FORMATION OF NOVEL Cu3Au ALLOY PHASE UNDER CONFINEMENT

2005 ◽  
Vol 04 (05n06) ◽  
pp. 1011-1020
Author(s):  
SUBHENDU SARKAR ◽  
ALOKMAY DATTA ◽  
PURUSHOTTAM CHAKRABORTY

Our present work deals with the formation and thermal behavior of a nonbulk alloy phase confined within about 8 nm across the interfaces of Au/Cu multilayer systems. These multilayers deposited on silicon and float glass by DC magnetron sputtering have been studied by secondary ion mass spectrometry (SIMS), X-ray diffraction (XRD) and cross-sectional transmission electron microscopy (XTEM). Along with the highly oriented growth of the Cu and Au layers along [111], Cu 3 Au alloy was found to be present only at the Cu/Au interfaces in the nonbulk tetragonal D023 phase. Co -sputtering of Au and Cu under similar conditions produces only conventional fcc Cu 3 Au alloy phases, suggesting that interfacial confinement plays a significant role in producing the novel Cu 3 Au alloy phase in gold/copper multilayers. This novel phase is found to form only when the interfacial width is less than 10 nm. The D023 alloy phase tends to stabilize, rather than transforming to the bulk L12 phase, when the multilayer is vacuum-annealed at 150°C. As alloy formation spreads out of the interfaces (on vacuum annealing at 200°C), the dominant alloy is CuAu , consistent with the Cu:Au atomic ratio averaged over the multilayer.

2010 ◽  
Vol 25 (6) ◽  
pp. 1196-1203 ◽  
Author(s):  
M.A. Mat Yajid ◽  
H. Bagshaw ◽  
G. Möbus

Metallic multilayers of Cu/Al/Ti composition were studied by transmission electron microscopy (TEM) and plasmon energy-loss mapping as prototypes of nanoscale reactive multilayer systems with exothermic alloy formation in oxygen-free conditions. The selection and arrangement of alloy phases by the system during ex situ and in situ heating experiments were found to depend not only on temperature but strongly on the initial volume ratios of metals, and to a lesser degree on the dimensionality of the reactive sample. Here, a two-dimensional sample was represented by ex situ heating of the full multilayer structure, a one-dimensional sample refers to in situ heating of thin cross-sectional TEM specimens, while a zero-dimensional sample (or metallic dot-array) was obtained after cutting thin pillars using focused ion beams. Lamellar self-organized alternation between Heusler phase and Cu9Al4 was found.


1999 ◽  
Vol 14 (5) ◽  
pp. 1977-1981 ◽  
Author(s):  
J. Bonevich ◽  
D. van Heerden ◽  
D. Josell

The present investigation is the first comprehensive comparative study of x-ray diffraction (XRD) and transmission electron microscopy (TEM) results to address the important issue of fcc Ti formation in nanoscale multilayers. Ti/Al multilayers with 7.2 and 5.2 nm composition modulation wavelengths were studied by reflection and transmission XRD as well as transmission electron diffraction (ED), high-resolution TEM, and energy-filtered TEM. Previous reports have claimed deposition of fcc Ti in multilayer systems. Our results demonstrate that the Ti in Ti/Al multilayers deposits in the hcp form and that fcc Ti is merely an artifact of producing specimens for cross-sectional TEM.


2005 ◽  
Vol 20 (10) ◽  
pp. 2639-2646 ◽  
Author(s):  
Subhendu Sarkar ◽  
Alokmay Datta ◽  
Purushottam Chakraborty ◽  
Biswarup Satpati

A new D023 metastable phase of Cu3Au was found to grow at the interfaces of Au/Cu multilayers deposited by magnetron sputtering. The extent of formation of this novel alloy phase depends upon an optimal range of interfacial width primarily governed by the deposition wattage of the direct current magnetron used. Such interfacially confined growth is utilized to grow a ∼300-nm-thick Au/Cu multilayer with thickness of each layer nearly equal to the optimal interfacial width which was obtained from secondary-ion mass spectrometry (SIMS) data. This growth technique is observed to enhance the formation of the novel alloy phase to a considerable extent. The SIMS depth profile also indicates that the mass fragment corresponding to Cu3Au occupies the whole film while x-ray diffraction (XRD) shows almost all the strong peaks belonging to the D023 structure. High-resolution cross-sectional transmission electron microscopy shows the near-perfect growth of the individual layers and also the lattice image of the alloy phase in the interfacial region. Vacuum annealing of the alloy film and XRD studies indicate stabilization of the D023 phase at ∼150 °C. The role of interfacial confinement, the interplay between interfacial strain and free energy, and the hyperthermal species generated during the sputtering process are discussed.


