研究目的
To investigate the enhancement of upconverted green emission intensity from Ho3+/Yb3+ co-doped Y2Ti2O7 phosphor in the presence of Zn2+ ions.
研究成果
The synthesis of Y2Ti2O7:Ho3+/Yb3+/Zn2+ phosphors via solid-state reaction successfully enhanced green upconversion emission intensity by up to 92 times with 30 mol% Zn2+ co-doping. This enhancement is attributed to increased crystallinity, particle size, and crystal field asymmetry. The lifetime of the 5S2 level of Ho3+ increased with Zn2+ concentration, and the upconversion mechanism shifted from two-photon to three-photon processes in Zn2+ co-doped samples. The intense green emission makes these phosphors suitable for display devices and other fluorescence-based applications, with potential for further optimization in similar hosts.
研究不足
The study is limited to the specific host material Y2Ti2O7 and dopants Ho3+, Yb3+, and Zn2+. The enhancement mechanism relies on crystallinity, particle size, and crystal field asymmetry, which may not generalize to other systems. The optimum Zn2+ concentration is 30 mol%, beyond which emission intensity decreases due to interstitial occupancy creating defects. The upconversion process involves multiple photons, and the emission intensity is power-dependent, with thermal effects at higher powers. Future work could explore other host materials or dopants to further optimize performance.
1:Experimental Design and Method Selection:
The study synthesized a series of tridoped Y2-x-y-zHozYbyZnxTiO7 phosphor samples with fixed concentrations of Ho3+ and Yb3+ (z=1, y=3) and varying concentrations of Zn2+ (x=0–35 mol%) using the conventional solid state reaction route. The rationale was to study the effect of Zn2+ co-doping on the structural and optical properties, particularly upconversion emission. Theoretical models included the Debye-Scherrer method for crystallite size calculation and the Wood and Tauc formula for optical band gap determination.
2:Sample Selection and Data Sources:
Samples were prepared using analytical grade chemicals: yttrium oxide (Y2O3, 99.999%), holmium oxide (Ho2O3, 99.9%), ytterbium oxide (Yb2O3, 99.99%), zinc oxide (ZnO, 99%), and titanium dioxide (TiO2, 99%). The stoichiometric mixtures were homogenously mixed in an agate mortar with acetone as a mixing media, dried, and heated at 1200°C for 5 hours in ambient atmosphere.
3:999%), holmium oxide (Ho2O3, 9%), ytterbium oxide (Yb2O3, 99%), zinc oxide (ZnO, 99%), and titanium dioxide (TiO2, 99%). The stoichiometric mixtures were homogenously mixed in an agate mortar with acetone as a mixing media, dried, and heated at 1200°C for 5 hours in ambient atmosphere. List of Experimental Equipment and Materials:
3. List of Experimental Equipment and Materials: Equipment included X-ray diffractometer (MiniFlex600: D/teX Ultra Rigaku, Japan), scanning electron microscope (EVO 18 SEM, Carl Zeiss, Germany), Fourier transform infrared spectrometer (model Spectrum-65 Perkin Elmer spectrometer), UV–vis-NIR spectrometer (Lambda 750, Perkin Elmer), dispersive monochromator (model: iHR 320 Horiba JovinYvon) with PMT detector (model no.1424M), 980 nm diode laser (CW, 2 W tunable source), mechanical chopper (model no. SR-540, Stanford Research Systems Inc.), and 150 MHz oscilloscope (model no. HM 1507, Hameg Instruments). Materials included the aforementioned oxides and acetone.
4:Experimental Procedures and Operational Workflow:
The synthesis involved mixing precursors, heating in an alumina crucible, and cooling to room temperature. Characterization steps included XRD for phase identification, SEM for morphological analysis, FTIR for vibrational groups, UV–vis-NIR for absorption spectra, upconversion emission spectra monitoring with a 980 nm laser, and lifetime measurements using a modulated laser and oscilloscope.
5:Data Analysis Methods:
Data analysis involved using the Debye-Scherrer equation for crystallite size, Wood and Tauc formula for band gap, single exponential fitting for lifetime calculation, and power-dependent studies with log-log plots to determine the number of photons involved in upconversion processes.
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X-ray diffractometer
MiniFlex600: D/teX Ultra
Rigaku
Phase identification and impurity detection of samples using X-ray diffraction analysis.
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Scanning electron microscope
EVO 18 SEM
Carl Zeiss
Analysis of morphological structure and surface particles of samples.
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Fourier transform infrared spectrometer
Spectrum-65
Perkin Elmer
Measurement of characteristic vibrational frequencies of different groups in the host matrix.
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UV–vis-NIR spectrometer
Lambda 750
Perkin Elmer
Recording UV–vis-NIR spectra in diffuse reflectance mode.
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Diode laser
Excitation source for upconversion emission spectra and lifetime measurements.
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Monochromator
iHR 320
Horiba JovinYvon
Dispersive monochromator attached with PMT detector for monitoring upconversion emission spectra.
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Photomultiplier tube
1424M
Detection of upconversion emission signals.
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Mechanical chopper
SR-540
Stanford Research Systems Inc.
Modulation of the diode laser for lifetime measurements.
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Oscilloscope
HM 1507
Hameg Instruments
Recording temporal signals for lifetime measurements.
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Agate mortar
Homogeneous mixing of precursor chemicals with acetone.
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Alumina crucible
Container for heating the sample mixture in the furnace.
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