Multifunctional Lanthanide-Doped Binary Fluorides and Graphene Oxide Nanocomposites Via a Task-Specific Ionic Liquid.

Graphene oxide-based nanocomposites (NCMs) exhibit diverse photonic and biophotonic applications. Innovative nanoengineering using a task-specific ionic liquid (IL), namely, 1-butyl-3-methyl tetrafluoroborate [C4mim][BF4], allows one to access a unique class of luminescent nanocomposites formed between lanthanide-doped binary fluorides and graphene oxide (GO). Here the IL is used as a solvent, templating agent, and as a reaction partner for the nanocomposite synthesis, that is, "all three in one". Our study shows that GO controls the size of the NCMs; however, it can tune the luminescence properties too. For example, the excitation spectrum of Ce3+ is higher-energy shifted when GO is attached. In addition, magnetic properties of GdF3:Tb3+ nanoparticles (NPs) and GdF3:Tb3+-GO NCMs are also studied at room temperature (300 K) and very low temperature (2 K). High magnetization results for the NPs (e.g., 6.676 emu g-1 at 300 K and 184.449 emu g-1 at 2 K in the applied magnetic field from +50 to -50 kOe) and NCMs promises their uses in many photonic and biphotonic applications including magnetic resonance imaging, etc.

Lanthanide-Doped Luminescent Nanophosphors via Ionic Liquids.

Lanthanide (Ln3+) ion(s)-doped or rare-earth ion(s)-doped nanomaterials have been considered a very important class of nanophosphors for various photonic and biophotonic applications. Unlike semiconductors and organic-based luminescent particles, the optical properties of Ln3+-doped nanophosphors are independent of the size of the nanoparticles. However, by varying the crystal phase, morphology, and lattice strain of the host materials along with making core-shell structure, the relaxation dynamics of dopant Ln3+ ions can be effectively tuned. Interestingly, a judicious choice of dopant ions leads to unparallel photophysical dynamics, such as quantum cutting, upconversion, and energy transfer. Recently, ionic liquids (ILs) have drawn tremendous attention in the field of nanomaterials synthesis due to their unique properties like negligible vapor pressure, nonflammability, and, most importantly, tunability; thus, they are often called "green" and "designer" solvents. This review article provides a critical overview of the latest developments in the ILs-assisted synthesis of rare-earth-doped nanomaterials and their subsequent photonic/biophotonic applications, such as energy-efficient lighting and solar cell applications, photodynamic therapy, and in vivo and in vitro bioimaging. This article will emphasize how luminescence dynamics of dopant rare-earth ions can be tuned by changing the basic properties of the host materials like crystal phase, morphology, and lattice strain, which can be eventually tuned by various properties of ILs such as cation/anion combination, alkyl chain length, and viscosity. Last but not least, different aspects of ILs like their ability to act as templating agents, solvents, and reaction partners and sometimes their "three-in-one" use in nanomaterials synthesis are highlighted along with various photoluminescence mechanisms of Ln3+ ion like up- and downconversion (UC and DC).

The nano-bio interactions of rare-earth doped BaF2 nanophosphors shape the developmental processes of zebrafish.

Nanoparticles with biomedical applications should be evaluated for their biocompatibility. Rare-earth doped nanoparticles with unique spectral properties are superior in vivo optical probes in comparison with quantum dots and organic dyes, however, studies describing their nano-bio interactions are still limited. Here, we have evaluated the nano-bio interactions of green-synthesized, phase-pure BaF2 nanoparticles doped with rare-earth (RE3+ = Ce3+/Tb3+) ions using larval zebrafish. We found that zebrafish can tolerate a wide concentration range of these nanoparticles, as the maximal lethality was observed at very high concentrations (more than 200 mg L-1) upon five days of continuous exposure. At a concentration of 10 mg L-1, at which Zn2+, Ti4+ and Ag+ nanoparticles are reported to be lethal to developing zebrafish, continuous exposure to our nanoparticles for four days produced no developmental anomalies, craniofacial defects, cardiac toxicity or behavioural abnormalities in the developing zebrafish larvae. We have also found that the doping of rare-earth ions has no major effect on these biomarkers. Interestingly, the function of acetylcholinesterase (AChE) and the cellular metabolic activity of whole zebrafish larvae remained unchanged, even during continuous exposure to these nanoparticles at 150 mg L-1 for four days; however, severe developmental toxicities were evident at this high concentration. Based on these results, we can conclude that the biocompatibility of rare-earth doped nanoparticles is concentration dependent. Not all biomarkers are sensitive to these nanoparticles. The high concentration-dependent toxicity occurs through a mechanism distinct from changes in the metabolic or AChE activity. The significance of these findings lies in using these nanoparticles for bioimaging applications and biomarker studies, especially for prolonged exposure times.

