This study addresses the complementary metal-oxide-semiconductor-compatible fabrication of vertically stacked Si/SiO 2 /Si nanopillars (NPs) with embedded Si nanodots (NDs) as key functional elements of a quantum-dot-based, gate-all-around single-electron transistor (SET) operating at room temperature. The main geometrical parameters of the NPs and NDs were deduced from SET device simulations using the nextnano++ program package. The basic concept for single silicon ND formation within a confined oxide volume was deduced from Monte-Carlo simulations of ion-beam mixing and SiO x phase separation. A process flow was developed and experimentally implemented by combining bottom-up (Si ND self-assembly) and top-down (ion-beam mixing, electron-beam lithography, reactive ion etching) technologies, fully satisfying process requirements of future 3D device architectures. The theoretically predicted self-assembly of a single Si ND via phase separation within a confined SiO x disc of <500 nm 3 volume was experimentally validated. This work describes in detail the optimization of conditions required for NP/ND formation, such as the oxide thickness, energy and fluence of ion-beam mixing, thermal budget for phase separation and parameters of reactive ion beam etching. Low-temperature plasma oxidation was used to further reduce NP diameter and for gate oxide fabrication whilst preserving the pre-existing NDs. The influence of critical dimension variability on the SET functionality and options to reduce such deviations are discussed. We finally demonstrate the reliable formation of Si quantum dots with diameters of less than 3 nm in the oxide layer of a stacked Si/SiO 2 /Si NP of 10 nm diameter, with tunnelling distances of about 1 nm between the Si ND and the neighboured Si regions forming drain and source of the SET.
Germanium nanocrystals embedded in high- k dielectric matrices are of main interest for infrared sensing application, as a role model for Ge-based nanoelectronics passivation or for nonvolatile memory devices. The capability of the size control of those nanocrystals via rapid thermal processing of superlattice structures is shown for the [Ge–TaZrO x /TaZrO x ] n , [Ge–TaZrO x /SiO 2 /TaZrO x ] 6 , and [TaZrO x /Ge–SiO 2 ] n superlattice systems. All superlattices were deposited by radiofrequency magnetron sputtering. Transmission electron microscopy (TEM) imaging confirms the formation of spherically shaped nanocrystals. Raman scattering proved the crystallization of Ge above 700°C. The TaZrO x crystallizes above 770°C, associated with a phase separation of Ta 2 O 5 and ZrO 2 as confirmed by x-ray diffraction. For the composite layers having 3 nm and 6 nm thickness, the size of the Ge nanocrystals correlates with the deposited layer thickness. Thicker composite layers (above 9 nm) form two fractions of nanocrystals with different sizes. An additional SiO 2 layer in the [Ge–TaZrO x /SiO 2 /TaZrO x ] 6 superlattice stacks facilitates the formation of larger and better separated Ge nanocrystals. The deposition of Ge-SiO 2 composite layers separated by pure TaZrO x illustrates the barrier effect of TaZrO x against Ge diffusion. All three material systems allow the controlled formation of Ge nanocrystals in amorphous matrices at temperatures above 700 and below 770°C. Graphical abstract
This study analyzes feasibility of complementary metal–oxide–semiconductor (CMOS)-compatible manufacturing of a hybrid single electron transistor–field effect transistor (SET-FET) circuit. The fundamental element towards an operating SET at room temperature is a vertical nanopillar (NP) with embedded Si nanodot generated by ion-beam irradiation. The integration process from NPs to contacted SETs is validated by structural characterization. Then, the monolithic fabrication of planar FETs integrated with vertical SETs is presented, and its compatibility with standard CMOS technology is demonstrated. The work includes process optimization, pillar integrity validation, electrical characterization and simulations taking into account parasitic effects. The FET fabrication process is adapted to meet the requirements of the pre-fabricated NPs. Overall, this work establishes the groundwork for the realization of a hybrid SET-FET circuit operating at room temperature.
SETs (Single-Electron-Transistors) arouse growing interest for their very low energy consumption. For future industrialization, it is crucial to show a CMOS-compatible fabrication of SETs, and a key prerequisite is the patterning of sub-20 nm Si Nano-Pillars (NP) with an embedded thin SiO2 layer. In this work, we report the patterning of such multi-layer isolated NP with e-beam lithography combined with a Reactive Ion Etching (RIE) process. The Critical Dimension (CD) uniformity and the robustness of the Process of Reference are evaluated. Characterization methods, either by CD-SEM for the CD, or by TEM cross-section for the NP profile, are compared and discussed.
