High-entropy ceramics: Review of principles, production and applications
TL;DR: High-entropy ceramics with five or more cations have recently attracted significant attention due to their superior properties for various structural and functional applications as mentioned in this paper, and significant efforts were started to increase the entropy, minimize the Gibbs free energy, and achieve stable single-phase high-entropically stable ceramic films.
Abstract: High-entropy ceramics with five or more cations have recently attracted significant attention due to their superior properties for various structural and functional applications. Although the multi-component ceramics have been of interest for several decades, the concept of high-entropy ceramics was defined in 2004 by producing the first high-entropy nitride films. Following the introduction of the entropy stabilization concept, significant efforts were started to increase the entropy, minimize the Gibbs free energy and achieve stable single-phase high-entropy ceramics. High-entropy oxides, nitrides, carbides, borides and hydrides are currently the most popular high-entropy ceramics due to their potential for various applications, while the study of other ceramics, such as silicides, sulfides, fluorides, phosphides, phosphates, oxynitrides, carbonitrides and borocarbonitrides, is also growing fast. In this paper, the progress regarding high-entropy ceramics is reviewed from both experimental and theoretical points of view. Different aspects including the history, principles, compositions, crystal structure, theoretical/empirical design (via density functional theory, molecular dynamics simulation, machine learning, CALPHAD and descriptors), production methods and properties are thoroughly reviewed. The paper specifically attempts to answer how these materials with remarkable structures and properties can be used in future applications.
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TL;DR: In this paper , the authors comprehensively review recent advances on development of ultrafine-grained and nanostructured materials by severe plastic deformation and provide a brief history regarding the progress of this field.
Abstract: Severe plastic deformation (SPD) is effective in producing bulk ultrafine-grained and nanostructured materials with large densities of lattice defects. This field, also known as NanoSPD, experienced a significant progress within the past two decades. Beside classic SPD methods such as high-pressure torsion, equal-channel angular pressing, accumulative roll-bonding, twist extrusion, and multi-directional forging, various continuous techniques were introduced to produce upscaled samples. Moreover, numerous alloys, glasses, semiconductors, ceramics, polymers, and their composites were processed. The SPD methods were used to synthesize new materials or to stabilize metastable phases with advanced mechanical and functional properties. High strength combined with high ductility, low/room-temperature superplasticity, creep resistance, hydrogen storage, photocatalytic hydrogen production, photocatalytic CO2 conversion, superconductivity, thermoelectric performance, radiation resistance, corrosion resistance, and biocompatibility are some highlighted properties of SPD-processed materials. This article reviews recent advances in the NanoSPD field and provides a brief history regarding its progress from the ancient times to modernity. Abbreviations: ARB: Accumulative Roll-Bonding; BCC: Body-Centered Cubic; DAC: Diamond Anvil Cell; EBSD: Electron Backscatter Diffraction; ECAP: Equal-Channel Angular Pressing (Extrusion); FCC: Face-Centered Cubic; FEM: Finite Element Method; FSP: Friction Stir Processing; HCP: Hexagonal Close-Packed; HPT: High-Pressure Torsion; HPTT: High-Pressure Tube Twisting; MDF: Multi-Directional (-Axial) Forging; NanoSPD: Nanomaterials by Severe Plastic Deformation; SDAC: Shear (Rotational) Diamond Anvil Cell; SEM: Scanning Electron Microscopy; SMAT: Surface Mechanical Attrition Treatment; SPD: Severe Plastic Deformation; TE: Twist Extrusion; TEM: Transmission Electron Microscopy; UFG: Ultrafine Grained GRAPHICAL ABSTRACT IMPACT STATEMENT This article comprehensively reviews recent advances on development of ultrafine-grained and nanostructured materials by severe plastic deformation and provides a brief history regarding the progress of this field.
136 citations
TL;DR: In this paper , a review provides critical and in-depth details of laser-based technologies vastly applied for printing high entropy alloys (HEAs), including selective laser melting (SLM) and direct laser deposition (DLD).
32 citations
TL;DR: In this article, a dual-phase TiZrNbHfTaO11 synthesized by a two-step high-pressure torsion mechanical alloying and high-temperature oxidation was examined for CO2 conversion.
