Abstract:several mechanisms [4] including flexoelectric effect, [1] ferroelectric-ferroelastic switching [5,6] and chemical modifications on the surface [7] and in the bulk. [8,9] The electrochemical effect in the bulk can be induced by diffusion of oxygen vacancies, [10] which in turn can lead to electrostatic or Vegard strain. [4] The contribution of the aforementioned mechanisms in depicting mechanical switching of ferroelectrics has been discussed recently, [4,11] while further work is still required to gain a more… Show more
“…A) Summary of threshold force and thickness data in various mechanical ferroelectric switching. The blue region represents the switchable range for the mechanical switching on substrate‐supported films in reported ferroelectrics (BaTiO 3, [ 14 ] TbMnO 3 , [ 16 ] PbTiO 3 , [ 28 ] BiFeO 3 , [ 15,29 ] MoS 2 , [ 30 ] PbZr 0.2 Ti 0.8 O 3 (PZT_1), [ 31,32 ] PbZr 0.48 Ti 0.52 O 3 (PZT_2), [ 33 ] Hf 0.5 Zr 0.5 O 2 , [ 17 ] and HfO 2 [ 34 ] ), while its boundary represents the approximate threshold force to initiate domain switching. The yellow region highlights the results from the mechanical switching in suspended CIPS.…”
Deterministic control of ferroelectric domain is critical in the ferroelectric functional electronics. Ferroelectric polarization can be manipulated mechanically with a nano‐tip through flexoelectricity. However, it usually occurs in a very localized area in ultrathin films, with possible permanent surface damage caused by a large tip‐force. Here it is demonstrated that the deliberate engineering of transverse flexoelectricity offers a powerful tool for improving the mechanical domain switching. Sizable‐area domain switching under an ultralow tip‐force can be realized in suspended van der Waals ferroelectrics with the surface intact, due to the enhanced transverse flexoelectric field. The film thickness range for domain switching in suspended ferroelectrics is significantly improved by an order of magnitude to hundreds of nanometers, being far beyond the limited range of the substrate‐supported ones. The experimental results and phase‐field simulations further reveal the crucial role of the transverse flexoelectricity in the domain manipulation. This large‐scale mechanical manipulation of ferroelectric domain provides opportunities for the flexoelectricity‐based domain controls in emerging low‐dimensional ferroelectrics and related devices.
“…A) Summary of threshold force and thickness data in various mechanical ferroelectric switching. The blue region represents the switchable range for the mechanical switching on substrate‐supported films in reported ferroelectrics (BaTiO 3, [ 14 ] TbMnO 3 , [ 16 ] PbTiO 3 , [ 28 ] BiFeO 3 , [ 15,29 ] MoS 2 , [ 30 ] PbZr 0.2 Ti 0.8 O 3 (PZT_1), [ 31,32 ] PbZr 0.48 Ti 0.52 O 3 (PZT_2), [ 33 ] Hf 0.5 Zr 0.5 O 2 , [ 17 ] and HfO 2 [ 34 ] ), while its boundary represents the approximate threshold force to initiate domain switching. The yellow region highlights the results from the mechanical switching in suspended CIPS.…”
Deterministic control of ferroelectric domain is critical in the ferroelectric functional electronics. Ferroelectric polarization can be manipulated mechanically with a nano‐tip through flexoelectricity. However, it usually occurs in a very localized area in ultrathin films, with possible permanent surface damage caused by a large tip‐force. Here it is demonstrated that the deliberate engineering of transverse flexoelectricity offers a powerful tool for improving the mechanical domain switching. Sizable‐area domain switching under an ultralow tip‐force can be realized in suspended van der Waals ferroelectrics with the surface intact, due to the enhanced transverse flexoelectric field. The film thickness range for domain switching in suspended ferroelectrics is significantly improved by an order of magnitude to hundreds of nanometers, being far beyond the limited range of the substrate‐supported ones. The experimental results and phase‐field simulations further reveal the crucial role of the transverse flexoelectricity in the domain manipulation. This large‐scale mechanical manipulation of ferroelectric domain provides opportunities for the flexoelectricity‐based domain controls in emerging low‐dimensional ferroelectrics and related devices.
