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Title: On-Demand Nanoscale Manipulations of Correlated Oxide Phases

Journal Article · · Advanced Functional Materials
 [1];  [1];  [2];  [3];  [4];  [1];  [1];  [2];  [3];  [4]; ORCiD logo [1]
  1. West Virginia Univ., Morgantown, WV (United States)
  2. Pennsylvania State Univ., University Park, PA (United States). Dept. of Material Sciences and Engineering
  3. Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
  4. Carnegie Mellon Univ., Pittsburgh, PA (United States)

Controlling material properties at the nanoscale is a critical enabler of high performance electronic and photonic devices. A prototypical material example is VO2, where a structural phase transition in correlation with dramatic changes in resistivity, optical response, and thermal properties demonstrates particular technological importance. While the phase transition in VO2 can be controlled at macroscopic scales, reliable and reversible nanoscale control of the material phases has remained elusive. Here, reconfigurable nanoscale manipulations of VO2 from the pristine monoclinic semiconducting phase to either a stable monoclinic metallic phase, a metastable rutile metallic phase, or a layered insulating phase using an atomic force microscope is demonstrated at room temperature. The capability to directly write and erase arbitrary 2D patterns of different material phases with distinct optical and electrical properties builds a solid foundation for future reprogrammable multifunctional device engineering.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC02-06CH11357; SC‐0010399
OSTI ID:
1604898
Alternate ID(s):
OSTI ID: 1566899
Journal Information:
Advanced Functional Materials, Vol. 29, Issue 49; ISSN 1616-301X
Publisher:
WileyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 10 works
Citation information provided by
Web of Science

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