Imidazolium Based Ionic Liquids: A Promising Green Solvent for Water Hyacinth Biomass Deconstruction.

Water hyacinth (WH) is a troublesome aquatic weed of natural and artificial water bodies of India and other tropical countries and causing severe ecological problems. The WH biomass is low in lignin content and contains high amount of cellulose and hemicellulose, making it suitable material for conversion into liquid fuels for energy production. This study highlighted that, how different imidazolium based ionic liquids (ILs) [1-alkyl-3-methylimidazolium bromide, [Cnmim]Br (n = 2, 4, 6, 8, and 10)] with tunable properties can be employed for the degradation of WH biomass. Different characterizations techniques, such as XRD, FT-IR, SEM, and DSC are used to unravel the interplay between ILs and the biomass. In this study, it is observed that [Emim][Br] pretreated samples have maximum crystalline value (Crl = 26.38%) as compared to other ionic liquids pretreatments. FTIR data showed the removal of lignin from WH biomass by 12.77% for [Emim][Br] and 10.74% for [Edmim][Br]. SEM images have proven that [Emim][Br] pretreatment have altered the structure of biomass the most. Our results proved that IL pretreatment is a promising approach for effective treatment of WH biomass and causes high levels disruption of cellulose structure.

Adsorption-Driven Catalytic and Photocatalytic Activity of Phase Tuned In2S3 Nanocrystals Synthesized via Ionic Liquids.

Phase tuned quantum confined In2S3 nanocrystals are accessible solvothermally using task-specific ionic liquids (ILs) as structure directing agents. Selective tuning of size, shape, morphology, and, most importantly, crystal phase of In2S3 is achieved by changing the alkyl side chain length, the H-bonding, and aromatic π-stacking ability of the 1-alkyl-3- methylimidazolium bromide ILs, [Cnmim]Br (n = 2, 4, 6, 8, and 10). It is observed that crystallite size is significantly less when ILs are used compared to the synthesis without ILs keeping the other reaction parameters the same. At 150 °C, when no IL is used, pure tetragonal form of ß-In2S3 appears however in the presence of [Cnmim]Br [n = 2,4], at the same reaction condition, a pure cubic phase crystallizes. However, in case of methylimidazolium bromides with longer pendant alkyl chains such as hexyl (C6), octyl (C8) or decyl (C10), nanoparticles of the tetragonal polymorph form. Likewise, judicious choice of reaction temperature and precursors has a profound effect to obtain phase pure and morphology controlled nanocrystals. Furthermore, the adsorption driven catalytic and photocatalytic activity of as-prepared nanosized indium sulfide is confirmed by studying the degradation of crystal violet (CV) dye in the presence of dark and visible light. A maximum of 94.8% catalytic efficiency is obtained for the In2S3 nanocrystals using tetramethylammonium bromide (TMAB) ionic liquid.

Phase selective synthesis of quantum cutting nanophosphors and the observation of a spontaneous room temperature phase transition.

