Achieving excellent energy storage properties in lead-free ceramics via competing FE/AFE phase coexistence

被引:1
作者
Lv, Zhongqian [1 ,2 ]
Han, Bing [1 ,2 ]
Liu, Zhen [1 ]
Guo, Shaobo [1 ]
Dai, Kai [3 ]
Cao, Fei [1 ]
Hu, Zhigao [3 ]
Wang, Genshui [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, Key Lab Inorgan Funct Mat & Devices, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] East China Normal Univ, Tech Ctr Multifunct Magneto Opt Spect Shanghai, Engn Res Ctr Nanophoton & Adv Instrument, Sch Phys & Elect Sci,Minist Educ,Dept Mat, Shanghai 200241, Peoples R China
基金
上海市自然科学基金;
关键词
Lead-free; Energy storage; Sodium niobate; Phase coexistence; RELAXOR FERROELECTRICS; CAPACITORS; STABILITY; DENSITY;
D O I
10.1016/j.ensm.2025.104205
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dielectric capacitors are widely utilized in large-scale power systems, including applications in medical and military fields. However, their relatively low energy storage density limits further advancements in miniaturization and integration. Therefore, improving the energy storage density of dielectric capacitors is of paramount importance. In this work, novel lead-free Na0.70Sr0.15Nb0.75Ta0.25O3 (NSNT) ceramics were designed, which exhibit a unique combination of relaxor ferroelectric (FE) N phase and stabilized antiferroelectric (AFE) P phase, as confirmed through local structural analysis. The competing FE/AFE phase coexistence is attributed to the discrepancy in ion valence and radius. As a result, the NSNT ceramics demonstrate exceptional energy storage performance, featuring a recoverable energy density (Wrec) of 10.45 J/cm3 and an energy efficiency (eta) of 83.0 % at 850 kV/cm, along with excellent stability. These outstanding energy storage properties not only confirm the promising application prospects of NN-based ceramics with competing FE/AFE phase coexistence, but also provide an innovative approach for advancing high-performance ceramic capacitors.
引用
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页数:8
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