RESUMEN
The need for improved functionalities in extreme environments is fuelling interest in high-entropy ceramics1-3. Except for the computational discovery of high-entropy carbides, performed with the entropy-forming-ability descriptor4, most innovation has been slowly driven by experimental means1-3. Hence, advancement in the field needs more theoretical contributions. Here we introduce disordered enthalpy-entropy descriptor (DEED), a descriptor that captures the balance between entropy gains and enthalpy costs, allowing the correct classification of functional synthesizability of multicomponent ceramics, regardless of chemistry and structure. To make our calculations possible, we have developed a convolutional algorithm that drastically reduces computational resources. Moreover, DEED guides the experimental discovery of new single-phase high-entropy carbonitrides and borides. This work, integrated into the AFLOW computational ecosystem, provides an array of potential new candidates, ripe for experimental discoveries.
RESUMEN
Similar to Earth, many large planetesimals in the Solar System experienced planetary-scale processes such as accretion, melting, and differentiation. As their cores cooled and solidified, significant chemical fractionation occurred due to solid metal-liquid metal fractionation. Iron meteorites -- core remnants of these ancient planetesimals -- record a history of this process. Recent Fe isotope analyses of iron meteorites found δ57/54Fe to be heavier than chondritic by approximately 0.1 to 0.2 for most meteorites, indicating that a common parent body process was responsible. However, the mechanism for this fractionation remains poorly understood. Here we experimentally show that the Fe isotopic composition of iron meteorites can be explained solely by core crystallization. In our experiments of core crystallization at 1300 °C, we find that solid metal becomes enriched in δ57/54Fe by 0.13 relative to liquid metal. Fractional crystallization modelling of the IIIAB iron meteorite parent body shows that observed Ir, Au and Fe isotopic compositions can be simultaneously reproduced during core crystallization. The model implies the formation of complementary S-rich components of the iron meteorite parental cores that remain unsampled by meteorite records and may be the missing reservoir of isotopically-light Fe. The lack of sulfide meteorites and previous trace element modeling predicting significant unsampled volumes of iron meteorite parent cores support our findings.