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Local Enhancement of Polarization at PbTiO3/BiFeO3 Interfaces Mediated by Charge Transfer | |
Liu, Ying1; Zhu, Yin-Lian1; Tang, Yun-Long1; Wang, Yu-Jia1; Jiang, Yi-Xiao1; Xu, Yao-Bin1; Zhang, Bin2; Ma, Xiu-Liang1,3 | |
2017-06 | |
发表期刊 | NANO LETTERS |
ISSN | 1530-6984 |
卷号 | 17期号:6页码:3619-3628 |
摘要 | Ferroelectrics hold promise for sensors, transducers, and telecommunications. With the demand of electronic devices scaling down, they take the form of nanoscale films. However, the polarizations in ultrathin ferroelectric films are usually reduced dramatically due to the depolarization field caused by incomplete charge screening at interfaces, hampering the integrations of ferroelectrics into electric devices. Here, we design and fabricate a ferroelectric/multiferroic PbTiO3/BiFeO3 system, which exhibits discontinuities in both chemical valence and ferroelectric polarization across the interface. Aberration-corrected scanning transmission electron microscopic study reveals an 8% elongation of out-of-plane lattice spacing associated with 104%, 107%, and 39% increments of delta(Ti), delta(O1), and delta(O2) in the PbTiO3 layer near the head-to-tail polarized interface, suggesting an over similar to 70% enhancement of polarization compared with that of bulk PbTiO3. Besides that in PbTiO3, polarization in the BiFeO3 is also remarkably enhanced. Electron energy loss spectrum and X-ray photoelectron spectroscopy investigations demonstrate the oxygen vacancy accumulation as well as the transfer of Fe3+ to Fe2+ at the interface. On the basis of the polar catastrophe model, FeO2/PbO interface is determined. First-principles calculation manifests that the oxygen vacancy at the interface plays a predominate role in inducing the local polarization enhancement. We propose a charge transfer mechanism that leads to the remarkable polarization increment at the PbTiO3/BiFeO3 interface. This study may facilitate the development of nanoscale ferroelectric devices by tailing the coupling of charge and lattice in oxide heteroepitaxy. |
关键词 | Perovskite oxide ferroelectric interface polarization enhancement aberration corrected scanning transmission electron microscope |
DOI | 10.1021/acs.nanolett.7b00788 |
收录类别 | SCI ; SCIE |
语种 | 英语 |
资助项目 | Key Research Program of Frontier Sciences CAS[QYZDJ-SSW-JSC010] |
WOS研究方向 | Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics |
WOS类目 | Chemistry, Multidisciplinary ; Chemistry, Physical ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary ; Physics, Applied ; Physics, Condensed Matter |
WOS记录号 | WOS:000403631600044 |
出版者 | AMER CHEMICAL SOC |
EI入藏号 | 20172503793097 |
EI主题词 | Polarization |
EI分类号 | 482.2 Minerals - 525.4 Energy Losses (industrial and residential) - 531.2 Metallography - 602.2 Mechanical Transmissions - 701.1 Electricity: Basic Concepts and Phenomena - 708.1 Dielectric Materials - 761 Nanotechnology - 802.2 Chemical Reactions - 804 Chemical Products Generally - 804.2 Inorganic Compounds - 921 Mathematics - 933.1 Crystalline Solids - 951 Materials Science |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://ir.lut.edu.cn/handle/2XXMBERH/33256 |
专题 | 材料科学与工程学院 材料科学与工程学院_特聘教授组 |
通讯作者 | Zhu, Yin-Lian; Ma, Xiu-Liang |
作者单位 | 1.Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Wenhua Rd 72, Shenyang 110016, Peoples R China; 2.Chinese Acad Sci, Inst Met Res, Anal & Testing Dept, Wenhua Rd 72, Shenyang 110016, Peoples R China; 3.Lanzhou Univ Technol, Sch Mat Sci & Engn, Langongping Rd 287, Lanzhou 730050, Peoples R China |
通讯作者单位 | 材料科学与工程学院 |
推荐引用方式 GB/T 7714 | Liu, Ying,Zhu, Yin-Lian,Tang, Yun-Long,et al. Local Enhancement of Polarization at PbTiO3/BiFeO3 Interfaces Mediated by Charge Transfer[J]. NANO LETTERS,2017,17(6):3619-3628. |
APA | Liu, Ying.,Zhu, Yin-Lian.,Tang, Yun-Long.,Wang, Yu-Jia.,Jiang, Yi-Xiao.,...&Ma, Xiu-Liang.(2017).Local Enhancement of Polarization at PbTiO3/BiFeO3 Interfaces Mediated by Charge Transfer.NANO LETTERS,17(6),3619-3628. |
MLA | Liu, Ying,et al."Local Enhancement of Polarization at PbTiO3/BiFeO3 Interfaces Mediated by Charge Transfer".NANO LETTERS 17.6(2017):3619-3628. |
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