journal article·2019-02-26Open access

Large Negative Thermal Expansion Induced by Synergistic Effects of Ferroelectrostriction and Spin Crossover in PbTiO3-Based Perovskites

Zhao Pan, Jun Chen, Runze Yu, Lokanath Patra, Ponniah Ravindran, Andrea Sanson, Ruggero Milazzo, Alberto Carnera, Lei Hu, Lu Wang, Hajime Yamamoto, Yang Ren, Qingzhen Huang, Yuki Sakai, Takumi Nishikubo, Takahiro Ogata, Xi’an Fan, Yawei Li, Guangqiang Li, Hajime Hojo, Masaki Azuma, Xianran Xing

Chemistry of Materials· Volume 31· Issue 4

Abstract

The discovery of unusual negative thermal expansion (NTE) provides the opportunity to control the common but much desired property of thermal expansion, which is valuable not only in scientific interests but also in practical applications. However, most of the available NTE materials are limited to a narrow temperature range, and the NTE effect is generally weakened by various modifications. Here, we report an enhanced NTE effect that occurs over a wide temperature range (α̅V = −5.24 × 10–5 °C–1, 25–575 °C), and this NTE effect is accompanied by an abnormal enhanced tetragonality, a large spontaneous polarization, and a G-type antiferromagnetic ordering in the present perovskite-type ferroelectric of (1–x)PbTiO3–xBiCoO3. Specifically, for the composition of 0.5PbTiO3–0.5BiCoO3, an extensive volumetric contraction of ∼4.8 % has been observed near the Curie temperature of 700 °C, which represents the highest level in PbTiO3-based ferroelectrics. According to our experimental and theoretical results, the large NTE originates from a synergistic effect of the ferroelectrostriction and spin crossover of cobalt on the crystal lattice. The actual NTE mechanism is contrasted with previous functional NTE materials, in which the NTE is simply coupled with one ordering such as electronic, magnetic, or ferroelectric ordering. The present study sheds light on the understanding of NTE mechanisms, and it attests that NTE could be simultaneously coupled with different orderings, which will pave a new way toward the design of large NTE materials.
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Research context

OpenAlex topics: Thermal Expansion and Ionic Conductivity · Ferroelectric and Piezoelectric Materials · Microwave Dielectric Ceramics Synthesis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, China

Laboratory for Materials and Structures, Tokyo Institute of Technology, 4259 Nagatsuta, Midori, Yokohama 226-8503, Japan

Department of Physics and Astronomy, University of Padova, Padova I-35131, Italy

X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439, United States

Center for Neutron Research, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland 20899-6102, United States

Funding

Ministry of Education of the People's Republic of China · China Postdoctoral Science Foundation · National Natural Science Foundation of China · Central Committee of the Communist Party of China

References (40)

Show source-provided references
1. 10.1021/ic980253h10.1021/ic980253h ↗
2. 10.1039/A904297K10.1039/A904297K ↗
3. 10.1088/1468-6996/13/1/01300110.1088/1468-6996/13/1/013001 ↗
4. 10.1088/1468-6996/16/3/03490410.1088/1468-6996/16/3/034904 ↗
5. 10.1039/C4CS00461B10.1039/C4CS00461B ↗
6. 10.1038/s41467-018-04113-y10.1038/s41467-018-04113-y ↗
7. 10.1126/science.272.5258.9010.1126/science.272.5258.90 ↗
8. 10.1021/ja106711v10.1021/ja106711v ↗
9. 10.1063/1.214772610.1063/1.2147726 ↗
10. 10.1021/ja510693a10.1021/ja510693a ↗
11. 10.1103/PhysRevB.58.84710.1103/PhysRevB.58.847 ↗
12. 10.1103/PhysRevLett.105.17720310.1103/PhysRevLett.105.177203 ↗
13. Xing X. R. · Rare Metals · 2003 · 22 · 294
14. 10.1126/science.115144210.1126/science.1151442 ↗
15. 10.1038/nature0781610.1038/nature07816 ↗
16. 10.1038/ncomms136110.1038/ncomms1361 ↗
17. 10.1103/PhysRevB.61.868710.1103/PhysRevB.61.8687 ↗
18. 10.1143/JJAP.40.599910.1143/JJAP.40.5999 ↗
19. 10.1021/ja710027810.1021/ja7100278 ↗
20. 10.1021/cm052334z10.1021/cm052334z ↗
21. 10.1021/ja102987d10.1021/ja102987d ↗
22. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
23. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
24. 10.1103/PhysRevB.74.22441210.1103/PhysRevB.74.224412 ↗
25. 10.1088/0305-4608/14/7/00810.1088/0305-4608/14/7/008 ↗
26. 10.1038/nature0645910.1038/nature06459 ↗
27. 10.1143/JJAP.41.209910.1143/JJAP.41.2099 ↗
28. 10.1126/science.108061510.1126/science.1080615 ↗
29. 10.1038/2177810.1038/21778 ↗
30. 10.1021/ja507748710.1021/ja5077487 ↗
31. 10.1021/ja056460f10.1021/ja056460f ↗
32. 10.1021/ja044959o10.1021/ja044959o ↗
33. 10.1038/srep0245810.1038/srep02458 ↗
34. 10.1021/jacs.7b0862510.1021/jacs.7b08625 ↗
35. 10.1038/ncomms1410210.1038/ncomms14102 ↗
36. 10.1016/j.jssc.2012.01.02510.1016/j.jssc.2012.01.025 ↗
37. 10.1002/xrs.110310.1002/xrs.1103 ↗
38. 10.1103/PhysRevLett.90.22720110.1103/PhysRevLett.90.227201 ↗
39. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
40. 10.1103/PhysRev.71.80910.1103/PhysRev.71.809 ↗