Engineering Phase Separation in Niobate Glass through Ab Initio Molecular Dynamics for Enhanced Energy Storage Performance and Unprecedented Thermal Stability in Niobate-Based Glass Ceramics

Abstract

The advancement of lead-free glass ceramics (GCs) possessing appropriate energy storage characteristics is crucial for the renewable energy and electronics industry. In this study, we synthesized lead-free GCs predominantly composed of the tungsten bronze phase, Ba 3.3 Nb 10 O 28.3 . Ab initio molecular dynamics initially reveal nonuniform distribution within the Ba/Nb−O regions in niobite glassy melts, offering valuable insights for the subsequent crystallization process. The proposal of a B-site engineering strategy is suggested, which entails the concurrent reduction of grain size and augmentation of the band gap in tungsten bronze GCs doped with Ta. This approach results in a substantial enhancement of the dielectric breakdown strength (BDS). Phase-field simulations have indicated that the refinement of grain sizes plays a pivotal role in augmenting the local electric field distribution and breakdown path, thereby contributing to the enhancement of BDS. As a consequence of these modifications, a notably high recoverable energy density (W rec ) of 5.23 J/cm 3 can be achieved, accompanied by an ultrahigh efficiency (η) of 94%, and superior thermal stability in energy storage. These outcomes are particularly evident in the case of 2 mol % Ta 2 O 5 -doped P 2 O 5 −K 2 O−BaO−Bi 2 O 3 −TeO 2 − Nb 2 O 5 (PKBBTN-T) GCs, where the W rec and η can be determined to be 2.87 ± 3% J/cm 3 and 95.46 ± 4%, respectively, over a temperature range spanning from 20 to 150 °C. Additionally, this specimen exhibits an exceptionally high discharge energy density (W dis ) of 4.01 J/cm 3 . This comprehensive investigation, comprising experimental and theoretical analyses, establishes an effective pathway and paradigm for the development of dielectric materials with ultrahigh energy storage properties.