Publication:
Development of high-performance lead-free piezoelectric thin films and nanostructures for microelectronic devices

dc.contributor.advisor Wang, Danyang en_US
dc.contributor.advisor Li, Sean en_US
dc.contributor.author Lin, Qianru en_US
dc.date.accessioned 2022-03-22T12:16:54Z
dc.date.available 2022-03-22T12:16:54Z
dc.date.issued 2016 en_US
dc.description.abstract In this thesis, high-performance lead-free piezoelectric epitaxial thin films and nanostructures based on (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT) and (Bi0.5Na0.5)TiO3-BaTiO3 (BNBT) were prepared using pulsed laser deposition (PLD) and laser molecular beam epitaxy (LMBE). Firstly, by investigating the effects of deposition temperature and oxygen partial pressure on the physical properties of BZT-0.5BCT thin films, the optimal deposition temperature and oxygen partial pressure were determined to be 850 ˚C and 200 mTorr, respectively. A series of BZT-xBCT homogenous thin films were then prepared under the optimized conditions to study the compositional dependence of structural and electrical properties. A morphology phase boundary (MPB)-like behaviour was observed at the composition of x=0.5 with a high remanent polarization Pr of 17.8 μC/cm2 and a large piezoelectric coefficient d33 of 100 ± 5 pm/V. The compositional gradient BZT-xBCT multilayers were fabricated. A higher remanent polarization and a larger piezoelectric coefficient were attained in compositionally downgraded (DG) thin films compared to the compositionally upgraded (UG) one, owing to the retained in-plane compressive strain and large built-in electric field, respectively. The origin of the internal electric field was also confirmed to be the flexoelectric effect. The morphology engineering was extended to BCTm/BZTm (m presents the number of unit cells for BCT and BZT in one period) symmetric superlattices prepared by LMBE. The growth rate was precisely controlled with the aid of reflection high-energy electron diffraction (RHEED). A built-in electric field was observed in all superlattices and its strength was periodicity dependent, i.e. the longer the periodicity, the larger the built-in electric field. An excellent piezoelectric coefficient was obtained in BCT3/BZT3 superlattice with d33+ of 150 ± 5 pm/V. Finally, Mn doped BNBT (MnBNBT) thin film was fabricated with a high Pr of 33.0 μC/cm2 and a large d33 of 120.0 ± 20 pm/V. By changing the deposition temperature, the defect level was finely tuned and minimized in the MnBNBT thin film deposited at 700˚C, giving rise to the excellent ferroelectric and piezoelectric properties. In summary, the high-performance lead-free piezoelectric thin films and nanostructures fabricated in this work presented their promising prospect on substituting lead-based materials as well as potential on applications of piezoelectric microelectronic devices. en_US
dc.identifier.uri http://hdl.handle.net/1959.4/56167
dc.language English
dc.language.iso EN en_US
dc.publisher UNSW, Sydney en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.subject.other Nanostructure. en_US
dc.subject.other Piezoelectricity. en_US
dc.subject.other Thin film. en_US
dc.title Development of high-performance lead-free piezoelectric thin films and nanostructures for microelectronic devices en_US
dc.type Thesis en_US
dcterms.accessRights open access
dcterms.rightsHolder Lin, Qianru
dspace.entity.type Publication en_US
unsw.accessRights.uri https://purl.org/coar/access_right/c_abf2
unsw.identifier.doi https://doi.org/10.26190/unsworks/18987
unsw.relation.faculty Science
unsw.relation.originalPublicationAffiliation Lin, Qianru, Materials Science & Engineering, Faculty of Science, UNSW en_US
unsw.relation.originalPublicationAffiliation Wang, Danyang, Materials Science & Engineering, Faculty of Science, UNSW en_US
unsw.relation.originalPublicationAffiliation Li, Sean, Materials Science & Engineering, Faculty of Science, UNSW en_US
unsw.relation.school School of Materials Science & Engineering *
unsw.thesis.degreetype PhD Doctorate en_US
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