亚稳态
材料科学
碳化物
退火(玻璃)
热力学
密度泛函理论
微观结构
动能
空位缺陷
化学稳定性
化学物理
组态熵
溅射
熵(时间箭头)
高熵合金
热力学平衡
高能材料
俘获
相(物质)
离解(化学)
热力学自由能
溅射沉积
不稳定性
热力学状态
旋节分解
活化能
氢
势能
分子动力学
动力学
脉冲(物理)
作者
Delower Hossain,Tao Liang,Jaynal Abedin,Haixuan Xu,Robert Mayanovic,Jon-Paul Maria
标识
DOI:10.1021/acs.chemmater.6c00320
摘要
Abstract High-entropy carbides (HECs) can be stabilized as single-phase solid-solution microstructures by kinetically trapping a “high-entropy state” under ambient conditions; however, such microstructures may represent metastable states rather than true thermodynamic equilibrium. Here, we investigate the thermodynamic stability of HECs using an integrated theoretical–experimental framework. Density functional theory calculations of carbon vacancy formation energies reveal two distinct energy landscapes, from which we hypothesize that rugged profiles correspond to reduced effective configurational entropy and promote multiphase microstructures, whereas smoother profiles are indicative of higher configurational entropy and stabilize single-phase microstructures. High-power impulse magnetron sputtering synthesis validates these predictions, showing single-phase HECs in the as-deposited state due to kinetic barriers, whereas postdeposition annealing induces phase segregation in compositions exhibiting rugged energy landscapes. Furthermore, machine-learning-derived descriptors enable systematic mapping of these energy landscapes, providing a predictive pathway to accelerate understanding of defect profile and its critical role in delineating phase stability in HECs.
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