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CHEMICAL VAPOR DEPOSITION OF SAMARIUM COMPOUNDS FOR THE DEVELOPMENT OF THIN FILM OPTICAL SWITCHES BASED ON PHASE TRANSITION MATERIALS.HILLMAN, PAUL DALLAS. January 1984 (has links)
The physical properties of single crystals of samarium monosulfide exhibit a first order semiconductor-to-metal transition near 6.5 kbar. However, thin films of SmS show only a gradual change in their properties on applying pressure and this renders the technical utilization of the material difficult. Several mechanisms have been proposed as the cause of the smoothing of the transition. They include intrinsic stress, impurities, grain size, improper stoichiometry, and porosity, all of which can be traced to the physical vapor deposition techniques employed in preparing the films. In contrast, chemical vapor deposition was employed in this study because previous work had shown that it could minimize these detrimental modifications in thin films. A new CVD system was tested using a volatile organometallic as the samarium source and reacting it with H₂S. The deposited films contained considerable amounts of oxygen as evidenced by structure analysis, and the origin was traced to the samarium organometallic. The reaction of oxygen-free samarium tricyclopentadienyl with H₂S as well as chemical transport are suggested for deposition of stress-free SmS thin films in future work.
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Visible and infrared emission from Er₂O₃ nanoparticles, and Ho⁺³, Tm⁺³, and Sm⁺³ doped in AlN for optical and biomedical applicationsWilkinson, Lynda L. 21 July 2012 (has links)
Rare-earth ions holmium (Ho+3), Thulium (Tm+3), and Samarium (Sm+3) were investigated for
infrared emission and their possible biomedical applications by a photoluminescence (PL)
system. Holmium’s (Ho+3) emission peaks were the result of transitions
5
S2 →
5
I7,
and
5
S2 →
5
I5
respectively. Samarium’s (Sm+3) emission peaks were 936 nm and 1863 nm. Thulium’s (Tm+3)
emission peaks were the a result of transitions
3
H4 →
3
H6,
3
H5 →
3
H6 , and
3
F4 →
3
H6 respectively.
Erbium Oxide nanoparticles (Er2O3) mixed with water by a photoluminescence (PL) system.
Erbium Oxide’ (Er2O3) nanoparticle’s emission peaks were the a result of transitions
4
I15/2 →
4
S3/2
,
4
I15/2 →
4
I13/2 respectively. The process was also repeated in vacuum and it was found that
the green emission enhances tremendously when the nanoparticles are excited in vacuum. This
enhanced luminescence from the Erbium Oxide nanoparticles shows their potential importance
in the optical devices and Biomedical applications. / Department of Physics and Astronomy
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