Li Long, Zhang Na, Su Yaqiong, Zhao Jing, Song Zhongxiao, Qian Dan, Wu Hu, Tahir Muhammad, Saeed Alam, Ding Shujiang
School of Chemistry, Xi'an Key Laboratory of Sustainable Energy Materials Chemistry, State Key Laboratory of Electrical Insulation and Power Equipment, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, China.
ACS Appl Mater Interfaces. 2021 May 26;13(20):23787-23793. doi: 10.1021/acsami.1c04647. Epub 2021 May 17.
NaV(PO)F has been considered as a promising cathode material for sodium-ion batteries due to its high operating voltage and structural stability. However, the issues about poor cycling performance and lack of understanding for the capacity degradation mechanism are the major hurdle for practical application. Herein, we meticulously analyzed the evolution of the morphology, crystal structure, and bonding states of the cathode material during the cycling process. We observed that capacity degradation is closely related to the shedding of the active material from the collector caused by HF corrosion. Meanwhile, HF is produced through F anion dissolution from NaV(PO)F induced by trace HO during the cycling process. The F dissolution-induced degradation mechanism based on fluorine-containing cathode materials is proposed for the first time, providing a new insight for the understanding, modification, and performance improvement for fluorophosphate-based cathode materials.
由于其高工作电压和结构稳定性,NaV(PO)F被认为是一种有前途的钠离子电池正极材料。然而,循环性能差以及对容量衰减机制缺乏了解等问题是其实际应用的主要障碍。在此,我们仔细分析了正极材料在循环过程中形态、晶体结构和键合状态的演变。我们观察到容量衰减与HF腐蚀导致活性材料从集流体上脱落密切相关。同时,在循环过程中,痕量H₂O诱导NaV(PO)F中的F⁻阴离子溶解产生HF。首次提出了基于含氟正极材料的F⁻溶解诱导降解机制,为理解、改性和提高氟磷酸盐基正极材料的性能提供了新的见解。