铁电性
储能
反向
材料科学
陶瓷
主动学习(机器学习)
光电子学
能量(信号处理)
铁电陶瓷
计算机科学
纳米技术
工程物理
计算机数据存储
电子工程
空格(标点符号)
反问题
物理
高效能源利用
合理设计
潜热
逆温
作者
Zhaochen Xi,Zhentao Wang,Changqing Guo,Ke Xu,Weichen Zhao,Zhengqiao Li,Jian Bao,Haowei Zhou,Cong Zou,Houbing Huang,Di Zhou
标识
DOI:10.1038/s41467-026-70792-7
摘要
Ferroelectric ceramics are promising energy-storage candidates for miniaturizing high-power electronic systems, yet synergistically enhancing energy density and efficiency remains constrained by intricate coupling between chemical compositions and polarization configurations. Achieving high-throughput compositional exploration while solving real-time polarization dynamics is nearly impossible with traditional simulations due to prohibitive computational costs. Here, we propose an inverse design framework integrating a variational generative model with active learning optimization to accelerate the development of ferroelectrics with enhanced energy-storage performance under limited electric fields. By formulating the time-dependent Ginzburg-Landau equation governing domain structure evolution as conditional sampling within model latent space, achieving synergistic optimization of chemistry and polarization configurations. Through four-round closed-loop synthesis, we successfully obtain Bi0.5Na0.5TiO3-based relaxor-ferroelectrics exhibiting exceptional energy density of ~2.3 J cm-3 and ~80% efficiency at a low field of 200 kV cm-1. This work establishes an efficient, generalizable route for the inverse design of next-generation energy-storage dielectric materials. The authors demonstrate a generative model-based inverse design strategy that synergistically optimizes the composition and polarization configurations in Bi0.5Na0.5TiO3-based ceramics, achieving enhanced energy-storage performance under low fields.
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