RESUMO
The two-dimensional van der Waals ferromagnetic semiconductor CrSiTe3 has attracted growing interest as an intrinsic topological magnet. Both superconductivity and enhancement of ferromagnetism, usually competing for orders, have been observed in CrSiTe3 at high pressure. However, the high-pressure structure of CrSiTe3 is still unclear, setting obstacles in understanding pressure-induced novel physics. Here, combining the Raman spectra and first-principles calculations, the structure of CrSiTe3 at high pressure has been clarified. The interlayer breathing mode located at â¼42.1 cm-1 has been observed for the first time in CrSiTe3 by ultralow-frequency Raman spectroscopy at high pressure. Theoretical calculations confirm a phase transition from the R3Ì phase to the R3 phase accompanying noticeable enhancement of the Curie temperature. Our results highlight ultralow-frequency Raman spectroscopy combined with high pressure for detecting and modulating the structure and interlayer coupling of two-dimensional materials.
RESUMO
Carbon quantum dots (CDs) with favorable fluorescent properties have stimulated considerable effort to modulate their photoluminescence (PL) for bioimaging and sensing. However, the fluorescent mechanisms are still only partially understood due to the diverse physicochemical properties of CDs prepared by various synthesis methods and postpreparation processes. In this report, pressure-induced bifurcation of PL is reported in red carbon quantum dots (R-CDs) for the first time. The splitting of PL into an irreversible blue-shifted peak and a reversible red-shifted peak under pressure suggests the coexistence of multiple fluorescent mechanisms in R-CDs, i.e., emissions from surface groups and nitrogen-doped cores. The concentration and excitation laser energy dependencies of pressure-induced bifurcation, as well as the time-resolved PL, further support the coexistence of multiple emitters. Our results provide a method for distinguishing between the different fluorescent mechanisms related to surface groups and carbon cores in CDs.