Crystallization acceleration of amorphous Fe40Ni40P14B6 alloy by fluxing technique

The effect of fluxing on the structure and the crystallization of amorphous Fe₄₀Ni₄₀P₁₄B₆ alloy has been studied. Subjected to fluxing, the incubation time upon isothermal crystallization decreases, whereas, the onset crystallization temperature upon non-isothermal crystallization (with constant heating rate) decreases, and crystallization peaks become less sharp. via structural characterization, it is considered that fluxing promotes relaxation of the system; the atomic structure becomes more similar to the corresponding crystallized phase, thus alleviating the transient effect on nucleation and accelerates the crystallization.     

Reaction of a Ni-coated Al nanoparticle to form B2-NiAl: A molecular dynamics study

The kinetic reaction in a Ni-coated Al nanoparticle with equi-atomic fractions and diameter of approximately 4.5 nm is studied by means of molecular dynamics simulation, using a potential of the embedded atom type to model the interatomic interactions. First, the large driving force for the alloying of Ni and Al initiates solid state amorphization of the nanoparticle with the formation of Ni₅₀Al₅₀ amorphous alloy. Amorphization makes intermixing of the components much easier compared to the crystalline state. The average rate of penetration of Ni atoms can be estimated to be about two times higher than Al atoms, whilst the total rate of inter-penetration can be estimated to be of the order of 10^?2 m/s. The heat of the intermixing with the formation of Ni₅₀Al₅₀ amorphous alloy can be estimated at approximately ?0.34 eV/at. Next, the crystallization of the Ni₅₀Al₅₀ amorphous alloy into B2-NiAl ordered crystal structure is observed. The heat of the crystallization can be estimated as approximately ?0.08 eV/at. Then, the B2-NiAl ordered nanoparticle melts at a temperature of approximately 1500 K. It is shown that, for the alloying reaction in the initial Ni-coated Al nanoparticle, the ignition temperature can be as low as approximately 200 K, while the adiabatic temperature for the reaction is below the melting temperature of the nanoparticle with the B2-NiAl ordered structure.     

Effect of heat treatment on the NO2-sensing properties of sputter-deposited indium tin oxide thin films

Transparent conducting indium tin oxide (ITO) films were deposited onto glass substrates by radio-frequency magnetron sputtering at 648?K, under an oxygen partial pressure of 1?Pa. The effect of annealing on the electrical properties of the films was studied. Characterization of the coatings revealed an electrical resistivity below 6.5?×?10^??3?Ω?cm. The ITO films deposited at 648?K were amorphous, while the crystallinity improved after annealing at 700?K. The surface morphology examined by scanning electron microscopy appears to be uniform over the entire surface area after annealing. The NO₂-sensing properties of the ITO films were investigated and showed sensitivity at concentrations lower than 50?ppm, at a working temperature of 600?K.     

Correlation between heat- and deformation-induced crystallization of amorphous Al alloys

Deformation-induced crystallization is correlated with thermal-induced crystallization in alloys with different compositions in a single amorphous alloy system. In Al₈₇Y₆Ni₅Co₂ and Al₈₅Y₈Ni₅Co₂ alloys, which undergo primary crystallization during heating, deformation-induced crystallization of fcc-Al has been observed. In Al₈₃Y₁₀Ni₅Co₂ alloy, which undergoes eutectic-like crystallization, no deformation-induced crystallization was observed. These observations can be explained by the presence or absence of quenched-in nuclei and the work required for the creation of an amorphous/crystalline interface under compressive stress.     

Microstructure and martensitic transformation behaviors of a Ti–Ni–Hf–Cu high-temperature shape memory alloy ribbon

The Ti₃₆Ni₄₁Hf₁₅Cu₈ melt-spun ribbon undergoes a B2 ? B19′ transformation upon cooling and heating. When the Ti₃₆Ni₄₁Hf₁₅Cu₈ melt-spun ribbon is annealed at 873 K for 1 h, the spherical (Ti, Hf)₂Ni particles with a diameter of 20–40 nm precipitate in the grain interior. The fine (Ti, Hf)₂Ni precipitates improve the stability of phase transformation temperatures and cause martensite domains, with (001) compound twins in three orientations dominant instead of (011) type I twins. {111}-, {113}- and (001)//{111}-type boundaries are observed among these martensite domains. When the (Ti,Hf)₂Ni precipitates coarsen, (011) type I twins become main martensite structures in the ribbon annealed at 973 K for 1 h.     

