Electrochemical Development of Magnetic Long-Range Correlations with Tc = 128 K in a Tetraoxolene-Bridged Fe-Based Framework
Electrochemical Development of Magnetic Long-Range Correlations with Tc = 128 K in a Tetraoxolene-Bridged Fe-Based Framework
复制标题
四氧乙烯桥铁基框架中 Tc = 128 K 的磁长程相关性的电化学发展
DOI:
10.1016/j.jmmm.2019.165818
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发表时间:
2020
期刊:
影响因子:
--
通讯作者:
and Hitoshi Miyasaka
中科院分区:
文献类型:
--
作者:
Jian Chen;Kouji Taniguchi;Yoshihiro Sekine;and Hitoshi Miyasaka
The generation of the paramagnetic radical (Cl2Anradical dot3−) in the framework-edge moieties of an Fe-based two-dimensional honeycomb framework with 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinonate (Cl2Ann−), (H3O)2(phz)3[Fe2(Cl2An)3] (phz = phenazine), allowed the formation of long-range magnetic correlations over the network with a relative high magnetic phase transition temperature (Tc) of 128 K. The original compound is a paramagnet with a diamagnetic Cl2An2−linker that significantly separates paramagnetic FeIIions (S= 2), where the [(H3O)2(phz)3]2+cation is located between layered frameworks. Post-synthetic electron-doping, i.e., reduction in the solid state, using a lithium-ion battery (LIB) system, finally produced (Li+)3(H3O+)2(phz)3[(Fe2+)2(Cl2Anradical dot3−)3], which demonstrated a drastic magnetic change.