Spinodal decomposition and the luminescence of Er in AlxIn1−xN:Er layers. Issue 1 (29th November 2012)
- Record Type:
- Journal Article
- Title:
- Spinodal decomposition and the luminescence of Er in AlxIn1−xN:Er layers. Issue 1 (29th November 2012)
- Main Title:
- Spinodal decomposition and the luminescence of Er in AlxIn1−xN:Er layers
- Authors:
- Yang, Miao
Weng, Ye
Strunk, Horst P. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Integrated photoluminescence intensities of the green lines from Er centers (<sup>2</sup>H<sub>11/2</sub>–<sup>4</sup>I<sub>15/2</sub> and <sup>4</sup>S<sub>3/2</sub>–<sup>4</sup>I<sub>15/2</sub>) embedded in Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N films are investigated in dependence of excitation energy and band gap energy of the film host. The films are deposited onto silicon and sapphire substrates by sputtering and subsequently annealed for optimization of the luminescence intensity. Two significant maxima of integrated intensity are observed. The first maximum appears, if the excitation energy matches the band gap energy of the Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N matrix. It can be explained by a bound exciton mediated energy transfer to Er centers. The second maximum occurs at below band gap energy excitation of some films with special compositions. These observations call for an adequate path for the excitation of Er. We propose a mechanism based on spinodal decomposition of Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N. In fact, our calculations and experiments (structure analysis in a transmission electron microscope) confirm that nanoparticles form of an In‐rich Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N phase, which can be assumed as quantum dots. Resonant energy transfer from these quantum dots<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Integrated photoluminescence intensities of the green lines from Er centers (<sup>2</sup>H<sub>11/2</sub>–<sup>4</sup>I<sub>15/2</sub> and <sup>4</sup>S<sub>3/2</sub>–<sup>4</sup>I<sub>15/2</sub>) embedded in Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N films are investigated in dependence of excitation energy and band gap energy of the film host. The films are deposited onto silicon and sapphire substrates by sputtering and subsequently annealed for optimization of the luminescence intensity. Two significant maxima of integrated intensity are observed. The first maximum appears, if the excitation energy matches the band gap energy of the Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N matrix. It can be explained by a bound exciton mediated energy transfer to Er centers. The second maximum occurs at below band gap energy excitation of some films with special compositions. These observations call for an adequate path for the excitation of Er. We propose a mechanism based on spinodal decomposition of Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N. In fact, our calculations and experiments (structure analysis in a transmission electron microscope) confirm that nanoparticles form of an In‐rich Al<sub><italic>x</italic></sub>In<sub>1−<italic>x</italic></sub>N phase, which can be assumed as quantum dots. Resonant energy transfer from these quantum dots into the luminescent centers can explain the Er luminescence enhancement.</p> </abstract> … (more)
- Is Part Of:
- Physica status solidi. Volume 210:Issue 1(2013:Jan.)
- Journal:
- Physica status solidi
- Issue:
- Volume 210:Issue 1(2013:Jan.)
- Issue Display:
- Volume 210, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 210
- Issue:
- 1
- Issue Sort Value:
- 2013-0210-0001-0000
- Page Start:
- 209
- Page End:
- 212
- Publication Date:
- 2012-11-29
- Subjects:
- Solid state physics -- Periodicals
Solids -- Industrial applications -- Periodicals
530.41 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/pssa.201200410 ↗
- Languages:
- English
- ISSNs:
- 1862-6300
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.210000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3533.xml