An explanation for the low-temperature H evolution peak in hydrogenated amorphous silicon films deposited 'on the edge of crystallinity'

The puzzling existence of a sharp low-temperature (T = 400°C) H evolution peak in compact hydrogenated amorphous silicon (a-Si : H) films deposited 'on the edge of crystallinity' is examined. From infrared absorption and X-ray diffraction (XRD) measurements, we show that none of the standard methods used to explain the existence of this peak in a-Si : H materials is applicable to the present films. From the Si-H wag-mode peak frequency, we postulate the existence of very small Si crystallites contained within the amorphous matrix. While the crystallite volume fraction is too small to be detected by XRD in the as-grown films, crystallization is observed for this material at anneal temperatures as low as 500°C. It is proposed that these crystallites catalyse the crystallization of the remainder of the amorphous matrix upon moderate annealing, enabling H surface desorption and H₂ out-diffusion to the sample surface along newly formed grain boundaries at low anneal temperatures.     

Comparative study of local structure in Zr70Al10Ni20 and quasi-crystal-forming Zr70Al9Ni20Pd1 metallic glasses

The local structure of Zr₇₀Al₉Ni₂₀Pd₁ metallic glass, in which a nano-icosahedral quasi-crystalline phase (I-phase) is formed in the primary stage of crystallization, has been examined and compared with that of Zr₇₀Al₁₀Ni₂₀, the supercooled liquid state of which has a high stability. Since the local environments around the Zr and Ni atoms do not change drastically by the addition of 1 at.% Pd to Zr₇₀Al₁₀Ni₂₀, as evidenced by radial distribution function (RDF) and extended x-ray absorption fine structure (EXAFS) studies, we deduce that the icosahedral phase formed in the Zr₇₀Al₉Ni₂₀Pd₁ metallic glass has a local structure similar to that in Zr₇₀Al₁₀Ni₂₀. Although a very slight rearrangement of Zr–Zr atomic pairs occurs during quasi-crystallization, the I-phase formation is achieved without disturbing the dominant local structure in the glassy state of the Zr₇₀Al₉Ni₂₀Pd₁. An icosahedral local structure is proposed for Zr–Al–Ni metallic glass system as well as for primary quasi-crystal (QC)-forming Zr-based metallic glasses.     

Evolution of a sharp {110} texture in microcrystalline Fe78Si9B13 during magnetic crystallization from the amorphous phase

The effect of magnetic crystallization on texture evolution and control in nanocrystalline materials has been studied using a melt-spun amorphous Fe₇₈Si₉B₁₃ alloy. The magnetic crystallization was conducted at temperatures ranging from 653 to 853?K in a magnetic field up to 6?T. The temperatures used for magnetic crystallization were chosen on the basis of the Curie and crystallization temperatures of the amorphous phase, and the Curie temperature of the crystallized phase. The resultant microstructure was characterized by X-ray diffraction and FE-SEM/EBSP/OIM techniques. It was found that a sharp {110} texture developed when the amorphous precursor was crystallized at 853?K in a magnetic field of 6?T applied in a direction parallel to the ribbon surface.     

Crystallization behaviour of Al-based amorphous alloy and nanocomposites by rapid quenching

The microstructure and crystallization behaviour of melt-spun Al₈₈Ni₉Ce₂Fe₁ amorphous alloy and nanophase composites have been studied by means of X-ray diffraction, transmission electron microscopy and scanning and isothermal calorimetry. The diffraction patterns from Al₈₈Ni₉Ce₂Fe₁ amorphous alloys are diffuse, indicating a basically amorphous structure but contain two rings presumed to be associated with quenched-in nuclei. In the cases of Al₈₈Ni₉Ce₂Fe₁ nanophase composites, nanoscale precipitated particles are homogeneously dispersed in an amorphous matrix, and the crystallite diameter and volume fraction are sensitive to quenching conditions. During thermal crystallization, a two-step phase transformation occurs in the amorphous alloy and nanocomposites, which is characterized by a diffusion-controlled precipitation of nanoscale Al particles and the growth of a Al₃(Ni, Fe) nanophase prior to a Al₁₁Ce₃ nanophase. This study gives insight into structure-control for obtaining nanophases dispersed in an amorphous matrix by rapid quenching.     

