Intense Red Catho- and Photoluminescence from 200 nm Thick Samarium Doped Amorphous AlN Thin Films
© to the authors 2009
Received: 21 January 2009
Accepted: 2 April 2009
Published: 25 April 2009
Samarium (Sm) doped aluminum nitride (AlN) thin films are deposited on silicon (100) substrates at 77 K by rf magnetron sputtering method. Thick films of 200 nm are grown at 100–200 watts RF power and 5–8 m Torr nitrogen, using a metal target of Al with Sm. X-ray diffraction results show that films are amorphous. Cathodoluminescence (CL) studies are performed and four peaks are observed in Sm at 564, 600, 648, and 707 nm as a result of4G5/2 → 6H5/2,4G5/2 → 6H7/2,4G5/2 → 6H9/2, and4G5/2 → 6H11/2transitions. Photoluminescence (PL) provides dominant peaks at 600 and 707 nm while CL gives the intense peaks at 600 nm and 648 nm, respectively. Films are thermally activated at 1,200 K for half an hour in a nitrogen atmosphere. Thermal activation enhances the intensity of luminescence.
Rear-earth doped nitride semiconductors thin films are attracting increasing attention as phosphor materials, and are used for optical displays [1–5]. Sputter deposited AlN has been shown to be a viable host for luminescent rare earth (RE) ions due to its transparency over a wide range, including the UV, IR, and entire visible range [6–17]. Recent progress toward nitride-based light-emitting diode and electroluminescent devices (ELDs) has been made using crystalline and amorphous AlN doped with a variety of rare-earth elements [1–9]. The electronic structure of the RE ions differ from the other elements and are characterized by an incompletely filled 4fn shell. The 4f electrons lay inside the ion and are shielded from the surroundings by the filled 5s2 and 5p6 electron orbital . When these materials are excited by various means, intense sharp-line emission is observed due to intra-4f n -shells transitions of the rare-earth ion core [18–21]. The amorphous III-nitride semiconductors have the advantage over their crystalline counterpart because the amorphous material can be grown at room temperature with little stress due to lattice mismatch . They may also be more suitable for waveguides and cylindrical and spherical laser cavities because of the elimination of grain boundaries at low-temperature growth .
High thermal conductivity, stability, and chemical inertness of AlN also make it very useful for its electrical and thermal applications.
In the present work, luminescence properties of Samarium (Sm) are studied when deposited in AlN host. The spectra obtained provide data in a broad range from 300 to 800 nm. Thus luminescence from the films in UV, visible, and IR are obtained and studied simultaneously. The effect of thermal activation is also studied by activating these materials in a tube furnace up to 1,200 K.
Thin films of amorphous AlN:Sm were prepared at 77 K by rf magnetron sputtering of an aluminum target of 99.999% purity in a pure nitrogen atmosphere. Doping of thin films with Sm was accomplished by drilling a small hole (0.5 cm diameter) in the aluminum target (4.2 cm diameter) and placing a slug of Sm in the hole. Sm was then co-sputtered with the aluminum. The rf power was varied between 100 and 200 watts. All films were deposited onto 2 cm × 2 cm, or less, p-silicon (100) substrates. The background pressure in the chamber was <3 × 10−5 Torr. Liquid nitrogen was used to keep the temperature of the film at 77 K. The metallic substrate holder was designed such that it had a half inch diameter cylindrical hole from the top. The substrate was pasted on the metal base of the holder below the liquid nitrogen. Liquid nitrogen was constantly poured in the holder to provide a constant low-temperature to the substrate during film growth.
The as-deposited films were characterized for their characteristic emissions. The thickness of the films was 200 nm, measured with a quartz crystal thickness monitor in the growth chamber. X-rays diffraction (XRD) was used to determine the structure of the films. No diffraction peaks were observed, indicating that the as-deposited films were amorphous.
