Abstract
We present a systematic study of leadsalt nanocrystals (NCs) doped with Mn. We have developed a theoretical simulation of electronic and magnetooptical properties by using a multiband calculation including intrinsic anisotropies and magnetic field effects in the diluted magnetic semiconductor regime. Theoretical findings regarding both broken symmetry and critical phenomena were studied by contrasting two different host materials (PbSe and PbTe) and changing the confinement geometry, dot size, and magnetic doping concentration. We also pointed out the relevance of optical absorption spectra modulated by the magnetic field that characterizes these NCs.
Keywords:
Nanocrystals; Quantum dots; DMS; IIVI semiconductors; Lead salts; Magnetooptical propertiesReview
Recently, the successful fabrication of IVVI nanocrystals doped with Mn has shown
possible effective tuning of the emission energy from infrared (dot radius ≃ 200 Å)
up to nearultraviolet (dot radius ≃ 20 Å) regions
[1]. The IVVI semiconductors, such as PbSe nanocrystals (NCs), provide access to the
limit of strong quantum confinement where, besides the changes induced by very small
dot size, the direct narrow bandgap that can also be engineered by the gradual addition
of dilute amounts of magnetic Mn ions to the dot structure. The members of the leadsalt
family, such as PbSe and PbTe, have rocksalt crystalline structure with a direct
bandgap in the Lpoint and the energy branches are fourfold degenerate. The bottom of the conduction
band has
In this letter, we contrast quantum dot electronic properties of two IVVI semiconductor materials by modifying the quantum confinement from spherical to semispherical and varying the diluted concentration of incorporated Mn^{2 + } ions. The electronic, magnetic, and optical properties are studied as a function of Mn content for varying temperature. The total Hamiltonian of the system is H = H_{kp} + V + H_{x} where H_{kp} is the hyperbolic or KaneDimmock [3]k · p Hamiltonian model for IVVI semiconductors, V is a hard wall confinement potential and H_{x} is the exchange interaction between ^{Mn2 + } ions and conduction band (valence band) spins. Here, H_{kp }was slightly modified to explore spherical symmetries of the confinements
where
Also, H_{x }= − x/2〈S_{z}(BT)〉N_{0} · α(·β), where 〈S_{z}(BTx)〉 is the mean field magnetization at temperature T, represented as a Brillouin function in dilute doped sample containing N_{0} unit cells and Mn content, x[6]. Finally, α and β are the exchange constants for the semimagnetic materials, N_{0} · α = −0.08 eV and N_{0}·β = 0.02 eV for PbMnSe, while N_{0}·α = −0.45 eV and N_{0}·β = 0.29 eV for PbMnTe [5].
A complete set of eigenfunctions for the total Hamiltonian H can be spanned in terms of products of periodic Bloch functions J,J_{z}〉 near the Lpoint and envelope functions. For spherical confinement, we expand the fourcomponent spinor wave functions in two Hilbert subspaces with the general form [7,8].
For the spherical model, these states fulfill the boundary condition
Figure 1a,b shows the changes in the magnetic energy dispersions for the first few levels in Pb_{1−x}Mn_{x}Se dots with R = 300 A when the confinement is changed from spherical to semispherical. The broken symmetry induces stronger changes on the electron than on the hole energy dispersions by inducing anticrossing regions. The exchange coupling affects mainly the conduction carrier dispersion. However, for Pb_{1−x}Mn_{x}Te dots with the same size R, shown in Figure 2a,b with both broken symmetry and exchange interaction, induce strong changes on both carrier magnetic dispersions but with the valenceband being more sensitive. The interplay between the usual Zeeman effect and the exchange interaction gives place to the crossing between spinsplit levels at certain critical field, B_{c}, as displayed in Figure 2 for both spherical and semispherical dot spatial confinements.
Figure 1. Conduction and valence band energy levels as function of magnetic field in Pb_{1−x}Mn_{x}Se NCs with spherical (a) and semispherical (b) confinements of radius R = 300 A andT = 1.8 K. The subbands structure with (solid line) and without Mndoping (dashed line) were calculated using E^{c(v)} − Eg(x).
Figure
3a,b shows that the critical field strength for Pb_{1−x}Mn_{x}Te dots, at a fixed temperature, increases with increasing Mn content for different dot
sizes. Note that the smaller the dot size R, the larger the critical concentration x_{c }where
Figure 3. Critical magnetic field as function of the Mn concentration for different Pb_{1−x}Mn_{x }Te NC radii Critical magnetic field as function of the Mn concentration for different
Pb_{1−x}Mn_{x }Te NC radii (a,b); Landè g factor in the limit
As noted in Figure 3c,d, there are Mn concentration regions where the g factor becomes strictly positive or negative, independent of the confinement shape. For fixed dot radius, it is possible to predict the existence of a zero critical field value for a certain value x_{c }for different dot and confinement geometries. For large dot sizes, a nonlinear increasing of B_{c} is observed for low values of x and a quasilinear behavior otherwise.
