scholarly journals Towards Reconfigurable Electronics: Silicidation of Top-Down Fabricated Silicon Nanowires

2019 ◽  
Vol 9 (17) ◽  
pp. 3462 ◽  
Author(s):  
Muhammad Bilal Khan ◽  
Dipjyoti Deb ◽  
Jochen Kerbusch ◽  
Florian Fuchs ◽  
Markus Löffler ◽  
...  

We present results of our investigations on nickel silicidation of top-down fabricated silicon nanowires (SiNWs). Control over the silicidation process is important for the application of SiNWs in reconfigurable field-effect transistors. Silicidation is performed using a rapid thermal annealing process on the SiNWs fabricated by electron beam lithography and inductively-coupled plasma etching. The effects of variations in crystallographic orientations of SiNWs and different NW designs on the silicidation process are studied. Scanning electron microscopy and transmission electron microscopy are performed to study Ni diffusion, silicide phases, and silicide–silicon interfaces. Control over the silicide phase is achieved together with atomically sharp silicide–silicon interfaces. We find that {111} interfaces are predominantly formed, which are energetically most favorable according to density functional theory calculations. However, control over the silicide length remains a challenge.

2017 ◽  
Vol 8 ◽  
pp. 440-445 ◽  
Author(s):  
Marta Agati ◽  
Guillaume Amiard ◽  
Vincent Le Borgne ◽  
Paola Castrucci ◽  
Richard Dolbec ◽  
...  

Scanning transmission electron microscopy (STEM) was successfully applied to the analysis of silicon nanowires (SiNWs) that were self-assembled during an inductively coupled plasma (ICP) process. The ICP-synthesized SiNWs were found to present a Si–SiO2 core–shell structure and length varying from ≈100 nm to 2–3 μm. The shorter SiNWs (maximum length ≈300 nm) were generally found to possess a nanoparticle at their tip. STEM energy dispersive X-ray (EDX) spectroscopy combined with electron tomography performed on these nanostructures revealed that they contain iron, clearly demonstrating that the short ICP-synthesized SiNWs grew via an iron-catalyzed vapor–liquid–solid (VLS) mechanism within the plasma reactor. Both the STEM tomography and STEM-EDX analysis contributed to gain further insight into the self-assembly process. In the long-term, this approach might be used to optimize the synthesis of VLS-grown SiNWs via ICP as a competitive technique to the well-established bottom-up approaches used for the production of thin SiNWs.


2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract


2012 ◽  
Vol 531 ◽  
pp. 211-214 ◽  
Author(s):  
Jun Jie Jing ◽  
Ji Min Xie ◽  
Hui Ru Qin ◽  
Wen Hua Li ◽  
Ming Mei Zhang

Nickel(Ni)-silver(Ag) core-shell nanoparticles with different shell thickness were synthesized with Ni nanoparticles by liquid phase reduction technique form water solution. The product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and inductively coupled plasma spectroscopy (ICP). The results showed that the Ni nanoparticles are in sphere shape and the average diameter is 104nm , the nickel(Ni)-silver(Ag) core-shell nanoparticles has good crystallinity and the thinkness of Ag nanoshells could be effectively controlled by changing the concentration of silver nitrate. The product can be used for nickel-based conductive paste preparation because of the surface character of Ag and the magnetic property of Ni


Chemija ◽  
2020 ◽  
Vol 31 (2) ◽  
Author(s):  
Jolita Jablonskienė ◽  
Dijana Šimkūnaitė ◽  
Jūratė Vaičiūnienė ◽  
Giedrius Stalnionis ◽  
Audrius Drabavičius ◽  
...  

The carbon supported manganese(IV)–cobalt (II/III) oxides nanoparticles labelled as MnO2–Co3O4/C nanocomposites have been prepared by a simple one-step microwave-assisted heating method using different precursor materials. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and inductively coupled plasma optical emission spectroscopy (ICP-OES) have been used for the characterization of morphology, structure and composition of the synthesized nanocomposites, whereas the electrochemical performance of the prepared nanocomposites has been evaluated by using cyclic voltammetry (CV). It was determined that the use of different precursor materials for the synthesis of the carbon supported MnO2 and Co3O4 nanocomposites results in a different morphology of the prepared substances. A high specific capacitance (Cs) of 658.8 F g−1 at a scan rate of 10 mV s−1 in a 1 M Na2SO4 solution has been obtained for the MnO2–Co3O4/C-2 nanocomposite that has a spherical shape of nanoparticles. Moreover, it significantly outperforms the MnO2–Co3O4/C-1 nanocomposite that has a lamellar shape of nanoparticles.


