M. C. Carmo
University of Aveiro
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by M. C. Carmo.
Journal of Applied Physics | 2005
A.J. Neves; M. C. Carmo; M.J. Soares; Marco Peres; J Wang; E. Alves; E Rita; Ulrich Wahl
We report the observation of slow emission bands overlapped with the near-band-edge steady-state luminescence of nominally undoped ZnO crystals. At low temperatures the time-resolved spectra are dominated by the emission of several high-energy bound exciton lines and the two-electron satellite spectral region. Furthermore, two donor-acceptor pair transitions at 3.22 and 3.238eV are clearly identified in temperature-dependent time-resolved spectroscopy. These donor-acceptor pairs involve a common shallow donor at 67meV and deep acceptor levels at 250 and 232meV.
Applied Physics Letters | 2003
F. Guffarth; R. Heitz; M. Geller; C. M. A. Kapteyn; H. Born; R. L. Sellin; A. Hoffmann; Dieter Bimberg; N. A. Sobolev; M. C. Carmo
The interaction between point defects in the matrix and excitons localized in self-organized InGaAs/GaAs quantum dots is investigated for structures irradiated by protons. The exciton ground state is demonstrated to be unaffected by radiation doses up to 1014 p/cm2. The close proximity of radiation-induced defects leads to a strong nonmonotonous temperature dependence of the luminescence yield: Carriers are lost via tunneling from excited quantum dot states to irradiation-induced defects below ∼100 K, whereas at higher temperatures, carriers escape to the barrier and are captured by defects.
Journal of Applied Physics | 2007
A. O. Ankiewicz; M. C. Carmo; N. A. Sobolev; W. Gehlhoff; Evgeni M. Kaidashev; A. Rahm; M. Lorenz; Marius Grundmann
The wide-band-gap zinc oxide-based diluted magnetic semiconductors currently attract considerable attention due to their possible use in spintronic devices. In this work, we studied ZnO nanowire samples synthesized on 10×10 mm2 a-plane sapphire substrates by high-pressure pulsed laser deposition. The samples were characterized by scanning electron microscopy (SEM) and electron paramagnetic resonance (EPR) in the X-band (≃9.3 GHz) from T=4 to 300 K. According to the SEM pictures, the nanowires exhibit a length of about 1 μm and are aligned perpendicular to the substrate surface. The structures have a hexagonal cross section and their diameter ranges from 60 nm up to 150 nm. For the lowest nominal concentrations of xMn=3 at. % and xCo=5 at. %, we detect the anisotropic EPR spectra of isolated Mn2+ (3d5, S6) and Co2+ (3d7, F4), respectively, on Zn sites. The detection of the well-resolved anisotropic spectra proves a coherent crystallographic orientation of the nanowires. The linewidth was larger than the be...
Applied Physics Letters | 2005
A.J. Neves; M.J. Soares; M. C. Carmo; Marco Peres; E. Alves; E. Rita
We report on the up-converted ultraviolet near-band edge emission of bulk ZnO generated by visible and ultraviolet photons with energies below the band gap. This up-converted photoluminescence was observed in samples intentionally doped with Tm ions, suggesting that the energy levels introduced by the rare earth ion in the ZnO band gap are responsible for this process.
Applied Physics Letters | 2005
C.J. Tang; A.J. Neves; M. C. Carmo
We present an infrared (IR) optical absorbance study of hydrogen incorporation in nanocrystalline diamond films. The thick nanocrystalline diamond films were synthesized by microwave plasma-assisted chemical vapor deposition and a high growth rate about 3.0μm∕h was achieved. The morphology, phase quality, and hydrogen incorporation were assessed by means of scanning electron microscopy, Raman spectroscopy, and Fourier-transform infrared spectroscopy (FTIR). Large amount of hydrogen bonded to nanocrystalline diamond is clearly evidenced by the huge CH stretching band in the FTIR spectrum. The mechanism of hydrogen incorporation is discussed in light of the growth mechanism of nanocrystalline diamond. This suggests the potential of nanocrystalline diamond for IR electro-optical device applications.
Journal of Applied Physics | 2008
A. Chahboun; Mikhail Vasilevskiy; N. V. Baidus; A. Cavaco; N. A. Sobolev; M. C. Carmo; E. Alves; B. N. Zvonkov
The possibility of controlling the photoluminescence (PL) intensity and its temperature dependence by means of in-growth and postgrowth technological procedures has been demonstrated for InAs∕GaAs self-assembled quantum dots (QDs) embedded in an InGaAs quantum well (QW). The improvement of the QD emission at room temperature (RT), achieved due to a treatment with tetrachloromethane used during the growth, is explained by the reduction of the point defect concentration in the capping layer. It is shown that the PL quenching at RT appears again if the samples are irradiated with protons, above a certain dose. These findings are accounted for by the variations in the quasi-Fermi level position of the minority carriers, which are related to the concentration of trapping centers in the GaAs matrix and have been calculated using a photocarrier statistical model including both radiative and nonradiative recombination channels. By taking into consideration the temperature dependent distribution of the majority an...
