O'Donnell Shaun, Leahy Ian A, Jana Subhendu, Gabilondo Eric A, Halasyamani P Shiv, Maggard Paul A, Smaha Rebecca W
Materials Science Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
Department of Chemistry and Biochemistry, Baylor University, Waco, Texas 76798, United States.
Chem Mater. 2025 Jul 9;37(14):5036-5042. doi: 10.1021/acs.chemmater.5c00421. eCollection 2025 Jul 22.
Eu-(II)-containing chalcogenides are an emerging class of materials that are of great interest due to their high optical activity and intriguing magnetism. Here, we synthesized EuSiSe as red-colored single crystals and characterized its structure with single-crystal X-ray diffraction, confirming the reported chiral monoclinic 2 symmetry at room temperature. The crystal structure of EuSiSe comprises distorted SiSe tetrahedral units and charge-balancing Eu-(II) cations. Here, we develop a two-step solid-state synthesis method for EuSiSe and compare it to the known boron chalcogenide method. We find the second-harmonic generation (SHG) activity of polycrystalline EuSiSe to be ∼7 × AgGaS, placing it among the highest-known SHG-active chalcogenides. No symmetry lowering is observed down to 100 K in single-crystal X-ray diffraction, although an anomalous expansion in the -axis lattice parameter occurs and may be correlated to lattice modes of the SiSe tetrahedra. We investigate the physical properties of EuSiSe using magnetometry and heat capacity measurements and find a transition to an antiferromagnetic ground state at ≈ 5.5 K. The low-temperature transition releases less entropy than expected, which may be due to the complex crystal electric field effects of Eu-(II).
含铕(II)的硫族化物是一类新兴材料,因其具有高光学活性和引人入胜的磁性而备受关注。在此,我们合成了红色单晶EuSiSe,并通过单晶X射线衍射对其结构进行了表征,证实了在室温下报道的手性单斜2对称性。EuSiSe的晶体结构由扭曲的SiSe四面体单元和电荷平衡的Eu(II)阳离子组成。在此,我们开发了一种用于EuSiSe的两步固态合成方法,并将其与已知的硼硫族化物方法进行了比较。我们发现多晶EuSiSe的二次谐波产生(SHG)活性约为7×AgGaS,使其成为已知SHG活性最高的硫族化物之一。在单晶X射线衍射中,直至100 K都未观察到对称性降低,尽管在a轴晶格参数中出现了异常膨胀,这可能与SiSe四面体的晶格模式相关。我们使用磁力测量和热容量测量研究了EuSiSe的物理性质,发现在T≈5.5 K时转变为反铁磁基态。低温转变释放的熵比预期的少,这可能是由于Eu(II)的复杂晶体电场效应所致。