Formation of Tetravalent Fe Ions in LaFeO3 Perovskite Through Mechanochemical Modification by Ball Milling

Mechanochemical modification of previously synthesized LaFeO₃ perovskite‐type oxide by a high‐energy ball milling was investigated to introduce Fe⁴⁺ ions or transform some Fe³⁺ into Fe⁴⁺ in LaFeO₃. X‐ray absorption fine structure studies revealed that the formation of Fe⁴⁺ ions into LaFeO₃ perovskite has been achieved at first time by ball milling at room temperature without any additives or replacement of La³⁺ ions by some divalent cations. The structural model of Fe⁴⁺ containing LaFeO₃ could be described as with a modified perovskite having equal amounts of La and Fe vacancies, which is supported by a good correlation between the results of Fe K‐edge XANES spectra and O₂‐TPD. The synthesis of Fe⁴⁺‐containing LaFeO₃ perovskite by ball milling was able to produce the O₂ adsorption capacity of nonsubstituted perovskite‐type oxide.     

Bisanthracene‐Based Donor–Acceptor‐type Light‐Emitting Dopants: Highly Efficient Deep‐Blue Emission in Organic Light‐Emitting Devices

Deep‐blue fluorescent compounds are particularly important in organic light‐emitting devices (OLEDs). A donor–accepotor (DA)‐type blue‐emitting compound, 1‐(10‐(4‐methoxyphenyl)anthracen‐9‐yl)‐4‐(10‐(4‐cyanophenyl)anthracen‐9‐yl)benzene ( BD3 ), is synthesized, and for comparison, a nonDA‐type compound, 1,4‐bis(10‐phenylanthracene‐9‐yl)benzene ( BD1 ) and a weak DA‐type compound, 1‐(10‐phenylanthracen‐9‐yl)‐4‐(10‐(4‐cyanophenyl)anthracen‐9‐yl)‐benzene ( BD2 ), are also synthesized. The twisted conformations of the two anthracene units in the compounds, confirmed by single crystal X‐ray analysis, effectively prevent π‐conjugation, and the compound shows deep‐blue photoluminescence (PL) with a high PL quantum efficiency, almost independent of the solvent polarity, resulting from the absence of an intramolecular charge transfer state. The DA‐type molecule BD3 in a non‐doped device exhibits a maximum external quantum efficiency (EQE) of 4.2% with a slight roll‐off, indicating good charge balance due to the DA‐type molecular design. In the doped device with 4,4′‐bis(N‐carbazolyl)‐1,1′‐biphenyl (CBP) host, the BD3 exhibits higher EQE than 10% with Commission International de L'Eclairge (CIE) coordinates of (0.15, 0.06) and a narrow full‐width at half‐maximum of 45 nm, which is close to the CIE of the high definition television standard blue.     

Lithium Phenolate Complexes with a Pyridine‐Containing Polymer for Solution‐Processable Electron Injection Layers in PLEDs

A series of (vinylphenyl)pyridine‐based polymer binders, PVPh2Py, PVPh3Py, and PVPh4Py, are designed and synthesized and it is found that mixtures of Liq and the polymers exhibit superior electron injection characteristics as ultrathin (1.6 nm) electron injection layer (EIL) films. They are comparable to those of EILs composed only of Liq. The addition of the polymers does not deteriorate the performance of Liq EILs. Additionally, when the EIL thickness is increased from 1.6 nm to 16 nm, the driving voltages increase and the external quantum efficiencies decrease. The increase in the voltage and decrease in the EQE are suppressed in the device with mixed EILs compared to those observed for the device composed of 100 wt% Liq. Furthermore, the position of the nitrogen in the pyridine ring is considered to influence the electron transport properties of the EILs. The mixing PVPh4Py with Liq improves the driving voltage of the fabricated devices, even with a thick mixed EIL. This reduced dependence of the performance of EILs on their thickness will be advantageous for the coating of large areas using solution processes.     

Tandem MIG welding of aluminium alloys

Welding processes used in transport system manufacturing, such as the automotive industry, have in recent years seen a pronounced trend towards fabrication of lower-cost welded structures through efficiency enhancement focused on weld quality improvement. In this context, arc welding processes providing sufficient weld reinforcing ability, while allowing higher-speed welding are expected to emerge. In welding of aluminium alloys, MIG welding conferring superior economy and profitability holds out particularly high expectations, in future set to be the mainstream process for fabrication of welded structures. In MIG welding, however, straightforward adoption of higher welding speeds for efficiency enhancement purposes leads to loss of joint quality and weldpool turbulence due to increased current. Welding speeds therefore normally have an upper limit of around 1.5 m/min.¹ More recently, however, further welding speed increases have been sought through improvement of wire feed¹ and power supply² systems.     

Effect of zeolite in surface discharge plasma on the decomposition of toluene

Toluene was decomposed in a surface discharge plasma reactor packed with various zeolites. The positioning effect of the zeolite bed was also investigated Reactor-B, in which the zeolite bed was located upstream, performed much better than Reactor-A, in which the zeolite bed was located downstream. Furthermore, the decomposition efficiency in Reactor-B increased with the capacity for toluene adsorption on zeolite, while that in Reactor-A did not. The toluene adsorbed in micropores was not decomposed effectively by direct electron impact, but was decomposed by active oxygen species generated in the plasma zone on the zeolite surface. A good correlation was also observed between toluene decomposition and ozone consumption in the downward-type reactor.     

Bildungsmechanismen im Primärschlackegebiet des Hochofens

Neues Verfahren zur Herstellung von großen Wüstitkristallen. Erörterung der Reaktionen zwischen Wüstit und Kalk-Kieselsäure-Gemischen. Deutung des Bildungsmechanismus im Primärschlackegebiet durch Erläuterung des Aufbaus hohler Körper aus reduzierten Eisenoxiden in Eiszapfenformen.