Amitava Patra
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The organizations/institutes from the scholar's latest article
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Amitava Patra has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
Glauco S. Maciel
2 shared publications- Márcio André Rodrigues Cavalcanti de Alencar
Universidade Federal de Sergipe (UFS)
2 shared publications - Pushpal Ghosh
School of Chemical Science and Technology Department of Chemistry Dr. Harisingh Gour University (a Central University) Sagar Madhya Pradesh India
2 shared publications Cid B. de Araújo
1 shared publicationNikifor Rakov
Sol−Gel Division, Central Glass & Ceramic Research Institute, Jadavpur, Kolkata, 700 032, India, Departamento de Física, Universidade Federal de Pernambuco, 50670-901 Recife, PE, Brazil, and Universidade Federal do Vale do São Francisco, 56306-410 Petrolina, PE, Brazil
1 shared publicationParamita Saha Chowdhury
Sol−Gel Division, Central Glass & Ceramic Research Institute, Jadavpur, Kolkata, 700 032, India, Departamento de Física, Universidade Federal de Pernambuco, 50670-901 Recife, PE, Brazil, and Universidade Federal do Vale do São Francisco, 56306-410 Petrolina, PE, Brazil
1 shared publication
Latest Publications
- 1 December 2008
- Published by American Scientific Publishers in Journal of Nanoscience and Nanotechnology
- Vol. 8 (12) , 6564-6568
Red to Green Upconversion in Er3+-Doped BaTiO3 Nanorods
We investigated the frequency upconversion (UC) process in BaTiO3:Er3+ nanocrystals for excitation wavelengths in the range 638 to 660 nm. Green upconversion emissions at 526 and 547 nm corresponding to 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 to transitions of the Er3+ were observed. The excitation spectrum for UC emissions presented three bands, due to ground state and excited state absorption of Er3+ ions. The UC intensity as a function of the laser power was investigated and it was found this a two-photon absorption process.
- 1 December 2008
- Published by American Scientific Publishers in Journal of Nanoscience and Nanotechnology
- Vol. 8 (12) , 6564-6568
Red to Green Upconversion in Er3+-Doped BaTiO3 Nanorods
We investigated the frequency upconversion (UC) process in BaTiO3:Er3+ nanocrystals for excitation wavelengths in the range 638 to 660 nm. Green upconversion emissions at 526 and 547 nm corresponding to 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 to transitions of the Er3+ were observed. The excitation spectrum for UC emissions presented three bands, due to ground state and excited state absorption of Er3+ ions. The UC intensity as a function of the laser power was investigated and it was found this a two-photon absorption process.
- Open Access
- 1 November 2005
- Published by Springer Nature in Pramana
- Vol. 65 (5) , 901-907
Understanding the influence of nanoenvironment on luminescence of rare-earth ions
- 1 November 2005
- Published by Springer Nature in Pramana
- Vol. 65 (5) , 901-907
Open AccessUnderstanding the influence of nanoenvironment on luminescence of rare-earth ions
- 28 April 2005
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 109 (20) , 10142-10146
Red to Blue Tunable Upconversion in Tm3+-Doped ZrO2 Nanocrystals
The effect of dopant concentration on the blue upconversion (UPC) emission of Tm3+ -doped ZrO2 nanocrystals under different excitation wavelengths in the red region is reported. The UPC emissions are due to the f−f electronic transitions from excited states 1G4 and 1D2 of Tm3+. We observed a chromatic change in the UPC with tuning the excitation wavelength. The UPC emission bands at 475, 488, and 501 nm are observed under excitation at 649 nm, but bands centered at 454 and 460 nm are observed when the excitation wavelength is tuned to 655 nm. The UPC emission could be tuned from 501 to 454 nm (∼47 nm) by changing the excitation wavelength from 649 to 655 nm (∼6 nm). The pump power dependence of the emission bands at 475, 488, and 501 nm were investigated on excitation intensity at 649 nm, and the emission bands at 454 and 460 nm are investigated on excitation intensity at 655 nm, which confirms that all of these UPC emission lines are a two-photon absorption process.
- 28 April 2005
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 109 (20) , 10142-10146
Red to Blue Tunable Upconversion in Tm3+-Doped ZrO2 Nanocrystals
The effect of dopant concentration on the blue upconversion (UPC) emission of Tm3+ -doped ZrO2 nanocrystals under different excitation wavelengths in the red region is reported. The UPC emissions are due to the f−f electronic transitions from excited states 1G4 and 1D2 of Tm3+. We observed a chromatic change in the UPC with tuning the excitation wavelength. The UPC emission bands at 475, 488, and 501 nm are observed under excitation at 649 nm, but bands centered at 454 and 460 nm are observed when the excitation wavelength is tuned to 655 nm. The UPC emission could be tuned from 501 to 454 nm (∼47 nm) by changing the excitation wavelength from 649 to 655 nm (∼6 nm). The pump power dependence of the emission bands at 475, 488, and 501 nm were investigated on excitation intensity at 649 nm, and the emission bands at 454 and 460 nm are investigated on excitation intensity at 655 nm, which confirms that all of these UPC emission lines are a two-photon absorption process.