Anhydrous sodium ultraphosphate glasses were prepared with Na,O conten
ts between O and 50 mol% and were characterized by several structurall
y sensitive spectroscopic probes to determine the nature of the phosph
ate tetrahedra that constitute the short-range glass structure. Solid
state P-31 magic angle spinning nuclear magnetic resonance (MAS-NMR) s
pectroscopy reveals that Na2O depolymerizes the branched (Q(3)) P-O ne
twork of P2O5 to form metaphosphate (Q(2)) sites, in quantitative agre
ement with Van Water's 'chemically simple' model. X-ray photoelectron
spectroscopy reveals that the concomitant increase in non-bridging oxy
gen with increasing Na2O content is also in quantitative agreement wit
h this structural model. Raman spectroscopic analyses of glasses with
approximately 40 mol% Na2O suggest that some intermediate-range order,
perhaps associated with strained rings, also exists within the glass
network. Strained sites are eliminated when the solid glass is heated
to melt temperatures.