TY - JOUR
T1 - Tunable magnetic and optical properties of transition metal dihalides by cation alloying
AU - Blei, Mark
AU - Kapeghian, Jesse
AU - Banerjee, Rounak
AU - Kolari, Pranvera
AU - Povilus, Blake
AU - Attarde, Yashika
AU - Botana, Antia S.
AU - Tongay, Sefaattin
N1 - Funding Information:
This paper was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award No. SC0020653 (Crystal growth and magnetism), Applied Materials Inc. (crystallography), National Science Foundation (NSF) Division of Materials Research (DMR) 1904716 (computational studies), NSF CMMI-1933214 (defect characterization), NSF ECCS 2052527 (electronic characterization), and DMR 2111812 (optical characterization). A.S.B and J. K acknowledge NSF Grant No. DMR 1904716 (computational efforts) and the ASU Research Computing Center for high-performance computing resources. S.T. acknowledges NSF Grant No. DMR 2206987.
Publisher Copyright:
© 2022 American Physical Society.
PY - 2022/7
Y1 - 2022/7
N2 - Alloying has been a tradition in materials science that has enabled groundbreaking discoveries in semiconductor technologies, optics, and photovoltaics, among others. While alloying in traditional systems is relatively well established, the effects of alloying in the emerging van der Waals (vdW) two-dimensional (2D) magnets are still in their infancy. Using Co1-xNixCl2 as a testbed system, our results show that chemical vapor transport of stoichiometric mixtures of TeCl4, Co, and Ni enables the synthesis of highly crystalline vdW magnetic alloys with excellent control over the Ni concentration (x) without any tellurium impurities or phase separation. The method is advantageous compared to binary CoCl2 and NiCl2 precursor mixtures which only produce small-sized crystals with a large compositional variation. Magnetic measurements show that the degree of magnetic anisotropy, Weiss temperature, and Néel temperature (TN) strongly correlate to the Ni concentration, offering a tune-knob to engineer the magnetic behavior of transition metal dihalides. First-principles calculations offer further insights into how the increasing Ni content influences the interlayer and intralayer magnetic couplings and the resulting magnetic response. Overall, our findings provide an important avenue toward metal cation alloying in dihalide 2D vdW magnets and offer means to tune their magnetic behavior on demand.
AB - Alloying has been a tradition in materials science that has enabled groundbreaking discoveries in semiconductor technologies, optics, and photovoltaics, among others. While alloying in traditional systems is relatively well established, the effects of alloying in the emerging van der Waals (vdW) two-dimensional (2D) magnets are still in their infancy. Using Co1-xNixCl2 as a testbed system, our results show that chemical vapor transport of stoichiometric mixtures of TeCl4, Co, and Ni enables the synthesis of highly crystalline vdW magnetic alloys with excellent control over the Ni concentration (x) without any tellurium impurities or phase separation. The method is advantageous compared to binary CoCl2 and NiCl2 precursor mixtures which only produce small-sized crystals with a large compositional variation. Magnetic measurements show that the degree of magnetic anisotropy, Weiss temperature, and Néel temperature (TN) strongly correlate to the Ni concentration, offering a tune-knob to engineer the magnetic behavior of transition metal dihalides. First-principles calculations offer further insights into how the increasing Ni content influences the interlayer and intralayer magnetic couplings and the resulting magnetic response. Overall, our findings provide an important avenue toward metal cation alloying in dihalide 2D vdW magnets and offer means to tune their magnetic behavior on demand.
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U2 - 10.1103/PhysRevMaterials.6.084003
DO - 10.1103/PhysRevMaterials.6.084003
M3 - Article
AN - SCOPUS:85137264005
SN - 2475-9953
VL - 6
JO - Physical Review Materials
JF - Physical Review Materials
IS - 8
M1 - 084003
ER -