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A core–shell structured nanocomposite of NiO with carbon nanotubes as positive electrode material of high capacitance for supercapacitors

Highlights: • A core–shell structured NiO@CNTs nanocomposite is synthesized by a simple hydrothermal method. • The CNTs core effectively improves the capacitance, rate and cycling performance of NiO. • A supercapacitor is assembled when activated carbon is used as the negative electrode. • The supercapacitor presents an energy density up to 52.6 Wh kg{sup −1}. - Abstract: A nanocomposite of carbon nanotubes coated with nickel oxide was prepared by a simple hydrothermal method. The structure, morphology and electrochemical performance of the nanocomposite were investigated by X-ray diffraction, scanning electron microscopy and transmission electron microscopy, electrochemical tests including cyclic voltammogram, galvanostatic charge–discharge and electrochemical impedance spectroscopy, respectively. It presents the highest specific capacitance of 1844 F g{sup −1} at 1 A g{sup −1} and 1145 F g{sup −1} at current density of 10 A g{sup −1} with 88.9% (at 1 A g{sup −1}) capacitance retention after 1000 cycles. The specific capacitance of the nanocomposite is almost double of that of the virginal NiO (972 F g{sup −1} at 1 A g{sup −1}). Its cycling behavior is also very good. When combined with activated carbon as the negative electrode, the energy density can be up to 52.6 Wh kg{sup −1}. Such good electrochemical behavior indicates that the nanocomposite is a promising electrode material for supercapacitors.

36 MATERIALS SCIENCE↗

Synthesis and characterization of Bi{sub 1.56}Sb{sub 1.48}Co{sub 0.96}O{sub 7} pyrochlore sun-light-responsive photocatalyst

Graphical abstract: Heterogeneous photo Fenton process with dye sensitized mechanism of RhB by Bi{sub 1.56}Sb{sub 1.48}Co{sub 0.96}O{sub 7} compound. - Highlights: • Bi{sub 1.56}Sb{sub 1.48}Co{sub 0.96}O{sub 7} (BSCO) catalyst was synthesized by improved solid state reaction method. • BSCO/H{sub 2}O{sub 2}/UVA and BSCO/H{sub 2}O{sub 2}/SL catalyst systems exhibit excellent photocatalytic activities for rhodamine B. • The photocatalytic degradation was preceded via heterogeneous photo Fenton mechanism process. • ·OH radicals are the main reactive species for the degradation of RhB. - Abstract: Novel nanostructure pyrochlore Bi{sub 1.56}Sb{sub 1.48}Co{sub 0.96}O{sub 7} was successfully synthesized via solid state reaction method in air. The as-synthesized photocatalyst was characterized by X-ray diffraction, Scanning electron microscopy and UV–vis diffuse reflectance spectroscopy techniques. The results showed that the BSCO was crystallized with the pyrochlore-type structure, cubic crystal system and space group Fd3m. The average particle size and band gap for BSCO were D = 76.29 nm and E{sub g} = 1.50 eV respectively. Under the optimum conditions for discoloration of the dye: initial concentration of 20 mg L{sup −1} RhB, pH 7, 25 °C, 0.5 mL H{sub 2}O{sub 2} and BSCO/dye mass ration of 1 g L{sup −1}, 97.77 and 90.16% of RhB were removed with BSCO/H{sub 2}O{sub 2} photocatalytic system within 60 min of irradiation time under UVA- and SL irradiations respectively. Pseudo-second-order kinetic model gave the best fit, with highest correlation coefficients (R{sup 2} ≥ 0.99). On the base of these results, the mechanism of the enhancement of the discoloration efficiency was discussed. .

36 MATERIALS SCIENCE↗

Electrical properties of films of zinc oxide nanoparticles and its hybrid with reduced graphene oxide

Free-standing films of ZnO nanoparticles (NPs) and reduced graphene oxide (rGO)-ZnO NPs hybrid are prepared at a liquid/liquid interface. The films are characterized by UV-visible spectroscopy, X-ray diffraction, scanning electron microscopy and atomic force microscopy. ZnO film consists of spherical aggregated NPs while the hybrid film contains folded sheets of rGO with embedded ZnO NPs. Electrical properties of the films and its photoresponse in presence of UV radiation are investigated using current sensing atomic force microscopy (CSAFM) at nanoscale and bulk measurements using two probe methods. Enhancement in photocurrent is observed in both cases and the current imaging reveals an inhomogeneous contribution by different ZnO grains in the film.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Effects of a refractory metal protective barrier on uranium carbonitride ceramic–metallic composites exposed to a high temperature hydrogen environment

