20% off DeltaTime Fluorescence Lifetime System Upgrade

There are 2 related live offers.

Horiba - DeltaTime - 20% Off | DeltaTime TCSPC Half Price | See All
Related Offers

Nanophotonics and Optical Spectroscopy, Tools and Processes from Horiba Scientific

Topics Covered

Background
Studying the Fluorescence Properties of RE-Doped Nanopowders
Synthesizing Rare Earth-Doped Nanopowders with Dopant Concentrations
How the Level of Fluorescence was Measured
The Results that Emerged from this Experiment
Conclusion
Instruments and Components Used in this Experiment

Background

Nanophotonics is one of the most exciting new fields to come out of nanotechnology. The quantum confinement effects implicit in these very small (~ 10 nm) particles can lead to unique optical properties. Rare-earth (RE) doped materials are particularly of interest due to their fluorescence emissions in the visible and infrared regions of the spectrum.

Studying the Fluorescence Properties of RE-Doped Nanopowders

There is an interest in examining the effects of particle size on the fluorescence properties of RE-doped nanopowders as the optical characteristics of RE ions are strongly influenced by their local bonding. Since most photonic devices require these powders be incorporated into a host matrix (i.e. polymer, glass, solvent), there is a need to investigate the emission properties in different host materials. A fully-integrated HORIBA Scientific spectroscopy system (sample chamber, Triax 550 monochromator, detectors) was employed to study the effects of different solvents on RE-doped nanopowders.  

Synthesizing Rare Earth-Doped Nanopowders with Dopant Concentrations - a Description of the Experimental Process

Optically-active, RE-doped nanopowders containing the rare-earth ions (Er3+,Yb3+) were synthesized with several dopant concentrations. The powders were first analyzed out-of-solution in order to obtain the as prepared fluorescence characteristics. This was done by placing a small amount of powder between two glass slides. Measurements were made in reflectance mode using the SampleMax Solid State Sample Holder (600 gr/mm grating blazed at 1.5 micron) with the sample placed approximately 45° off the entrance slit focal axis. Solid state laser diodes or a Ti:Sapphire ring laser were used to pump the absorption bands of the RE-doped nanopowders.

Figure 1. Diagram showing an illustration of the experimental process and the instruments used.

How the Level of Fluorescence was Measured

Fluorescence was measured using HORIBA Scientific TEcooled InGaAs and PbS detectors, with the output sent directly to a Stanford Research SR850 lock-in amplifier (using the integrated optical chopper for beam modulation). Subsequently, dilute solutions containing various solvents (methanol, ethanol, and cyclohexane) were prepared for in-solution measurements. The samples were placed in cuvettes then placed into the SampleMax rotating turret for fluorescence measurement.        

The Results that Emerged from this Experiment

The fluorescence emissions of the nanopowder/alcohol solutions, even in the most dilute samples, were accurately measured with the constructed system. The high resolution of the system allowed for examination of the effects of the host matrix on the emission characteristics of the RE-doped nanopowders. Small shifts in fluorescence peaks are normally very difficult to see with noisier (lower intensity) signals like the dilute powder/methanol solution. However, due to sensitivity of the HORIBA Scientific system, small shifts were easily observed.  

Figure 2. Chart showing Spectra collected with the Jobin Yvon TE Cooled InGaAs Detector.

Conclusion

The HORIBA Scientific Triax 550, coupled with the solid state laser diodes, proved valuable to the successful observation of the effects of solvents on RE-doped nanopowders. This high resolution fluorescence system experienced minimal noise, allowing for effective data collection and analysis. The ability to measure liquids, powders, bulk glasses, and thin films in a matter of minutes, was found to drastically increase productivity. The ability to quickly interchange detectors eliminated the need for lengthy alignment procedures when monitoring materials which have emissions across a broad range of wavelengths.   

Instruments and Components Used in this Experiment

  • Triax 550 Monochromator Triax 550,
  • Solid State Detector Interface 1427B,
  • Detector, InGaAs, TE Cooled (800 nm–1650 nm) DSS-IGA020T,
  • Detector, PbS, TE Cooled (1000 nm–3000 nm) DSS-PBS020T,
  • Detector, Silicon, Ambient (200 nm–1100 nm) DSS-S025A,
  • SampleMax, Visible ASC-VIS,
  • Sample Compartment Turret ASC-STUR,
  • SampleMax Optical Rail ASC-ORAIL,
  • SampleMax Solid Sample Holder ASC-SSOL,
  • Chopper ACH-C,
  • Lock-in Amplifier SR850,
  • Cable for Silicon Detector +/- 15V CCA-LKDS,

Note: A complete set of references can be found by referring to the original document.

Source: NIR Systems for Nanophotonics, Application Note #106 from Horiba Scientific.

For more information on this source please visit Horiba Scientific.

Date Added: Aug 17, 2005 | Updated: Jun 11, 2013
Ask A Question

Do you have a question you'd like to ask regarding this article?

Leave your feedback
Submit