Hexa-Alkoxytriphenylenes As Hole Transporting Materials Inc Stable Oleds Using ALQ3 As Emitting Layer

1999 ◽  
Vol 598 ◽  
Author(s):  
Markus Emerich ◽  
S. Tasch ◽  
R. Resel ◽  
G. Leising ◽  
R. Freudenmann ◽  
...  

ABSTRACTDevices consisting of hexa-alkoxythriphenylene derivatives as hole transport materials and 8-hydroxyquinoline aluminium (Alq3) as emitting layer with ITO as anode and magnesium as cathode are presented. Moreover X-ray diffraction studies of evaporated triphenylene films were performed leading to a better understanding of crystal structure, morphology and the alignment of the triphenylene molecules on the surface of the substrate.

2010 ◽  
Vol 447-448 ◽  
pp. 734-739
Author(s):  
R. Cai ◽  
W.K. Tan ◽  
Fern Lan Ng ◽  
Chang Q. Sun

In this paper, three types of titanium dioxide structures (anatase, heated amorphous and amorphous) from peroxo titanium complex were deposited on glass and wafer substrates by spraying technique. Influences of crystal structure, morphology and sodium ion on UV induced hydrophilicity were studied. X-ray diffraction revealed that crystalline anatase coatings are extremely hydrophilic (<10°) under UV irradiation (indoor) while the amorphous coatings are still hydrophobic on both glass and wafer substrate with contact angles as high as 70º. When amorphous coating was heated at 450°C, its structure was converted into crystalline anatase, and hence its UV induced hydrophilicity behavior on wafer substrate became similar to that of anatase. However, this UV induced hydrophilicity was inhibited on heated glass (450°C), suggesting that sodium ions in the glass might be responsible for the differences between silicon wafer and glass. With increasing coating thickness, such inhibition effect was reduced, but the hydrophilicity still could not reach the level of anatase. After 6 months of outdoor exposure, water contact angle for amorphous, heated amorphous and anatase were 61°, 26.6° and 12.1°, respectively. Also, X-ray diffraction suggested that amorphous is not converted into anatase after long period of UV exposure, although coating morphologies are changed based on Scanning Electron Microscopic observation. It is concluded that the crystal structure, coating morphology and sodium ion concentration have key impact on the photocatalytic properties on glass substrate.


2020 ◽  
Vol 11 (1) ◽  
pp. 9-15
Author(s):  
Zulhadjri Zulhadjri ◽  
Firmanul Qadri Amir ◽  
Marsal Mahmud ◽  
Upita Septiani ◽  
Syukri Arief

Synthesis of four-layer Aurivillius CaBi3LaTi4O15 has been successfully carried out by hydrothermal technique using NaOH 4 M as mineralizer. The reaction was carried out at 220 °C for 72 h. Crystal structure, morphology, and dielectric properties were analyzed in this study. X-ray diffraction confirmed that the single-phase product was successfully obtained. The refinement result shows the product has orthorhombic crystal structure with space group A21am. The morphology analyzed using SEM shows plate-like grains are observed, which is characteristic of Aurivillius phase. Dielectric curves show peaks at 585 °C which indicate ferroelectric transition temperature.


2014 ◽  
Vol 989-994 ◽  
pp. 755-758
Author(s):  
Yun Jie Zhang ◽  
Jie Zhao ◽  
Da Jian Wang ◽  
Jian Ma

CaS:Eu2+phosphors were prepared by two steps method at a relatively low temperature (1050°C) using NH4Cl as a flux. The influences of NH4Cl flux concentrations on the crystal structure, morphology and photoluminescent properties of CaS:Eu2+phosphors were investigated by X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL), respectively. XRD analysis shows that when the raw materials added with the NH4Cl flux, the crystal structure was not changed .The SEM images indicate that increase of the NH4Cl flux enlarged the grain size of the phosphor particles. The luminescence intensity of CaS:Eu2+was enhanced with adding NH4Cl flux and up to the maximum emission intensity when the addition of NH4Cl flux is 1wt%.


Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group


2002 ◽  
Vol 67 (4) ◽  
pp. 479-489 ◽  
Author(s):  
Michal Hušák ◽  
Bohumil Kratochvíl ◽  
Ivana Císařová ◽  
Ladislav Cvak ◽  
Alexandr Jegorov ◽  
...  

