多主元高熵合金AlFeCuCoNiCr的微观结构

依据多主元高熵合金的设计理念,采用真空电弧炉熔炼等摩尔比多主元高熵合金AlFeCuCoNiCr,研究合金的组织结构。研究发现:AlFeCuCoNiCr合金的铸态组织是典型的树枝晶,并有纳米析出相和非晶相形成;合金存在严重的成分偏析现象,铜偏聚于枝晶间;合金形成了简单的面心立方+体心立方(FCC+BCC)结构和少量金属间化合物。     

Employing Interfaces with Metavalently Bonded Materials for Phonon Scattering and Control of the Thermal Conductivity in TAGS‐x Thermoelectric Materials

The thermoelectric compound (GeTe)_x(AgSbTe₂)_1?x, in short (TAGS‐x), is investigated with a focus on two stoichiometries, i.e., TAGS‐50 and TAGS‐85. TAGS‐85 is currently one of the most studied thermoelectric materials with great potential for thermoelectric applications. Yet, surprisingly, the lowest thermal conductivity is measured for TAGS‐50, instead of TAGS‐85. To explain this unexpected observation, atom probe tomography (APT) measurements are conducted on both samples, revealing clusters of various compositions and sizes. The most important role is attributed to Ag₂Te nanoprecipitates (NPs) found in TAGS‐50. In contrast to the Ag₂Te NPs, the matrix reveals an unconventional bond breaking mechanism. More specifically, a high probability of multiple events (PME) of ≈60% is observed for the matrix by APT. Surprisingly, the PME value decreases abruptly to ≈20–30% for the Ag₂Te NPs. These differences can be attributed to differences in chemical bonding. The precipitates' PME value is indicative of normal bonding, i.e., covalent bonding with normal optical modes, while materials with this unconventional bond breaking found in the matrix are characterized by metavalent bonding. This implies that the interface between the metavalently bonded matrix and covalently bonded Ag₂Te NP is partly responsible for the reduced thermal conductivity in TAGS‐50.     

Multipoint Defect Synergy Realizing the Excellent Thermoelectric Performance of n‐Type Polycrystalline SnSe via Re Doping

SnSe has attracted much attention due to the excellent thermoelectric (TE) properties of both p‐ and n‐type single crystals. However, the TE performance of polycrystalline SnSe is still low, especially in n‐type materials, because SnSe is an intrinsic p‐type semiconductor. In this work, a three‐step doping process is employed on polycrystalline SnSe to make it n‐type and enhance its TE properties. It is found that the Sn_0.97Re_0.03Se_0.93Cl_0.02 sample achieves a peak ZT value of ≈1.5 at 798 K, which is the highest ZT reported, to date, in n‐type polycrystalline SnSe. This is attributed to the synergistic effects of a series of point defects: $V_{\mathrm{Se}}^{\mathrm{..}},{\mathrm{Cl}}_{\mathrm{Se}}^{.},V_{\mathrm{Sn}}^{,,},{\mathrm{Re}}_{\mathrm{Sn}}^{\times },{\mathrm{Re}}_{}^0$. In those defects, the $V_{\mathrm{Se}}^{\mathrm{..}}$ compensates for the intrinsic Sn vacancies in SnSe, the ${\mathrm{Cl}}_{\mathrm{Se}}^{.}$ acts as a donor, the $V_{\mathrm{Sn}}^{,,}$acts as an acceptor, all of which contribute to optimizing the carrier concentration. Rhenium (Re) doping surprisingly plays dual‐roles, in that it both significantly enhances the electrical transport properties and largely reduces the thermal conductivity by introducing the point defects, ${\mathrm{Re}}_{\mathrm{Sn}}^{\times },{\mathrm{Re}}_{}^0$. The method paves the way for obtaining high‐performance TE properties in SnSe crystals using multipoint‐defect synergy via a step‐by‐step multielement doping methodology.     

High-temperature strength-coercivity balance in a FeCo-based soft magnetic alloy via magnetic nanoprecipitates

Precipitation strengthening is an effective approach to enhance the strength of soft magnetic alloys for applications at high temperatures,while inevitably results in deterioration in coercivity due to the pinning effect on the domain wall movement.Here,we realize a good combination of high-temperature strength and ductility (ultimate tensile strength of 564 MPa and elongation of ～ 20 ％,respectively) as well as low coercivity (6.97 Oe) of FeCo-2V-0.3Cr-0.2Mo soft magnetic alloy through introducing high-density magnetic nanoprecipitates.The magnetic nanoprecipitates are characterized by FeCo-based phase with disordered body-centered cubic structure,whichenables the alloy to have a low coercivity.In addition,these nanoprecipitates can impede the dislocation motion and suppress the brittle fracture,which lead to a high tensile strength and ductility.This work provides a guideline to enhance strength and ductility while maintaining low coercivity in soft magnetic alloys via magnetic nanoprecipitates.     

Ultrastrong High-Ductility Ni35Co35Fe10Al10Ti8B2 High-Entropy Alloy Strengthened with Super-High Concentration L12 Precipitates

L1₂ phase hardening alloys with excellent mechanical properties are of great significance for structural applications. However, low volume fractions of L1₂ precipitates in conventional alloys (nearly lower than 60%) tend to limit their practical usage, while the strengths of the alloys generally increase with L1₂ precipitation contents. Herein, a novel high-entropy alloy (HEA) Ni₃₅Co₃₅Fe₁₀Al₈Ti₁₀B₂ with ultrahigh concentration L1₂ precipitates is successfully designed aided by the calculation of phase diagrams (CALPHAD). The volume fraction of L1₂ precipitates in this HEA is up to 75% and outperforms that of most of traditional superalloys. The novel L1₂-strengthened Ni₃₅Co₃₅Fe₁₀Al₈Ti₁₀B₂ has an ultrahigh tensile yield strength of ≈1.45 GPa, ultimate tensile strength of ≈1.9 GPa, and great ductility of ≈23% at room temperature. The desirable strength–ductility combination is superior to most of conventional superalloys and reported HEAs, mainly due to the presence of ultrahigh concentration L1₂ precipitates that act as dislocation obstacles and the formation of numerous stacking faults and deformation twining. This work is expected to provide guidance for developing new high-performance HEAs with an excellent combination of strength and ductility.