Urbach tail and optical characterization of gadolinium-doped TlGaSe 2 single crystals


Gurbulak B., Duman S.

Physica Scripta, cilt.77, sa.2, 2008 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 77 Sayı: 2
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1088/0031-8949/77/02/025702
  • Dergi Adı: Physica Scripta
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Atatürk Üniversitesi Adresli: Evet

Özet

TlGaSe(2) and TlGaSe(2) : Gd single crystals were grown by the Stockbarger method. There are no cracks or voids on the surface of ingots. The samples were cleaved along the cleavage planes (001). The freshly cleaved crystals had mirror-like surfaces even before using mechanical treatment. The phonon energies in TlGaSe(2) and TlGaSe(2) : Gd have been calculated as (35.7 +/- 4) and (38.3 +/- 4) meV at 200 K, respectively. At 10 K, the direct band gaps of TlGaSe(2) and TlGaSe(2) : Gd are 2.293 and 2.297 eV and the indirect bandgaps are 2.196 and 2.106 eV, respectively. There is an abrupt change in the energy spectrum of TlGaSe(2) and TlGaSe(2) : Gd in the temperature ranges 105-115 and 210-215 K, respectively. The values obtained from the energy peak change may be related phase transition temperatures. The defect levels were found to be at 2.162, 2.143, 2.136 and 2.108 eV for TlGaSe(2) : Gd at 10, 100, 200 and 300 K, respectively. The defect levels, which exist in TlGaSe(2) : Gd, but not in pure TlGaSe(2) can be observed by adding Gd in the temperature range of 10-320 K. The steepness parameters and Urbach energies for TlGaSe(2) and TlGaSe(2) : Gd samples increased with increasing sample temperature in the range of 10-320 K. The other important results obtained are: (i) the defect levels and defect absorption peaks due to Gd which have been observed (figure 9(b)). (ii) Gd and Gd related defect levels which exist in Gd-doped TlGaSe(2) and can be observed by adding Gd in the range of 10-320 K. Adding of the rare earth elements to the TlGaSe(2) causes the new appearance and changing of the absorption peak intensity (figure 9( b)).