TY - JOUR
T1 - High Energy Density Performance of Polymer Nanocomposites Induced by Designed Formation of BaTiO3@sheet-likeTiO2 Hybrid Nanofillers
AU - Su, Ran
AU - Luo, Zhengdong
AU - Zhang, Dawei
AU - Liu, Yang
AU - Wang, Zhipeng
AU - Li, Junning
AU - Bian, Jihong
AU - Li, Yanxi
AU - Hu, Xinghao
AU - Gao, Jinghui
AU - Yang, Yaodong
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/6/9
Y1 - 2016/6/9
N2 - Nanocomposites incorporating inorganic nanoparticles (NPs) within ferroelectric polymeric matrices have great potential for high density energy capacitors. In this strategy, employing the nanostructures with specially designed morphology as fillers would notably improve the energy storage. However, this strategy is extremely challenging and has not been largely explored. Here, the BaTiO3@sheet-likeTiO2 core-shell NPs have been successfully synthesized, and can be well-dispersed into polyvinylidene fluoride (PVDF) matrices. The nanocomposites with the volume fraction 2.5% BT@TiO2 NPs have higher the electric displacement (6.0 μm/cm2) than that of PVDF films with the 2.5 vol % BaTiO3 (BT) NPs (5.1 μm/cm2) under the same electric field of 350 kV/mm, which is mainly ascribed to the hierarchical interfacical polarization induced by the large surface area of TiO2 sheet assembled on BT NPs in the nanocomposites. Simultaneously, the medium permittivity TiO2 with medium ϵr as a buffer layer between the BT NPs and polymer matrix could minimize the inhomogeneous electric field in the nanocomposites, which results in the enhancement of the breakdown strength (490 kV/mm with 2.5 vol % BT@TiO2 NPs) compared to pristine PVDF. As a result of a gratifying EB and D, the energy density of the nanocomposites with 2.5 vol % BT@TiO2 NPs reached 17.6 J/cc.
AB - Nanocomposites incorporating inorganic nanoparticles (NPs) within ferroelectric polymeric matrices have great potential for high density energy capacitors. In this strategy, employing the nanostructures with specially designed morphology as fillers would notably improve the energy storage. However, this strategy is extremely challenging and has not been largely explored. Here, the BaTiO3@sheet-likeTiO2 core-shell NPs have been successfully synthesized, and can be well-dispersed into polyvinylidene fluoride (PVDF) matrices. The nanocomposites with the volume fraction 2.5% BT@TiO2 NPs have higher the electric displacement (6.0 μm/cm2) than that of PVDF films with the 2.5 vol % BaTiO3 (BT) NPs (5.1 μm/cm2) under the same electric field of 350 kV/mm, which is mainly ascribed to the hierarchical interfacical polarization induced by the large surface area of TiO2 sheet assembled on BT NPs in the nanocomposites. Simultaneously, the medium permittivity TiO2 with medium ϵr as a buffer layer between the BT NPs and polymer matrix could minimize the inhomogeneous electric field in the nanocomposites, which results in the enhancement of the breakdown strength (490 kV/mm with 2.5 vol % BT@TiO2 NPs) compared to pristine PVDF. As a result of a gratifying EB and D, the energy density of the nanocomposites with 2.5 vol % BT@TiO2 NPs reached 17.6 J/cc.
UR - https://www.scopus.com/pages/publications/84974625456
U2 - 10.1021/acs.jpcc.6b01853
DO - 10.1021/acs.jpcc.6b01853
M3 - 文章
AN - SCOPUS:84974625456
SN - 1932-7447
VL - 120
SP - 11769
EP - 11776
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 22
ER -