Park Jehee, Yang Yingjie, Park Haesun, Sundar Aditya, Lee Sungsik, Kinnibrugh Tiffany L, Son Seoung-Bum, Lee Eungje, Zapol Peter, Klie Robert F, Kim Jae Jin
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
Department of Physics, University of Illinois -Chicago, Chicago Illinois 60607, United States.
ACS Appl Mater Interfaces. 2024 Oct 23;16(42):57151-57161. doi: 10.1021/acsami.4c12920. Epub 2024 Oct 10.
Metal fluorides (e.g., FeF and FeF) have received attention as conversion-type cathode materials for Li-ion batteries due to their higher theoretical capacity compared to that of common intercalation materials. However, their practical use has been hindered by low round-trip efficiency, voltage hysteresis, and capacity fading. Cation substitution has been proposed to address these challenges, and recent advancements in battery performance involve the introduction of entropy stabilization in an attempt to facilitate reversible conversion reactions by increasing configurational entropy. Building on this concept, high entropy fluorides with five cations were synthesized by using a simple mechanochemical route. In order to examine the impact of element selection, CoCuNiZnFeF (HEF-Fe) was compared with CoCuNiZnMgF (HEF-Mg), replacing electrochemically inactive Mg with Fe as an active participant in the conversion reaction. Combining electrochemical measurements with first-principles calculations, high-resolution electron microscopy, and synchrotron X-ray analysis, HEFs' battery performances and conversion reaction mechanisms were investigated in detail. The results highlighted that replacement of Mg with Fe was beneficial, with enhanced capacity, rate capability, and surface stability. In addition, it was found that HEF-Fe showed similar cycle stability without an electrochemically inactive element. These findings provide valuable insights for the design of high entropy multielement fluorides for improved Li-ion battery performance.
金属氟化物(如FeF和FeF)作为锂离子电池的转换型阴极材料受到了关注,因为与常见的嵌入材料相比,它们具有更高的理论容量。然而,它们的实际应用受到低往返效率、电压滞后和容量衰减的阻碍。有人提出阳离子取代来应对这些挑战,最近电池性能的进展涉及引入熵稳定,试图通过增加构型熵来促进可逆转换反应。基于这一概念,通过简单的机械化学路线合成了含有五种阳离子的高熵氟化物。为了研究元素选择的影响,将CoCuNiZnFeF(HEF-Fe)与CoCuNiZnMgF(HEF-Mg)进行了比较,用作为转换反应中活性参与者的Fe取代了电化学惰性的Mg。结合电化学测量与第一性原理计算、高分辨率电子显微镜和同步加速器X射线分析,对高熵氟化物的电池性能和转换反应机制进行了详细研究。结果表明,用Fe取代Mg是有益的,容量、倍率性能和表面稳定性都有所提高。此外,还发现HEF-Fe在没有电化学惰性元素的情况下表现出相似的循环稳定性。这些发现为设计用于改善锂离子电池性能的高熵多元素氟化物提供了有价值的见解。