Optical absorption of Co2+ in MgIn2S4, CdIn2S4, and HgIn2S4 spinel crystals

2003 ◽  
Vol 18 (3) ◽  
pp. 733-736 ◽  
Author(s):  
Seok-Joo Lee ◽  
Jae-Eun Kim ◽  
Hae Yong Park

The optical absorption spectra of cobalt-doped MgIn2S4, CdIn2S4, and HgIn2S4 single crystals grown by a chemical transport reaction were investigated at 7 K. The values of Dq and B calculated from the observed spectra show that the d electrons are more delocalized in the order of MgIn2S4, CdIn2S4, and HgIn2S4. Because this order corresponds to the decreasing order of the electronegativity differences between the metal and sulfur atoms of the host crystals, we conclude that as the metal-sulfur bonds in the host crystals are more covalent, the d electrons of the cobalt impurities are more spread out and the cobalt-sulfur bonds are also more covalent.

2001 ◽  
Vol 16 (4) ◽  
pp. 975-978 ◽  
Author(s):  
Hidong Kim ◽  
Seok-Joo Lee ◽  
Jae-Eun Kim ◽  
Hae Yong Park ◽  
Seok-Kyun Oh ◽  
...  

The optical absorption spectra of AgInS2:Co2+ single crystals grown by chemical transport reaction using iodine as a transporting medium have been studied at 6 K. The peaks can be explained by the transitions of Co2+ in the Td symmetry with the spin-orbit coupling, which means that the deviations of the atomic sites from those of the ideal wurtzite structure can be considered negligibly small. The consideration of both the crystal field parameters and the electronegativity difference between atoms may indicate that Co atoms substitute In atoms.


1966 ◽  
Vol 44 (1) ◽  
pp. 413-414 ◽  
Author(s):  
Gerhard Closs ◽  
Clyde A. Hutchison ◽  
Bryan E. Kohler

1974 ◽  
Vol 9 (9) ◽  
pp. 1267-1272 ◽  
Author(s):  
A. Paja̧czkowska ◽  
P. Peshev ◽  
M. Ivanova ◽  
R. Gałazka

2010 ◽  
Vol 7 (2) ◽  
pp. 425-432
Author(s):  
P. Eswaran ◽  
A. Anbagi ◽  
S. Nagarajan

Optical absorption spectra of KBr:Tl+(0.0125 mol%) single crystals shows A, B and C bands around 258, 220 and 210 nm respectively. In KCl0.1Br0.9:Tl+(0.0125 mol%) mixed crystals exhibit slightly broadening of the A-band towards lower wavelength side. The broadening of the absorption spectra are suggested to be due to some complex Tl+centers involving Br-and Cl-ions formed in the mixed crystals. When excited at A, B and C-bands of Tl+ions, PL of KBr:Tl+showed emission band around 320 with a prominent shoulder around 365 nm. In KCl0.1Br0.9mixed crystals the shoulder around 365 nm is not prominent due to the perturbing influence of Cl-ions. Addition bands in the excitation spectra are attributed to the presence of Tl+dimmers. PSL observed in X-ray irradiated crystals resembled their respective PL emissions indicating that PSL in them is due to Tl+ions.


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