4.8 Article

Heterogeneous integration of single-crystalline complex-oxide membranes

期刊

NATURE
卷 578, 期 7793, 页码 75-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41586-020-1939-z

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资金

  1. Defense Advanced Research Projects Agency (DARPA) [027049-00001]
  2. Army Research Office [W911NF-17-1-0462]
  3. SMART Center - NIST
  4. SRC
  5. NSF CAREER award [1453924]
  6. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2018R1D1A1B07050484]
  7. National Science Foundation (Platform for the Accelerated Realization, Analysis and Discovery of Interface Materials (PARADIM)) [DMR-1539918]
  8. National Research Foundation of Korea [2018R1D1A1B07050484] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  9. Division Of Materials Research
  10. Direct For Mathematical & Physical Scien [1453924, GRANTS:13652099] Funding Source: National Science Foundation

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Complex-oxide materials exhibit a vast range of functional properties desirable for next-generation electronic, spintronic, magnetoelectric, neuromorphic, and energy conversion storage devices(1-4). Their physical functionalities can be coupled by stacking layers of such materials to create heterostructures and can be further boosted by applying strain(5-7). The predominant method for heterogeneous integration and application of strain has been through heteroepitaxy, which drastically limits the possible material combinations and the ability to integrate complex oxides with mature semiconductor technologies. Moreover, key physical properties of complex-oxide thin films, such as piezoelectricity and magnetostriction, are severely reduced by the substrate clamping effect. Here we demonstrate a universal mechanical exfoliation method of producing freestanding single-crystalline membranes made from a wide range of complex-oxide materials including perovskite, spinel and garnet crystal structures with varying crystallographic orientations. In addition, we create artificial heterostructures and hybridize their physical properties by directly stacking such freestanding membranes with different crystal structures and orientations, which is not possible using conventional methods. Our results establish a platform for stacking and coupling three-dimensional structures, akin to two-dimensional material-based heterostructures, for enhancing device functionalities(8,9).

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