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arXiv 1302.2192cond-mat.mtrl-sci
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普鲁士蓝中Fe2+的混合轨道基态

Mixed Orbital Ground States of Fe2+ in Prussian Blues

Mössbauer Effect Data Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences(中国科学院大连化学物理研究所);School of Engineering, The University of Tokyo(东京大学工学部)

A. I. Rykov, J. Wang, T. Zhang, K. Nomura

AI总结:

本研究发现普鲁士蓝类似物中Fe2+存在轨道二重态与单态混合基态,其占比受温度、碱金属种类及离子交换调控,且扭曲异构可在合成中同步改变Fe2+电荷分布与晶体尺寸。

摘要:

我们报道了与混合价化合物类似的混合轨道基态化合物。在普鲁士蓝类似物AyFe3-y[Co(CN)6]·2xH2O(y<1)的穆斯堡尔谱中,Fe2+离子的轨道二重态和单态基态在A=K、Na时会随温度变化相互转化。轨道单态基态的相对权重随温度降低而增加。在无碱金属的钴氰化物中,穆斯堡尔谱以同源的四极分裂双峰为主,具有Fe2+物种的大分裂特征,该Fe2+由至少两个顺式构型的水分子氧原子配位。在A=Rb、Cs的A位填充钴氰化物中,Fe2+的单一类型八面体配位是孤立的,其特征是与轨道二重态基态相关的更窄四极谱。KFe[Co(CN)6]·H2O中K与Cs的离子交换导致轨道单态占优,即Fe2+价电子的各向异性增强。我们因此发现,由于扭曲异构现象,Fe2+的电荷分布可在合成步骤中与晶体尺寸一起被调控。

英文摘要:

We report on the mixed-orbital ground state compounds analogous to the mixed-valence ones. Orbital doublet and singlet ground states of the Fe2+ ion displayed in Moessbauer spectra of the Prussian blue analogues AyFe3-y[Co(CN)6]2xH2O (y<1) are interconverting to each other as temperature changes for A = K, Na. Relative weight of orbital singlet ground states increases with lowering temperature. In the alcali-free cobalticyanides, the Moessbauer spectra are dominated by quadrupole-splt doublets of the same origin with a large splitting characteristic of the Fe2+ species coordinated by two (at least) oxygen atoms of water molecules in cis-configuration. Single type octahedral coordination of Fe2+ is isolated in A-filled cobalticyanides for A=Rb, Cs to be characterized by the narrower quadrupole spectrum associated with the orbital doublet ground states. Ionic exchange of K for Cs in KFe[Co(CN)6]H2O results in predominance of the orbital singlet, i.e., in enhanced anisotropy of the Fe2+ valence electrons. We found hence that the Fe2+ charge distribution can be modified together with crystal size at the step of synthesis owing to distortion isomerism.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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