Abstract: High-entropy oxides (HEOs), as a new family of materials with five or more principal cations, have shown promising properties for various applications. In this work and inspired by inherent defective and strained structure of HEOs, photocatalytic CO2 conversion is examined on a dual-phase TiZrNbHfTaO11 synthesized by a two-step high-pressure torsion mechanical alloying and high-temperature oxidation. The HEO, which had various structural defects, showed simultaneous photocatalytic activity for CO2 to CO and H2O to H2 conversion without the addition of a co-catalyst. The photocatalytic activity of this HEO for CO2 conversion was better than conventional photocatalysts such as anatase TiO2 and BiVO4 and similar to P25 TiO2. The high activity of HEO was discussed in terms of lattice defects, lattice strain, light absorbance, band structure, photocurrent generation and charge carrier mobility to activation centers. The current study confirms the high potential of HEOs as a new family of photocatalysts for CO2 conversion.
27 citations
TL;DR: In this article , a dual-phase TiZrNbHfTaO11 synthesized by a two-step high-pressure torsion mechanical alloying and high-temperature oxidation was used for CO2 conversion.
Abstract: High-entropy oxides (HEOs), as a new family of materials with five or more principal cations, have shown promising properties for various applications. In this work and inspired by inherent defective and strained structure of HEOs, photocatalytic CO2 conversion is examined on a dual-phase TiZrNbHfTaO11 synthesized by a two-step high-pressure torsion mechanical alloying and high-temperature oxidation. The HEO, which had various structural defects, showed simultaneous photocatalytic activity for CO2 to CO and H2O to H2 conversion without the addition of a co-catalyst. The photocatalytic activity of this HEO for CO2 conversion was better than conventional photocatalysts such as anatase TiO2 and BiVO4 and similar to P25 TiO2. The high activity of HEO was discussed in terms of lattice defects, lattice strain, light absorbance, band structure, photocurrent generation and charge carrier mobility to activation centers. The current study confirms the high potential of HEOs as a new family of photocatalysts for CO2 conversion.
27 citations
TL;DR: In this article , oxygen vacancies and lattice strain are simultaneously introduced in this oxide using a high-pressure torsion process to overcome the drawbacks of BiVO4, and the enhancement of photocatalytic activity is discussed based on the modification of band structure, enhanced light absorbance, and role of oxygen vacancies as activation sites for CO2 photoreduction.
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TL;DR: A comprehensive review of 1D nanostructures can be found in this article, where the authors provide a comprehensive overview of current research activities that concentrate on one-dimensional (1D) nanostructure (wires, rods, belts and tubes).
Abstract: This article provides a comprehensive review of current research activities that concentrate on one-dimensional (1D) nanostructures—wires, rods, belts, and tubes—whose lateral dimensions fall anywhere in the range of 1 to 100 nm. We devote the most attention to 1D nanostructures that have been synthesized in relatively copious quantities using chemical methods. We begin this article with an overview of synthetic strategies that have been exploited to achieve 1D growth. We then elaborate on these approaches in the following four sections: i) anisotropic growth dictated by the crystallographic structure of a solid material; ii) anisotropic growth confined and directed by various templates; iii) anisotropic growth kinetically controlled by supersaturation or through the use of an appropriate capping reagent; and iv) new concepts not yet fully demonstrated, but with long-term potential in generating 1D nanostructures. Following is a discussion of techniques for generating various types of important heterostructured nanowires. By the end of this article, we highlight a range of unique properties (e.g., thermal, mechanical, electronic, optoelectronic, optical, nonlinear optical, and field emission) associated with different types of 1D nanostructures. We also briefly discuss a number of methods potentially useful for assembling 1D nanostructures into functional devices based on crossbar junctions, and complex architectures such as 2D and 3D periodic lattices. We conclude this review with personal perspectives on the directions towards which future research on this new class of nanostructured materials might be directed.
8,259 citations
TL;DR: A new approach for the design of alloys is presented in this paper, where high-entropy alloys with multi-principal elements were synthesized using well-developed processing technologies.
Abstract: A new approach for the design of alloys is presented in this study. These high-entropy alloys with multi-principal elements were synthesized using well-developed processing technologies. Preliminary results demonstrate examples of the alloys with simple crystal structures, nanostructures, and promising mechanical properties. This approach may be opening a new era in materials science and engineering.
