Compositional Evolution of the Structure and Connectivity in Binary P-Se Glasses: Results from 2D Multinuclear NMR and Raman Spectroscopy.
2021
The atomic structure of binary PxSe100-x glasses with 5 ≤ x ≤ 70 is investigated using Raman spectroscopy and two-dimensional 77Se and 31P isotropic/anisotropic correlation nuclear magnetic resonance (NMR) spectroscopy. These spectroscopic results, when taken together, demonstrate that the structure of PxSe100-x glasses with x ≤ 50 consists primarily of -Se-Se-Se- chain elements, pyramidal P(Se1/2)3 units, ethylene-like 2/2SeP-PSe2/2 units, and Se=P(Se1/2)3 tetrahedral units. The chain structure of Se becomes increasingly cross-linked by P-Se polyhedral units, and the degree of connectivity increases with a progressive increase in P content up to x ∼ 50, at which point the -Se-Se-Se- chain elements completely disappear, and the structure becomes highly rigid. The compositional variation of the Se-Se-Se environments as obtained from the 77Se isotropic NMR spectra reveals that the connectivity between the Se-Se and P-Se units in glasses with x ≤ 50 is intermediate to that of the random and the fully clustered scenarios. A further increase in P content results in the formation of P4Se3 molecules such that at x = 63, the structure becomes predominantly molecular, consisting of P4Se3 molecules likely held together via van der Waals forces. The structure of glasses with x > 63 is characterized by P4Se3 molecules and likely nonmolecular P4Se3-like species, along with amorphous red phosphorus-like regions. These P4Se3-like moieties and the amorphous red phosphorus-like units can connect to each other via P-P bonds, and their relative concentrations increase with increasing P content. This compositional evolution of structural connectivity of PxSe100-x glasses is shown to be consistent with the corresponding variation in the glass transition temperature.
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