Modifications of magnetic and magneto-optical properties of Pt/Co(dCo)/Pt upon Ar+ irradiation (with energy 1.2, 5 and 30 keV) and fluence, F at the range from 2 · 1013–2 · 1016 Ar+ cm−2) were studied. Two ‘branches’ of increased perpendicular magnetic anisotropy (PMA) and enhanced magneto-optical response are found on 2D (dCo, F) diagrams. The difference in F between ‘branches’ is driven by ion energy. Structural features correlated with magnetic properties have been analysed thoroughly by x-ray diffraction, Rutherford backscattering spectrometry and positron annihilation spectroscopy. Experimental results are in agreement with TRIDYN numerical calculations of irradiation-induced layers intermixing. Our work discusses particularly structural factors related to crystal lattice defects and strain, created and modified by irradiation, co-responsible for the increase in the PMA.
A helium ion microscope, known for high resolution imaging and modification with helium or neon ions, has been equipped with a time-of-flight spectrometer for compositional analysis. Here we report on its design, implementation and show first results of this powerful add-on. Our design considerations were based on the results of detailed ion collision cascade simulations that focus on the physically achievable resolution for various detection limits. Different secondary ion extraction geometries and spectrometer types are considered and compared with respect to the demands and limitations of the microscope. As a result the development and evaluation of a secondary ion extraction optics and time-of-flight spectrometer that allows the parallel measurement of all secondary ion masses is reported. First experimental results demonstrate an excellent mass resolution as well as high-resolution secondary ion imaging capabilities with sub-8 nm lateral resolution. The combination of high resolution secondary electron images and mass-separated sputtered ion distributions have a high potential to answer open questions in microbiology, cell biology, earth sciences and materials research.
We demonstrate the conversion of lattice-matched InGaAs/InAlAs quantum-cascade-laser (QCL) active-region material into an effective current-blocking layer via proton implantation. A 35-period active region of an 8.4 μm-emitting QCL structure was implanted with a dose of 5 × 1014 cm−2 protons at 450 keV to produce a vacancy concentration of ∼1019 cm−3. At room temperature, the sheet resistance, extracted from the Hall measurements, increases by a factor of ∼240 with respect to that of an unimplanted material. Over the 160–320 K temperature range, the activation energy of the implanted-material Hall sheet-carrier density is 270 meV. The significant increase in room-temperature sheet resistance indicates that upon implantation deep carrier traps have been formed in the InAlAs layers of the superlattice. Fabricated mesas show effective current blocking, at voltages ≥10 V, up to at least 350 K. Thus, the implanted InGaAs/InAlAs superlattices are highly resistive to at least 350 K heat sink temperature. Such implanted material should prove useful for effective current confinement in 8–15 μm-emitting InP-based single-emitter QCL structures as well as in resonant leaky-wave coupled phase-locked arrays of QCLs.
Ge-rich ZrO2 films, fabricated by confocal RF magnetron sputtering of pure Ge and ZrO2 targets in Ar plasma, were studied by multi-angle laser ellipsometry, Raman scattering, Auger electron spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction for varied deposition conditions and annealing treatments. It was found that as-deposited films are homogeneous for all Ge contents, thermal treatment stimulated a phase separation and a formation of crystalline Ge and ZrO2. The “start point” of this process is in the range of 640–700 °C depending on the Ge content. The higher the Ge content, the lower is the temperature necessary for phase separation, nucleation of Ge nanoclusters, and crystallization. Along with this, the crystallization temperature of the tetragonal ZrO2 exceeds that of the Ge phase, which results in the formation of Ge crystallites in an amorphous ZrO2 matrix. The mechanism of phase separation is discussed in detail.
Epitaxial thin ZnO films grown by Atomic Layer Deposition were implanted with 150keV Pr ions to a fluence of 1×1015at/cm2. Implanted samples were subjected to two different kinds of annealing: rapid thermal annealing (RTA) and millisecond-range flash lamp annealing (FLA). Structural properties of implanted and annealed ZnO and the optical response were evaluated by the Channeling Rutherford Backscattering Spectrometry (RBS/c), High-resolution X-ray diffraction and Photoluminescence Spectroscopy (PL), respectively. The results shown, that both annealing techniques lead to recrystallization of the ZnO lattice, that was damaged during the ion implantation. Upon RTA performed at 800°C a return of Zn atoms from interstitial to their regular site positions is accompanied by rejection of primarily substitutional Pr atoms to the interstitial sites. Consequently, it leads to the out-diffusion and precipitation of Pr atoms on the surface. In contrast to RTA, the diffusion of implanted Pr during a millisecond range FLA treatment is completely suppressed. Despite differences in location of Pr inside the ZnO matrix after FLA and RTA, both annealing techniques lead to the optical activation of Pr3+. Interestingly, our RBS/c study for as implanted layers also revealed the anomalous damage peak, called intermediate peak (IP) located between the expected surface and the bulk damage peak. The PL spectra clearly suggest, that the defect which forms the IP, can be assigned to Zn interstitials. The long-time annealing at 800°C in oxygen atmosphere causes the complete removal of the IP.
