Baumgärtner Julian F, Stoian Dragos C, Marshall Kenneth P, Jafarpour Mohammad, Klimpel Matthias, Zhang Huanyu, Okur Faruk, van Beek Wouter, Chernyshov Dmitry, Abdolhosseinzadeh Sina, Wörle Michael, Kovalenko Maksym V, Kravchyk Kostiantyn V
Laboratory of Inorganic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zürich, CH-8093 Zürich, Switzerland.
Laboratory for Thin Films and Photovoltaics, Laboratory for Functional Polymers, Empa - Swiss Federal Laboratories for Materials Science & Technology, CH-8600 Dübendorf, Switzerland.
ACS Energy Lett. 2025 Feb 6;10(2):1082-1088. doi: 10.1021/acsenergylett.5c00218. eCollection 2025 Feb 14.
3D transition metal fluorides have long been recognized as appealing low-cost, high-energy-density cathode materials for Li-ion batteries, but their conversion-type lithiation mechanism induces structural and morphological changes, limiting their cycling stability. Our findings now suggest that metal fluorides may undergo single-phase lithiation when crystallized in a pyrochlore structure, enabled by the presence of Li-ion storage sites within interconnected hexagonal channels. By conducting a detailed analysis of pyrochlore iron(III) hydroxy fluorides during lithiation using X-ray absorption spectroscopy, X-ray total scattering, and electron microscopy, we provide evidence for a possible single-phase lithiation mechanism and robust structural stability. These results challenge the traditional view of conversion-type lithiation in metal fluorides and highlight their potential for achieving high cycling stability and eventual commercialization in Li-ion batteries.
长期以来,三维过渡金属氟化物一直被认为是用于锂离子电池的有吸引力的低成本、高能量密度阴极材料,但其转换型锂化机制会引起结构和形态变化,限制了它们的循环稳定性。我们现在的研究结果表明,当金属氟化物以焦绿石结构结晶时,可能会发生单相锂化,这是由相互连接的六边形通道内存在锂离子存储位点所促成的。通过使用X射线吸收光谱、X射线全散射和电子显微镜对锂化过程中的焦绿石铁(III)羟基氟化物进行详细分析,我们为可能的单相锂化机制和强大的结构稳定性提供了证据。这些结果挑战了金属氟化物中转换型锂化的传统观点,并突出了它们在锂离子电池中实现高循环稳定性并最终商业化的潜力。