8,175 citations
TL;DR: It is reported that electrodes made of nanoparticles of transition-metal oxides (MO), where M is Co, Ni, Cu or Fe, demonstrate electrochemical capacities of 700 mA h g-1, with 100% capacity retention for up to 100 cycles and high recharging rates.
Abstract: Rechargeable solid-state batteries have long been considered an attractive power source for a wide variety of applications, and in particular, lithium-ion batteries are emerging as the technology of choice for portable electronics. One of the main challenges in the design of these batteries is to ensure that the electrodes maintain their integrity over many discharge-recharge cycles. Although promising electrode systems have recently been proposed, their lifespans are limited by Li-alloying agglomeration or the growth of passivation layers, which prevent the fully reversible insertion of Li ions into the negative electrodes. Here we report that electrodes made of nanoparticles of transition-metal oxides (MO, where M is Co, Ni, Cu or Fe) demonstrate electrochemical capacities of 700 mA h g(-1), with 100% capacity retention for up to 100 cycles and high recharging rates. The mechanism of Li reactivity differs from the classical Li insertion/deinsertion or Li-alloying processes, and involves the formation and decomposition of Li2O, accompanying the reduction and oxidation of metal nanoparticles (in the range 1-5 nanometres) respectively. We expect that the use of transition-metal nanoparticles to enhance surface electrochemical reactivity will lead to further improvements in the performance of lithium-ion batteries.
7,404 citations
01 Jul 2004-Materials Science and Engineering A-structural Materials Properties Microstructure and Processing
TL;DR: In this paper, it was shown that the confusion principle does not apply, and other factors are more important in promoting glass formation of late transition metal rich multicomponent alloys.
Abstract: Multicomponent alloys containing several components in equal atomic proportions have been manufactured by casting and melt spinning, and their microstructures and properties have been investigated by a combination of optical microscopy, scanning electron microscopy, electron probe microanalysis, X-ray diffractrometry and microhardness measurements. Alloys containing 16 and 20 components in equal proportions are multiphase, crystalline and brittle both as-cast and after melt spinning. A five component Fe20Cr20Mn20Ni20Co20 alloy forms a single fcc solid solution which solidifies dendritically. A wide range of other six to nine component late transition metal rich multicomponent alloys exhibit the same majority fcc primary dendritic phase, which can dissolve substantial amounts of other transition metals such as Nb, Ti and V. More electronegative elements such as Cu and Ge are less stable in the fcc dendrites and are rejected into the interdendritic regions. The total number of phases is always well below the maximum equilibrium number allowed by the Gibbs phase rule, and even further below the maximum number allowed under non-equilibrium solidification conditions. Glassy structures are not formed by casting or melt spinning of late transition metal rich multicomponent alloys, indicating that the confusion principle does not apply, and other factors are more important in promoting glass formation.
5,289 citations
TL;DR: In this paper, the authors report the feasibility to approach such capacities by creating highly ordered interwoven composites, where conductive mesoporous carbon framework precisely constrains sulphur nanofiller growth within its channels and generates essential electrical contact to the insulating sulphur.
Abstract: The Li-S battery has been under intense scrutiny for over two decades, as it offers the possibility of high gravimetric capacities and theoretical energy densities ranging up to a factor of five beyond conventional Li-ion systems. Herein, we report the feasibility to approach such capacities by creating highly ordered interwoven composites. The conductive mesoporous carbon framework precisely constrains sulphur nanofiller growth within its channels and generates essential electrical contact to the insulating sulphur. The structure provides access to Li+ ingress/egress for reactivity with the sulphur, and we speculate that the kinetic inhibition to diffusion within the framework and the sorption properties of the carbon aid in trapping the polysulphides formed during redox. Polymer modification of the carbon surface further provides a chemical gradient that retards diffusion of these large anions out of the electrode, thus facilitating more complete reaction. Reversible capacities up to 1,320 mA h g(-1) are attained. The assembly process is simple and broadly applicable, conceptually providing new opportunities for materials scientists for tailored design that can be extended to many different electrode materials.
5,151 citations