Oxygen-free Eu(3+)-doped NaGdF4 nanocrystals with high quantum cutting efficiency are accessible at low temperatures (room temperature to 80 °C) using task-specific ionic liquids (ILs) as structure directing agents and only water as solvent. Selective tuning of the shape, morphology and, most importantly, the crystal phase of the host lattice is achieved by changing the alkyl side length, the H-bonding capabilities and the concentration of 1-alkyl-3-methylimidazolium bromide ILs, [C(n)mim]Br. When using [C2mim]Br, hexagonal NaGdF4 nanoparticles are obtained. In the case of methylimidazolium bromides with longer pendant alkyl chains such as butyl (C4), octyl (C8) or decyl (C10), extremely small nanoparticles of the cubic polymorph form, which then convert even at room temperature (RT) to the thermodynamically favored hexagonal modification. To the best of our knowledge, this kind of spontaneous phase transition is not yet reported. The hexagonal nanomaterial shows a substantial quantum cutting efficiency (154%) whilst in the cubic material, the effect is negligible (107%). The easy yet highly phase selective green synthesis of the materials promises large scale industrial application in environmentally benign energy efficient lighting.

Highly luminescent salts containing well-shielded lanthanide-centered complex anions and bulky imidazolium countercations.

Four salts containing imidazolium cations and europium(III)- or terbium(III)-centered complex anions have been successfully synthesized from an ethanol/H2O solution. The single-crystal X-ray diffraction analyses reveal that these compounds have a common formula of [R][Ln(DETCAP)4] [R = 1-ethyl-3-methylimidazolium (C2mim), Ln = Eu (1) and Tb (2); R = 1-butyl-3-methylimidazolium (C4mim), Ln = Eu (3) and Tb (4); DETCAP = diethyl-2,2,2-trichloroacetylphosphoramidate], in which the lanthanide centers are chelated by four chelating pseudo-ß-diketonate ligands (DETCAP)(-), forming the respective complex anions. Their thermal behaviors and stabilities were also investigated to study the role of the length of the side chain in the cations. Fluorescence measurements at both room temperature and liquid-nitrogen temperature show that these materials show intense characteristic europium(III) or terbium(III) emissions and have long decay times. Their overall quantum yields were determined to be in the range of 30-49%.

Energy transfer study between Ce3+ and Tb3+ ions in doped and core-shell sodium yttrium fluoride nanocrystals.

Here, we report the preparation of Ce(3+) and Tb(3+) co-doped sodium yttrium fluoride nanorods and NaYF(4):Ce(3+)/Tb(3+) core-shell nanoparticles by the emulsion method. The core-shell nanoparticles are confirmed by X-ray diffraction study and transmission electron microscopy (TEM) analysis. The hexagonal crystal phase of Ce(3+)-doped sodium yttrium fluoride nanocrystals is converted to the cubic polymorph after surface coating by TbF(3). Cell volume, cell parameters and lattice strain have been modified due to core-shell structure. The decay times are found to be 8.4 ms and 5.4 ms for doped nanorods and core-shell nanoparticles, respectively, which reveals that non-radiative decay is higher in the case of core-shell nanoparticles than doped nanorods. Energy transfer efficiencies from Ce(3+) to Tb(3+)are 65% and 45% for doped Na(Y(1.5)Na (0.5))F(6):Ce:Tb material and NaYF(4):Ce/Tb core-shell materials, respectively. Quantum yields are found to be 75% and 42% for doped and core-shell samples, respectively.

Crystal phase, shape and luminescence properties of LaPO4:Eu3+ nanocrystals.

We demonstrated the change of shape and crystal phase of LaPO4:Eu3+ nanomaterials by tuning the temperature of heating. The mechanism related to morphology control of LaPO4:Eu nanorods/nanoparticles are proposed and discussed. We describe the "oriented attachment" growth mechanism for nanorod-to-nanoparticles transformation with increasing the temperature of heating. It is found that the photoluminescence properties of LaPO4:Eu3+ nanostructures are sensitive to the crystal phase and shape. The drastic increase in luminescence intensity (12 times) and decay time increases from 2.66 to 3.34 ms with changing the shape (nanorod to nanoparticle) and crystal phase (hexagonal to monoclinic phase) for the samples prepared by emulsion based method. Our analysis suggests that the manipulation of the photoluminescence property can be done by changing the crystal phase of nanomaterials.

