Abstract:In the presence of strain, high temperature magnetic ordering in Cr2Ge2Te6 was observed with electronic phase crossover from semiconducting to half-metallic state. On coupling strain and electric field, the Curie temperature reaches 331 K.
“…Alternately, it is also plausible that smaller strain on higher layer numbers can also boost the T c to RT and beyond because the same percentage of strain on higher layer number demonstrates elevated T c and MAE. Recent computational works have also predicted rapid elevation of T c to RT in bulk CGT with increasing strain percentage . Therefore, it is conceivable that for thicker layers T c tends to augment under smaller strain application.…”
Section: Resultsmentioning
confidence: 99%
“…Recent computational works have also predicted rapid elevation of T c to RT in bulk CGT with increasing strain percentage. 34 Therefore, it is conceivable that for thicker layers T c tends to augment under smaller strain application. Hence it is reasonable to speculate that bulk CGT under application of strain would lead to a T c above RT with enhanced magnetism.…”
Emergent magnetism in van der Waals materials offers
exciting opportunities
in fabricating atomically thin spintronic devices. One pertinent obstacle
has been the low transition temperatures (T
c) inherent to these materials, precluding room temperature applications.
Here, we show that large structural gradients found in highly strained
nanoscale wrinkles in Cr2Ge2Te6 (CGT)
lead to significant increases of T
c. Magnetic
force microscopy was utilized in characterizing multiple strained
CGT nanostructures leading to experimental evidence of elevated T
c, depending on the strain percentage estimated
from finite element analysis. Our findings are further supported by ab initio and DFT studies of the strained material, which
indicates that strain directly augments the ferromagnetic coupling
between Cr atoms in CGT, influenced by superexchange interaction;
this provides strong insight into the mechanism of the enhanced magnetism
and T
c.
“…Alternately, it is also plausible that smaller strain on higher layer numbers can also boost the T c to RT and beyond because the same percentage of strain on higher layer number demonstrates elevated T c and MAE. Recent computational works have also predicted rapid elevation of T c to RT in bulk CGT with increasing strain percentage . Therefore, it is conceivable that for thicker layers T c tends to augment under smaller strain application.…”
Section: Resultsmentioning
confidence: 99%
“…Recent computational works have also predicted rapid elevation of T c to RT in bulk CGT with increasing strain percentage. 34 Therefore, it is conceivable that for thicker layers T c tends to augment under smaller strain application. Hence it is reasonable to speculate that bulk CGT under application of strain would lead to a T c above RT with enhanced magnetism.…”
Emergent magnetism in van der Waals materials offers
exciting opportunities
in fabricating atomically thin spintronic devices. One pertinent obstacle
has been the low transition temperatures (T
c) inherent to these materials, precluding room temperature applications.
Here, we show that large structural gradients found in highly strained
nanoscale wrinkles in Cr2Ge2Te6 (CGT)
lead to significant increases of T
c. Magnetic
force microscopy was utilized in characterizing multiple strained
CGT nanostructures leading to experimental evidence of elevated T
c, depending on the strain percentage estimated
from finite element analysis. Our findings are further supported by ab initio and DFT studies of the strained material, which
indicates that strain directly augments the ferromagnetic coupling
between Cr atoms in CGT, influenced by superexchange interaction;
this provides strong insight into the mechanism of the enhanced magnetism
and T
c.
“…The energy needed to synthesize a monolayer is represented by the formation energy, as expressed by the following equationEnormalfnormalonormalrnormalm=EhBN/NbSe2−EnormalhnormalBnormalN−ENbSe2where EhBN/NbSe2 represents the total energy of the hBN/NbSe 2 vdW heterostructure. E hBN and ENbSe2 represent the total energies of single phase hBN monolayer and NbSe 2 monolayers, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…The energy needed to synthesize a monolayer is represented by the formation energy, 39 as expressed by the following equation…”
Despite the availability of a variety of two-dimensional (2D) materials for potential use as Li-ion battery electrodes, it is difficult to find all the desirable qualities of an electrode in a single material. Therefore, research efforts are ongoing in designing a heterostructure to incorporate the desirable characteristics that are not available in the parent structures. In our work, we have designed a van der Waals heterostructure made of a conducting 2D NbSe 2 -layer and insulating hexagonal boron nitride (h-BN) and applied interlayer twist at different twist angles for potential applications as an electrode in the Li-ion battery. The heterostructure offers a metallic character, which makes the insulating h-BN capable of battery application. The adsorption site changes for different twist angles. For the twist angles of 5.21 and 54.79°, the H-site is the most favorable adsorption site, but for all other twist angles, T-site stays the most favorable adsorption site. When the angle between surfaces is 19.11°, the heterostructure shows better stability as compared to all other configurations in different twist angles. The adsorption energy gets enhanced compared to the individual monolayers, indicating better intercalation. At a twist angle of 19.11°, our structure shows a minimum diffusion barrier of 0.6 eV, whereas at all other twist angles, it shows a nearly 0.9 eV barrier. The open circuit voltage is found to be 0.62 V. The structure shows a specific capacity of 185 mA h g m −1 .
“…Most of these materials are non-magnetic and according to Mermin-Wagner theorem [4,5], the presence of long-range magnetic ordering in 2D materials is not possible due to thermal fluctuations [6,7]. Despite this, recently several intrinsically magnetic 2D materials have been discovered [8] with finite critical temperature ( T c ), like CrI 3 [9], Cr 2 Ge 2 Se 6 [10], and Cr 2 Ge 2 Te 6 [11,12]. Their electronic properties are varied and among them, 2D ferromagnetic semiconductors are specifically interesting for their use in spin circuits, MRAM and high density storage devices etc.…”
In the post graphene era, the discovery of magnetism in two-dimensional (2D) intrinsic nanomagnets has opened up exciting possibilities for low-dimensional spintronics. In this article, we have reported three new 2D Janus nanomagnets VBrCl 2 , VBrI 2 , and VClBrI for the first time. First-principles based density functional theory calculations reveal that these monolayers are intrinsically magnetic with indirect band gap semiconducting properties and further the magnetic and electronic properties of these monolayers are enhanced with the application of biaxial strain and electric field. We observe interesting electronic and magnetic phase transitions, tunable band gap, and supreme enhancement of the Curie temperature (~ 686%). Large magnetic anisotropic energy (MAE) with high magnetic moment and tunable band gap property make these Janus materials useful candidates for future information storage, optoelectronics, and 2D spin circuit development.
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