Uranium nitride has been under consideration at NASA and the Department of Energy for nuclear thermal propulsion applications intended for deep space exploration vehicles. It is critical to the success of the technology development that the behavior of the fuel system is properly characterized in operational environments. This body of work fabricated ceramic metal composites consisting of uranium ceramic fuel in a molybdenum and molybdenum–tungsten metal matrix, both with and without an exterior molybdenum barrier. Specimens were introduced to a high temperature hydrogen environment and characterized through x-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy to identify characteristic changes. A portion of the specimens was fabricated with a 1.27 mm thick molybdenum barrier in order to isolate the material from the hydrogen environment. Instability of the uranium nitride occurred as low as 2073 K, leading to aggressive instability approaching 2658 K. Carbon reactions with the metal matrix were observed as well as alloying between the uranium and metal matrix constituents. The liquid uranium resulting from the instability of the uranium nitride was observed to attack the grain boundaries of the refractory metal, resulting in the formation of a liquid uranium molybdenum eutectic melt. Specimens encased in a barrier experienced similar results. The authors conclude this is a significant challenge to applications of this cermet at these temperatures. Alternate configurations with resilient hermetic seals or lower temperature applications such as power reactors may have more success.

36 MATERIALS SCIENCE↗

Cu{sub 2}O and CuO Films Produced by Chemical and Anodic Oxidation on the Surface of Copper Foil

The processes underlying the chemical and anodic oxidation of the surface of copper foil have been studied by X-ray diffraction, scanning electron microscopy, and Raman spectroscopy. It has been shown that, in the case of anodic oxidation, at a given process duration (τ) the composition and density of initially forming Cu(OH){sub 2} films depend not only on the current density (j{sub a}) but also on whether or not the electrolyte is stirred. A Cu{sub 2}O film with an optimal, coral-like structure has been produced by the anodic oxidation of copper foil for τ = 10 min at j{sub a} = 5 mA/cm{sup 2} without stirring, followed by the thermal reduction of the Cu(OH){sub 2} in a nitrogen atmosphere for 1 h at 500°C. In the case of the chemical oxidation of the copper foil surface, similar Cu{sub 2}O films with a coral-like structure can also be produced by the thermal reduction of initially forming Cu(OH){sub 2} at 500°C for 1 h.

36 MATERIALS SCIENCE↗

Effect of Ag in CdSe thin films prepared using thermal evaporation

It has been a general practice to dope thin films with suitable dopants to modify the properties of the films to make them more suitable for potential applications. When the dopant concentrations are low, they do not normally affect the structure and morphology of the films. However, it may lead to drastic changes in electronic properties of the films. This might result from the dopant getting incorporated into the lattice of the material of the films. Cadmium selenide is an important compound semiconductor material with an attractive energy band gap. The present work relates to an attempt made to dope CdSe thin films with silver. CdSe:Ag (1–5%) thin films were deposited on glass substrates at an optimized substrate temperature of 453 K using thermal evaporation technique. The grown films were analyzed using X-ray diffraction, scanning electron microscopy (SEM), energy dispersive analysis of X-ray (EDX) techniques. It is observed that undoped CdSe thin films and CdSe:Ag films have hexagonal structure. The grain size was found to increase marginally with an increase in the Ag concentration. The optical band gap of the films determined by optical transmission measurements agree with that of CdSe. Electrical conductivity is observed to increase from 10{sup –4} to 3.66 (Ω cm){sup –1} on addition of silver. The variation of resistance with temperature indicates that the prepared films consist of CdSe and Ag existing as two separate phases coexisting and contributing individually to the resistivity of the films.

