Structural, ferromagnetic and optical properties of pure bismuth A-site polar perovskite Bi(Mg3/8Fe2/8Ti3/8)O3 synthesized at ambient pressure

Two-dimensional lead halide perovskite nanoplatelets (2D LHP NPLs) have been emerging as one of the most promising semiconductor nanomaterials due to their narrow absorption and emission line widths, tunable bandgaps, high exciton binding energies, high defect tolerance as well as highly localized energy states. Colloidal synthesis of 2D LHP NPLs is generally performed using hot-injection or ligand assisted precipitation techniques (LARP). In the LARP method, perovskites are synthesized in polar solvents, which decrease the stability of the 2D LHP NPLs due to their weakly bonded nature. In fact, the presence of residual polar solvent in the LHP NPL colloid can cause deterioration of thickness uniformity, degradation of NPLs to parent precursors, and undesired phase transformations. Herein, for the first time, we report facile seed-mediated synthesis route of monolayer, 2-monolayers, and thicker lead halide perovskite nanoplatelets without using A site cation halide salt (AX; A = Cesium, methylammonium, formamidinium and, X = Cl, Br, I) and long chain alkylammonium halide salts (LX; L = oleylammonium, octylammonium, butylammonium and, X = Cl, Br, I). The seed solution has been synthesized by reacting lead (II) halide salt and coordinating ligands (oleylamine or octylamine and oleic acid) in nonpolar high boiling solvent (1-octadecene). The seed mediated synthesis has been carried out in hexane by reacting seed solution with A-site cation precursors (Cs-oleate, FA-oleate, or diluted MA solution in hexane) under ambient conditions. More importantly, the seed mediated growth of NPLs has been tracked for the first time by performing in-situ optical measurements. Furthermore, the optical properties and morphologies of the seeds have been extensively studied. We find that our facile synthesis route provides highly stable, monodisperse NPLs with narrow absorption, and photoluminescence line widths (68-201 meV), and high PLQY (37.6-1.66% for 2ML NPLs). Furthermore, anion exchange reactions have been performed by mixing pre-synthesized LHP NPLs with counter halide seeds. The optical properties of NPLs have been affectively tuned by postsynthetic chemical reactions without changing the thickness of the NPLs. We anticipate that our new synthetic route provides further understanding of growth dynamics of LHP NPLs.

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Effect of Annealing on Structural and Optical Properties of Pulsed Laser Deposited Titanium Dioxide Thin Films

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.67.65 ◽

2009 ◽

Vol 67 ◽

pp. 65-70 ◽

Cited By ~ 1

Author(s):

Gaurav Shukla ◽

Alika K. Khare

Keyword(s):

Thin Films ◽

Optical Properties ◽

Pulsed Laser Deposition ◽

Annealing Temperature ◽

Ambient Pressure ◽

Pulsed Laser ◽

Laser Deposition ◽

Tio2 Thin Films ◽

Post Annealing ◽

Post Annealing Temperature

TiO2 is a widely studied material for many important applications in areas such as environmental purification, photocatalyst, gas sensors, cancer therapy and high effect solar cell. However, investigations demonstrated that the properties and applications of titanium oxide films depend upon the nature of the crystalline phases present in the films, i.e. anatase and rutile phases. We report on the pulsed laser deposition of high quality TiO2 thin films. Pulsed Laser deposition of TiO2 thin films were performed in different ambient viz. oxygen, argon and vacuum, using a second harmonic of Nd:YAG laser of 6 ns pulse width. These deposited films of TiO2 were further annealed for 5hrs in air at different temperatures. TiO2 thin films were characterized using x-ray diffraction, SEM, photoluminescence, transmittance and reflectance. We observed effect of annealing over structural, morphological and optical properties of TiO2 thin films. The anatase phase of as-deposited TiO2 thin films is found to change into rutile phase with increased annealing temperature. Increase in crystalline behaviour of thin films with post-annealing temperature is also observed. Surface morphology of TiO2 thin films is dependent upon ambient pressure and post- annealing temperature. TiO2 thin films are found to be optically transparent with very low reflectivity hence will be suitable for antireflection coating applications.

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Role of Sr Addition on the Structure Stability and Electrical Conductivity of Sr-Doped Lanthanum Copper Oxide Perovskites

Journal of Materials Research ◽

10.1557/jmr.2004.19.3.943 ◽

2004 ◽

Vol 19 (3) ◽

pp. 943-949 ◽

Cited By ~ 13

Author(s):

Ho-Chieh Yu ◽

Kuan-Zong Fung

Keyword(s):

