Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95777
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorZhang, Yen_US
dc.creatorChen, Jen_US
dc.creatorZhang, Qen_US
dc.creatorLu, Yen_US
dc.creatorHuang, Hen_US
dc.creatorHe, Yen_US
dc.date.accessioned2022-10-06T06:04:28Z-
dc.date.available2022-10-06T06:04:28Z-
dc.identifier.issn0002-7820en_US
dc.identifier.urihttp://hdl.handle.net/10397/95777-
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.rights© 2021 American Ceramic Societyen_US
dc.rightsThis is the peer reviewed version of the following article: Zhang, Y, Chen, J, Zhang, Q, Lu, Y, Huang, H, He, Y. Ultrasensitive self-powered UV PDs via depolarization and heterojunction fields jointly enhanced carriers separation. J Am Ceram Soc. 2021; 105: 392– 401, which has been published in final form at https://doi.org/10.1111/jace.18074. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectFerroelectricity/ferroelectric materialsen_US
dc.subjectLead lanthanum zirconate titanateen_US
dc.subjectSelf-powered ultraviolet photodetectorsen_US
dc.subjectThin filmsen_US
dc.subjectTitanium oxideen_US
dc.titleUltrasensitive self-powered UV PDs via depolarization and heterojunction fields jointly enhanced carriers separationen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage392en_US
dc.identifier.epage401en_US
dc.identifier.volume105en_US
dc.identifier.issue1en_US
dc.identifier.doi10.1111/jace.18074en_US
dcterms.abstractIn current semiconductor-based self-powered ultraviolet (UV) photodetectors (PDs), because the built-in electric field only exits in the space-charge region of p-n junction or Schottky junction interfaces, the photo-generated carriers can't be efficiently separated and thus the photoelectric response is low. To solve this issue, in this work, we design and fabricate new-type Pb,La(Zr,Ti)O3 ferroelectrics/TiO2 semiconductors heterojunction self-powered UV photodetectors. The results indicate that by introducing Pb,La(Zr,Ti)O3 ferroelectric layers, the photocurrent of the PDs is greatly improved and at a negative poling electric voltage, the device exhibits excellent self-powered UV photoelectric properties with a large responsivity of 21 mA/W, high specific detectivity of 2.4 × 1011 Jones, and fast response speed (rise time of 2.4 ms, decay time of 3.2 ms). These values are far superior to those of all recently reported self-powered UV PDs and their huge improvement is primarily because the depolarization field caused by the high remnant polarization of Pb,La(Zr,Ti)O3 and the built-in electric field resulting from the heterojunction interfaces of the Pb,La(Zr,Ti)O3 and the TiO2 thin films jointly enhance the separation efficiency of photo-generated electrons and holes. Besides, the heterojunction PDs also show good weak UV light detection ability. This work opens new avenue for designing and fabricating next-generation self-powered UV PDs by a simple, low-cost, and easy to mass-produce way.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of the American Ceramic Society, Jan. 2022, v. 105, no. 1, p. 392-401en_US
dcterms.isPartOfJournal of the American Ceramic Societyen_US
dcterms.issued2022-01-
dc.identifier.scopus2-s2.0-85113576604-
dc.identifier.eissn1551-2916en_US
dc.description.validate202210 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera1749-
dc.identifier.SubFormID45874-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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