The formation of orthorhombic (Zr,Ta)O2 was found in annealed thin Zr-Ta-O films with various tantalum concentrations deposited by co-sputtering a ZrO2 target and a mixed ZrO2/Ta2O5 target. In the as-deposited state, all films were amorphous. After annealing, tetragonal (Zr,Ta)O2 for [Ta]/([Ta] + [Zr]) ≤ 0.19 and orthorhombic (Zr,Ta)O2 for [Ta]/([Ta] + [Zr]) > 0.19 were formed. Thin films with excess of tantalum ([Ta]/([Ta] + [Zr]) ≥ 0.5) decomposed into two orthorhombic phases upon crystallization: (Zr,Ta)O2 and tantalum-rich (Ta,Zr)2O5. The Rietveld analysis of X-ray diffraction patterns revealed that the crystal structure of (Zr,Ta)O2 can be described with the non-centrosymmetric space group Pbc21. The broad range of tantalum concentrations, in which orthorhombic (Zr,Ta)O2 is formed as a single crystalline phase, is promising for the use of this compound in ferroelectric field effect transistors.
The recently installed and unique PIXE (particle-induced X-ray emission) set-up at the Helmholtz-Zentrum Dresden-Rossendorf (HZDR) is mainly dedicated to applications for a detailed overview of elemental composition over large sample areas within a short time even at trace level. The so-called High-Speed-PIXE (HS-PIXE), a combination of a pnCCD-based pixel-detector with polycapillary X-ray optics, offers simultaneous imaging of sample areas up to 12×12mm2 with a lateral resolution better than 100μm. Each of the 264×264 individual pixels detects X-ray photons in an energy range from 2keV to 20keV with an energy resolution of 152eV (@Mn-Kα). A high precision sample manipulator offers the inspection of areas up to 250×250mm2. During first experiments the determined resolution is (76±23)μm using a sample of well-known sharp-edged chromium patterns. Trace element analysis has been performed using a geological sample, a tin ore, with an average Ta-concentration below 0.1at.%. Fine-zoned structures became visible in the Ta-Lα intensity map within only 45min. The High-Speed-PIXE closes a gap in the analytical process flow chain especially for geoanalytical characterisations. It is a unique and fast detection system to identify areas of interest in comparably short time at large-area scale for further analysis.
Time of flight backscattering spectrometry (ToF-BS) was successfully implemented in a helium ion microscope (HIM). Its integration introduces the ability to perform laterally resolved elemental analysis as well as elemental depth profiling on the nm scale. A lateral resolution of ≤54nm and a time resolution of Δt≤17ns(Δt/t≤5.4%) are achieved. By using the energy of the backscattered particles for contrast generation, we introduce a new imaging method to the HIM allowing direct elemental mapping as well as local spectrometry. In addition laterally resolved time of flight secondary ion mass spectrometry (ToF-SIMS) can be performed with the same setup. Time of flight is implemented by pulsing the primary ion beam. This is achieved in a cost effective and minimal invasive way that does not influence the high resolution capabilities of the microscope when operating in standard secondary electron (SE) imaging mode. This technique can thus be easily adapted to existing devices. The particular implementation of ToF-BS and ToF-SIMS techniques are described, results are presented and advantages, difficulties and limitations of this new techniques are discussed.
Ge-nanocrystals (NCs) were synthesized in amorphous TaZrOx by thermal annealing of co-sputtered Ge-TaZrOx layers. Formation of spherical shaped Ge-NCs with small variation of size, areal density, and depth distribution was confirmed by high-resolution transmission electron microscopy. The charge storage characteristics of the Ge-NCs were investigated by capacitance-voltage and constant-capacity measurements using metal-insulator-semiconductor structures. Samples with Ge-NCs exhibit a maximum memory window of 5 V by sweeping the bias voltage from −7 V to 7 V and back. Below this maximum, the width of the memory window can be controlled by the bias voltage. The fitted slope of the memory window versus bias voltage characteristics is very close to 1 for samples with one layer Ge-NCs. A second layer Ge-NCs does not result in a second flat stair in the memory window characteristics. Constant-capacity measurements indicate charge storage in trapping centers at the interfaces between the Ge-NCs and the surrounding materials (amorphous matrix/tunneling oxide). Charge loss occurs by thermal detrapping and subsequent band-to-band tunneling. Reference samples without Ge-NCs do not show any memory window.
