Inter-Cation Charge Transfer Mediated Antiferromagnetism in Co$_{1+x}$Ir$_{2-x}$S$_4$
Liang-Wen Ji, Si-Qi Wu, Bai-Zhuo Li, Wu-Zhang Yang, Shi-Jie Song, Yi, Liu, Jing Li, Zhi Ren, and Guang-Han Cao

TL;DR
This paper reports a new spinel compound Co$_{1+x}$Ir$_{2-x}$S$_4$ exhibiting high-temperature antiferromagnetism mediated by inter-cation charge transfer, expanding traditional superexchange theory to complex multi-cation systems.
Contribution
It introduces a novel mechanism of inter-cation charge transfer facilitating superexchange in a new spinel compound, broadening understanding of magnetic interactions in complex materials.
Findings
Antiferromagnetic transition at 292 K in Co$_{1+x}$Ir$_{2-x}$S$_4$
First-principle calculations show antiferromagnetic alignment of Co spins
Inter-cation charge transfer enhances superexchange interaction
Abstract
The antiferromagnetism in transition metal compounds is mostly mediated by the bridging anions through a so-called superexchange mechanism. However, in materials like normal spinels with local moments only at the site, such an anion-mediated superexchange needs to be modified. Here we report a new spinel compound CoIrS ( = 0.3). The physical property measurements strongly suggest an antiferromagnetic-like transition at 292 K in the Co() diamond sublattice. The first-principle calculations reveal that the nearest-neighbor Co() spins align antiferromagnetically with an ordered magnetic moment of 1.67 , smaller than the expected for Co. In the antiferromagnetic state, there exists an inter-cation charge-transfer gap between the non-bonding Ir- orbitals at the valence band maximum and the Co-S…
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