The magnetic properties of 2H phase of MoS2 (2H-MoS2) and 1T phase of MoS2 (1T-MoS2) were investigated both experimentally and theoretically. Lithium (Li) intercalation method was used to prepare single-layer MoS2 sheets. It was found that pristine MoS2 (2H-MoS2) exhibited weak diamagnetism. After exfoliating by Li intercalation, the crystal structure transformed from 2H to 1T phase, and the magnetism was significantly enhanced from diamagnetism to paramagnetism accordingly. With further annealing in argon atmosphere, the 2H phase recovered gradually from 1T phase, and the magnetism decreased correspondingly. Using crystal field theory and combining the results of first principle calculation, we conclude that the enhanced magnetism can be attributed to the Mo atoms of 1T-MoS2.

Hydrogen reduction treatments with variations in isothermal reduction temperature, duration, and partial pressure of hydrogen (PH2) are carried out on CeO2 nanoparticles (NPs) to investigate the relationship between the surface chemical states and magnetic properties of the samples. The phenomenon of surface reduction degree dependence of the ferromagnetism of CeO2 NPs is observed. Semiquantitative calculated concentrations of surface Ce3+ ions from x-ray photoelectron spectroscopy data demonstrate that ferromagnetism does not relate to the surface oxygen vacancies but to the surface Ce3+/Ce4+ pairs. The higher the number of surface Ce3+/Ce4+ pairs, the more robust the ferromagnetism appears.

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