Abstract

Herein, a ternary system of TeO2–ZnO–Na2O (TZN) with competitive roles of covalent Zn–O and ionic Na–O bonds in tellurite glassy network is examined for high‐temperature in situ X‐ray diffraction (XRD) and Raman spectroscopy. TZN glasses are doped with Nd2O3 and the effects of Nd doping on the crystallization of glasses are also written. In situ high‐temperature XRD permits the assignment of each of the differential scanning calorimetry (DSC) crystallization peaks (the first crystallization peak (T c1) is related to sodium‐based crystalline phases, while the second crystallization peak (T c2) is correlated with tellurium‐/zinc‐based crystalline phases). The study of in situ high‐temperature Raman spectroscopy shows that T c1 shows γ‐TeO2 crystallized phase‐like peaks while T c2 crystallization has more α‐TeO2‐crystallized phase‐like peaks. Comparison at the same temperature (430 °C) permits a first understanding of the structural changes of the glasses in terms of the evolution first to α‐TeO2, ZnO, ZnTeO3, and Zn2Te3O8 crystalline phases compared with Na10Zn4O9 phase. The ZnTeO3 and Zn2Te3O8 crystallization evolution is also compared between the Nd‐doped and nondoped glasses, which gives more insight into the tellurite glass structures.

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