TY - JOUR
T1 - Spectroscopic properties of cerium in sol-gel glasses
AU - Reisfeld, Renata
AU - Patra, Amitava
AU - Panczer, Gerard
AU - Gaft, Michael
N1 - Funding Information:
We acknowledge the support of India–Israel research Grant and the Israely Ministry of Science that allowed the visit of A. Patra in Jerusalem and the help of Dr. H. Minti for steady-state spectra.
PY - 1999/10
Y1 - 1999/10
N2 - Glasses containing Ce were prepared by the sol-gel method at elevated temperatures. Two parallel series, one in air and one in nitrogen atmosphere, were obtained. The main constituent of the glasses was silica SiO2 obtained by hydrolysis of ethoxysilane (TEOS). Spectroscopic properties of the glasses were studied by time-resolved and steady-state luminescence spectroscopy. In the present paper we made an effort to distinguish between the blue luminescence arising from Ce(III) and that obtained from the silica host which is connected with defects in the matrix. While the spectra of both pure silica and Ce activated silica excited at 337 nm or longer wavelength have the similar emission peaking between 400 and 450 nm, the emission of silica is broader and its decay time shorter than that of Ce(III). It seems that Ce quenches the luminescence of the silica centers. When excited at 308 nm by an excimer laser we detect short-lived emission of Ce(III) peaking between 350-380 nm which may be due to excitation to the conductivity band and subsequent recombination of the excited electrons with a hole.
AB - Glasses containing Ce were prepared by the sol-gel method at elevated temperatures. Two parallel series, one in air and one in nitrogen atmosphere, were obtained. The main constituent of the glasses was silica SiO2 obtained by hydrolysis of ethoxysilane (TEOS). Spectroscopic properties of the glasses were studied by time-resolved and steady-state luminescence spectroscopy. In the present paper we made an effort to distinguish between the blue luminescence arising from Ce(III) and that obtained from the silica host which is connected with defects in the matrix. While the spectra of both pure silica and Ce activated silica excited at 337 nm or longer wavelength have the similar emission peaking between 400 and 450 nm, the emission of silica is broader and its decay time shorter than that of Ce(III). It seems that Ce quenches the luminescence of the silica centers. When excited at 308 nm by an excimer laser we detect short-lived emission of Ce(III) peaking between 350-380 nm which may be due to excitation to the conductivity band and subsequent recombination of the excited electrons with a hole.
UR - http://www.scopus.com/inward/record.url?scp=0033208115&partnerID=8YFLogxK
U2 - 10.1016/S0925-3467(99)00015-4
DO - 10.1016/S0925-3467(99)00015-4
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AN - SCOPUS:0033208115
SN - 0925-3467
VL - 13
SP - 81
EP - 88
JO - Optical Materials
JF - Optical Materials
IS - 1
T2 - Proceedings of the 1997 1st Spanish-Israeli Workshop on Solid State Lasers
Y2 - 14 December 1997 through 16 December 1997
ER -