36 MATERIALS SCIENCE↗

Sol–gel Synthesis and Upconversion Luminescent Properties of Yb{sup 3+},Er{sup 3+},Eu{sup 3+} Triply-Doped in YVO{sub 4} Phosphors

Yb{sup 3+},Er{sup 3+},Eu{sup 3+} triply-doped in YVO{sub 4} with varying molar ratio of Er/Eu were synthesized in a sol–gel method with a subsequent heat treatment for the first time. The optimal molar ratio of Er/Eu for the maximum energy transfer efficiency was 1/39. After molar ratio, the influences of different heat treatment temperatures were also researched and the maximal heat temperature was 1300 °C. Besides, the properties of YVO{sub 4}:Yb{sup 3+},Er{sup 3+},Eu{sup 3+} upconversion phosphors were investigated by X-ray diffraction, scanning electron microscopy and photo luminescent spectra, respectively. In sum, XRD results indicate the crystal structure of as-prepared samples, which is the tetragonal phase of YVO{sub 4} with no other diffraction peaks. SEM images show the morphology of as-prepared samples, which are granular-like nanoparticles. PL spectra demonstrate the upconversion luminescence of as-prepared samples, which emit strong green lights (at 525 nm, 550 nm) and slight red lights (at 590 nm, 615 nm, 695 nm) under the NIR irradiation at 980 nm. Two strong green emissions are attributed to the {sup 2}H{sub 11/2}→{sup 4}I{sub 15/2} and {sup 4}S{sub 3/2}→{sup 4}I{sub 15/2} transitions of Er{sup 3+} ions. Meanwhile, three slight red emissions are attributed to the {sup 5}D{sub 0}→{sup 7}F{sub 1}, {sup 5}D{sub 0}→{sup 7}F{sub 2} and {sup 5}D{sub 0}→{sup 7}F{sub 4} transitions of Eu{sup 3+} ions. All in all, the colorful emissions endow YVO{sub 4}:Yb{sup 3+},Er{sup 3+},Eu{sup 3+} phosphors great potential for some applications, such as display devices, bio-labeling and infrared detection.

36 MATERIALS SCIENCE↗

Complex magnetic properties associated with competing local and itinerant magnetism in \({\text {Pr}}_2 {\text {Co}}_{0.86} {\text {Si}}_{2.88}\)

Ternary intermetallic compound \({\text {Pr}}_2 {\text {Co}}_{0.86} {\text {Si}}_{2.88}\) has been synthesized in single phase and characterized by x-ray diffraction, scanning electron microscopy with energy dispersive x-ray spectroscopy (SEM-EDX) analysis, magnetization, heat capacity, neutron diffraction and muon spin rotation/relaxation ( \(\mu\) SR) measurements. The polycrystalline compound was synthesized in single phase by introducing necessary vacancies in Co/Si sites. Magnetic, heat capacity, and zero-field neutron diffraction studies reveal that the system undergoes magnetic transition below \(\sim\) 4 K. Neutron diffraction measurement further reveals that the magnetic ordering is antiferromagnetic in nature with an weak ordered moment. The high temperature magnetic phase has been attributed to glassy in nature consisting of ferromagnetic clusters of itinerant (3 d ) Co moments as evident by the development of internal field in zero-field \(\mu\) SR below 50 K. The density-functional theory (DFT) calculations suggest that the low temperature magnetic transition is associated with antiferromagnetic coupling between Pr 4 f and Co 3 d spins. Pr moments show spin fluctuation along with unconventional orbital moment quenching due to crystal field. The evolution of the symmetry and the crystalline electric field environment of Pr-ions are also studied and compared theoretically between the elemental Pr and when it is coupled with other elements such as Co. The localized moment of Pr 4 f and itinerant moment of Co 3 d compete with each other below \(\sim\) 20 K resulting in an unusual temperature dependence of magnetic coercivity in the system.

36 MATERIALS SCIENCE↗

Reduction Mechanism of Iron Oxide Briquettes by Carbonaceous Materials Extracted from Blast Furnace Dust

The reducibility of carbonaceous powder extracted from blast furnace dust was investigated. In this study, pickling treatment was used for BF bag dust and BF gravitational dust to extract the carbonaceous material. The structural characteristics of carbonaceous material were studied by X-ray diffraction, scanning electron microscope, and energy-dispersive spectrometer. The reduction of ferric oxide and carbon gasification experiments were researched by thermogravimetry. The results show that the pickled raw coal gives the highest reducibility, which is followed by BF bag dust and BF gravitational dust. The reason for this is that the higher disordered crystalline structure leads to stronger gasification reactivity, and further results in stronger reduction reactivity. Based on the randomized nucleation model, the kinetic analysis shows that the activation energies for the reduction reaction of BF gravitational dust, BF bag dust, and raw coal after pickling are 300.14, 180.43, and 124.62 kJ mol{sup −1}, respectively.

