associated structural relaxation are shown to be responsible for the observed superstructure. 相似文献
49.
Tao Zhang Qingxue Ji Jiayi Song Haiming Li Xing Wang Haiqiang Shi Meihong Niu Tingting Chu Fengshan Zhang Yanzhu Guo 《Molecules (Basel, Switzerland)》2022,27(22)
The poor water solubility, large particle size, and low accessibility of cellulose, the most abundant bioresource, have restricted its generalization to carbon dots (CDs). Herein, nitrogen and sulfur co-doped fluorescent carbon dots (N, S-CDs) were hydrothermally synthesized using cellulose nanocrystals (CNC) as a carbon precursor, exhibiting a small particle size and excellent aqueous dispersion. Thiourea was selected as a nitrogen and sulfur dopant to introduce abundant fluorescent functional groups into N, S-CDs. The resulting N, S-CDs exhibited nanoscale size (6.2 nm), abundant functional groups, bright blue fluorescence, high quantum yield (QY = 27.4%), and high overall yield (16.2%). The excellent optical properties of N, S-CDs endowed it to potentially display a highly sensitive fluorescence “turn off” response to rutin. The fluorescence response for rutin allowed a wide linear range of 0–40 mg·L−1, with a limit of detection (LOD) of 0.02 μM, which revealed the potential of N, S-CDs as a rapid and simple sensing platform for rutin detection. In addition, the sustainable and large-scale production of the N, S-CDs in this study paves the way for the successful high-value utilization of cellulose. 相似文献
50.
Ran Lu Wei Wang Bo Dong Chao Xu Bo Li Yong Sun Junchao Liu Biao Hong 《Molecules (Basel, Switzerland)》2022,27(23)
Cardiovascular disease caused by atherosclerosis (AS) seriously affects human health. Photothermal therapy (PTT) brings hope to the diagnosis and treatment of AS, with the development of nanotechnology. To improve treatment efficiency, self-assembled CuCo2S4 nanocrystals (NCs) were developed as a drug-delivery nanocarrier, triggered by near-infrared (NIR) light for efficient chemophotothermal therapy of arterial inflammation. The as-prepared self-assembled CuCo2S4 NCs exhibited excellent biocompatibility and a very high chloroquine (CL)-loading content. In addition, the self-assembled CuCo2S4 NCs/CL nanocomposites showed good photothermal performance, due to strong absorption in the NIR region, and the release of CL from the NCs/CL nanocomposites was driven by NIR light. When illuminated by NIR light, both PTT from the NCs and chemotherapy from the CL were simultaneously triggered, resulting in killing macrophages with a synergistic effect. Moreover, chemo-photothermal therapy with CuCo2S4 NCs/CL nanocomposites showed an effective therapeutic effect for arterial inflammation, in vivo. Our work demonstrated that chemo-photothermal therapy could be a promising strategy for the treatment of arterial inflammation against atherosclerosis. 相似文献