Materials Science and Engineering B-advanced Functional Solid-state Materials | 1989
Maria Helena Nazaré; M. C. Carmo; A.J. Duarte
Abstract Results of an investigation of the luminescence from silicon doped with silver and nickel in the spectral energy range 0.7–1.1 eV are reported. Two emission bands are described. The electronic structure and vibronic properties of the defects where the emission occurs, deduced from the temperature dependence of the luminescence, are compared with those of luminescent defects that result from doping silicon crystals with other transition metal elements.
Journal of Applied Physics | 2008
Angela S. Pereira; A. O. Ankiewicz; W. Gehlhoff; A. Hoffmann; S. Pereira; Tito Trindade; Marius Grundmann; M. C. Carmo; N. A. Sobolev
A series of chemically prepared Co2+-doped ZnO colloids has been surface modified either by growing shells of ZnSe or by the in situ encapsulation in poly(styrene). The surface modification effects using these two distinct chemical strategies on the magnetic properties of the nanocrystals were probed by electron paramagnetic resonance (EPR). Structural characterization by means of x-ray diffraction and transmission electron microscopy gave no evidence of second phase formation within the detection limits of the used equipment. The EPR analysis was carried out by simulations of the powderlike EPR spectra. The results confirm that in the core of these nanocrystals Co was incorporated as Co2+, occupying the Zn2+ sites in the wurtzite structure of ZnO. Additionally we identify two Co signals stemming from the nanocrystals’ shell. The performed surface modifications clearly change the relative intensity of the EPR spectrum components, revealing the core and shell signals.
Journal of Experimental and Theoretical Physics | 2006
N. P. Stepina; A. I. Yakimov; A. V. Nenashev; A. V. Dvurechenskiĭ; N. A. Sobolev; J. P. Leitão; V. V. Kirienko; A. I. Nikiforov; E. S. Koptev; L. Pereira; M. C. Carmo
The photoconduction in a tunnel-coupled Ge/Si quantum dot (QD) array has been studied. The photoconductance (PC) sign can be either positive or negative, depending on the initial filling of QDs with holes. The PC kinetics has a long-term character (102−104 s at T = 4.2 K) and is accompanied by persistent photoconduction (PPC), whereby the PC value is not restored on the initial level even after relaxation for several hours. These phenomena are observed upon illumination by light with photon energies both greater and smaller than the silicon bandgap. A threshold light wavelength corresponding to a long-term PC kinetics depends on the QD filling with holes. A model describing the observed PC kinetics is proposed, according to which the main contribution to the PC is related to the degree of QD filling with holes. By applying the proposed model to the analysis of PC kinetics at various excitation levels, it is possible to determine the dependence of the hopping conductance on the number of holes per QD. The rate of the charge carrier density relaxation exponentially depends on the carrier density.
Journal of Physics: Condensed Matter | 2007
C.J. Tang; A.J. Neves; A.J.S. Fernandes; J. Gracio; M. C. Carmo
Nanocrystalline diamond (NCD) films have been synthesized by using either nitrogen addition or oxygen addition to conventional CH4/H2 mixtures besides the most commonly used Ar/CH4 with or without H2 chemistry. However, the synthesis of NCD films using both nitrogen and oxygen addition simultaneously into CH4/H2 gases has not been reported thus far. In this work, we investigate the effect of simultaneous O2 and N2 addition to CH4/H2 plasma on the growth of nanocrystalline diamond (NCD) films, focusing particularly on the ratio between the amount of O2 and N2 additives into conventional CH4/H2 gas mixtures on the morphology, microstructure, texture, and crystalline quality of the NCD films. The NCD samples were produced by using a high microwave power (3 kW) in a microwave plasma-assisted chemical vapour deposition reactor with a maximum power of 5 kW on large silicon wafers, 2 inches in diameter, and characterized by high-resolution scanning electron microscopy, x-ray diffraction and micro-Raman spectroscopy. Our work demonstrates that, under the conditions investigated here, NCD films can be formed when the ratio of O2/N2 addition is increased from 0 through 1 up to 7/3 (at higher than 7/3, for example 4, a large-grained polycrystalline diamond film will form), and the crystalline quality is significantly enhanced with the increase of oxygen addition. The mechanism of O2 and N2 additives on the formation of NCD films is briefly studied.