Two Er3+/Yb3+ monolithic silica-alumina xerogels doped with different Yb3+ concentrations were prepared by sol-gel route. The samples were thermally treated in air at 950 C for 120 h, and Raman and UVvisible-NIR spectroscopy were used to monitor the degree of densification of the glasses and the residual OH content. Back energy transfer from Er3+ to Yb3+ was demonstrated by measurement of Yb3+ emission upon Er3+ excitation at 514.5 nm. Photoluminescence excitation spectroscopy over the 880-1010 nm wavelength range, spanning the energy range of the Yb3+- 2F5/2 and Er3+-4I11/2 excited states, was used to obtain information about the effective excitation efficiency of Er3+ ions by co-doping with Yb ions. The emission of 4I13/2->4 I 15/2 of Er3+ ion transition with a 47 nm bandwidth was observed upon excitation at 514.5 nm and a lifetime of the 4I13/2 metastable state of 8.7 ms was measured.
Photoluminescence spectroscopy of Er3+/Yb3+ co-activated silica-alumina monolithic xerogels
A Chiasera;M Ferrari;S Pelli;
2003
Abstract
Two Er3+/Yb3+ monolithic silica-alumina xerogels doped with different Yb3+ concentrations were prepared by sol-gel route. The samples were thermally treated in air at 950 C for 120 h, and Raman and UVvisible-NIR spectroscopy were used to monitor the degree of densification of the glasses and the residual OH content. Back energy transfer from Er3+ to Yb3+ was demonstrated by measurement of Yb3+ emission upon Er3+ excitation at 514.5 nm. Photoluminescence excitation spectroscopy over the 880-1010 nm wavelength range, spanning the energy range of the Yb3+- 2F5/2 and Er3+-4I11/2 excited states, was used to obtain information about the effective excitation efficiency of Er3+ ions by co-doping with Yb ions. The emission of 4I13/2->4 I 15/2 of Er3+ ion transition with a 47 nm bandwidth was observed upon excitation at 514.5 nm and a lifetime of the 4I13/2 metastable state of 8.7 ms was measured.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