Two new structures of semisynthetic ergot alkaloid terguride created by unusual number of symmetry-independent molecules were determined by X-ray diffraction methods at 150 K. Form A (monoclinic, P212121, Z = 12) contains three symmetry-independent terguride molecules and two molecules of water in the asymmetric part of the unit cell. The form CA (monoclinic, P21, Z = 8) is an anhydrate remarkable by the presence of four symmetry-independent molecules in the crystal structure. Conformations of twelve symmetry-independent molecules that were found in four already described terguride structures are compared with torsion angles obtained by ab initio quantum-mechanical calculations for the simplified model of N-cyclohexyl-N'-diethylurea.


2019 ◽  
Vol 74 (4) ◽  
pp. 357-363
Author(s):  
Daniela Vitzthum ◽  
Hubert Huppertz

AbstractThe mixed cation triel borate Ga4In4B15O33(OH)3 was synthesized in a Walker-type multianvil apparatus at high-pressure/high-temperature conditions of 12.5 GPa and 1300°C. Although the product could not be reproduced in further experiments, its crystal structure could be reliably determined via single-crystal X-ray diffraction data. Ga4In4B15O33(OH)3 crystallizes in the tetragonal space group I41/a (origin choice 2) with the lattice parameters a = 11.382(2), c = 15.244(2) Å, and V = 1974.9(4) Å3. The structure of the quaternary triel borate consists of a complex network of BO4 tetrahedra, edge-sharing InO6 octahedra in dinuclear units, and very dense edge-sharing GaO6 octahedra in tetranuclear units.


1985 ◽  
Vol 63 (6) ◽  
pp. 1166-1169 ◽  
Author(s):  
John F. Richardson ◽  
Ted S. Sorensen

The molecular structures of exo-7-methylbicyclo[3.3.1]nonan-3-one, 3, and the endo-7-methyl isomer, 4, have been determined using X-ray-diffraction techniques. Compound 3 crystallizes in the space group [Formula: see text] with a = 15.115(1), c = 7.677(2) Å, and Z = 8 while 4 crystallizes in the space group P21 with a = 6.446(1), b = 7.831(1), c = 8.414(2) Å, β = 94.42(2)°, and Z = 2. The structures were solved by direct methods and refined to final agreement factors of R = 0.041 and R = 0.034 for 3 and 4 respectively. Compound 3 exists in a chair–chair conformation and there is no significant flattening of the chair rings. However, in 4, the non-ketone ring is forced into a boat conformation. These results are significant in interpreting what conformations may be present in the related sp2-hybridized carbocations.


2015 ◽  
Vol 71 (4) ◽  
pp. 330-337 ◽  
Author(s):  
Sabina Kovač ◽  
Ljiljana Karanović ◽  
Tamara Đorđević

Two isostructural diarsenates, SrZnAs2O7(strontium zinc diarsenate), (I), and BaCuAs2O7[barium copper(II) diarsenate], (II), have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The three-dimensional open-framework crystal structure consists of corner-sharingM2O5(M2 = Zn or Cu) square pyramids and diarsenate (As2O7) groups. Each As2O7group shares its five corners with five differentM2O5square pyramids. The resulting framework delimits two types of tunnels aligned parallel to the [010] and [100] directions where the large divalent nine-coordinatedM1 (M1 = Sr or Ba) cations are located. The geometrical characteristics of theM1O9,M2O5and As2O7groups of known isostructural diarsenates, adopting the general formulaM1IIM2IIAs2O7(M1II= Sr, Ba, Pb;M2II= Mg, Co, Cu, Zn) and crystallizing in the space groupP21/n, are presented and discussed.


2020 ◽  
Vol 75 (8) ◽  
pp. 727-732
Author(s):  
Chen Zhang ◽  
Jian-Qing Tao

AbstractA new Cu(II) metal-organic framework, [Cu(L)(OBA)·H2O]n (1) [H2OBA = 4,4′-oxybis(benzoic acid), L = 3,5-di(1H-benzimidazol-1-yl)pyridine] was hydrothermally synthesized and characterized through IR spectroscopy, elemental and thermal analysis and single-crystal X-ray diffraction. Complex 1 is a four-connected uni-nodal 2D net with a (44·62) topology which shows an emission centered at λ ∼393 nm upon excitation at λ = 245 nm. Moreover, complex 1 possesses high photocatalytic activities for the decomposition of Rhodamine B (RhB) under UV light irradiation.


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