Preparation and photoluminescence properties of Y2SiO5:Eu3+ nanocrystals.

The sol-emulsion-gel method is used for the preparation of about 5-7 nm size Eu2O3 doped and coated Y2SiO5 nanoparticles at 1300 degrees C. Here, we report the role of surface coating, dopant concentration and temperature of heating on the modification of crystal structure and the photoluminescence properties of Y2SiO5:Eu3+ nanocrystals. It is found that photoluminescence properties are sensitive to the crystal structure which is again controlled by surface coating, concentration and heating temperature. The decay times are 0.76, 1.14, 1.23 and 1.40 ms for 0.25, 0.5, 1.0 and 2.5 mol% Eu2O3 doped Y2SiO5 nanocrystals prepared at 1100 degrees C (X1-Y2SiO5). However, in X2-Y2SiO5 crystal phase (at 1300 degrees C) the average decay times are 1.05, 1.35, 1.55 and 1.60 ms for 0.25, 0.5, 1.0 and 2.5 mol% Eu2O3 doped Y2SiO5 nanocrystals, indicating the photoluminescence properties depend on both the crystal structure and the concentration of ions. The emission intensity of the peak at 612 nm (5D0-->7F2) of the Eu3+-ions is found to be sensitive to the doping and surface coating of Y2SiO5 nanocrystals. The decay times are 1.55 and 1.70 ms for 1300 degrees C heated 1.0 mol% Eu2O3 doped and coated Y2SiO5 nanocrystals, respectively. Our analysis suggests that the site symmetry of ions plays a most important role in the modification of radiative relaxation mechanisms and as a result on the overall photoluminescence properties.

Role of surface coating in ZrO2/Eu3+ nanocrystals.

The sol-emulsion-gel method is used for the preparation of Eu3+ ion-doped and coated ZrO2 nanocrystals. Here, we report the role of surface coating, dopant concentration, and temperature of heating in the modification of their crystal structure and photoluminescence properties. It is found that the volume fraction of the tetragonal phase increases from 28.08 to 91.56% because of surface coating. This is a significant modification of the crystal phase in ZrO2 nanocrystals due to surface coating by Eu2O3. It is found that the photoluminescence properties are sensitive to the crystal structure, which is again controlled by surface coating, concentration, and heating temperature. It is found that the decay time (tau) of Eu-doped ZrO2 nanocrystals increases with increasing the concentration of dopant and with increasing the temperature of heating because of changes in their crystal phase. The emission intensity of the peak at 611-617 nm (5D0 --> 7F2) of the Eu3+ ion-activated ZrO2 nanocrystals (doped and coated) is also found to be sensitive to the nanoenvironment. The average decay times are 770 and 488 mus for 1100 degrees C-heated 1.0 mol % Eu2O3-doped and coated ZrO2 nanocrystals, respectively. Our analysis suggests that the site symmetry of the ions plays the most important role in the modifications of the radiative and nonradiative relaxation mechanisms as a result of the overall photoluminescence properties.

Red to blue tunable upconversion in Tm3+-doped ZrO2 nanocrystals.

The effect of dopant concentration on the blue upconversion (UPC) emission of Tm(3+) -doped ZrO(2) nanocrystals under different excitation wavelengths in the red region is reported. The UPC emissions are due to the f-f electronic transitions from excited states (1)G(4) and (1)D(2) of Tm(3+). We observed a chromatic change in the UPC with tuning the excitation wavelength. The UPC emission bands at 475, 488, and 501 nm are observed under excitation at 649 nm, but bands centered at 454 and 460 nm are observed when the excitation wavelength is tuned to 655 nm. The UPC emission could be tuned from 501 to 454 nm ( approximately 47 nm) by changing the excitation wavelength from 649 to 655 nm ( approximately 6 nm). The pump power dependence of the emission bands at 475, 488, and 501 nm were investigated on excitation intensity at 649 nm, and the emission bands at 454 and 460 nm are investigated on excitation intensity at 655 nm, which confirms that all of these UPC emission lines are a two-photon absorption process.