Nanoporous YVO4 as a luminescent host for probing molecular encapsulation.

Control of phase separation of VO43- and rare earth precursors in reverse microemulsions afforded ∼35 nm YVO4 nanoparticles with functionalisable ∼7 ± 3 nm nanopores. Doping by Eu3+ allowed luminescent probing of interfacial crystallisation while xylenol orange absorption showed molecular encapsulation in particle cavities. This provides potential multifunctional systems combining UV-Vis-NIR luminescence and (photo)active molecules for optical sensing.

Spectroscopic characterization of rare events in colloidal particle stochastic thermodynamics.

Given the remarkable developments in synthetic control over chemical and physical properties of colloidal particles, it is interesting to see how stochastic thermodynamics studies may be performed with new, surrogate, or hybrid model systems. In the present work, we apply stochastic dynamics and nonlinear optical light-matter interaction simulations to study nonequilibrium trajectories of individual Yb (III):Er (III) colloidal particles driven by two-dimensional dynamic optical traps. In addition, we characterize the role of fluctuations at the single-particle level by analyzing position trajectories and time-dependent upconversion emission intensities. By integrating these two complementary perspectives, we show how the methods developed here can be used to characterize rare events.

A Highly Stable Yttrium Organic Framework as a Host for Optical Thermometry and D2 O Detection.

The yttrium organic framework (Y0.89 Tb0.10 Eu0.01 )6 (BDC)7 (OH)4 (H2 O)4 (BDC=benzene-1,4-dicarboxylate) is hydrothermally stable up to at least 513 K and thermally stable in air in excess of 673 K. The relative intensities of luminescence of Tb3+ and Eu3+ are governed by Tb3+ -to-Eu3+ phonon-assisted energy transfer and Tb3+ -to-ligand back transfer and are responsible for the differing temperature-dependent luminescence of the two ions. This provides a ratiometric luminescent thermometer in the 288-573 K temperature range, not previously seen for MOF materials, with a high sensitivity, 1.69±0.04 % K-1 at 523 K. In aqueous conditions, loosely bound H2 O can be replaced by D2 O in the same material, which modifies decay lifetimes to yield a quantitative luminescent D2 O sensor with a useful sensitivity for practical application.

Tuning morphology, surface, and nanocrystallinity of rare earth vanadates by one-pot colloidal conversion of hydroxycarbonates.

We show that particle size, morphology, nanocrystallinity, surface area, and defect density of (Y,Eu)VO4 structures can be tuned by one-pot colloidal conversion of rare earth hydroxycarbonates in water/ethylene glycol (EG) suspensions. Using small angle X-ray scattering, transmission electron microscopy and dynamic light scattering, we show how volume fractions of EG direct the amorphous to crystalline conversion at 1 atm/95 °C by controlling size and aggregation of hydroxycarbonate precursors. A template effect due to a Kirkendall-type conversion occurs for low EG contents, yielding solids with high densities of oxygen defects, as demonstrated by O2 uptakes in thermogravimetry and X-ray photoelectron spectroscopy profiles. Starting from small and aggregated hydroxycarbonates high-porosity (Y,Eu)VO4 nanoparticles were produced with expanded unit cells and short-range (<100 Å) crystalline ordering. We explored the effects of synthesis on the textural, microstructure, and defects of (Y,Eu)VO4 solids, which were further correlated to the spectroscopic profiles of Eu3+-activated samples. We show that the ratios between Eu3+ 5D0 internal quantum yields and particle diameters can be directly correlated to the particle surface areas, opening new perspectives for theoretical detailing of f-f luminescence in YVO4 solids, and enabling accurate tuning of structure and applicability of colloidal vanadate nanoparticles for sensing and catalysis applications.

Lanthanoid-Doped Phosphate/Vanadate Mixed Hollow Particles as Ratiometric Luminescent Sensors.