“…This effect has been demonstrated in, for example, BaTiO 3 , [ 4,5 ] BiFeO 3 , [ 6 ] and PbZr 0.2 Ti 0.8 O 3 [ 7 ] or PbZr 0.52 Ti 0.48 O 3 . [ 8 ]…”
Section: Introductionmentioning
confidence: 99%
“…This effect has been demonstrated in, for example, BaTiO 3 , [4,5] BiFeO 3 , [6] and PbZr 0.2 Ti 0.8 O 3 [7] or PbZr 0.52 Ti 0.48 O 3 . [8] conductive layer used as a bottom electrode and deposited at 620 °C on a SrTiO 3 (STO) single crystal substrate by radio frequency sputtering. The PZT crystalline phase was obtained after a rapid thermal annealing at 650 °C under O 2 atmosphere for 1 min.…”
The mechanical switching of ferroelectric domains is achieved in PbZr0.2Ti0.8O3 thin films obtained by the sol-gel method for thicknesses up to 200 nm. The dielectric polarization can be switched when a force higher than a given threshold value in the order of some µNewtons is applied with the tip of an atomic force microscope. This threshold is determined as a function of the thickness of the films, and local hysteresis loops are recorded under mechanical stress. The possibility of switching the polarisation in such unusually thick films is related to the existence in their volume of physical nanoscale defects, which might play the role of pinning centers for the domains.
“…Since 180° polarization switching was accomplished in 4.8 nm thick tetragonal BaTiO 3 thin films via mechanical manipulation, [ 25 ] considerable effort has been devoted to manipulating the polarization switching in ferroelectric thin films, for example, 3–5 nm thick PbZr 0.2 Ti 0.8 O 3 (001) film, 1.6–45 nm thick BaTiO 3 (001) film, 50 nm thick PbZr 0.1 Ti 0.9 O 3 (001) film, and 10 nm thick PbZr 0.48 Ti 0.52 O 3 (001) film, and flexoelectric effect is proposed to explain the mechanical manipulation of the domain and domain wall structures. [ 25–40 ] It is accepted that using tip force turns to be an effective alternative to electric field for switching ferroelectric domains. [ 32–40 ] However, mechanical manipulation based on flexoelectricity has proved ineffective when going beyond a critical thickness (tens of nanometers), [ 40 ] because tip induced flexoelectricity is usually negligible in thick films due to the small strain gradient, and the flexoelectricity in thin films substantially decreases when the film thickness is above a certain thickness.…”
Ferroelectric materials feature a switchable spontaneous electric polarization and can enable low-power logic and nonvolatile memories. These applications require reliable and precise control of ferroelectric domains and domain walls in ferroelectric thin films. Mechanical manipulation is a promising route to engineer ferroelectric domains, but it has proved ineffective when going beyond a critical thickness. Here, multi-step 90° switching polarization reversal processes in ( 111)-oriented PbZr 0.2 Ti 0.8 O 3 thin films by applying mechanical forces along the direction parallel to the domain bands are reported. By probing the interrelationships between the relevant order parameters, coupled lattice distortion and piezoelectricity is revealed to facilitate domain switching from downward to upward in PbZr 0.2 Ti 0.8 O 3 , a mechanism that is supported by the evolution of domains and electrical performances at different temperatures and under varying pressures, respectively. The multistep domain reversal processes render PbZr 0.2 Ti 0.8 O 3 thin films an excellent candidate for multilevel data storage. The study's results have implications for the manipulation of polarization switching in ferroelectrics and open an avenue to domain reversal driven by mechanical loads for the development of next-generation ferroelectric devices.
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