4.8 Article

Ferroelastic-switching-driven large shear strain and piezoelectricity in a hybrid ferroelectric

期刊

NATURE MATERIALS
卷 20, 期 5, 页码 612-+

出版社

NATURE RESEARCH
DOI: 10.1038/s41563-020-00875-3

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资金

  1. Soochow University
  2. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
  3. National Natural Science Foundation of China [12074278, 12074277]
  4. Key University Science Research Project of Jiangsu Province [20KJA140001]
  5. Natural Science Foundation of Jiangsu Province [BK20201404]
  6. AME Individual Research Grant [A1883c0004]
  7. Agency for Science, Technology, and Research (A*STAR)
  8. Ministry of Education, Singapore (AcRF Tier 1) [118/17, 189/18]
  9. Southern University of Science and Technology (SUSTech), China

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The study demonstrates a large shear strain in the hybrid ferroelectric C6H5N(CH3)(3)CdCl3, achieving up to 21.5% strain, two orders of magnitude greater than traditional piezoelectrics. This is attributed to organic molecules preventing 180 degrees polarization switching, showing potential for lightweight and high-energy-density devices.
Materials that can produce large controllable strains are widely used in shape memory devices, actuators and sensors(1,2), and great efforts have been made to improve the strain output(3-6). Among them, ferroelastic transitions underpin giant reversible strains in electrically driven ferroelectrics or piezoelectrics and thermally or magnetically driven shape memory alloys(7,8). However, large-strain ferroelastic switching in conventional ferroelectrics is very challenging, while magnetic and thermal controls are not desirable for practical applications. Here we demonstrate a large shear strain of up to 21.5% in a hybrid ferroelectric, C6H5N(CH3)(3)CdCl3, which is two orders of magnitude greater than that in conventional ferroelectric polymers and oxides. It is achieved by inorganic bond switching and facilitated by structural confinement of the large organic moieties, which prevents undesired 180 degrees polarization switching. Furthermore, Br substitution can soften the bonds, allowing a sizable shear piezoelectric coefficient (d(35) approximate to 4,830 pm V-1) at the Br-rich end of the solid solution, C6H5N(CH3)(3)CdBr3xCl3(1-x). The electromechanical properties of these compounds suggest their potential in lightweight and high-energy-density devices, and the strategy described here could inspire the development of next-generation piezoelectrics and electroactive materials based on hybrid ferroelectrics. Reversible strains are widely used in high-technology systems, with piezoelectrics showing fast response but low strain. Here, ferroelectric C6H5N(CH3)(3)CdCl3 is shown to produce a strain of 21.5%, two orders of magnitude larger than other piezoelectrics, due to organic molecules preventing 180 degrees polarization switching.

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