标题: 以吸收光谱研究钙钛矿结构中钴氧化物自旋态与钴离子价数
Spin configurations and valence states of cobalt ions in perovskite structure revealed by the XAS spectroscopy
作者: 高政男
Kao, Cheng-Nan
林俊源
Lin, Jiunn-Yuan
物理研究所
关键字: 钙钛矿;钴氧化物;自旋态;价态;吸收光谱;同步辐射;perovskite;Spin configurations;valence;XAS;cobalt ions
公开日期: 2011
摘要: 在许多过度金属氧化物之中,钴氧化物在价态与自旋态上展现了
非常丰富的变化。本实验是以Re1-xCaxCoO3-δ(Re=Eu、Sm ; x=0, 0.1, 0.2,
0.3, 0.4)与等样品进行一系列变温之O K-edge、Co K-edge 和Co L-edge
之X 光近缘吸收光谱(XANES),研究Re1-xCaxCoO3-δ(Re=Eu、Sm ; x=0,
0.1, 0.2, 0.3, 0.4)光谱权重随钙参杂之含量变化,进而探讨在电子自旋
态与价态变化之机制。由结果推论钴离子在低掺杂(x=0.1, 0.2)时,价
数与氧缺陷共同平衡离子价数,因此可以同时观察到价数增加与自旋
态改变的特征;而高掺杂样品,钴离子价数不在随着钙含量而增加,
平衡离子价数的工作则全由氧缺陷贡献,进而使自旋态由低自旋转变
为高自旋态。
本论文亦在ReCo0.5Mn0.5O3(其中Re=Eu、La 和Pr)样品以及
PrSrCoMnO6-δ 样品进行Co 和Mn 的L、K-edge 及O K-edge XANES
光谱实验,探讨不同稀土族化合物其过渡金属离子之电子组态,并讨
论是否有可能在钙态矿结构中发现Co+3 离子高自旋态的贡献。由实
验结果判断,ReCo0.5Mn0.5O3(其中Re=Eu、La 和Pr)样品钴、锰离子
价数分别为+2 价与+4 价。但当我们利用Sr 取代Pr 后可以观察出,
锰离子维持在+4 价,而钴离子价数已转变为+3 价,并且自旋态也与
低自旋态之光谱形状大为不同。
Soft x-ray absorption spectroscopy at the Co L2,3- ,K-edge and O
K-edges was employed as an idea tool to examine the valence states and
spin configurations of the Co ions in the perovskite compounds, such as
Re1-xAxCoO3 (Re is Eu or Sm, A is Co). Depending on the substitution
level x of calcium, our spectra show the existence of low-spin and
high-spin Co+3 and a few high-spin Co+4 ions associated with octahedral
and pyramidal oxygen coordinations in the compounds. The valence
changes of Co ions are not propotional to the levels of calcium (x).
We also measured Co and Mn L, K-edge XAS on Re2CoMnO6
(Re=Eu, Pr, and La) and PrSRCoMnO6-δ samples. Our XAS spectra clarify the valence states of Co and Mn ions in the samples. We also
found that the valence states of the transition-metal ions is Mn+4/Co+2
which cannot be understood by the simple estimation of ionization energy.
And the valence states of the Co ions in PrSRCoMnO6 is +3 , and the spin
state is high spin different from low spin in Pr2CoMnO6.
URI: http://140.113.39.130/cdrfb3/record/nctu/#GT079927546
http://hdl.handle.net/11536/49950
显示于类别:Thesis


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