Polycrystalline alumina samples (α-Al2O3, purity: 99.8%) were irradiated with 63Cu5+ ions of 32MeV kinetic energy (≈0.5MeV/u) up to fluences of 1014ions/cm2 at various temperatures ranging from 295 to 973K. Ion beam induced luminescence and emission spectra were monitored at wavelengths from 320 to 800nm. Optical absorption measurements were performed to deduce color center formation. Results were evaluated by the Birks model to determine the material’s radiation hardness. The applicability of alumina as scintillation screens for ion beam diagnostics could be extended by enhanced temperature operation. Analysis of the emission spectra shows a complex color center formation behavior as a function of fluence and temperature.
We present results of recent development of the color X‐ray camera, type SLcam®, allowing detection of X‐ray images with few microns resolution. Such spectral resolution is achieved with the use of high‐quality polycapillary optics combined with sub‐pixel resolution. Imaging of Siemens star resolution test chart reveals that the resolution limit of SLcam® can go down to nearly 5μm. Several real sample examples of measurements carried out at the laboratory, synchrotron, and particle‐induced X‐ray emission beamlines are shown. This is the first time SLcam® is used as particle‐induced X‐ray emission detector. Copyright © 2015 John Wiley & Sons, Ltd.
ZrO2/ZrGe2O3 superlattices were deposited on Si wafers and thermally treated at different temperatures to form Ge nanocrystals embedded in a ZrO2 matrix. The formation process of Ge nanocrystals has been investigated by means of methods like Raman spectroscopy, X-ray diffraction, and transmission electron microscopy. With increasing temperature, there is first a separation process leading to flat Ge clusters between amorphous ZrO2 layers and then at about 630 °C a crystallization process of both the Ge clusters and the ZrO2 layers starts simultaneously. An orientation relation of the Ge and ZrO2 nanocrystals could be proven by high-resolution transmission electron microscopy.
LaLuO3 and LaScO3 high-k layers were treated by flash lamp annealing (FLA) at temperatures between 1000 degrees C and 1200 degrees C for 3 or 20 ms. This procedure mimics the effect of an source/drain activation annealing by FLA on the electrical and microstructural properties of these alternative high-k dielectrics in a gate-first processing scheme. Related MOS capacitors with a TiN metal gate were processed in a gate-first like processing scheme. It is shown that 3 nm thick oxide layers resist crystallization even at 1200 degrees C for 3 ms, while nanocrystallites are formed in thicker layers. The influence of the FLA treatment on capacitance-voltage (C-V) and current-voltage (I-V) characteristics are investigated. From these measurements, the effects on the relative dielectric constant (k), the fixed oxide charge density (Q(ox)) as well as the leakage current through the insulators are deduced. (C) 2013 Elsevier B.V. All rights reserved.
Rare earth oxides are promising candidates for future integration into nano-electronics. A key property of these oxides is their ability to form silicates in order to replace the interfacial layer in Si-based complementary metal-oxide field effect transistors. In this work a detailed study of lanthanum lutetium oxide based gate stacks is presented. Special attention is given to the silicate formation at temperatures typical for CMOS processing. The experimental analysis is based on hard x-ray photoemission spectroscopy complemented by standard laboratory experiments as Rutherford backscattering spectrometry and high-resolution transmission electron microscopy. Homogenously distributed La silicate and Lu silicate at the Si interface are proven to form already during gate oxide deposition. During the thermal treatment Si atoms diffuse through the oxide layer towards the TiN metal gate. This mechanism is identified to be promoted via Lu-O bonds, whereby the diffusion of La was found to be less important.
The phase separation of Si: ZrO2 and Ge:ZrO2 films in superlattice geometries were investigated by X-ray diffraction and reflectometry as well as by high resolution transmission electron microscopy. In case of the Si containing films, round-shaped clusters within a crystalline ZrO2 matrix have been observed after annealing at 1,000 degrees C. The appearance of nanocrystalline Si could not be shown, whereas amorphous clusters within the crystalline ZrO2 matrix were formed. For the Ge containing films, the formation of nanocrystalline Ge layers was observed after annealing at 650 degrees C. In both material systems the ZrO2 matrix crystallized in the tetragonal phase. (C) 2012 The Electrochemical Society. All rights reserved.