Rare earth (RE) phosphates and vanadates are structurally similar compositions that display distinct but complementary luminescent properties. The properties of these phosphors can be combined in REPO4-REVO4 heterostructures during the development of new sensing technologies for biological applications. This work presents the synthesis of hollow RE phosphate/vanadate colloidal particles and evaluates their applicability as luminescent markers. Hydrothermal treatments of RE hydroxycarbonate particles in the presence of the PO43- and VO43- precursors afforded the final REPO4-REVO4 solids in a two-step template synthesis. We converted precursor hydroxycarbonate particles into the final heterostructures and characterized their structure and morphology. According to our detailed study into the spectroscopic properties of Eu3+-doped particles and their luminescence response to several species, the presence of the phosphate and vanadate phases in a single particle provided different chemical environments and enabled the design of a ratiometric approach to detect H2O2. These results open new perspectives for the development of new intracellular luminescent markers.

Thermal, vibrational and optical properties of PrLuO3 interlanthanides from hydrothermally-derived precursors.

PrLuO3 interlanthanides were prepared at temperatures ranging from 800 °C to 1600 °C using hydrothermally-derived precursors. The chemical reactions observed include the conversion and segregation of Pr(OH)3 and LuO(OH), respectively, into PrO2 and Lu2O3 cubic oxides below 1200 °C, followed by the production of a mixture of hexagonal P63/mmc and orthorhombic Pnma PrLuO3 phases at 1400 °C. Phase-pure orthorhombic PrLuO3 was obtained at 1600 °C, which was corroborated by Raman and micro far-infrared spectroscopic analyses. Photoluminescence, colorimetric and lifetime measurements were carried out in PrLuO3 samples. Dominant emission verified in samples calcined at 1400 °C corresponds to the hypersensitive 3P0 → 3F2 transition with a color purity of 97% (decay times of 12 µs and 3 µs), while emissions for the phase-pure samples correspond to the 3P0 → 3H6 and 3P0 → 3H5 transitions with a color purity of 94% (a single luminescence lifetime of 12 µs). The optical properties of PrLuO3 interlanthanides thereby suggest that they can be used as luminescent materials in both structural arrangements.

Metalloporphyrins immobilized in Fe3O4@SiO2 mesoporous submicrospheres: Reusable biomimetic catalysts for hydrocarbon oxidation.

We successfully immobilized metalloporphyrins (MeP) in mesoporous silica coating magnetite spheres. In this sense, we prepared two different classes of core@shell supports, which comprise aligned (Fe3O4-AM-MeP, MeP=FeP or MnP) and non-aligned (Fe3O4-NM-MeP, MeP=FeP or MnP) mesoporous magnetic structures. X-ray diffractometry and energy dispersive X-ray spectroscopy confirmed the mesoporous nature of the silica shell of the materials. Magnetization measurements, scanning and transmission electron microscopies (SEM/TEM), electrophoretic mobility (ζ-potential), and infrared spectroscopy (FTIR) also confirm the composition and structure of the materials. The catalysts maintained their catalytic activity during nine reaction cycles toward hydrocarbon oxidation processes without detectable catalyst leaching. The catalysis results revealed a biomimetic pattern of cytochrome P450-type enzymes, thus confirming that the prepared materials are can effectively mimic the activity of such groups.

Tripolyphosphate as precursor for REPO(4):Eu (3+) (RE = Y, La, Gd) by a polymeric method.

A modification of the Pechini method was applied to obtain luminescent rare earth orthophosphates. The developed synthetic route is based on the ability of the tripolyphosphate anion (P(3)O(5-)(10)) to act both as a complexing agent and as an orthophosphate precursor. Heating of aqueous solutions containing RE(3+), Eu(3+), P(3)O(5-)(10), citric acid, and ethylene glycol led to polymeric resins. The ignition of these resins at different temperatures yielded luminescent orthophosphates. The produced nanosized phosphors (YPO(4):Eu(3+), (Y,Gd)PO(4):Eu(3+), and LaPO(4):Eu(3+)) were analyzed by infrared and luminescence spectroscopies, X-ray diffractometry, and scanning electron microscopy.