Epitaxial Ni-Al thin films on NaCl using a Ag buffer layer

Epitaxial nanoscale [001] films of Ni _x Al_100-x (x = 62.5) have been prepared by physical vapour deposition on to a thin film of Ag [001] on NaCl (001) faces with occasional hillocks. The Ag film contains numerous dislocations and stacking faults and has a rms surface roughness of 2 nm. The Ni-Al film is ordered in the B2 structure and reveals many dislocations as well as antiphase boundaries between ordered domains. The formation of subgrains in the Ni-Al film results in severe height variations up to 30 nm across the surface. A cross-sectional model for the growth of both films is presented.     

Precipitation of an icosahedral quasicrystalline phase in Hf59Ni8Cu20Al10Ti3 metallic glass

The crystallization process of a Hf₅₉Ni₈Cu₂₀Al₁₀Ti₃     

Effect of cooling rate on size-dependent atomic ordering of CoPt nanoparticles

We report on the effect of cooling rate on the size-dependent atomic ordering of CoPt nanoparticles using aberration corrected high-resolution transmission electron microscopy. It was found that cooling rate plays a crucial role in promoting atomic ordering during the cooling process after annealing. Nanoparticles of ≈3?nm in diameter show the A1-disordered phase after annealing at 873?K for 1?h followed by rapid cooling (110?K/min), while the L1₀-ordered phase is obtained when the cooling rate is slow (1.5?K/min). The disordered phase is also obtained by rapid cooling after annealing at 973?K for 1?h. These results unambiguously indicate that the order–disorder transformation temperature is reduced to a temperature at least lower than 873?K for CoPt nanoparticles smaller than 3?nm in diameter. The slow cooling process promotes the atomic ordering, which resulted in an enhancement of magnetic coercivity as high as 2200?Oe. This study demonstrates that hard magnetic properties of the CoPt nanoparticles can be improved by controlling the cooling rate after heat treatments.     

Effects of Ag and Pd on the nucleation and growth of the nano-icosahedral phase in Zr65Al7.5Ni10Cu7.5M10 (M = Ag or Pd) metallic glasses

The nucleation and growth of a nano-icosahedral phase from a supercooled liquid region of Zr₆₅Al_7.5Ni₁₀Cu_7.5M₁₀ (M = Ag or Pd) glasses have been examined by differential scanning calorimetry and transmission electron microscopy. The growth rate of the icosahedral phase is nearly constant at the initial stage and much slower than that of the Zr₂Ni phase in the Zr₆₅Al_7.5Ni₁₀Cu_17.5 metallic glass. The homogeneous nucleation rate has a maximum value of 4.4 x 10²⁰ m^-3 s^-1 at 695 K in the Zr₆₅Al_7.5Ni₁₀Cu_7.5Ag₁₀ glass, which is approximately 10² times higher than that for the formation of quasicrystalline phase in the Zr_69.5Al_7.5Ni₁₁Cu₁₂ glass and 10⁴ times higher than that of the Zr₂Ni phase in the Zr₆₅Al_7.5Ni₁₀Cu_17.5 glass. With increasing Pd content, the nucleation rate of the primary phase increases significantly and the growth rate decreases at the crystallization temperature. Thus, the addition of Ag and Pd is effective for an increase in the number of nucleation sites and the suppression of grain growth, which is the main reason for the formation of icosahedral nanoparticles. The significant increase in the nucleation rate is due to an increase in the number of nucleation sites resulting from the short-range ordering consisting of Zr-(Ag or Pd) strong pairs. It is implied that the strong pair Zr-(Ag or Pd) also contributes to the restraint of the long-range rearrangements of the constitutional elements. The formation of the nanoicosahedral phase suggests that icosahedral short-range order exists in the glassy state in the present alloys.     

Highly inhomogeneous compressive plasticity in nanocrystal-toughened Zr–Cu–Ni–Al bulk metallic glass

A Zr₆₂Cu_15.5Al₁₀Ni_12.5 bulk metallic glass with a large supercooled liquid region of 90 K, produced by copper-mould casting, exhibits a high strength of 1730 MPa and superior but highly inhomogeneous plasticity under uniaxial compression at ambient temperature. Micro-X-ray diffraction shows that compressive loading facilitates crystallization in the monolithic glassy alloy, resulting in room-temperature plasticity. The plastic deformation of the Zr₆₂Cu_15.5Al₁₀Ni_12.5 BMG may be attributed to in situ precipitation of nanocrystals during compression in heavily deformed areas.     

