TY - JOUR
T1 - Defect-Superstructure-Engineered Vanadium Dioxide Films for Electric-Field-Driven Phase Reconfiguration and Overload Protection
AU - Yang, Junlin
AU - Li, Qianyi
AU - Liu, Shiqiao
AU - Xing, Fangyuan
AU - Li, Xiaolong
AU - Wang, Chengzhi
AU - Li, Yong
AU - Jin, Haibo
AU - Li, Jingbo
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/7/14
Y1 - 2026/7/14
N2 - Electric-field-induced phase switching in vanadium dioxide (VO2) is central to its integration into adaptive electronic systems. However, the role of oxygen defects in governing structural stability and switching behavior remains insufficiently understood. Here, we engineer oxygen-deficient VO2 (VO2-δ) films to investigate the structure of VO2-δ and the electrical switching behavior systematically. The preferential occupation of oxygen vacancies was identified, which induces a 3-fold superstructure of (011)R and stacking faults with a certain degree of long-range ordering along (110)R and (020)R. Even so, the VO2-δ maintains the rutile-like coordination structure as VO2. Notably, the VO2-δ films exhibit high conductivity at room temperature. An irreversible metal–insulator transition can be triggered at 20 V for the VO2-δ film, enabled by localized Joule-heating-assisted reorganization of the oxygen-vacancy defect structure. The resulting abrupt resistance jump highlights the potential of VO2-δ as an ultrathin active medium for fast electronic overload protection. This work establishes vacancy ordering as a powerful lever for tailoring phase behavior in VO2, offering a defect-engineering pathway toward reconfigurable oxide electronic devices.
AB - Electric-field-induced phase switching in vanadium dioxide (VO2) is central to its integration into adaptive electronic systems. However, the role of oxygen defects in governing structural stability and switching behavior remains insufficiently understood. Here, we engineer oxygen-deficient VO2 (VO2-δ) films to investigate the structure of VO2-δ and the electrical switching behavior systematically. The preferential occupation of oxygen vacancies was identified, which induces a 3-fold superstructure of (011)R and stacking faults with a certain degree of long-range ordering along (110)R and (020)R. Even so, the VO2-δ maintains the rutile-like coordination structure as VO2. Notably, the VO2-δ films exhibit high conductivity at room temperature. An irreversible metal–insulator transition can be triggered at 20 V for the VO2-δ film, enabled by localized Joule-heating-assisted reorganization of the oxygen-vacancy defect structure. The resulting abrupt resistance jump highlights the potential of VO2-δ as an ultrathin active medium for fast electronic overload protection. This work establishes vacancy ordering as a powerful lever for tailoring phase behavior in VO2, offering a defect-engineering pathway toward reconfigurable oxide electronic devices.
UR - https://www.scopus.com/pages/publications/105044894819
U2 - 10.1021/acs.chemmater.6c00776
DO - 10.1021/acs.chemmater.6c00776
M3 - Article
AN - SCOPUS:105044894819
SN - 0897-4756
VL - 38
SP - 6604
EP - 6614
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 13
ER -