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Two-dimensional (2D) materials that exhibit charge density waves (CDWs)—spontaneous reorganization of their electrons into a periodic modulation—have generated many research endeavors in the hopes of employing their exotic properties for various quantum-based technologies. Early investigations surrounding CDWs were mostly focused on bulk materials. However, applications for quantum devices require few-layer materials to fully utilize the emergent phenomena. The CDW field has greatly expanded over the decades, warranting a focus on the computational efforts surrounding them specifically in 2D materials. In this review, we cover ground in the following relevant theory-driven subtopics for TaS2 and TaSe2: summary of general computational techniques and methods, resulting atomic structures, the effect of electron–phonon interaction of the Raman scattering modes, the effects of confinement and dimensionality on the CDW, and we end with a future outlook. Through understanding how the computational methods have enabled incredible advancements in quantum materials, one may anticipate the ever-expanding directions available for continued pursuit as the field brings us through the 21st century. 

We report the polarization-dependent Raman spectra of exfoliated MoI3, a van der Waals material with a “true one-dimensional” crystal structure that can be exfoliated to individual atomic chains. The temperature evolution of several Raman features reveals an anomalous behavior suggesting a phase transition of magnetic origin. Theoretical considerations indicate that MoI3 is an easy-plane antiferromagnet with alternating spins along the dimerized chains and with inter-chain helical spin ordering. The calculated frequencies of phonons and magnons are consistent with the interpretation of the experimental Raman data. The obtained results shed light on the specifics of the phononic and magnonic states in MoI3 and provide a strong motivation for further study of this unique material with potential for future spintronic applications.

 

Abstract The Joint Automated Repository for Various Integrated Simulations (JARVIS) is an integrated infrastructure to accelerate materials discovery and design using density functional theory (DFT), classical force-fields (FF), and machine learning (ML) techniques. JARVIS is motivated by the Materials Genome Initiative (MGI) principles of developing open-access databases and tools to reduce the cost and development time of materials discovery, optimization, and deployment. The major features of JARVIS are: JARVIS-DFT, JARVIS-FF, JARVIS-ML, and JARVIS-tools. To date, JARVIS consists of ≈40,000 materials and ≈1 million calculated properties in JARVIS-DFT, ≈500 materials and ≈110 force-fields in JARVIS-FF, and ≈25 ML models for material-property predictions in JARVIS-ML, all of which are continuously expanding. JARVIS-tools provides scripts and workflows for running and analyzing various simulations. We compare our computational data to experiments or high-fidelity computational methods wherever applicable to evaluate error/uncertainty in predictions. In addition to the existing workflows, the infrastructure can support a wide variety of other technologically important applications as part of the data-driven materials design paradigm. The JARVIS datasets and tools are publicly available at the website: https://jarvis.nist.gov . 

In targeting reduced valent lanthanide chalcogenides, we report the first nanoparticle synthesis of the mixed‐valent ferromagnets Eu₃S₄and EuSm₂S₄. Using divalent lanthanide halides with bis(trimethylsilyl)sulfide and oleylamine, we prepared nanoparticles of EuS, Eu₃S₄, EuSm₂S₄, SmS_1.9, and Sm₃S₄. All nanoparticle phases were identified using powder X‐ray diffraction, transmission electron microscopy was used to confirm morphology and nanoparticle size, and magnetic susceptibility measurements for determining the ordering temperatures and valence. The UV/Vis, Raman and X‐ray photoelectron spectroscopies for each phase were compared. Surprisingly, the phase is influenced by the halide and the reaction temperature, where EuCl₂formed EuS while EuI₂formed Eu₃S₄, highlighting the role of kinetics in phase stabilization. Interestingly, at lower temperatures EuI₂initially forms EuS, and converts over time to Eu₃S₄.

 

In targeting reduced valent lanthanide chalcogenides, we report the first nanoparticle synthesis of the mixed‐valent ferromagnets Eu₃S₄and EuSm₂S₄. Using divalent lanthanide halides with bis(trimethylsilyl)sulfide and oleylamine, we prepared nanoparticles of EuS, Eu₃S₄, EuSm₂S₄, SmS_1.9, and Sm₃S₄. All nanoparticle phases were identified using powder X‐ray diffraction, transmission electron microscopy was used to confirm morphology and nanoparticle size, and magnetic susceptibility measurements for determining the ordering temperatures and valence. The UV/Vis, Raman and X‐ray photoelectron spectroscopies for each phase were compared. Surprisingly, the phase is influenced by the halide and the reaction temperature, where EuCl₂formed EuS while EuI₂formed Eu₃S₄, highlighting the role of kinetics in phase stabilization. Interestingly, at lower temperatures EuI₂initially forms EuS, and converts over time to Eu₃S₄.