研究目的
Investigating the energy-transfer processes between Er3+ and Dy3+ ions in lead-cadmium-fluorogermanate glass under 405 nm excitation to understand their mutual interactions and visible luminescence.
研究成果
The study confirmed a one-way energy transfer from Er3+ to Dy3+ in the codoped glass, evidenced by decreased Er3+ emission intensity and lifetime with increasing Dy3+ concentration. This mechanism enables tunable visible luminescence with potential applications in solid-state lighting, emphasizing the importance of understanding donor/acceptor relationships for optimizing doping concentrations.
研究不足
The conclusions are based on a specific glass matrix (PbGeO3:PbF2:CdF2) and excitation at 405 nm. Further studies are needed with different pump schemes, wavelengths, and hosts to verify if the donor/acceptor relationship is maintained. The concentration ranges used were limited to investigating energy transfer, not optimized for white light generation.
1:Experimental Design and Method Selection:
The study involved preparing codoped glass samples with varying concentrations of Er3+ and Dy3+ to investigate energy transfer mechanisms. Absorption, excitation, and emission spectra were measured, and time-resolved spectroscopy was used to analyze decay times. Theoretical models for energy transfer efficiency were applied.
2:Sample Selection and Data Sources:
Glass samples were prepared with a composition of 80%PbGeO3:10%PbF2:10%CdF
3:Two codoped sample groups were made:
one with fixed Er3+ concentration (0.50 mol%) and varying Dy3+ (0.25, 0.50, 0.75 mol%), and another with fixed Dy3+ concentration (0.75 mol%) and varying Er3+ (0.25, 0.50, 0.75 mol%). Single-doped samples with 1.0 mol% Er3+ and 1.0 mol% Dy3+ were also prepared.
4:50 mol%) and varying Dy3+ (25, 50, 75 mol%), and another with fixed Dy3+ concentration (75 mol%) and varying Er3+ (25, 50, 75 mol%). Single-doped samples with 0 mol% Er3+ and 0 mol% Dy3+ were also prepared. List of Experimental Equipment and Materials:
3. List of Experimental Equipment and Materials: Equipment included a LAMBDA 1050 UV/VIS/NIR spectrophotometer (Horiba, Japan) for absorption measurements, a spectrofluorometer (TCSPC Nanolog, Horiba) for excitation spectra, a laser source at 405 nm (OBIS, Coherent) for luminescence, a fiber-integrated UV-VIS-NIR spectrograph (HR 4000, Ocean Optics) for emission spectra, and a time-resolved measurement system with a pulsed pump lamp (FL1040-1457B-3714, Horiba), spectrometer (iHR 320, Horiba), data acquisition module (SpectrAcq2, Horiba), and photomultiplier tube detector. Materials included the glass host and dopant ions.
5:Experimental Procedures and Operational Workflow:
Samples were excited at 405 nm, and emissions were collected. Absorption spectra were measured from 400 to 1800 nm. Excitation spectra were collected from 330 to 500 nm. Time-resolved measurements were performed for specific emission bands using bandpass filters. Lifetimes were calculated using the integral method for decay curves.
6:Data Analysis Methods:
Data were analyzed by normalizing emission spectra, measuring intensity changes, and calculating lifetimes and energy transfer efficiencies using statistical methods and software tools associated with the equipment.
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laser source
OBIS
Coherent
Providing excitation at 405 nm for luminescence measurements
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spectrograph
HR 4000
Ocean Optics
Collecting and directing luminescence signals for spectral analysis
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UV/VIS/NIR spectrophotometer
LAMBDA 1050
Horiba
Performing optical absorption measurements in the 400-1800 nm range
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spectrofluorometer
TCSPC Nanolog
Horiba
Collecting excitation spectra and performing time-resolved measurements
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pulsed pump lamp
FL1040-1457B-3714
Horiba
Providing pulsed excitation at 405 nm for time-resolved measurements
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spectrometer
iHR 320
Horiba
Used in the time-resolved measurement system for spectral analysis
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data acquisition module
SpectrAcq2
Horiba
Acquiring data in the time-resolved measurement system
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photmultiplier tube detector
Detecting signals in the time-resolved measurement system
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