Low-Temperature Formation and Photophysics of Phloroglucinol-Derived Carbonaceous Materials Under Air and Vacuum.

Phloroglucinol is an oxygen-rich aromatic precursor whose thermal evolution can yield emissive carbonaceous materials with excitation-dependent photoluminescence. However, the influence of the reaction atmosphere on its low-temperature transformation remains insufficiently understood. In this work, phloroglucinol was thermally treated at 200 °C under air or static vacuum for 5 and 10 h. The resulting materials were investigated by electron microscopy, energy-dispersive X-ray spectroscopy, Raman spectroscopy, steady-state and time-resolved photoluminescence, transient absorption spectroscopy, and density functional theory calculations. The reaction atmosphere mainly affected the early stages of structural evolution. Air-treated samples formed irregular networks of filamentous substructures, whereas vacuum-treated samples displayed more compact quasi-spherical aggregates with a fibrous internal organization. Raman spectra indicated the progressive transformation of crystalline phloroglucinol into a disordered carbonaceous network containing small sp2-rich domains. Optical measurements revealed violet/deep-blue and cyan emissive centers whose relative contributions depended on atmosphere and treatment time. Transient absorption supported a multi-center photophysical picture involving ultrafast relaxation, intermediate trapping or interconversion, and longer-lived decay. Calculations on representative molecular motifs identified furan-containing conjugated domains as plausible candidates for the violet/deep-blue centers and compact triangular phloroglucinol-derived structures for the cyan center. Overall, oxygen availability and treatment duration modulate the morphology and emissive-center distribution of phloroglucinol-derived carbonaceous materials.