Cathodoluminescence (CL) studies of the films were performed at room temperature in a vacuum chamber at a pressure of about 3 × 10−6 Torr, which was maintained with an Alcatel CFF 450 turbo pump. Films were excited with electron beam energy of 2.85 kV and beam current of 100 μA. The films were placed an angle of 45° to the incident electron beam coming out of electron gun. The detector was placed at an angle of 45° to the film such that lines joining electron gun, the film and detector were making and angle of 90°. Luminescence from the films was focused onto the entrance slit of a SPEX Industries double monochromator with gratings blazed at 500 nm and detected at a Thorn EMI fast high gain photomultiplier tube with a range of 200–900 nm. The resolution of the spectra was 1 nm.
A 488 nm line of Argon laser was used to obtain the photoluminescence spectra, analyzed by a spectrometer equipped with a cooled photomultiplier tube. The power of the laser beam was 9.3 mW.
Thermal activation was accomplished by placing the flat films in a tube furnace at 1,200 K in a nitrogen atmosphere for half an hour.
Results and Discussion
Summary of Sm3+ions emissions from AlN:Sm
Relative intensity non-annealed films.
Relative intensity of annealed films
4G5/2 → 6H5/2
4G5/2 → 6H7/2
4G5/2 → 6H9/2
4G5/2 → 6H11/2
4G5/2 → 6H7/2
4G5/2 → 6H11/2
Table 1 provides detail of all transitions from Sm3+. Column 2 and 3 give all transitions and the corresponding wavelengths of emission. The relative intensities of non-annealed and annealed samples are given in column 4 and 5, respectively. These relative intensities are determined by comparing the intensity of every peak to the intensity brightest peak (567 nm) in the non-annealed samples. Column 4 gives the ratio by which the intensity of luminescence is enhanced by thermal annealing. Careful consideration of these ratios tells that enhancement is higher for lower wavelengths and it goes down when one moves from ultraviolet to infrared region of the spectrum. The reason being, with increasing temperature the probability of populating higher energy levels increases and hence higher energy levels are thermally more populated as compared to lower energy levels at high-temperature . These thermally populated higher energy levels give rise to enhanced emission.
Both PL peaks indicate very strong emission from AlN:Sm when excited with 488 nm laser. Such a strong intensity clearly indicates that this material is a potential candidate for laser production. We are in the process of providing optimum conditions and laser power to achieve laser in AlN:Sm. Polarization study is also in progress and will be published soon once it is complete.
This significant increase in the intensities of luminescence from Sm3+ ions by thermal annealing has got a good explanation. Luminescence occurs from Sm3+ ions and not from Sm2+ or Sm1+. During the film deposition, it is most likely that some of Al3+ of AlN may be replaced by Sm3+ but there are also chances for imperfections and defects giving rise to Sm2+ or Sm1+ during film growth. These ions do not contribute to luminescence. Smaller the number of these ions, more will be Sm3+ ions and hence luminescence will be higher. When these films are activated thermally at a higher temperature then most of Sm2+ or Sm1+ impurities ionize and converts to Sm3+ ions giving path to enhanced luminescence [22–24]. Moreover when the films are transferred to the furnace and thermally activated after removed from the deposition chamber, they are exposed to air. Thus oxidation of the surface of the film cannot be ignored. Oxygen enhances the luminescence of rare-earth ions giving rise to the enhanced luminescence after thermal activation of the films .
The results show that amorphous AlN:Sm is a promising candidate for its use in nanoscale optical devices and communication tools. The strong red emission makes this material a potential candidate for making quantum dots.
Thin films of amorphous AlN:Sm are deposited by rf magnetron sputtering. Films were characterized for their surface morphology and luminescence properties by XRD, PL, and CL. Samarium ion emits mainly in visible region with the most intense transition in the orange-red portion of the spectrum. Thermal activation enhances the luminescence of films. PL provides very sharp emission in red making it a useful material for nanoscale optical devices applications.
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