In order to discuss the optical absorption spectrum, the probability for dipoleallowed
optical transitions between single electron and hole states has to be evaluated in
detail. Within the electrical dipole approximation, the oscillator strength is a linear
combination of the matrix elements of the optical transitions,
The corresponding selection rules for each optical transition in any polarization
can be precisely obtained according to Kang et al.
[2]. Due to the differences in the angular momenta L (symmetry and parity) of electron and hole spinor components, the allowed transitions
occur only between initial (hole) and final (electron) states belonging to different
Hilbert subspaces
where
with β = 2L + 1/2∓1/2. In the same way, the
where α_{0} is a magnitude which includes the bulk P parameter and the dielectric constant. The material parameters can be found in [4,5]. For the linear light polarization Π^{z}, the optical matrix element becomes
where
and the related absorption coefficient turns
In the case of semispherical geometry, the selection rules for the circular light polarization are the same as for the spherical case; meanwhile, for the linear light polarization, these allow transitions within the same subspace due to the parities of the components of the wave functions in the subspaces.
The excitonic resonances for Π^{z }and σ^{+} , calculated as a function of the magnetic field for each Mndoped leadsalt dot and confinements, are shown in Figure 4a,b,c,d,e,f,g,h. In Figure 5, we displayed the corresponding excitonic resonances for σ^{+} of the reference samples (without Mn doping) for spherical confinement. Comparing Figures 4e and 5a and Figures 4g and 5b, we confirm that the effect of Mn doping on the absorption spectra is stronger on the bandgap renormalization than on the subband levels in the doped saltselenide unlike the salttelluride, where the Mn presence strongly modifies all the band structure [11,12]. The resonant transitions shown in Figure 5a,b involve just the conduction band ground state of spherical and semispherical PbMnSe dots. The corresponding spectra for PbMnTe, shown in Figure 4c,d, correspond to the transitions to the first crossing conduction band levels. Figure 4d displays an absorption bottleneck due to the level crossing (see Figure 2a,b) for PbMnSe spherical dots. Another absorption quenching appears at B = 1.2T in Figure 4e caused by the character admixture close to a level crossing. In turn, Figure 4f displays a single transition to the conduction band ground state. In Figures 4g,h two transitions appear that fadeoff for lower and higher fields, respectively. This effect is produced by the modulation of the oscillator strength. For small nanocrystal size, the spectra will show quantitative variation due to the effective gap modulation and the subsequent weakening of the intersubband coupling.
Figure 4. Interband absorption spectra as function of magnetic field for polarization Π^{z }(ad) and σ^{+ }(eh) Pb_{0.99}Mn_{0.01}Se NCs with spherical (a,e) and semispherical (b,f) confinements and Pb_{0.99}Mn_{0.01}Te NC with spherical (c,g) and semispherical (d,h) confinements. The same parameters were as referred in Figures 1 and 2.
Figure 5. Interband absorption spectra as function of magnetic field for polarization σ^{+ }of PbSe (a) and PbTe NCs (b) with spherical confinement of R = 300 A and temperatures 1.8 and 4.8 K, respectively.
Conclusions
Summarizing, we have investigated the electronic and magnetooptical properties of Pb_{1−x}Mn_{x }Se and Pb_{1−x}Mn_{x} Te semimagnetic dots by taking advantage of their strong sensitivity to spatial confinement asymmetry and properties induced by the Mn doping. We have shown the appearance of the critical phenomena as the spin level crossing for certain concentration of Mn on the Pb_{1−x}Mn_{x }Te and the modulation of the optical absorption controlled by field B and confinement anisotropy. Subtle effects of Mn content variation were predicted for the energy spectra of the Pb_{1−x}Mn_{x }Se dots, whereas important consequences are expected for Pb_{1−x}Mn_{x }Te dots. We believe that these results may stimulate research groups working on these important materials to explore device applications working on the wide spectral range.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
SJP carried out the calculation of the band structure and absorption spectra and participated in the study of the electronic and magnetooptical properties. LVL, VLR and GEM participated in the design of the problem, and its study and coordination. AMA conceived of the study and participated in the design of the problem and first stages of calculation. All authors read and approved the final manuscript.
Acknowledgements
The authors acknowledge the financial support from the Brazilian agencies, FAPEMIG (SJP, LVL), INCTIQ (AMA) and FAPESP and CNPq (VLR, GEM).
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