Yakubovich Olga V, Shvanskaya Larisa V, Kiriukhina Galina V, Simonov Sergey V, Volkov Anatoly S, Dimitrova Olga V, Glazkov Vasiliy N, Ignatenko Andrey N, Chung Seung Hwan, Koo Hyun-Joo, Whangbo Myung-Hwan, Vasiliev Alexander N
Lomonosov Moscow State University, Moscow 119991, Russia.
National University of Science and Technology "MISiS", Moscow 119049, Russia.
Inorg Chem. 2023 Sep 4;62(35):14180-14190. doi: 10.1021/acs.inorgchem.3c01100. Epub 2023 Aug 18.
-Pyrovanadate (or -diorthovanadate) KMnMnO(OH)(VO)(VO) synthesized hydrothermally crystallizes in the orthorhombic space group with = 17.9155(5), = 5.8940(2), = 10.9971(3) Å, = 1161.23(6) Å, and = 4. Its crystal structure features linear chains of edge-sharing MnO octahedra with every second pair of MnO octahedra condensed with a MnO octahedron on one side of a chain in a sawtooth pattern so that each sawtooth chain consists of a triangular trimer. These sawtooth chains, running parallel to the axis and linked by the VO and VO groups, form a framework with channels populated by K atoms. The new compound is a structural analogue of the mineral zoisite CaAlO(OH)(SiO)(SiO), showing a striking example of very different chemical compositions. KMnO(OH)(VO)(VO) undergoes a phase transition into an ordered antiferromagnetic (AFM) state at = 14.4 K, which was detected by high-frequency electron spin resonance as well as by both specific heat and Fisher's specific heat d(χ)/d measurements. However, this phase transition was not detected by magnetic susceptibility measurements. The origin of this puzzling observation was resolved by evaluating the spin exchanges of KMnO(OH)(VO)(VO), which revealed that each triangular trimer is a ferromagnetically coupled cluster, and the observed ordering involves an AFM ordering between the ferromagnetic (FM) clusters. This ordering is shrouded in magnetic susceptibility measurements due to the susceptibility contributions from the individual FM triangular trimers even below . We showed that the magnetic susceptibility of KMnO(OH)(VO)(VO) between ∼30 K and room temperature is satisfactorily described by an AFM chain made up of ferromagnetically coupled triangular clusters, as described by a few spin-exchange parameters.
水热合成的焦钒酸盐(或二正钒酸盐)KMnMnO(OH)(VO)(VO) 结晶于正交空间群,其晶格参数为:a = 17.9155(5) Å,b = 5.8940(2) Å,c = 10.9971(3) Å,V = 1161.23(6) ų,Z = 4。其晶体结构的特征是由共边MnO八面体形成的线性链,每隔一对MnO八面体在链的一侧以锯齿状与一个MnO八面体缩合,使得每个锯齿链由一个三角形三聚体组成。这些平行于c轴排列并通过VO和VO基团相连的锯齿链形成了一个由K原子填充通道的框架。这种新化合物是矿物黝帘石CaAlO(OH)(SiO)(SiO)的结构类似物,展现了化学成分差异极大的显著例子。KMnO(OH)(VO)(VO)在T = 14.4 K时发生相变进入有序反铁磁(AFM)态,这通过高频电子自旋共振以及比热和费舍尔比热d(χ)/dT测量得以检测。然而,该相变通过磁化率测量未被检测到。通过评估KMnO(OH)(VO)(VO)的自旋交换解决了这一令人困惑的观测结果,结果表明每个三角形三聚体是一个铁磁耦合簇,所观测到的有序化涉及铁磁(FM)簇之间的AFM有序化。由于即使在T以下单个FM三角形三聚体的磁化率贡献,这种有序化在磁化率测量中被掩盖。我们表明,KMnO(OH)(VO)(VO)在约30 K至室温之间的磁化率可以由由铁磁耦合三角形簇组成的AFM链令人满意地描述,这由几个自旋交换参数所描述。