36 MATERIALS SCIENCE↗

Effect of Silicon Content on the Hardenability and Mechanical Properties of Link-Chain Steel

Heavy-section link-chains are increasingly required to satisfy industrial demands of shipping, lifting, and mining machinery. In this study, the hardenability of link-chain steels with different Si contents was investigated using end-quench tests. The microstructures of the end-quenched specimens were examined by x-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The mechanical properties were investigated by tension tests and impact tests. The effect of the Si content on the phase-transformation temperature during cooling was analyzed by differential scanning calorimetry. It was found that increasing the Si content from 0.24 to 0.74% led to a significant increase in hardenability; the ideal diameter (i.e., the diameter of given steel that would produce 50% martensite at the center when quenched in a hypothetical quenching medium that reduces the surface temperature of the heated steel to the bath temperature in zero time) increased from 187 to 248 mm. Si enhances the hardenability of link-chain steel by affecting its phase-transition behaviors during cooling, including suppressing ferrite formation, inhibiting carbide precipitation, and lowering the temperature of maximum transformation of bainite. The suggested Si content is 0.70-0.75% to produce link-chain steel with high hardenability and good mechanical properties.

36 MATERIALS SCIENCE↗

Photon up-conversion production in Tb{sup 3+}–Yb{sup 3+} co-doped CaF{sub 2} phosphors prepared by combustion synthesis

Graphical abstract: Up-conversion luminescence from Tb{sup 3+} obtained by energy transfer from Yb{sup 3+} pairs in CaF{sub 2} powder prepared by combustion synthesis. - Highlights: • Calcium fluoride (CaF{sub 2}) powders were prepared by combustion synthesis. • Rare-earth ions doped in this material were found in interstitial sites. • Cooperative up-conversion was observed in Tb{sup 3+}:Yb{sup 3+}:CaF{sub 2} powder. • Energy transfer between Tb{sup 3+} and pairs of Yb{sup 3+} was analyzed using rate equations. - Abstract: Calcium fluoride (CaF{sub 2}) crystalline powders were successfully prepared by the combustion synthesis method. The powder material containing luminescent rare-earth ions, more specifically terbium (Tb{sup 3+}) and ytterbium (Yb{sup 3+}), was studied by X-ray diffraction, scanning electronic microscopy and optical spectroscopy. These ions are allocated in charge compensated interstitial positions of tetragonal (C{sub 4v}) and trigonal (C{sub 3v}) symmetry sites of the cubic (O{sub h}) CaF{sub 2} lattice. Up-conversion (UC) luminescence in Tb{sup 3+} was achieved using a low power diode laser operating at 975 nm. Tb{sup 3+} is insensitive to near-infrared radiation but UC can be achieved via energy transfer from pairs of Yb{sup 3+} ions to Tb{sup 3+} ions. The UC luminescence dynamics of Tb{sup 3+} was used to study the energy transfer mechanism.

36 MATERIALS SCIENCE↗

Enhanced photocatalytic degradation of methylene blue dye under UV-sunlight irradiation by cesium doped chromium oxide thin films

Highlights: • Cs doped thin films has been prepared by the low- cost spray pyrolysis technique. • Enhanced photocatalytic activity of Cr2O3 thin films for MB photogegradation(MB) dye was achieved through Cs doping. • 6 % Cs doped Cr{sub 2}O{sub 3} thin film photocatalyst with the merits of low band gap and more oxygen vacancies, exhibits the highest sun-light photocatalytic activity. • High photostability and recyclability was achieved under sun-light irradiation. - Abstract: The present contribution highlights the photocatalytic degradation of methylene blue dye over chromium oxide Cr{sub 2}O{sub 3} thin films based photocatalysts illuminated by ultraviolet and sunlight. Cr{sub 2}O{sub 3} photocatalyst was synthesized as thin film by the spray pyrolysis method on glass substrate at temperature of 350 °C. The physical properties of the thin films were studied by X-ray diffraction, scanning electron microscopy (SEM), infrared spectroscopy (IR), Raman spectroscopy, photoluminescence (PL) probing and UV–vis spectroscopy. XRD results showed that all samples were well crystallized with rhomoboedric curudum structure. Emissions of all films have been observed in visible region at 325 nm excitation. UV–vis-NIR spectrophotometry analysis showed that the band gap energy value of chromium oxide is shortened with cesium doping. Results indicate that both the cesium doping and the introduction of oxygen vacancies promote good photocatalytic activity of Cs doped Cr{sub 2}O{sub 3} thin films under sunlight for MB degradation.

