H.F. Wong

Water dispersible ultra-small multifunctional KGdF4:Tm3+, Yb3+ nanoparticles with near-infrared to near-infrared upconversion

Ultra-small multifunctional KGdF4:Tm3+,Yb3+ nanoparticles with near-infrared to near-infrared upconversion are synthesized. The average sizes of KGdF4:Tm3+ 2%, Yb3+ 20% core-only and KGdF4:Tm3+ 2%, Yb3+ 20%/KGdF4 core–shell nanoparticles are ∼3.7 nm and ∼7.4 nm, respectively, which fall within the reported optimal sizes (<10 nm) for bioimaging probes. The excitation and emission at 980 and 803 nm are favorable to deeper tissue penetration and reduced autofluorescence. The weak upconversion luminescence of the ultra-small core-only nanoparticles is overcome by the use of the core–shell approach. The magnetic mass susceptibility and magnetization of the ultra-small core-only and core–shell nanoparticles were determined, and are close to those of large nanoparticles (26 and 50 nm) used for magnetic resonance imaging and bio-separation. There is no variation in the magnetic properties with the nanoparticles’ sizes between the core-only (∼3.7 nm) and core–shell (∼7.4 nm) nanoparticles, which differs from the size-dependent luminescence. The oleate-capped core–shell nanoparticles were further encapsulated with a PEG-phospholipid shell to endow them with dispersibility in water, which is indispensable for future biological applications.

Magnetic and luminescent properties of multifunctional GdF3:Eu3+ nanoparticles

Multifunctional GdF3:Eu3+ nanoparticles were synthesized using a hydrothermal method. Photoluminescent excitation and emission spectra, and lifetime were measured. The average lifetime of the nanoparticles is about 11 ms. The nanoparticle exhibits paramagnetism at both 293 and 77 K, ascribing to noninteracting localized nature of the magnetic moment in the compound. The magnetic properties of GdF3:Eu3+ is intrinsic to the Gd3+ ions, which is unaffected by the doping concentration of the Eu3+ luminescent centers. A measured magnetization of approximately 2 emu/g is close to reported values of other nanoparticles for bioseparation.

Towards pure near-infrared to near-infrared upconversion of multifunctional GdF 3 :Yb 3+ ,Tm 3+ nanoparticles

Nearly pure near-infrared to near-infrared (NIR-to-NIR) upconversion in GdF(3) host with 23% Yb(3+) and 1% Tm(3+) under 980 nm excitation is firstly reported. The ratio of the intensity of the emission at 807 nm to that at 478 nm can reach to 105, and the intensity of the emission at 807 nm is preserved. Moreover, the excitation and the emission at 980 and 807 nm are away from the visible region. These are beneficial to deeper tissue penetration and reduced autofluorescence. Raman spectroscopy measurements suggest the high probability of NIR emission in GdF(3) host. Our results indicate that the reported multifunctional nanoparticles are promising in bio-imaging and bio-separation.

In vitro cell imaging using multifunctional small sized KGdF4:Yb3+,Er3+ upconverting nanoparticles synthesized by a one-pot solvothermal process.

Multifunctional KGdF4:18%Yb(3+),2%Er(3+) nanoparticles with upconversion fluorescence and paramagnetism are synthesized. The average sizes of the nanoparticles capped with branched polyethyleneimine (PEI) and 6-aminocaproic acid (6AA) are ~14 and ~13 nm, respectively. Our KGdF4 host does not exhibit any phase change with the decrease of particle size, which can prevent the detrimental significant decrease in upconversion luminescence caused by this effect observed in the well-known NaYF4 host. The branched PEI and 6AA capping ligands endow our nanoparticles with water-dispersibility and biocompatibility, which can favor internalization of our nanoparticles into the cytoplasm of HeLa cells and relatively high cell viability. The strong upconversion luminescence detected at the cytoplasm of HeLa cells incubated with the branched PEI-capped nanoparticles is probably attributed to the reported high efficiency of cellular uptake. The magnetic mass susceptibility of our nanoparticle is 8.62 × 10(-5) emu g(-1) Oe(-1). This is the highest value ever reported in trivalent rare-earth ion-doped KGdF4 nanoparticles of small size (≤14 nm), and is very close to that of nanoparticles used as T1 contrast agents in magnetic resonance imaging. These suggest the potential of our KGdF4:Yb(3+),Er(3+) nanoparticles as small-sized multifunctional bioprobes.

Multiple-mode excitation in spin-transfer nanocontacts with dynamic polarizer

We report our study on the emission response of a magnetic nanocontact with dynamic polarizer in perpendicular magnetic field. In this configuration three modes are accessible, two of which correspond to the precessional motion of a vortex in one of the two ferromagnetic layers with the other working as a static polarizer. At high currents a third mode can be observed that is ascribed to the simultaneous precession of two vortices, one in each layer, with the other layer working as a dynamic polarizer.

Spin-Valve Junction With Transfer-Free MoS 2 Spacer Prepared by Sputtering

The prospect of spintronic devices based on two-dimensional metal dichalcogenide material (2DMX2) originate from their long spin life time [1] and 100% out-of-plane spin polarization [2].

Patterning of L1(0) FePt nanoparticles with ultra-high coercivity for bit-patterned media

L10-ordered FePt nanoparticles (NPs) with ultra-high coercivity were directly prepared from a new metallopolyyne using a one-step pyrolysis method. The chemical ordering, morphology and magnetic properties of the as-synthesized FePt NPs have been studied. Magnetic measurements show the coercivity of these FePt NPs is as high as 3.6 T. Comparison of NPs synthesized under the Ar and Ar/H2 atmospheres shows that the presence of H2 in the annealing environment influences the nucleation and promotes the growth of L10-FePt NPs. Application of this metallopolymer for bit-patterned media was also demonstrated using nanoimprint lithography.