Optical transitions in GaNAs quantum wells with variable nitrogen content embedded in AlGaAs
Source abstract
Abstract
We investigate the optical transitions of GaNxAs1−x quantum wells (QWs) embedded in wider band gap AlGaAs. A combination of absorption and emission spectroscopic techniques is employed to systematically investigate the properties of GaNAs QWs with N concentrations ranging from 0 – 3%. From measurement of the photocurrent spectra, we find that besides QW ground state and first excited transition, distinct increases in photocurrent generation are observed. Their origin can be explained by N-induced modifications in the density of states at higher energies above the QW ground state. Photoluminescence experiments reveal that peak position dependence with temperature changes with N concentration. The characteristic S-shaped dependence for low N concentrations of 0.5% changes with increasing N concentration where the low temperature red-shift of the S-shape gradually disappears. This change indicates a gradual transition from impurity picture, where localized N induced energy states are present, to alloying picture, where an impurity-band is formed. In the highest-N sample, photoluminescence emission shows remarkable temperature stability. This phenomenon is explained by the interplay of N-induced energy states and QW confined states.
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Research context
OpenAlex topics: Semiconductor Quantum Structures and Devices · GaN-based semiconductor devices and materials · Quantum and electron transport phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Institute for Materials Science 1 International Center for Young Scientists, , 305-0047 Tsukuba, Japan
National Institute for Materials Science 2 Photovoltaic Materials Unit, , 305-0047 Tsukuba, Japan
National Institute for Materials Science 3 Photonic Materials Unit, , 305-0047 Tsukuba, Japan
Funding
Japan Society for the Promotion of Science
References (30)
Show source-provided references
1. Phys. Rev. B · 2001 · 64 · 08532010.1103/PhysRevB.64.085320 ↗
2. Phys. Rev. Lett. · 1996 · 76 · 66410.1103/PhysRevLett.76.664 ↗
3. Appl. Phys. Lett. · 2009 · 94 · 01190710.1063/1.3055605 ↗
4. Appl. Phys. Lett. · 2001 · 78 · 156210.1063/1.1354153 ↗
5. J. of Appl. Phys. · 2002 · 92 · 144610.1063/1.1488240 ↗
6. Appl. Phys. Lett. · 2008 · 93 · 03190410.1063/1.2958232 ↗
7. J. of Appl. Phys. · 2002 · 92 · 436110.1063/1.1507817 ↗
8. J. of Appl. Phys. · 2013 · 113 · 23350810.1063/1.4810920 ↗
9. J. of Appl. Phys. · 2014 · 116 · 02310310.1063/1.4886178 ↗
10. J. Appl. Phys. · 2003 · 94 · 231910.1063/1.1591416 ↗
11. Appl. Phys. Lett. · 2006 · 89 · 03211010.1063/1.2227618 ↗
12. App. Phys. Lett. · 2002 · 80 · 208710.1063/1.1463208 ↗
13. Mater. Sci. Eng. C · 2002 · 21 · 24510.1016/S0928-4931(02)00074-7 ↗
14. Opt. Mater. · 2003 · 24 · 30310.1016/S0925-3467(03)00140-X ↗
15. Phys. Rev. B · 2011 · 84 · 04530210.1103/PhysRevB.84.045302 ↗
16. J. of Appl. Phys. · 2005 · 98 · 06351810.1063/1.2058192 ↗
17. J. Vac. Sci. Technol. B · 2002 · 20 · 115810.1116/1.1473176 ↗
18. Sol. Energ. Mat. Sol. Cells · 2014 · 124 · 150-15810.1016/j.solmat.2014.01.044 ↗
19. Jap. J. Appl. Phys. · 1996 · 35 · 127310.1143/JJAP.35.1273 ↗
20. Phys. Rev. Lett. · 1997 · 78 · 501410.1103/PhysRevLett.78.5014 ↗
21. Jap. J. of Appl. Phys. · 2012 · 51 · 06FF1510.7567/JJAP.51.06FF15 ↗
22. Appl. Phys. Express · 2011 · 4 · 12500110.1143/APEX.4.125001 ↗
23. Appl. Phys. Lett. · 1999 · 75 · 50110.1063/1.124429 ↗
24. J. Phys.: Condens. Matter · 2008 · 20 · 01521710.1088/0953-8984/20/01/015217 ↗
25. J. of Appl. Phys. · 1982 · 53 · R12310.1063/1.331665 ↗
26. Appl. Phys. Lett. · 2000 · 76 · 128510.1063/1.126010 ↗
27. J. of Appl. Phys. · 1985 · 57 · 534010.1063/1.334852 ↗
28. 1999 · 190
29. Phys. Rev. B · 2005 · 72 · 04522210.1103/PhysRevB.72.045222 ↗
30. Phys. Rev. Lett. · 1999 · 82 · 122110.1103/PhysRevLett.82.1221 ↗