36 MATERIALS SCIENCE↗

Synthesis, Structural Characterization, and Growth Mechanism of Li 1+ x V 3 O 8 Submicron Fibers for Lithium-Ion Batteries

Here, we report on the synthesis of submicron Li 1+x V 3 O 8 fibers through a facile mixed ethanol/water solution-mediated solvothermal route in the absence of surfactants. All the raw materials used are commercially available, relatively inexpensive, and low-toxic, and these can be handled in an ambient atmosphere, rendering this synthetic route as reasonably facile and efficient. To ensure a desirable and acceptable sample crystallinity and purity, we introduced a postannealing treatment at 500°C. The monoclinic phase formation of the fiber sample was probed in detail using a series of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, X-ray photoelectron spectroscopy, high resolution transmission electron microscopy, and selected area electron diffraction measurements. Both morphology and chemical composition could be carefully and systematically tuned in terms of generating a class of novel, pure, and well-defined motifs of Li 1+x V 3 O 8 . A plausible mechanism for the formation of submicron-diameter fibers has been discussed in addition to the expected phase transformation within our Li-V-O materials. Our comprehensive study should provide for needed fundamental insights into putting forth a viable synthesis strategy for the generation of well-defined morphological variants of layered oxide materials for battery applications.

25 ENERGY STORAGE↗

Oxidation Behavior of Zirconium Diboride Nanoparticles

The products of oxidation of ZrB{sub 2} powders with average particle sizes of ~100 and ~30 nm by atmospheric oxygen under isothermal conditions and during heating have been characterized by thermal analysis, X-ray diffraction, scanning electron microscopy, IR frustrated total internal reflection spectroscopy, energy dispersive X-ray analysis, and elemental analysis. The oxidation onset has been observed at 594 and 396°C, respectively. Oxidation at temperatures of ≥800°C leads to the formation of boron oxide and monoclinic ZrO{sub 2}, independent of the particle size of ZrB{sub 2}. The reaction rate constants for the oxidation of ZrB{sub 2} nanoparticles ~100 and ~30 nm in size have been determined to be 0.03, 0.15, and 0.31 h{sup –1} at 600, 650, and 700°C and 0.11, 0.35, and 0.81 h{sup –1} at 500, 600, and 700°C, respectively. The apparent activation energies for the oxidation of the ZrB{sub 2} nanoparticles ~100 and ~30 nm in size are 161 ± 4 and 62 ± 3 kJ/mol, respectively, as evaluated from the temperature dependence of the rate constants at the above temperatures.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Fabrication and Magnetic Characterization of CFO/NiO and CFO/NiS Heterostructures

Magnetic analysis of different magnetic bilayers and multilayers is an important step for designing next-generation multiferroic heterostructures. In this study, we have investigated the magnetic interaction at the interface in CFO/NiO hetero-structures grown by pulsed laser deposition on sapphire substrates. The thin film heterostructure samples were characterized by means of X-ray diffraction, scanning electron microscopy (SEM), energy disruptive X-ray spectroscopy (EDS), and superconducting quantum interference device (SQUID) for magnetic measurements. The XRD analysis on different samples shows the crystalline growth of the thin films. The SEM-EDS analysis provides information about structural and elemental compositions of the heterostructure films. A SQUID magnetometer was used to investigate the temperature and field-dependent magnetic properties. To better understand the magnetic properties of the thin film heterostructure samples, zero field cool (ZFC) and field cool (FC) magnetization data were analyzed. At low temperature, ferromagnetic hysteresis loop was observed. A shift in the M-H hysteresis curve was observed for the FC data from the ZFC data, which indicates the presence of exchange bias effect. In addition, we have examined the effect of antiferromagnetic NiS thin films on ferromagnetism of CFO. This study on the magnetic interaction between a ferromagnetic layer and an antiferromagnetic layer can advance the frontier for applications in spin valves, magnetic sensors, and magnetic random access memory.

36 MATERIALS SCIENCE↗

Effect of Molybdenum Content on Structural, Mechanical, and Tribological Properties of Hot Isostatically Pressed β-Type Titanium Alloys for Orthopedic Applications

Aiming to develop alloys with better properties for orthopedic applications, the focus of the present research was to evaluate the effect of Mo at.% content on structural, mechanical, and tribological properties of hot isostatically pressed Ti-xMo (x = 4, 8, 12, 15, and 20 at.%) alloys. The structural evolution, mechanical properties, and tribological behavior of the nanostructured Ti-xMo alloys were evaluated using x-ray diffraction, scanning electron microscope, and ball-on-disk tribometer. Wear tests were conducted under different applied loads of 2, 8, and 16 N. Experimental results indicated that the structural evolution and morphological changes of the milled alloys were sensitive to their molybdenum (Mo) content. The morphological characterization showed that the crystallite size and the particle size decreased with increasing Mo content (at.%) reaching the lowest values of 27 and 26 nm in the case of Ti-15Mo and Ti-20Mo, respectively. On the other hand, the coefficient of friction and wear rates were found to be decreasing with increasing Mo content.