2005 ◽  
Vol 20 (2) ◽  
pp. 456-463 ◽  
Author(s):  
Jiin-Long Yang ◽  
J.S. Chen ◽  
S.J. Chang

The distribution of Au and NiO in NiO/Au ohmic contact on p-type GaN was investigated in this work. Au (5 nm) films were deposited on p-GaN substrates by magnetron sputtering. Some of the Au films were preheated in N2 ambient to agglomerate into semi-connected structure (abbreviated by agg-Au); others were not preheated and remained the continuous (abbreviated by cont-Au). A NiO film (5 nm) was deposited on both types of samples, and all samples were subsequently annealed in N2 ambient at the temperatures ranging from 100 to 500 °C. The surface morphology, phases, and cross-sectional microstructure were investigated by scanning electron microscopy, glancing incident angle x-ray diffraction, and transmission electron microscopy. I-V measurement on the contacts indicates that only the 400 °C annealed NiO/cont-Au/p-GaN sample exhibits ohmic behavior and its specific contact resistance (ρc) is 8.93 × 10−3 Ω cm2. After annealing, Au and NiO contact to GaN individually in the NiO/agg-Au/p-GaN system while the Au and NiO layers become tangled in the NiO/cont-Au/p-GaN system. As a result, the highly tangled NiO-Au structure shall be the key to achieve the ohmic behavior for NiO/cont-Au/p-GaN system.


1997 ◽  
Vol 483 ◽  
Author(s):  
S. A. Ustin ◽  
C. Long ◽  
L. Lauhon ◽  
W. Ho

AbstractCubic SiC films have been grown on Si(001) and Si(111) substrates at temperatures between 600 °C and 900 °C with a single supersonic molecular beam source. Methylsilane (H3SiCH3) was used as the sole precursor with hydrogen and nitrogen as seeding gases. Optical reflectance was used to monitor in situ growth rate and macroscopic roughness. The growth rate of SiC was found to depend strongly on substrate orientation, methylsilane kinetic energy, and growth temperature. Growth rates were 1.5 to 2 times greater on Si(111) than on Si(001). The maximum growth rates achieved were 0.63 μm/hr on Si(111) and 0.375μm/hr on Si(001). Transmission electron diffraction (TED) and x-ray diffraction (XRD) were used for structural characterization. In-plane azimuthal (ø-) scans show that films on Si(001) have the correct 4-fold symmetry and that films on Si(111) have a 6-fold symmetry. The 6-fold symmetry indicates that stacking has occurred in two different sequences and double positioning boundaries have been formed. The minimum rocking curve width for SiC on Si(001) and Si(111) is 1.2°. Fourier Transform Infrared (FTIR) absorption was performed to discern the chemical bonding. Cross Sectional Transmission Electron Microscopy (XTEM) was used to image the SiC/Si interface.


2012 ◽  
Vol 583 ◽  
pp. 86-90 ◽  
Author(s):  
Hai Bin Li ◽  
Xin Yong Li ◽  
Yan De Song ◽  
Shu Guang Chen ◽  
Ying Wang ◽  
...  

TiO2nanotubes were prepared via a hydrothermal route. CeO2nanoparticles with diameters around 5nm were loaded onto the surface of TiO2nanotubes via a deposition approach followed by a calcination process. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and UV-vis diffuse reflectance spectroscopy (UV-vis) were applied for the characterization of the as-prepared CeO2/TiO2nanotubes composites. The results show that CeO2particles are highly dispersed on the surface of TiO2nanotubes. The TiO2 nanotubes are modified to response to the visible light due to the combination with CeO2. The CeO2/TiO2nanotubes composites with a CeO2/TiO2atomic ratio of 2.5% show a further improvement on the photocatalytic activity for degradation of Rhodamine B in water. The presence of CeO2improves the light absorption of TiO2nanotubes and inhibits the electron-hole recombination.


