Stabilization of mixed valencies in Cu, Zn-based oxides

2005 ◽  
Vol 891 ◽  
Author(s):  
Anne Le Nestour ◽  
Manuel Gaudon ◽  
Mona Tréguer-Delapierre ◽  
Ronn Andriessen ◽  
Alain Demourgues

ABSTRACTCu and Zn-based oxides have been developed for the last decades because of their remarkable electronic properties and their relevant UV-Visible-NIR absorption properties. Cu in oxides can adopt various oxidation states (+I, +II, +III) stabilized in various environments (h, Td, D4h, C4v, D2h, Oh). Divalent copper cations can occupy Td or Oh sites in zinc aluminate spinel network. Solid state routes lead to homogeneous phases with Zn1−xCuxAl2O4 compositions. Depending on the inversion rate in the spinel matrix, various absorption bands have been identified in the UV-Visible-CNIR spectrum. The synthesis of the zinc-aluminate spinel solid solution Zn1−xCuxAl2O4 by an esterification route led to monocrystalline nanosized oxides. Two intense absorption bands at 300 and 500 nm can be attributed to charge transfer phenomena between oxygen and Cu2+ cations in tetrahedral and octahedral coordinations. Two other less intense absorption bands centred at 800 nm and 1500 nm are also appearing when the copper rate in the spinel increases but their relative intensity are not in good agreement with those observed in the case of the solid-state synthesis. In the case of the esterification route, the absorption band at 800 nm is much more intense than in the case of the solid-state synthesis. It can only be explained either by a deviation to the centrosymmetric character of octahedral sites or by the occurence of a non negligible amount of monovalent copper cations which give electronic transitions in this energy range. A magnetic study correlated to EPR measurements confirms the occurence of a mixed valence state for copper cations in the solid solution Zn1−xCuxAl2O4. EPR spectra at T=4K show for the small concentration of Cu2+ (x<0.10) a strong anisotropic signal due to the presence of Cu2+ ions in a distorted octahedral symmetry (gx=2.07, gy= 2.15 gz=2.23). Moreover the hyperfine structure, identified on EPR spectra tend to disappear as the compounds are annealed under air because the content of paramagnetic centers Cu2+ (3d9) as well as their interactions become significant. Furthermore, the color changes drastically with the Cu+ (3d10) content. Finally the structural features and UV-Visible-NIR absorption properties of copper-zinc aluminates will be discussed and compared to Cu-doped ZnO.

2007 ◽  
Vol 61 (17) ◽  
pp. 3755-3757 ◽  
Author(s):  
Ping Yin ◽  
Yucai Hu ◽  
Yanzhi Sun ◽  
Yingxia Yang ◽  
Chunnuan Ji ◽  
...  

2016 ◽  
Vol 233 ◽  
pp. 244-251 ◽  
Author(s):  
R.N. Rai ◽  
Shiva Kant ◽  
R.S.B. Reddi ◽  
S. Ganesamoorthy ◽  
P.K. Gupta

2002 ◽  
Vol 755 ◽  
Author(s):  
Barbara Malic ◽  
Darja Jenko ◽  
Janez Bernard ◽  
Jena Cilensek ◽  
Marija Kosec

ABSTRACTStoichiometric K0.5Na0.5NbO3 solid solution(KNN) was prepared by solid-state synthesis from alkaline carbonates and niobium oxide. Thermal decomposition of the powder mixture occurs upon heating to 700 °C followed by crystallization of the perovskite phase. After sintering at 1100 °C, 2h the stoichiometric KNN reaches 94 % of theoretical density. Dielectric constant of stoichiometric KNN is 620, and the losses 0.03.


2012 ◽  
Vol 529 ◽  
pp. 154-158
Author(s):  
Mei Zhang ◽  
Ping Wang ◽  
Xin He ◽  
Qing Guang Zeng ◽  
Jin Xiu Wen

A series of Ba1.91-xSrxSiO4:Eu2+, Dy3+phosphors were synthesized by the high-temperature solid-state reaction. The structure of powder samples were characterized by X-ray powder diffraction. The photoluminescence emission and excitation spectra are also studied. It can be proved the formation of the solid solution of Ba1.91-xSrxSiO4:Eu2+, Dy3+ compounds, and the phosphors can be efficiently excited by UV-visible light from 300 to 480 nm. The as-synthesized Ba1.91-xSrxSiO4:Eu2+, Dy3+ phosphors are promising candidates applicable to near-UV and blue LEDs for solid-state lighting.


2014 ◽  
Vol 10 ◽  
pp. 599-612 ◽  
Author(s):  
Christian Muschelknautz ◽  
Robin Visse ◽  
Jan Nordmann ◽  
Thomas J J Müller

Novel triene merocyanines, i.e. 1-styryleth-2-enylidene and 4-(1,3,3-trimethylindolin-2-ylidene)but-2-en-1-ylideneindolones are obtained in good to excellent yields in a consecutive three-component insertion Sonogashira coupling–addition sequence. The selectivity of either series is remarkable and has its origin in the stepwise character of the terminal addition step as shown by extensive computations on the DFT level. All merocyanines display intense absorption bands in solution and the film spectra indicate J-aggregation. While 1-styryleth-2-enylideneindolones show an intense deep red emission in films, 4-(1,3,3-trimethylindolin-2-ylidene)but-2-en-1-ylideneindolones are essentially nonemissive in films or in the solid state. TD-DFT computations rationalize the charge-transfer nature of the characteristic broad long-wavelength absorptions bands.


2005 ◽  
Vol 88 (6) ◽  
pp. 1651-1654 ◽  
Author(s):  
Chuanyong Huang ◽  
Ruyan Guo ◽  
Zilong Tang ◽  
Zhongtai Zhang

2011 ◽  
Vol 3 (7) ◽  
pp. 335-340
Author(s):  
Ashok Vishram Borhade ◽  
◽  
Vishwas Bhaskar Gaikwad ◽  
Yogeshwar Rajaram Baste

2012 ◽  
Vol 29 (10) ◽  
pp. 1117
Author(s):  
Abdiryim Tursun ◽  
Jamal Ruxangul ◽  
Awut Tunsagul ◽  
Nurulla Ismayil ◽  
Feng XU ◽  
...  

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