2000 ◽  
Vol 638 ◽  
Author(s):  
Jordi Arbiol ◽  
Ana Ruiz ◽  
Albert Cirera ◽  
Francisca Peiró ◽  
Albert Cornet ◽  
...  

AbstractIn this work, we studied the Pt particles embedded on crystalline TiO2 nanopowders. As it is well known, metal nanoparticles distributed on TiO2 surface can improve dramatically the reaction rate and selectivity of reaction in gas sensing. We prepared a wide set of TiO2 samples with different nominal Pt concentration. The aim of this study was to analyse the Pt distribution on TiO2 surface (density of Pt, particle size distribution, etc.), as well as the Pt phases existing in our samples. We used High Resolution Transmission Electron Microscopy (HRTEM) as a powerful tool to study Pt particles morphology. The HRTEM images were compared with computer simulations to confirm the results obtained. The chemical composition of the material has been also investigated by Inductively Coupled Plasma (ICP).


2020 ◽  
Vol 84 (2) ◽  
pp. 313-334 ◽  
Author(s):  
Marion Turuani ◽  
Flavien Choulet ◽  
Aurélien Eglinger ◽  
Philippe Goncalves ◽  
Julie Machault ◽  
...  

AbstractBrannerite (UTi2O6) is among the major uranium-bearing minerals found in ore deposits, however as it has been long considered as a refractory mineral for leaching it is currently disregarded in ore deposits. Brannerite is found in a variety of geological environments with the most common occurrences being hydrothermal and pegmatitic. On the basis of scanning electron microscopy observations coupled with electron probe micro-analyses and laser ablation inductively-coupled plasma mass spectrometer analyses, this study describes the morphological features and the major- and trace-element abundances of brannerite samples from five hydrothermal and five pegmatitic localities across the world. Mineral compositions are also compared with observations from transmission electron microscopy and Raman spectrometry showing that brannerite is amorphous. Significant results include the definition of substitution trends and REE patterns, which are characteristics of either an occurrence or genetic type (hydrothermal and pegmatitic). Hence, in combination, it is possible to obtain reliable constraints for establishing a geochemical classification of brannerite. Inferred fingerprints have direct implications for forensic science and the exploration industry; they also contribute to a better understanding of metallogenic processes and to optimising the extraction of uranium.


Clay Minerals ◽  
2001 ◽  
Vol 36 (3) ◽  
pp. 447-464 ◽  
Author(s):  
J. M. Huggett ◽  
A. S. Gale ◽  
N. Clauer

AbstractVariegated palaeosols, which formed from weathering of clays, silts and brackish to freshwater limestones, are present in the Late Eocene–Early Oligocene Solent Group of the Hampshire Basin, southern UK. The composition and origin of the clay in three segments of the lower part of the Solent Group have been investigated by X-ray diffraction, microprobe analysis, inductively coupled plasma-mas spectrometry, K/Ar dating, high resolution scanning electron microscopy, analytical transmission electron microscopy and wet chemistry. The detrital clay mineral suite is dominated by illite and smectite with minor kaolinite and chlorite. Seasonal wetting and drying in gley soils has resulted in replacement of smectite by Fe-rich, or illite-rich illitesmectite. Illite has also formed with gypsum and calcite in ephemeral hypersaline alkaline lakes that periodically dried out. This illite may have precipitated directly from solution. X-ray diffraction data and probe analyses indicate that the neoformed illite is Fe-rich. The K and Fe for the illitization are thought to be derived from weathered glauconite reworked from the underlying Bracklesham Group and Barton Beds.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1340
Author(s):  
Davide Motta ◽  
Ilaria Barlocco ◽  
Silvio Bellomi ◽  
Alberto Villa ◽  
Nikolaos Dimitratos

In the present work, an Ir/CeO2 catalyst was prepared by the deposition–precipitation method and tested in the decomposition of hydrazine hydrate to hydrogen, which is very important in the development of hydrogen storage materials for fuel cells. The catalyst was characterised using different techniques, i.e., X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) equipped with X-ray detector (EDX) and inductively coupled plasma—mass spectroscopy (ICP-MS). The effect of reaction conditions on the activity and selectivity of the material was evaluated in this study, modifying parameters such as temperature, the mass of the catalyst, stirring speed and concentration of base in order to find the optimal conditions of reaction, which allow performing the test in a kinetically limited regime.


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