Giant electrostrictive effect in lead-free barium titanate-based ceramics via A-site ion-pairs engineering. Issue 29 (8th July 2019)
- Record Type:
- Journal Article
- Title:
- Giant electrostrictive effect in lead-free barium titanate-based ceramics via A-site ion-pairs engineering. Issue 29 (8th July 2019)
- Main Title:
- Giant electrostrictive effect in lead-free barium titanate-based ceramics via A-site ion-pairs engineering
- Authors:
- Huang, Yanli
Zhao, Chunlin
Yin, Jie
Lv, Xiang
Ma, Jian
Wu, Jiagang - Abstract:
- Abstract : We propose a novel strategy to arouse the potential capacity of electrostriction in BaTiO3 -based materials by A-site Li + –Ho 3+ ion-pairs engineering. Abstract : Electrostrictors offer unique advantages over piezoelectrics, including no poling process, temperature stability and hysteresis-free strain characteristics. Learning from the distinction between disordered and ordered ABI0.5BII0.5O3 perovskite-structured electrostrictors, the electrostrictive effect enhances with a smaller active space for B ions. Here, we propose a novel design strategy to arouse the potential capacity of electrostriction in BaTiO3 -based materials by A-site Li + –Ho 3+ ion-pairs engineering. In this way, limited active space for a Ti-site is expected due to the contracted oxygen octahedron around ion-pairs, resulting in smaller polarization per unit magnitude of electric field but a larger strain per unit magnitude of polarization and therefore an enhanced longitudinal electrostrictive coefficient Q 33 . A systematic analysis evidenced that Li + and Ho 3+ ions tend to occupy the neighboring Ba-sites in one unit cell of BaTiO3, and directly form Li + –Ho 3+ ion-pairs along the [001] direction. Besides, partial fragmented domain patterns induced by local structural heterogeneity due to the involvement of ion-pairs are detected in samples with higher dopants, benefiting suppression of hysteresis in strain curves. Consequently, the (Li, Ho) co-doped BaTiO3 ceramics by A-site engineeringAbstract : We propose a novel strategy to arouse the potential capacity of electrostriction in BaTiO3 -based materials by A-site Li + –Ho 3+ ion-pairs engineering. Abstract : Electrostrictors offer unique advantages over piezoelectrics, including no poling process, temperature stability and hysteresis-free strain characteristics. Learning from the distinction between disordered and ordered ABI0.5BII0.5O3 perovskite-structured electrostrictors, the electrostrictive effect enhances with a smaller active space for B ions. Here, we propose a novel design strategy to arouse the potential capacity of electrostriction in BaTiO3 -based materials by A-site Li + –Ho 3+ ion-pairs engineering. In this way, limited active space for a Ti-site is expected due to the contracted oxygen octahedron around ion-pairs, resulting in smaller polarization per unit magnitude of electric field but a larger strain per unit magnitude of polarization and therefore an enhanced longitudinal electrostrictive coefficient Q 33 . A systematic analysis evidenced that Li + and Ho 3+ ions tend to occupy the neighboring Ba-sites in one unit cell of BaTiO3, and directly form Li + –Ho 3+ ion-pairs along the [001] direction. Besides, partial fragmented domain patterns induced by local structural heterogeneity due to the involvement of ion-pairs are detected in samples with higher dopants, benefiting suppression of hysteresis in strain curves. Consequently, the (Li, Ho) co-doped BaTiO3 ceramics by A-site engineering exhibit giant Q 33 up to 0.06 m 4 C −2 which is superior to other lead-bearing/free electrostrictive materials, meeting the requirement of a thermal stability (20–150 °C) – low hysteresis (<10%) – large strain (0.12–0.2%) combination stimulated by the outstanding electrostrictive effect. Our research provides a new paradigm for designing applicable high-performance electrostrictive materials through A-site engineering. This is expected to benefit a wide range of functional materials. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 7:Issue 29(2019)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 7:Issue 29(2019)
- Issue Display:
- Volume 7, Issue 29 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 29
- Issue Sort Value:
- 2019-0007-0029-0000
- Page Start:
- 17366
- Page End:
- 17375
- Publication Date:
- 2019-07-08
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ta05681e ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11157.xml