Abstract:Sm3+ doped YPO4 spherical nanoparticles are prepared by wet chemical route. Pure YPO4 shows the tetragonal phase, which is stable up to 900 °C, whereas pure SmPO4 shows the phase transition from hexagonal to monoclinic when heated above 800 °C. The (2-10 at.%) Sm3+ doped YPO4 shows the mixture of phases of tetragonal and hexagonal, which transform to the tetragonal phase above 800 °C. Infra-red study could distinguish confined water in the pore of hexagonal phase from water present on the surface of particles.… Show more
“…Figure (a) represents the TGA‐DTA curves of YPO 4 NPs prepared in ethylene glycol medium. There are two steps of weight loss in TGA curve, one below 300 °C due to loss of surface water and another below 500 °C due to the loss of bound water present in the prepared NPs . There is also an exothermic peak at around 279 nm due to the decomposition of ethylene glycol.…”
Spherical MnFe2O4 and MnFe2O4@YPO4:5 Eu3+ magnetic nanoparticles have been prepared by co‐precipitation method. Crystal structure, morphology, elemental composition and surface structure were characterised by X‐ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and Infra‐red spectroscopy (IR). Their calculated average crystallite sizes are found to be 28 and 35 nm respectively. And the prepared nanoparticles are having spherical morphology. The composite bond formation between MnFe2O4 and YPO4:5 Eu3+ is confirmed by more intense bending vibrations of PO43− group for hybrid nanoparticles. The magnetization of hybrid nanoparticles shows magnetization per gram of MnFe2O4, Ms= 34.355 emu/g with negligible coercivity indicating superparamagnetic behaviour. Prepared magnetic nanoparticles achieve hyperthermia temperature (42 °C to 47 °C) under AC magnetic field indicating potential material for biological application. The prepared nanoparticles are showing red luminescence peaks at 615 nm and 702 nm, which are included in the range of biological window.
“…Figure (a) represents the TGA‐DTA curves of YPO 4 NPs prepared in ethylene glycol medium. There are two steps of weight loss in TGA curve, one below 300 °C due to loss of surface water and another below 500 °C due to the loss of bound water present in the prepared NPs . There is also an exothermic peak at around 279 nm due to the decomposition of ethylene glycol.…”
Spherical MnFe2O4 and MnFe2O4@YPO4:5 Eu3+ magnetic nanoparticles have been prepared by co‐precipitation method. Crystal structure, morphology, elemental composition and surface structure were characterised by X‐ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and Infra‐red spectroscopy (IR). Their calculated average crystallite sizes are found to be 28 and 35 nm respectively. And the prepared nanoparticles are having spherical morphology. The composite bond formation between MnFe2O4 and YPO4:5 Eu3+ is confirmed by more intense bending vibrations of PO43− group for hybrid nanoparticles. The magnetization of hybrid nanoparticles shows magnetization per gram of MnFe2O4, Ms= 34.355 emu/g with negligible coercivity indicating superparamagnetic behaviour. Prepared magnetic nanoparticles achieve hyperthermia temperature (42 °C to 47 °C) under AC magnetic field indicating potential material for biological application. The prepared nanoparticles are showing red luminescence peaks at 615 nm and 702 nm, which are included in the range of biological window.
“…Chemically and thermally stable, highly crystalline, photostable and efficiently emitting, these particles are admitted to be an attractive candidate for a wide range of applications, from optoelectronics (display and LED production) to biomedicine. The biomedical application include such areas as cell labeling [1], the detection of molecules [2], while YPO 4 containing composite nanoparticles were suggested for hyperthermia treatment [3]. Apart from high fluorescence intensity and stability, the latter impose additional requirements on the material properties, namely, low toxicity, high biocompatibility and dispersability in aqueous media.…”
“…Therefore one of the main problems for the NPs development for bioimaging is protection of NPs against the inner and surface water. Fluorescence quenching is enhanced further by placing nanoparticles in aqueous environment, which is a necessary stage of cancer diagnostics, as well as any other medical treatment 15 . Moreover, the concentration of nanoparticles in colloidal solution during in vivo experiments should be as low as possible to avoid or at least minimize intoxication.…”
Tetragonal xenotime-type yttrium orthophosphate (YPO4) Nd(3+) doped nanoparticles suitable for biomedical applications were prepared by microwave-hydrothermal treatment. We applied the energy transfer probing based on the analysis of kinetics of impurity quenching to determine the presence and spatial position of -OH fluorescence quenching acceptors in the impurity-containing nanoparticles. We show that the impurity quenching kinetics of the 0.1 at% Nd(3+) doped YPO4 nanoparticles is a two stage (ordered and disordered) static kinetics, determined by a direct energy transfer to the -OH acceptors. Analyzing the ordered stage, we assume that the origin of the -OH groups is the protonation of the phosphate groups, while analyzing the disordered stage, we assume the presence of water molecules in the mesopores. We determine the dimension of the space of the -OH acceptors as d = 3 and quantify their absolute concentration using the disordered Förster stage of kinetics. We use the late stage of kinetics of fluorescence hopping (CDD ≫ CDA) quenching (the fluctuation asymptotics) at 1 at% Nd(3+) concentration as an energy transfer probe to quantify the relative concentration of -OH molecular groups compared to an optically active rare-earth dopant in the volume of NPs, when energy migration over Nd(3+) donors to the -OH acceptors accelerates fluorescence quenching. In doing so we use just one parameter α = γ(A)/γ(D) = n(A)√[C(DA)]/n(D)√[C(DD)], defined by the relation of concentration of the -OH acceptors to the concentration of an optically active dopant. The higher is the α, the higher is the relative concentration of -OH acceptors in the volume of nanoparticles. We find α = 2.95 for the 1 at% Nd(3+):YPO4 NPs that, according to the equation for α, and the results obtained for the values of the microparameters CDD(Nd-Nd) = 24.6 nm(6) ms(-1) and CDA(Nd-OH) = 0.6 nm(6) ms(-1), suggests twenty times higher concentration for acceptors other than donors. As the main result we have established that the majority of -OH acceptors is located not on the surface of the Nd(3+):YPO4 nanoparticles, as many researchers assumed, but in their volume, and can be either associated with crystal structure defects or located in the mesopores.
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