Charge compensation mechanisms in favor of the incorporation of the Eu 3+ ion into the ZnO host lattice

2018 ◽  
Vol 537 ◽  
pp. 296-300 ◽  
Author(s):  
M. Baira ◽  
A. Bekhti-Siad ◽  
K. Hebali ◽  
H. Bouhani-Benziane ◽  
M. Sahnoun
2011 ◽  
Vol 01 (02) ◽  
pp. 215-221 ◽  
Author(s):  
GUANPING HUANG ◽  
WEN DONG ◽  
LIANG FANG ◽  
FENGANG ZHENG ◽  
MINGRONG SHEN

In this paper, Eu3+ -doped CaTiO3 (CTO) nanoparticles were prepared by a sol-gel method. Three different charge compensation mechanisms were realized by substituting Eu ion at different sites. (i) Ca site substitution with Ca vacancy compensation (CTO-A); (ii) Ti site substitution with O vacancy compensation (CTO-B); (iii) simultaneous substitution at both Ca and Ti sites with self-compensation (CTO-AB). Strongly related to the site substitution, the photoluminescent (PL) intensities were increasing in the sequence of CTO-B > CTO-AB > CTO-A. The absorbance spectra analysis of pure CTO nanoparticles showed absorption in the UV light region, while the absorption of Eu -doped CTO samples exhibited the blue shift owing to the presence of Eu3+ . Moreover, the photocatalytic activities of samples for decomposing dyes were reverse to the sequence of PL intensities. The PL properties and photocatalytic activity of the Eu3+ -doped CTO nanoparticles were thus discussed in detail from the viewpoints of the microstructures and charge transfer-related processes.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 444
Author(s):  
María Taeño ◽  
David Maestre ◽  
Julio Ramírez-Castellanos ◽  
Shaohui Li ◽  
Pooi See Lee ◽  
...  

Achieving nanostructures with high surface area is one of the most challenging tasks as this metric usually plays a key role in technological applications, such as energy storage, gas sensing or photocatalysis, fields in which NiO is gaining increasing attention recently. Furthermore, the advent of modern NiO-based devices can take advantage of a deeper knowledge of the doping process in NiO, and the fabrication of p-n heterojunctions. By controlling experimental conditions such as dopant concentration, reaction time, temperature or pH, NiO morphology and doping mechanisms can be modulated. In this work, undoped and Sn doped nanoparticles and NiO/SnO2 nanostructures with high surface areas were obtained as a result of Sn incorporation. We demonstrate that Sn incorporation leads to the formation of nanosticks morphology, not previously observed for undoped NiO, promoting p-n heterostructures. Consequently, a surface area value around 340 m2/g was obtained for NiO nanoparticles with 4.7 at.% of Sn, which is nearly nine times higher than that of undoped NiO. The presence of Sn with different oxidation states and variable Ni3+/Ni2+ ratio as a function of the Sn content were also verified by XPS, suggesting a combination of two charge compensation mechanisms (electronic and ionic) for the substitution of Ni2+ by Sn4+. These results make Sn doped NiO nanostructures a potential candidate for a high number of technological applications, in which implementations can be achieved in the form of NiO–SnO2 p-n heterostructures.


2014 ◽  
Vol 69 (2) ◽  
pp. 171-182 ◽  
Author(s):  
Mika Lastusaari ◽  
Högne Jungner ◽  
Aleksei Kotlov ◽  
Taneli Laamanen ◽  
Lucas C. V. Rodrigues ◽  
...  

Similar to many other Eu2+,RE3+-co-doped persistent luminescence materials, for Sr2MgSi2O7:Eu2+,RE3+ the initial intensity and duration of persistent luminescence was also found to depend critically on the rare-earth (RE) co-doping. An enhancement of 1 - 2 orders of magnitude in these properties could be obtained by Dy3+ co-doping whereas total quenching of persistent luminescence resulted from the use of Sm3+ and Yb3+. To solve this drastic disparity, the effects of the individual RE3+ ions were studied with thermoluminescence (TL) spectroscopy to derive information about the formation of traps storing the excitation energy. The charge compensation defects were concluded to be the origin of the complex TL glow curve structure. The tuning of the band gap of the Sr2MgSi2O7 host and especially the position of the bottom of the conduction band due to the Eu2+,RE3+ co-doping was measured with the synchrotron radiation vacuum UV (VUV) excitation spectra of the Eu2+ dopant. The model based on the evolution of the band gap energy with RE3+ co-doping was found to explain the intensity and duration of the persistent luminescence.


