AgNbO3-Based Multilayer Capacitors: Heterovalent-Ion-Substitution Engineering Achieves High Energy Storage Performances

被引:7
|
作者
Tang, Ting [1 ]
Liu, Dong [1 ]
Wang, Qi [1 ]
Zhao, Lei [3 ]
Zhang, Bo-Ping [1 ]
Qi, He [2 ]
Zhu, Li-Feng [1 ]
机构
[1] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
[2] Univ Sci & Technol Beijing, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing, Peoples R China
[3] Hebei Univ, Coll Phys Sci & Technol, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
dielectric capacitor; multilayer capacitors; AgNbO3; energy storage; heterovalention substitution; BDS; FREE ANTIFERROELECTRIC CERAMICS; DENSITY; EFFICIENCY; TEMPERATURE;
D O I
10.1021/acsami.3c10240
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The demand for miniaturization and integration in next-generation advanced high-/pulsed-power devices has resulted in a strong desire for dielectric capacitors with high energy storage capabilities. However, practical applications of dielectric capacitors have been hindered by the challenge of poor energy-storage density (U-rec) and efficiency (eta) caused by large remanent polarization (P-r) and low breakdown strength (BDS). Herein, we take a method of heterovalent ion substitution engineering in combination with the multilayer capacitor (MLCC) technology and thus achieve a large maximum polarization (P-max), zero P-r, and high BDS in the AgNbO3 (AN) system simultaneously and obtain excellent U-rec and eta. The substitution of Sm3+ for Ag+ in Sm(x)AN+Mn MLCCs at x >= 0.01 decreases the M-1-M-2 phase transition temperature, and the antiferroelectric (AFE) M-2 phase appears at room temperature, which is beneficial to achieving a low Pr value. Due to the low P-r value and high BDS similar to 1300 kV.cm(-1), an excellent U-rec similar to 9.8 J.cm(-3) and P-D,P-max similar to 34.8 MW.cm(-3) were achieved in Sm(x)AN+Mn MLCCs at x = 0.03. The work suggests a paradigm that can enhance the energy storage capabilities of AFE MLCCs to meet the demanding requirements of advanced energy storage applications.
引用
收藏
页码:45128 / 45136
页数:9
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