Avdeev Maxim, Ling Chris D, Tan Thiam Teck, Li Sean, Oyama Gosuke, Yamada Atsuo, Barpanda Prabeer
Bragg Institute, B87, Australian Nuclear Science and Technology Organization , Locked Bag 2001, Kirrawee DC NSW 2232, Australia.
Inorg Chem. 2014 Jan 21;53(2):682-4. doi: 10.1021/ic402513d. Epub 2013 Dec 26.
The magnetic structure and properties of sodium iron fluorophosphate Na2FePO4F (space group Pbcn), a cathode material for rechargeable batteries, were studied using magnetometry and neutron powder diffraction. The material, which can be described as a quasi-layered structure with zigzag Fe-octahedral chains, develops a long-range antiferromagnetic order below ∼3.4 K. The magnetic structure is rationalized as a super-exchange-driven ferromagnetic ordering of chains running along the a-axis, coupled antiferromagnetically by super-super-exchange via phosphate groups along the c-axis, with ordering along the b-axis likely due to the contribution of dipole-dipole interactions.
采用磁强计和中子粉末衍射研究了用于可充电电池的阴极材料氟磷酸钠铁(Na2FePO4F,空间群Pbcn)的磁结构和性质。该材料可描述为准层状结构,具有锯齿状铁八面体链,在约3.4 K以下呈现长程反铁磁有序。磁结构被解释为沿a轴方向的链通过超交换驱动的铁磁有序排列,沿c轴通过磷酸根基团的超超交换反铁磁耦合,沿b轴的有序排列可能归因于偶极-偶极相互作用的贡献。