36 MATERIALS SCIENCE↗

Mesoporous ZnO microcube derived from a metal-organic framework as photocatalyst for the degradation of organic dyes

A cube-like porous ZnO architecture was synthesized by direct two-step thermolysis of a zinc-based metal-organic framework [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}]. The obtained ZnO microcube was characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy and nitrogen adsorption and desorption isotherms. The mesoporous ZnO microcube was comprised by many nanoparticles, and inherited the cube shape from [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}] precursor. With large surface area and mesoporous structure, the ZnO microcube exhibits excellent photocatalytic activities against methyl orange (MO) and rhodamine B (RhB) under UV irradiation, and the degradation rates reached 99.7% and 98.1% within 120 min, respectively. - Graphical abstract: Mesoporous ZnO microcube was synthesized via two-step thermolysis of metal-organic framework [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}], and exhibit excellent photocatalytic activity towards MO and RhB. Display Omitted - Highlights: • Cubic MOF [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}] was prepared by solution-precipitation method. • Mesoporous ZnO microcube was obtained by a two-step calcination of MOF precursor. • ZnO microcube shows photocatalytic activity to MO and RhB under UV irradiation. • The h{sup +} and ∙O{sub 2}{sup -} are main active species during the photodegradation process.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Assessment of phase constitution on the Al-rich region of rapidly solidified Al-Co-Fe-Cr alloys

The formation of quasicrystalline approximants in rapidly solidified Al-Co-Fe-Cr alloys was investigated. Alloys of atomic composition Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8}, Al{sub 77}Co{sub 11}Fe{sub 6}Cr{sub 6} and Al{sub 76}Co{sub 19}Fe{sub 4}Cr{sub 1} were produced using melt spinning and arc melting methods and their microstructural characterization was carried out by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Up to the present there is no consensus in the literature regarding the formation of quasicrystalline phase or quasicrystalline approximants in the Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8} alloy. This work presents, for the first time, a detailed structural characterization of selected alloys in the Al-Co-Fe-Cr system close to the atomic composition Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8}. The results indicated the samples to be composed, mostly, by two intermetallic phases, which are quaternary extensions of Al{sub 5}Co{sub 2} and Al{sub 13}Co{sub 4} and are quasicrystalline approximants. Although the Al{sub 5}Co{sub 2} phase has already been reported in the Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8} alloy, the presence of the monoclinic Al{sub 13}Co{sub 4} is now identified for the first time in the as cast state. In the binary Al-Co system a quasicrystalline phase is known to form in a rapidly solidified alloy with composition close to the monoclinic and orthorhombic Al{sub 13}Co{sub 4} phases. This binary quasicrystalline phase presents an average valence electron per atom (e/a) between 1.7 and 1.9; thus, in addition to the Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8} alloy, the compositions Al{sub 77}Co{sub 11}Fe{sub 6}Cr{sub 6} and Al{sub 76}Co{sub 19}Fe{sub 4}Cr{sub 1} were chosen to be within the region of formation of the quaternary extension of the Al{sub 13}Co{sub 4} phase and also within the (e/a) of 1.7 to 1.9. However, no quasicrystalline phase is present in any of the studied alloys. The Al-Co-Fe-Cr system, around the compositions studied, is composed of quaternary extensions of Al-Co intermetallic phases, which present solubility of Fe and Cr at Co atomic sites. - Highlights: •The Al rich region of the AlCoFeCr system is studied concerning phase formation on rapidly solidified alloys. •The alloys were composed mostly by quaternary extensions of Al-Co intermetallic phases. •Al{sub 5}Co{sub 2} and Al{sub 13}Co{sub 4} were the major phases observed in the alloys and are approximants of a quasicrystalline phase. •No quasicrystalline phase was observed in the Al{sub 71}Co{sub 13}Fe{sub 8}Cr{sub 8} composition.

36 MATERIALS SCIENCE↗