Microstructural features of phase transformation in a binary Pd–Si metallic glass

Glassy ribbons of Pd–Si alloys were prepared by a combination of melt spinning and flux treatment. The crystallization behaviour of a Pd₈₁Si₁₉ glassy alloy was studied through isothermal annealing at temperatures ranging lower than the glass-transition temperature T _g to around the onset of crystallization. The evolution of microstructures arising from isothermal annealing was investigated by X-ray diffraction (XRD) and (high-resolution) transmission electron microscopy ((HR)TEM). XRD spectra showed that, after the sample was annealed at a sub-T _g temperature, its first diffraction peak was split into two overlapping broad peaks. TEM analysis revealed the formation of a spherical, particle-like glassy phase embedded in the glassy matrix together with a finely connected network morphology within both. Combining these observations with compositional analysis suggested that phase separation had taken place during sub-T _g annealing. When the glassy alloy was annealed at temperatures higher than T _g, nanocrystalline structures, composed of Pd₃Si and Pd phases plus a Pd₉Si₂ phase with a lamellar structure, was formed.     

A new highly ordered Al-Ni-Ru decagonal quasicrystal with 1.6 nm periodicity

A new decagonal quasicrystal (the D phase) with a period of about 1.6 nm was found to form in conventionally solidified and heat-treated Al₇₅Ni₁₅Ru₁₀ alloys. The electron diffraction patterns of the Al-Ni-Ru D phase exhibit a large number of quite sharp diffraction spots located at precise decagonal symmetry positions, indicating a highly ordered decagonal quasicrystal with a long-range quasiperiodic correlation. The D phase is formed with a composition close to Al₇₄Ni₁₅Ru₁₁, as determined by energy-dispersive X-ray analysis. By means of high-resolution electron microscopy, the structural features of the Al-Ni-Ru D phase, which are obviously different from that of the Al-Pd D phase (a typical decagonal quasicrystal with 1.6 nm periodicity reported previously), have been revealed.     

Formation of Al3Ni2-type nanocrystalline τ 3 phases in the Al–Cu–Ni system by mechanical alloying

An elemental powder mixture of Al (70 at.%), Ni (15 at.%) and Cu (15 at.%) was milled in a high-energy ball mill for various times ranging from 10 to 100?h to form ternary intermetallic alloys. X-ray diffraction and transmission electron microscopy techniques were employed for characterization of the samples. The dissolution of the individual elements into an alloy led to the formation of a τ₃ vacancy-ordered phase after 100?h of milling. This phase was found to be quite stable against milling, and no other crystalline and amorphous phases could be detected. The powder after 100?h of milling was found to contain mostly τ₃ nanophases with partial ordering, and with crystallite sizes in the range 10–20?nm along with a lattice strain of ～0.675%. The milled powder, after annealing at 700°C for 20, 40 and 60?h, revealed the formation of a strain-free and ordered τ₃ phase with a crystallite size of 80?nm, indicating grain coarsening. It is interesting to note that the mechanical energy imparted during milling could not completely destroy the vacancy ordering in the τ₃ phase, unlike other stoichiometric Al–Cu–transition metal (TM) systems, where the disordered B2 (bcc) phase is commonly observed instead of any vacancy-ordered phases.     

Crystal growth velocity in deeply undercooled Ni–Si alloys

The crystal growth velocity of Ni₉₅Si₅ and Ni₉₀Si₁₀ alloys as a function of undercooling is investigated using molecular dynamics simulations. The modified imbedded atom method potential yields the equilibrium liquidus temperatures T _L?≈?1505 and 1387?K for Ni₉₅Si₅ and Ni₉₀Si₁₀ alloys, respectively. From the liquidus temperatures down to the deeply undercooled region, the crystal growth velocities of both the alloys rise to the maximum with increasing undercooling and then drop slowly, whereas the athermal growth process presented in elemental Ni is not observed in Ni–Si alloys. Instead, the undercooling dependence of the growth velocity can be well-described by the diffusion-limited model, furthermore, the activation energy associated with the diffusion from melt to interface increases as the concentration increases from 5 to 10?at.% Si, resulting in the remarkable decrease of growth velocity.