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We meticulously study the individual effects of hydrogen irradiation and annealing on the electronic structure and magnetic properties of nanostructured MoS2 thin films grown through Chemical Vapor Deposition (CVD). The role of edge-terminated structure and point defects to induce room-temperature ferromagnetism (RTFM) is thoroughly investigated. The nanostructured pristine MoS2 thin films show the formation of a pure 2-H MoS2 phase, confirmed by X-ray diffraction (XRD) and Raman spectroscopy. Pristine MoS2 thin films are independently annealed in a reducing hydrogen environment and irradiated with low-energy hydrogen ions to study the significance of point defects like sulfur vacancies. RTFM with saturation magnetization value (Ms: 1.66 emu/g) has been observed in the pristine film. Magnetization increases after irradiation and annealing processes. However, hydrogen annealing at a temperature of 200oC exhibits a maximum Ms value of 2.7 emu/g at room temperature. The increase in ferromagnetism is attributed to an increment in sulfur vacancies, hydrogen adsorption with sulfur, and modification in edges, which is confirmed by the analysis of Electron probe micro-analyzer (EPMA), X-ray photoelectron spectroscopy (XPS), and Field emission scanning electron microscopy (FESEM) measurements. The Density Functional Theory (DFT) calculations have demonstrated that the edge-oriented structure of MoS2 exhibits a magnetization value of 3.2 {\mu}B. Additionally, introducing an S-vacancy and H-adsorption in a parallel position to the sulfur further enhances the magnetization value to 3.85 {\mu}B and 3.43 {\mu}B respectively. These findings align broadly with our experimental results., Comment: arXiv admin note: text overlap with arXiv:2406.09721

Room-temperature ferromagnetism (RTFM) exhibited by nanostructured two-dimensional semiconductors for spintronics applications is a fascinating area of research. The present work reports on the correlation between the electronic structure and magnetic properties of defect-engineered nano-structured MoS2 thin films. Low-energy light and heavy-mass ion irradiation have been performed to create defects and tune magnetic properties. Vertical nanosheets with edge state termination in the pristine sample have been examined by field emission scanning electron microscopy (FESEM). Deterioration of vertical nanosheets is observed in low-energy Ar+ and Xe+ irradiated samples. An appreciably high magnetization value of 1.7 emu/g was observed for edge-oriented nanostructured pristine MoS2 thin films, which decreased after ion irradiation. From X-ray photoelectron spectroscopy (XPS) data, it is evident that, due to oxygen incorporation in the sulfur vacancy sites, Mo5+ and 6+ states increase after ion irradiation. The density functional theory (DFT) calculations suggest that the edge-oriented spins of the prismatic edges of the vertical nanosheets are primarily responsible for the high magnetic moment in the pristine film, and the edge degradation and reduction in sulfur vacancies by the incorporation of oxygen upon irradiation result in a decrease in the magnetic moment.

In this paper, we report the growth of pure {\alpha}-MoO3 micro-flakes by CVD technique and their structural, electronic, optical, and magnetic properties. Samples are annealed at various temperatures in an H2 atmosphere to induce ferromagnetism. All the samples exhibit ferromagnetism at room temperature, and 250oC annealed sample shows the highest magnetic moment of 0.087 emu/g. It is evident from PL data that pristine as well as annealed samples contain different types of defects like oxygen vacancies, surface defects, interstitial oxygen, etc. It is deduced from the analysis of Mo3d and O1s core-level XPS spectra that oxygen vacancies increase up to an annealing temperature of 250oC that correlates with the magnetic moment. Significant changes in the total density of states and also in the magnetic moment for two and three oxygen vacancies are noticed through first-principle-based calculations. It is concluded that the magnetic moment is produced by oxygen vacancies or vacancy clusters, which is consistent with our experimental findings.