Copper Oxide ◽

Copper Ions ◽

Perovskite Phase ◽

Ambient Pressure ◽

Solubility Limit ◽

Structure Stability ◽

Lanthanum Copper Oxide ◽

Metallic Conductor ◽

Electron Holes ◽

A Site

The structural and electrical properties of lanthanum copper oxide were examined as a function of Sr addition. It was observed that the lanthanum oxide and copper oxide formed La2CuO4 with K2NiF4 structure when the powder mixture was heated at 800 °C in ambient pressure. Interestingly, the samples of Sr-doped (15∼25%) lanthanum copper oxides showed single perovskite-based phase after being heated at 800 °C. Without Sr addition, a single-perovskite phase of lanthanum copper oxide was observed only under the oxygen pressure as high as 65 kbar. The stabilization of perovskite structure in lanthanum copper oxide was effectively achieved by the addition of Sr. Based on the titration analysis and pertinent defect reactions, the enhancement of perovskite stability was due to the presence of trivalent copper ions that were created to balance the electrical charge of doping ion (SrLa′). With the increasing concentration of trivalent copper ions (or electron holes equivalently) in Sr-doped samples, lanthanum copper oxide also changed from a semiconductor to metallic conductor. When the Sr dopant exceeded its solubility limit of approximately 25% in the A-site sublattice, the Sr-rich second phases, La2SrCu2O6 and Cu2SrO3, appeared and suppressed the electronic conduction drastically.

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Structural, Elastic, and Electronic Properties of Antiperovskite Chromium-Based Carbides ACCr3(A = Al and Ga)

Advances in Condensed Matter Physics ◽

10.1155/2013/136274 ◽

2013 ◽

Vol 2013 ◽

pp. 1-7 ◽

Cited By ~ 6

Author(s):

D. F. Shao ◽

W. J. Lu ◽

S. Lin ◽

P. Tong ◽

Y. P. Sun

Keyword(s):

Fermi Level ◽

Density Functional ◽

Ambient Pressure ◽

Experimental Studies ◽

Lattice Parameter ◽

First Principles Calculation ◽

Functional Theory ◽

Multiple Band ◽

A Site ◽

Formation Energies

We theoretically investigated antiperovskite chromium-based carbides ACCr3through the first-principles calculation based on density functional theory (DFT). The structure optimization shows that the lattice parameter of ACCr3is basically proportional to the radius of A-site elements. The calculated formation energies show that AlCCr3and GaCCr3can be synthesized at ambient pressure and are stable with nonmagnetic ground states. Based on the calculation of elastic constants, some elastic, mechanical, and thermal parameters are derived and discussed. AlCCr3and GaCCr3show ductile natures and may have similar thermal properties. From the analysis of the electronic structures, it was found that there are electron and hole bands that cross the Fermi level for AlCCr3and GaCCr3, indicating multiple-band natures. The Fermi level locates at the vicinity of the density of states (DOSs) peak, which leads to a large DOS at Fermi level dominated by Cr-3d electrons. The band structures of AlCCr3and GaCCr3are very similar to those of the superconducting antiperovskite MgCNi3. The similarity may make AlCCr3and GaCCr3behave superconductively, which needs to be further investigated in theoretical and experimental studies.

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Role of Central Atom on the Pressure Response of 2D Perovskites Containing a Long Alkyl Chain (Decylammonium, DA): DA2PbI4 and DA2GeI4

10.26434/chemrxiv-2021-mfkh0 ◽

2021 ◽

Author(s):

Lorenzo Malavasi ◽

Marta Morana ◽

Boby Joseph ◽

Mauro Coduri ◽

Ausonio Tuissi ◽

...

Keyword(s):

Optical Properties ◽

Phase Separation ◽

Alkyl Chain ◽

Central Atom ◽

Ambient Pressure ◽

Pressure Response ◽

Lead Free ◽

White Lead ◽

Moderate Pressure ◽

Long Alkyl Chain

The application of an external pressure on Metal Halide Perovskite (MHPs) has become a fascinating way of tuning their optical properties, achieving also novel features. Here, the pressure response of 2D MHPs including a long alkyl chain made of ten carbon atoms, namely decylammonium (DA), has been investigated as a function of the central atom in DA2PbI4 and DA2GeI4. The two systems share a common trend in the phase stability, displaying a transition from an orthorhombic to a monoclinic phase around 2 GPa, followed by a phase separation in two monoclinic phases characterized by different c-axis. The optical properties show rather different behavior due to the presence of Pb or Ge. DA2PbI4 shows a progressive red shift of the band gap from 2.28 eV at ambient conditions, to 1.64 eV at 11.5 GPa, with a narrow PL emission composed by two components, with the second one appearing in concomitance with the phase separation and significantly shifted to lower energy. On the other hand, DA2GeI4, changes from a non-PL system at ambient pressure, to a clear broadband emitter centered around 730 nm (FWHM ~ 170 nm), with a large stoke shift, and an intensity maximum at about 3.7 GPa. This work sheds light on the structural stability of 2D perovskites characterized by extended alkyl chains, to date limited to four carbon atoms, and shows the pressure-induced emergence of broad emission in a novel lead-free perovskite, DA2GeI4. The evidence of wide emission by a moderate pressure in a germanium-based 2D MHP represents a novel result which may open the design, by chemical pressure, of efficient wide or even white lead-free emitters.

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