2020 ◽  
Vol 405 ◽  
pp. 33-39
Author(s):  
Elisabeth Rauchenwald ◽  
Mario Lessiak ◽  
Ronald Weissenbacher ◽  
Sabine Schwarz ◽  
Roland Haubner

Chemical vapour deposited HfN can be utilised as a component of multilayer systems in protective coatings on cutting tools. In this study, related AlHfN coatings were synthesized through a reaction of metallic hafnium and aluminium with HCl gas forming gaseous HfCl4 and AlCl3, which were subsequently transported into a heated coating reactor. Via high temperatures and separately introduced NH3 and N2 as reaction gases, AlHfN coatings were deposited on hardmetal inserts. By varying the ratio between AlCl3 and HfCl4, compositionally different AlHfN coatings were examined. Additionally, surface morphology, composition as well as crystalline phases of the obtained coatings were analysed by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction. Finally, the microstructure of the cross section of a coating was investigated via transmission electron microscopy. The observations revealed a great impact of the gas composition on the morphology and crystal structures of the coatings. Within the layer, the growth of columnar microstructures was detected. Additionally, the formation of an amorphous HfN intermediate layer between the substrate and the AlHfN with a thickness of approximately 2 nm was found.


1997 ◽  
Vol 485 ◽  
Author(s):  
G. M. Riker ◽  
M. M. Al-Jassim ◽  
F. S. Hasoon

AbstractWe have investigated CdS thin films as possible passivating window layers for InP. The films were deposited on single crystal InP by chemical bath deposition (CBD). The film thickness, as optically determined by ellipsometry, was varied from 500 to 840Å. The film morphology was investigated by high resolution scanning electron microscopy (SEM), whereas the film microstructure was studied by X-ray diffraction (XRD) and cross-sectional transmission electron microscopy (TEM). Most of the films were fine-grained polycrystalline CdS, with some deposition conditions resulting in epitaxial growth. Cross-sectional TEM examination revealed the presence of interface contaminants. The effect of such contaminants on the film morphology and microstructure was studied, and various approaches for InP surface cleaning/treatment were investigated. The epitaxial films were determined to be hexagonal on both the (111) and (100) InP substrates; however, they were heavily faulted.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Wei-Lin Wang ◽  
Chia-Ti Wang ◽  
Wei-Chun Chen ◽  
Kuo-Tzu Peng ◽  
Ming-Hsin Yeh ◽  
...  

Ta/TaN bilayers have been deposited by a commercial self-ionized plasma (SIP) system. The microstructures of Ta/TaN bilayers have been systematically characterized by X-ray diffraction patterns and cross-sectional transmission electron microscopy. TaN films deposited by SIP system are amorphous. The crystalline behavior of Ta film can be controlled by the N concentration of underlying TaN film. On amorphous TaN film with low N concentration, overdeposited Ta film is the mixture ofα- andβ-phases with amorphous-like structure. Increasing the N concentration of amorphous TaN underlayer successfully leads upper Ta film to form pureα-phase. For the practical application, the electrical property and reliability of Cu interconnection structure have been investigated by utilizing various types of Ta/TaN diffusion barrier. The diffusion barrier fabricated by the combination of crystallizedα-Ta and TaN with high N concentration efficiently reduces the KRc and improves the EM resistance of Cu interconnection structure.


2011 ◽  
Vol 672 ◽  
pp. 171-174
Author(s):  
Ionel Chicinaş ◽  
P. Cârlan ◽  
Florin Popa ◽  
Virgiliu Călin Prică ◽  
Lidia Adriana Sorcoi

The Ir-Al powder in the 1:1 atomic ratio was obtained by high energy mechanical alloying in a Pulverisette 4 Fritch planetary mill. The final product was obtained after 28 h of milling in argon atmosphere. Alloy formation was investigated by X-ray diffraction. After 4 h of milling the new structure of IrAl compound is found in the diffraction patterns. The obtained powders are nanocrystalline with a mean crystallite size of 11 nm after 28 h of milling. The particle morphology and the chemical homogeneity were studied using scanning electron microscopy (SEM) and energy dispersive spectrometry (EDX). It was found that the obtained compound present large particles composed by smaller one.


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