材料科学
纳米复合材料
电介质
反铁电性
磁滞
大气温度范围
透射电子显微镜
纳米尺度
功勋
相(物质)
纳米技术
分析化学(期刊)
铁电性
凝聚态物理
光电子学
热力学
物理
色谱法
有机化学
化学
作者
Jingzhe Xu,Yongbin Liu,Dong Wang,He Li,Lisheng Zhong,Jinghui Gao,Ming C. Wu,Ruifeng Yao,Nan Zhang,Xiaojie Lou,Shengtao Li,Xiaobing Ren
标识
DOI:10.1002/adma.202502788
摘要
Abstract A fundamental paradox in energy storage dielectrics lies in the challenge of achieving superior performance consistently across both room and elevated temperatures. This is addressed by designing a self‐organized nanocomposite (1−x)(Ba,Sr)(Ti,Sn)O 3 ‐xBi 1.5 ZnNb 1.5 O 7 composed of nano‐sized antiferroelectric(AFE) particles embedded into a trirelaxor(TRE) matrix through nanoscale phase separation process. The optimal composition at x = 0.11 exhibits outstanding energy storage performance from room temperature (energy density = 8.5 J cm −3 , efficiency = 94.8%, and figure of merit of 167 J cm −3 ) up to 200 °C (energy density = 4.85 J cm −3 , efficiency >90% and figure of merit of 49 J cm −3 ), outperforming existing Pb‐free dielectrics. High‐resolution transmission electron microscopy and synchrotron x‐ray diffractometry reveal that the coexisting nanometric antiferroelectric particles and the trirelaxor nanodomains sustain over a wide temperature range. Piezoresponse force microscopy and phase‐field simulation show that hysteresis‐free switching of trirelaxor nanodomains enables enhanced polarization and low hysteretic loss. Resistivity shows a 2–3 order of magnitude increases accompanying significant increase in breakdown strength up to high temperatures, attributable to deep charge trapping effect at high‐density TRE/AFE interfaces as evidenced by thermally stimulated depolarization current. These favorable effects in the nano‐composite are responsible for its high energy storage performance up to high temperatures.
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