Hong Liu, Wanfeng Zhuang, Ning Chen, Hao Chen, Weiling Wang, Jie Xing, Jianguo Zhu
{"title":"掺杂异价离子的 PZT 陶瓷的超高温稳定性","authors":"Hong Liu, Wanfeng Zhuang, Ning Chen, Hao Chen, Weiling Wang, Jie Xing, Jianguo Zhu","doi":"10.1016/j.jallcom.2024.177686","DOIUrl":null,"url":null,"abstract":"We achieved ultrahigh temperature stability of the piezoelectric coefficient <em>d</em><sub>33</sub> by doping heterovalent ions in the PbZr<sub>0.54</sub>Ti<sub>0.46</sub>O<sub>3</sub> ceramics at the A/B sites in the ABO<sub>3</sub> lattice. The Sm<sup>3+</sup>-ion amount at the A-site remains constant, while the Ta<sup>5+</sup>-ion amount at the B-site changes. We utilized electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) to investigate the reduction of oxygen vacancies, which are closely associated with the defect dipoles formed by heterovalent doping. We utilized piezoresponse force microscopy (PFM), temperature-dependent X-ray diffraction (XRD) combined with Rietveld refinement, and temperature-dependent Raman spectroscopy to understand the mechanism of the temperature stability of the piezoelectric coefficient <em>d</em><sub>33</sub>. When <em>x</em>=0.01, the performance of <em>x</em>Ta-0.01Sm-PbZr<sub>0.54</sub>Ti<sub>0.46</sub>O<sub>3</sub> ceramic is optimal: <em>d</em><sub>33</sub>=530 pC/N, electromechanical coupling factor <em>k</em><sub>p</sub>=0.72, Curie temperature <em>T</em><sub>C</sub> =343 °C, where the temperature stability of the piezoelectric coefficient is ultrahigh, and the <em>d</em><sub>33</sub> changes only 2.2% over the 25−200 °C temperature range.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"46 1","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrahigh temperature stability in heterovalent-ion doped PZT ceramics\",\"authors\":\"Hong Liu, Wanfeng Zhuang, Ning Chen, Hao Chen, Weiling Wang, Jie Xing, Jianguo Zhu\",\"doi\":\"10.1016/j.jallcom.2024.177686\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We achieved ultrahigh temperature stability of the piezoelectric coefficient <em>d</em><sub>33</sub> by doping heterovalent ions in the PbZr<sub>0.54</sub>Ti<sub>0.46</sub>O<sub>3</sub> ceramics at the A/B sites in the ABO<sub>3</sub> lattice. The Sm<sup>3+</sup>-ion amount at the A-site remains constant, while the Ta<sup>5+</sup>-ion amount at the B-site changes. We utilized electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) to investigate the reduction of oxygen vacancies, which are closely associated with the defect dipoles formed by heterovalent doping. We utilized piezoresponse force microscopy (PFM), temperature-dependent X-ray diffraction (XRD) combined with Rietveld refinement, and temperature-dependent Raman spectroscopy to understand the mechanism of the temperature stability of the piezoelectric coefficient <em>d</em><sub>33</sub>. When <em>x</em>=0.01, the performance of <em>x</em>Ta-0.01Sm-PbZr<sub>0.54</sub>Ti<sub>0.46</sub>O<sub>3</sub> ceramic is optimal: <em>d</em><sub>33</sub>=530 pC/N, electromechanical coupling factor <em>k</em><sub>p</sub>=0.72, Curie temperature <em>T</em><sub>C</sub> =343 °C, where the temperature stability of the piezoelectric coefficient is ultrahigh, and the <em>d</em><sub>33</sub> changes only 2.2% over the 25−200 °C temperature range.\",\"PeriodicalId\":344,\"journal\":{\"name\":\"Journal of Alloys and Compounds\",\"volume\":\"46 1\",\"pages\":\"\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alloys and Compounds\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jallcom.2024.177686\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jallcom.2024.177686","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Ultrahigh temperature stability in heterovalent-ion doped PZT ceramics
We achieved ultrahigh temperature stability of the piezoelectric coefficient d33 by doping heterovalent ions in the PbZr0.54Ti0.46O3 ceramics at the A/B sites in the ABO3 lattice. The Sm3+-ion amount at the A-site remains constant, while the Ta5+-ion amount at the B-site changes. We utilized electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) to investigate the reduction of oxygen vacancies, which are closely associated with the defect dipoles formed by heterovalent doping. We utilized piezoresponse force microscopy (PFM), temperature-dependent X-ray diffraction (XRD) combined with Rietveld refinement, and temperature-dependent Raman spectroscopy to understand the mechanism of the temperature stability of the piezoelectric coefficient d33. When x=0.01, the performance of xTa-0.01Sm-PbZr0.54Ti0.46O3 ceramic is optimal: d33=530 pC/N, electromechanical coupling factor kp=0.72, Curie temperature TC =343 °C, where the temperature stability of the piezoelectric coefficient is ultrahigh, and the d33 changes only 2.2% over the 25−200 °C temperature range.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.