TY - JOUR
T1 - Potential barrier engineered colossal permittivity CaCu3Ti4O12 ceramics with largely reduced dielectric loss
AU - Feng, Huimin
AU - Mao, Pu
AU - Sun, Jie
AU - Wang, Ting
AU - Shimoshili, Gerhard Marthin
AU - Tian, Yahui
AU - Liu, Zhiyong
AU - Xie, Bing
AU - Guo, Kun
AU - Gao, Jinghui
N1 - Publisher Copyright:
© 2026 The Authors. Published by Elsevier B.V. on behalf of The Chinese Ceramic Society. This is an open access article under the CC BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0/
PY - 2026/9
Y1 - 2026/9
N2 - CaCu3Ti4O12 (CCTO) ceramics exhibit a colossal permittivity response and good stability across wide temperature and frequency ranges, and play an indispensable role in microelectronic devices and energy storage applications. However, the advancements of CCTO-based ceramics are still impeded by a large dielectric loss. In this work, a potential barrier engineering was employed to fabricate the Sr2+ and Co2+ doped CCTO ceramics with improved dielectric properties via a solid-state method. The phase structure, microstructure and dielectric properties of the doped samples were systematically investigated. As anticipated, all the doped CCTO ceramics present a significant colossal permittivity characteristic and a reduced dielectric loss. Especially, the Ca0.9Sr0.1Cu2.9Co0.1Ti4O12 ceramic presents a significantly reduced dielectric loss of about 0.05, while maintaining a notably giant permittivity characteristic of about 3.24 × 104 at a frequency of 103 Hz. This ceramic is also characterized by a relatively dense microstructure, and the corresponding average grain size of about 15.31 μm. The pinning effect imposed by these defects on free charge carriers limits their mobility, thereby intensifying local polarization and reducing oxygen vacancies in this Sr2+/Co2+ co-doped CCTO ceramics. This phenomenon contributes to an increased barrier height of about 0.61 eV, which amplifies the grain boundary response and ultimately leads to reduced dielectric loss. This finding signifies that the potential barrier engineering is an effective strategy for designing giant permittivity materials with low dielectric loss.
AB - CaCu3Ti4O12 (CCTO) ceramics exhibit a colossal permittivity response and good stability across wide temperature and frequency ranges, and play an indispensable role in microelectronic devices and energy storage applications. However, the advancements of CCTO-based ceramics are still impeded by a large dielectric loss. In this work, a potential barrier engineering was employed to fabricate the Sr2+ and Co2+ doped CCTO ceramics with improved dielectric properties via a solid-state method. The phase structure, microstructure and dielectric properties of the doped samples were systematically investigated. As anticipated, all the doped CCTO ceramics present a significant colossal permittivity characteristic and a reduced dielectric loss. Especially, the Ca0.9Sr0.1Cu2.9Co0.1Ti4O12 ceramic presents a significantly reduced dielectric loss of about 0.05, while maintaining a notably giant permittivity characteristic of about 3.24 × 104 at a frequency of 103 Hz. This ceramic is also characterized by a relatively dense microstructure, and the corresponding average grain size of about 15.31 μm. The pinning effect imposed by these defects on free charge carriers limits their mobility, thereby intensifying local polarization and reducing oxygen vacancies in this Sr2+/Co2+ co-doped CCTO ceramics. This phenomenon contributes to an increased barrier height of about 0.61 eV, which amplifies the grain boundary response and ultimately leads to reduced dielectric loss. This finding signifies that the potential barrier engineering is an effective strategy for designing giant permittivity materials with low dielectric loss.
KW - CaCuTiO-Based ceramics
KW - Colossal dielectric constant
KW - Low dielectric loss
KW - Potential barrier
UR - https://www.scopus.com/pages/publications/105043639412
U2 - 10.1016/j.jmat.2026.101260
DO - 10.1016/j.jmat.2026.101260
M3 - 文章
AN - SCOPUS:105043639412
SN - 2352-8478
VL - 12
JO - Journal of Materiomics
JF - Journal of Materiomics
IS - 5
M1 - 101260
ER -