Stuffed Tridymite Structures: Synthesis, Structure, Second Harmonic Generation, Optical, and Multiferroic Properties.

The stuffed tridymite structure Ba(Zn/Co)1-x Si1-x M2x O4 (M=Al3+ and Fe3+ ) is explored for the possible multiferroic behavior and to develop new inorganic colored materials. The compounds were synthesized by employing conventional solid-state chemistry methods in the temperature range 1100-1175 °C for 24 h. The powder X-ray diffraction (PXRD) and Rietveld refinement studies indicate that the compounds stabilize in the P63 space group (no. 173). The refinement results were also rationalized by employing Raman spectroscopic studies. The compounds were found to be second harmonic generation (SHG) active and show weak ferroelectric behavior. The co-substitution of Co2+ and Fe3+ in the structure gives rise to a weak ferromagnetic behavior to the compound, BaCo0.75 Si0.75 Fe0.5 O4 , making it a multiferroic material. The optical studies on the prepared compounds exhibited blue color (Co2+ in Td geometry), purple color (Ni2+ in Td geometry), and simultaneous substitution of Co2+ and Fe3+ gives rise to blue-green color owing to metal-to-metal charge transfer (MMCT) effect.

Tuning the Langasite, La3SbZn3Si2O14, towards white light emission: synthesis, structure, SHG and photoluminescence studies.

A series of single-phase color-tunable Langasite, La3SbZn3Si2O14:RE3+ (RE = Eu, Tb, and Tm) phosphors have been prepared and characterized employing X-ray diffraction (XRD), Raman, and photoluminescence (PL) studies. The substituted compounds, La3SbZn3Si2O14:Eu3+, La3SbZn3Si2O14:Tb3+ and La3SbZn3Si2O14:Tm3+ exhibit the characteristic emissions of Eu3+ (red), Tb3+ (green) and Tm3+ (blue), respectively. By carefully adjusting the concentration of Eu3+ ions in the La3SbZn3Si2O14:1% Tm3+, 2% Tb3+, x% Eu3+ system, we achieved a white emission with a reasonable quantum yield. The compounds are found to be SHG (second-harmonic generation) active with the highest values of 3.6 × KDP (potassium dihydrogen phosphate). In addition, the compounds exhibit reasonable dielectric constants with low loss. The present study demonstrates the color tunability of the Langasite family of compounds and establishes it as an adaptable structure.

Visible-Light-Activated C-C Bond Cleavage and Aerobic Oxidation of Benzyl Alcohols Employing BiMXO5 (M=Mg, Cd, Ni, Co, Pb, Ca and X=V, P).

The synthesis, structure, optical and photocatalytic studies of a family of compounds with the general formula, BiMXO5 ; M=Mg, Cd, Ni, Co, Pb, Ca and X=V, P is presented. The compounds were prepared by regular solid-state reaction of constituents in the temperature range of 720-810 °C for 24 h. The compounds were characterized by powder X-ray diffraction (PXRD) methods. The Rietveld refinement of the PXRD patterns have been carried out to establish the structure. The optical absorption spectra along with the colors in daylight have been explained employing the allowed d-d transition. In addition, the observed colors of some of the V5+ containing compounds were explained using metal-to-metal charge transfer (MMCT) from the partially filled transition-metal 3d orbitals to the empty 3d orbitals of V5+ ions. The near IR (NIR) reflectivity studies indicate that many compounds exhibit good NIR reflectivity, suggesting that these compounds can be employed as 'cool pigments'. The experimentally determined band gaps of the prepared compounds were found to be suitable to exploit them for visible light activated photocatalysis. Photocatalytic C-C bond cleavage of alkenes and aerobic oxidation of alcohols were investigated employing visible light, which gave good yields and selectivity. The present study clearly demonstrated the versatility of the Paganoite family of compounds (BiMXO5 ) towards new colored inorganic materials, visible-light photocatalysts and 'cool pigments'.

New Members of SHG Active Dugganite Family, A3BC3D2O14 (A = Ba, Pb; B = Te, Sb; C = Al, Ga, Fe, Zn; D = Si, Ge, P, V): Synthesis, Structure, and Materials Properties.

A family of compounds, A3BC3D2O14 (A = Ba, Pb; B = Te, Sb; C = Al, Ga, Fe, Zn; D = Si, Ge, P, V), with the Dugganite structure was prepared employing traditional solid-state chemistry methods. PXRD and Rietveld refinement studies indicate that the compounds are stabilized in P321 space group (no. 150). The compounds are found to be SHG active with values ranging from 1.9 to 15.0 × KDP. The compounds exhibit high dielectric constants and low loss in our studies. The noncentrosymmetry related properties of the new Dugganites were understood by band structure calculations. We also explored the present Dugganite-structured oxides for the development of new inorganic colored materials by substituting Co2+, Ni2+, Cu2+, and Fe3+ in place of Zn2+. Thus, substitution of Co2+ and Fe3+ together tunes the blue color of the cobalt compound to blue-green color arising from metal-to-metal charge transfer (MMCT) of Fe3+ and Co2+ ions. The tetrahedrally coordinated Ni2+ in the Dugganite imparts a magenta color.

Color Tuning in Garnet Oxides: The Role of Tetrahedral Coordination Geometry for 3 d Metal Ions and Ligand-Metal Charge Transfer (Band-Gap Manipulation).

We explored garnet-structured oxide materials containing 3d transition-metal ions (e.g., Co2+ , Ni2+ , Cu2+ , and Fe3+ ) for the development of new inorganic colored materials. For this purpose, we synthesized new garnets, Ca3 Sb2 Ga2 ZnO12 (I) and Ca3 Sb2 Fe2 ZnO12 (II), that were isostructural with Ca3 Te2 Zn3 O12 . Substitution of Co2+ , Ni2+ , and Cu2+ at the tetrahedral Zn2+ sites in I and II gave rise to brilliantly colored materials (different shades of blue, green, turquoise, and red). The materials were characterized by optical absorption spectroscopy and CIE chromaticity diagrams. The Fe3+ -containing oxides showed band-gap narrowing (owing to strong sp-d exchange interactions between Zn2+ and the transition-metal ion), and this tuned the color of these materials uniquely. We also characterized the color and optical absorption properties of Ca3 Te2 Zn3-x Cox O12 (0

Electrochemical Dealloying of PdCu3 Nanoparticles to Achieve Pt-like Activity for the Hydrogen Evolution Reaction.

Manipulating the d-band center of the metal surface and hence optimizing the free energy of hydrogen adsorption (ΔGH ) close to the optimal adsorption energy (ΔGH =0) for hydrogen evolution reaction (HER), is an efficient strategy to enhance the activity for HER. Herein, we report a oleylamine-mediated (acting as the solvent, stabilizer, and reducing agent) strategy to synthesize intermetallic PdCu3 nanoparticles (NPs) without using any external reducing agent. Upon electrochemical cycling, PdCu3 transforms into Pd-rich PdCu (ΔGH =0.05 eV), exhibiting remarkably enhanced activity (with a current density of 25 mA cm-2 at ∼69 mV overpotential) as an alternative to Pt for HER. The first-principle calculation suggests that formation of low coordination number Pd active sites alters the d-band center and hence optimal adsorption of hydrogen, leading to enhanced activity. This finding may provide guidelines towards the design and development of Pt-free highly active and robust electrocatalysts.