Heavy metal lead germanate glasses doubly doped with Yb^3+ and Ln^3+ ions (Ln=Er, Tin) were investigated. Up-conversion spectra of Er^3+ and Tm^3+ were registered under diode-laser excitation of Yb^3+. Up-conve...Heavy metal lead germanate glasses doubly doped with Yb^3+ and Ln^3+ ions (Ln=Er, Tin) were investigated. Up-conversion spectra of Er^3+ and Tm^3+ were registered under diode-laser excitation of Yb^3+. Up-conversion luminescence bands corresponded to ^4S3/2→^4I15/2 (green) and ^4F9/2→^4I15/2 (red) transitions of Er^3+ as well as ^1G4→^3H6 (blue) and ^3Ha→^3H6 (N]R) transitions of Tm^3+, respectively.展开更多
Heavy metal glasses doubly doped with Yb3+ and Ln3+ ions (Ln=Er or Tm) were studied. Glass host matrices were limited to lead borate glass and lead germanate glass. Efficient resonant (yb3+-Er3+) and non-reson...Heavy metal glasses doubly doped with Yb3+ and Ln3+ ions (Ln=Er or Tm) were studied. Glass host matrices were limited to lead borate glass and lead germanate glass. Efficient resonant (yb3+-Er3+) and non-resonant (yb3+-Tm3+) energy transfer was ob- served for the studied systems. Near-infrared luminescence spectra at 1.53 μm (Er3+) and 1.9 gm (Tm3+) were detected under excita- tion of Yb3+ by 975 nm diode laser line. They corresponded to 4I13/2→4115/2 (Er3+) and 3F4→3H6 (Tm3+) transitions of rare earth ions, respectively. The unusual large spectral linewidth nearly close to 110 nm for 4I13/2→4I15/2 transition of Er3+ ions in lead borate glass was obtained, whereas long-lived near-infrared luminescence at 1.53 gm was detected in lead germanate glass. Quite different situa- tion was observed for yb3+-Tm3+ doubly doped glasses. In contrast to lead borate glass, near-infrared (3F4→3H6) luminescence spectra were registered for Tm3+ ions in lead germanate glasses, only. These phenomena strongly depended on stretching vibrations of glass host, which was confirmed by FT-IR spectroscopy.展开更多
基金Project supported by the Science and Higher Education (N N204 313937)
文摘Heavy metal lead germanate glasses doubly doped with Yb^3+ and Ln^3+ ions (Ln=Er, Tin) were investigated. Up-conversion spectra of Er^3+ and Tm^3+ were registered under diode-laser excitation of Yb^3+. Up-conversion luminescence bands corresponded to ^4S3/2→^4I15/2 (green) and ^4F9/2→^4I15/2 (red) transitions of Er^3+ as well as ^1G4→^3H6 (blue) and ^3Ha→^3H6 (N]R) transitions of Tm^3+, respectively.
文摘Heavy metal glasses doubly doped with Yb3+ and Ln3+ ions (Ln=Er or Tm) were studied. Glass host matrices were limited to lead borate glass and lead germanate glass. Efficient resonant (yb3+-Er3+) and non-resonant (yb3+-Tm3+) energy transfer was ob- served for the studied systems. Near-infrared luminescence spectra at 1.53 μm (Er3+) and 1.9 gm (Tm3+) were detected under excita- tion of Yb3+ by 975 nm diode laser line. They corresponded to 4I13/2→4115/2 (Er3+) and 3F4→3H6 (Tm3+) transitions of rare earth ions, respectively. The unusual large spectral linewidth nearly close to 110 nm for 4I13/2→4I15/2 transition of Er3+ ions in lead borate glass was obtained, whereas long-lived near-infrared luminescence at 1.53 gm was detected in lead germanate glass. Quite different situa- tion was observed for yb3+-Tm3+ doubly doped glasses. In contrast to lead borate glass, near-infrared (3F4→3H6) luminescence spectra were registered for Tm3+ ions in lead germanate glasses, only. These phenomena strongly depended on stretching vibrations of glass host, which was confirmed by FT-IR spectroscopy.