2008
DOI: 10.1063/1.2837537
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Auger recombination in InN thin films

Abstract: Auger recombination is studied in InN thin films using an ultrafast time-resolved photoluminescence apparatus. The decay rates are analyzed with nonlinear dependence of the photoluminescence intensity on the carrier concentration. The fitted radiative recombination coefficients at a temperature of 35K are consistent with the theoretical prediction. The Auger rates are small at low carrier concentrations but increase quadratically with the carrier concentration. The Auger activation energies of 4.3 and 9.0meV o… Show more

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Cited by 25 publications
(16 citation statements)
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“…measurements (at 1.58 eV) [4] and ultrafast time-resolved photoluminescence (TRPL at 1.53 eV pump) [5] revealed the Auger recombination process with the linear [4] or quadratic [5] ) at interband photoexcitation (hν = 1.17 eV). Monitoring of the spatial and temporal carrier dynamics via light diffraction provided a direct way to control the dynamics of photoexcited carrier density N (i.e.…”
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confidence: 98%
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“…measurements (at 1.58 eV) [4] and ultrafast time-resolved photoluminescence (TRPL at 1.53 eV pump) [5] revealed the Auger recombination process with the linear [4] or quadratic [5] ) at interband photoexcitation (hν = 1.17 eV). Monitoring of the spatial and temporal carrier dynamics via light diffraction provided a direct way to control the dynamics of photoexcited carrier density N (i.e.…”
mentioning
confidence: 98%
“…As the all recombination mechanisms were found of comparable decay rate (5 to 30 ns -1 for Auger and 10-20 ns -1 for SHR), the discrimination of their contributions as well as the determination of radiative and Auger coefficients seems not very reliable from ultrafast PL kinetics. Moreover, the authors of [4,5] did not account for carrier diffusion which can significantly contribute to carrier in-depth redistribution after short pulse photoexcitation by moving the nonequilibrium carriers out of the detection region of PL or DR techniques, thus leading to strongly non-exponential relaxation kinetics [7]. The latter peculiarity explained the origin of the fast PL signal decay component in nonhomogeneously excited high-quality HVPE, hetero-and homoepotaxial layers of GaN [7,8].…”
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confidence: 99%
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“…The phonon-assisted process has weaker temperature dependence compared to the band-to-band process [16]; therefore, the activation energy E C in nitrides would be smaller than typical values obtained for the band-to-band process. Although the Auger activation energy in InGaN materials is still debatable, we employ E C = 4.3 meV based on the results presented in [17]. Reported room-temperature SRH coefficient values in InGaN are between 4.0 × 10 6 s −1 [18] and 2.0 × 10 8 s −1 [19].…”
Section: Temperature-dependent Parametersmentioning
confidence: 99%
“…Reported room-temperature SRH coefficient values in InGaN are between 4.0 × 10 6 s −1 [18] and 2.0 × 10 8 s −1 [19]. In this paper SRH recombination was modelled assuming A = 3.0 × 10 7 s −1 at 300 K and using linear temperature decrease down to 2.0 × 10 7 s −1 at 150 K according to the experimental data [17] and theoretical calculations [20].…”
Section: Temperature-dependent Parametersmentioning
confidence: 99%