Nano sized La0.4F3：Ce0.45,Tb0.15（core）, La0.4F3：Ce0.45,Tb0.15（Ti O2）（core） shell, La0.55F：Ce0.45, and La0.85F3：Tb0.15 particles were synthesized by adopting co-precipitation technique in acidic environment a...Nano sized La0.4F3：Ce0.45,Tb0.15（core）, La0.4F3：Ce0.45,Tb0.15（Ti O2）（core） shell, La0.55F：Ce0.45, and La0.85F3：Tb0.15 particles were synthesized by adopting co-precipitation technique in acidic environment and coated with Ti O2 to form a core-shell structure by adopting a mechanical dispersion method at room temperature. The synthesized materials were characterized using X-ray diffraction（XRD）, transmission electron microscopy（TEM）, Fourier transform infrared spectroscopy（FTIR）, ultraviolet-visible spectroscopy（UV-Vis） absorption, photoluminescence and lifetime spectroscopy. The crystal structure of La0.4F3：Ce0.45,Tb0.15 remained the same as La F3 after being doped with Ce and Tb ions but with a slight decrease in the lattice parameter. TEM image confirmed the formation of a core-shell structure. The La0.4F3：Ce0.45,Tb0.15/Ti O2 exhibited Tb3＋ fluorescence enhancement by a factor of 1.76. Scintillation from the synthesized materials was also observed under X-ray excitation.展开更多
We study here the response of photonic hydrogels(PHs),made of photonic crystals of homogeneous silica particles in polyacrylamide hydrogels(SPHs),to the uranyl ions 22 UO_(2)^(2+) in aqueous solutions.It is found that...We study here the response of photonic hydrogels(PHs),made of photonic crystals of homogeneous silica particles in polyacrylamide hydrogels(SPHs),to the uranyl ions 22 UO_(2)^(2+) in aqueous solutions.It is found that the reflection spectra of the SPH show a peak due to the Bragg diffraction,which exhibits a blue shift in the presence of 22 UO_(2)^(2+).Upon exposure to the SPH,22 UO_(2)^(2+)gets adsorbed on the SPH and forms complex coordinate bonds with multiple ligands on the SPH,which causes shrinking of hydrogel and leads to the blue shift in the diffraction peak.The amount of the blue shift in the diffraction peak increases monotonically up to 22 UO_(2)^(2+)concentrations as high as 2300μM.The equilibration time for the shift in the Bragg peak upon exposure to 22 UO_(2)^(2+)is found to be~30 min.These results are in contrast to the earlier reports on photonic hydrogels of inhomogeneous microgel particles hydrogel(MPH),which shows the threshold 22 UO_(2)^(2+)concentration of~600μM,below which the diffraction peak exhibits a blue shift and a change to a red shift above it.The equilibration time for MPH is~300 min.The observed monotonic blue shift and the faster time response of the SPH to 22 UO_(2)^(2+)as compared to the MPH are explained in terms of homogeneous nature of silica particles in the SPH,against the porous and polymeric nature of microgels in the MPH.We also study the extraction of 22 UO_(2)^(2+)from aqueous solutions using the SPH.The extraction capacity estimated by the arsenazo-III analysis is found to be 112 mM/kg.展开更多
文摘Nano sized La0.4F3：Ce0.45,Tb0.15（core）, La0.4F3：Ce0.45,Tb0.15（Ti O2）（core） shell, La0.55F：Ce0.45, and La0.85F3：Tb0.15 particles were synthesized by adopting co-precipitation technique in acidic environment and coated with Ti O2 to form a core-shell structure by adopting a mechanical dispersion method at room temperature. The synthesized materials were characterized using X-ray diffraction（XRD）, transmission electron microscopy（TEM）, Fourier transform infrared spectroscopy（FTIR）, ultraviolet-visible spectroscopy（UV-Vis） absorption, photoluminescence and lifetime spectroscopy. The crystal structure of La0.4F3：Ce0.45,Tb0.15 remained the same as La F3 after being doped with Ce and Tb ions but with a slight decrease in the lattice parameter. TEM image confirmed the formation of a core-shell structure. The La0.4F3：Ce0.45,Tb0.15/Ti O2 exhibited Tb3＋ fluorescence enhancement by a factor of 1.76. Scintillation from the synthesized materials was also observed under X-ray excitation.
文摘We study here the response of photonic hydrogels(PHs),made of photonic crystals of homogeneous silica particles in polyacrylamide hydrogels(SPHs),to the uranyl ions 22 UO_(2)^(2+) in aqueous solutions.It is found that the reflection spectra of the SPH show a peak due to the Bragg diffraction,which exhibits a blue shift in the presence of 22 UO_(2)^(2+).Upon exposure to the SPH,22 UO_(2)^(2+)gets adsorbed on the SPH and forms complex coordinate bonds with multiple ligands on the SPH,which causes shrinking of hydrogel and leads to the blue shift in the diffraction peak.The amount of the blue shift in the diffraction peak increases monotonically up to 22 UO_(2)^(2+)concentrations as high as 2300μM.The equilibration time for the shift in the Bragg peak upon exposure to 22 UO_(2)^(2+)is found to be~30 min.These results are in contrast to the earlier reports on photonic hydrogels of inhomogeneous microgel particles hydrogel(MPH),which shows the threshold 22 UO_(2)^(2+)concentration of~600μM,below which the diffraction peak exhibits a blue shift and a change to a red shift above it.The equilibration time for MPH is~300 min.The observed monotonic blue shift and the faster time response of the SPH to 22 UO_(2)^(2+)as compared to the MPH are explained in terms of homogeneous nature of silica particles in the SPH,against the porous and polymeric nature of microgels in the MPH.We also study the extraction of 22 UO_(2)^(2+)from aqueous solutions using the SPH.The extraction capacity estimated by the arsenazo-III analysis is found to be 112 mM/kg.