2017 ◽  
Vol 489 ◽  
pp. 9-21 ◽  
Author(s):  
R. Bès ◽  
J. Pakarinen ◽  
A. Baena ◽  
S. Conradson ◽  
M. Verwerft ◽  
...  

1996 ◽  
Vol 465 ◽  
Author(s):  
B. D. Begg ◽  
E. R. Vance ◽  
R.A Day ◽  
M. Hambley ◽  
S. D. Conradson

ABSTRACTThe incorporation of Pu and Np in zirconolite (CaZrTi2O7) has been investigated over a range of redox conditions. Zirconolite formulations designed to favour either trivalent or tetravalent Pu and Np were prepared by limiting the amount of charge compensating additives available to maintain electroneutrality. From near-edge X-ray absorption spectroscopy the Pu valence state was found to vary with the processing atmosphere, from completely tetravalent when fired in air, and located on either the Ca or Zr sites, to trivalent, when substituted on the Ca site after annealing in 3.5% H2/N2. Np was predominantly tetravalent over the range of redox conditions examined and was readily incorporated on either of zirconolite's Ca or Zr sites. The charge compensation mechanisms at work in different zirconolites are also discussed.


CrystEngComm ◽  
2018 ◽  
Vol 20 (11) ◽  
pp. 1520-1526 ◽  
Author(s):  
M. V. Derdzyan ◽  
K. L. Hovhannesyan ◽  
A. V. Yeganyan ◽  
R. V. Sargsyan ◽  
A. Novikov ◽  
...  

Using a combination of experimental methods, the substitution tendencies of Li+ and involved charge compensation mechanisms are determined and compared in two important similar scintillators, LuAG:Ce and YAG:Ce.


2019 ◽  
Vol 34 (01n03) ◽  
pp. 2040014
Author(s):  
Huidong Tang ◽  
Rong Yang ◽  
Chao Xiong ◽  
Wei Gao

Novel red light-emitting [Formula: see text] ([Formula: see text][Formula: see text]–[Formula: see text][Formula: see text]) phosphors were prepared by solid state reaction. The crystal phase structure and powder morphology were measured by X-ray powder diffraction (XRD) and scanning electron microscope (SEM), respectively. The photoluminescence (PL) properties were investigated. The excitation spectrum shows a wide coverage in the UV-Vis region, and the [Formula: see text] transition with the maximum peak of 613 nm governs the emission spectrum. The lifetime of [Formula: see text] ([Formula: see text][Formula: see text]–[Formula: see text][Formula: see text]) phosphor is temperature-independent as well as the [Formula: see text] doping content because of the existence of defect. In [Formula: see text] lattice, the Eu[Formula: see text] ions substitute for the [Formula: see text] ions, and the charge compensation mechanism could be ascribed to the dipole complex ([Formula: see text]) combined by [Formula: see text] vacancy ([Formula: see text]) and positive charge ([Formula: see text]).


2020 ◽  
Vol 44 (18) ◽  
pp. 7300-7309 ◽  
Author(s):  
Debarati Das ◽  
Santosh K. Gupta ◽  
C. S. Datrik ◽  
P. Nandi ◽  
K. Sudarshan

The present work demonstrates the distinct role of alkali metal ion charge compensators on the luminescence of NIR-emitting Nd3+ Scheelite. The unit cell dimensions of the host lattice and excitation wavelength play a very important role.


2012 ◽  
Vol 100 (5) ◽  
pp. 052103 ◽  
Author(s):  
F. Gunkel ◽  
P. Brinks ◽  
S. Hoffmann-Eifert ◽  
R. Dittmann ◽  
M. Huijben ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document