Kinetics of N- to M-Polar Switching in Ferroelectric Al1−xScxN Capacitors

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Roberto Guido - , Professur für Nanoelektronik, NaMLab - Nanoelectronic materials laboratory gGmbH (Autor:in)
  • Haidong Lu - , University of Nebraska-Lincoln (Autor:in)
  • Patrick D. Lomenzo - , NaMLab - Nanoelectronic materials laboratory gGmbH (Autor:in)
  • Thomas Mikolajick - , Professur für Nanoelektronik, NaMLab - Nanoelectronic materials laboratory gGmbH (Autor:in)
  • Alexei Gruverman - , University of Nebraska-Lincoln (Autor:in)
  • Uwe Schroeder - , NaMLab - Nanoelectronic materials laboratory gGmbH (Autor:in)

Abstract

Ferroelectric wurtzite-type aluminum scandium nitride (Al1−xScxN) presents unique properties that can enhance the performance of non-volatile memory technologies. The realization of the full potential of Al1−xScxN requires a comprehensive understanding of the mechanism of polarization reversal and domain structure dynamics involved in the ferroelectric switching process. In this work, transient current integration measurements performed by a pulse switching method are combined with domain imaging by piezoresponse force microscopy (PFM) to investigate the kinetics of domain nucleation and wall motion during polarization reversal in Al0.85Sc0.15N capacitors. In the studied electric field range (from 4.4 to 5.6 MV cm−1), ferroelectric switching proceeds via domain nucleation and wall movement. The currently available phenomenological models are shown to not fully capture all the details of the complex dynamics of polarization reversal in Al0.85Sc0.15N. PFM reveals a non-linear increase of both domain nucleation rate and lateral wall velocity during the switching process, as well as the dependency of the domain pattern on the polarization reversal direction. A continuously faster N- to M-polar switching upon cycling is reported and ascribed to an increasing number of M-polar nucleation sites and density of domain walls.

Details

OriginalspracheEnglisch
Aufsatznummer2308797
Seitenumfang9
FachzeitschriftAdvanced science
Jahrgang11
Ausgabenummer16
Frühes Online-Datum14 Feb. 2024
PublikationsstatusVeröffentlicht - 24 Apr. 2024
Peer-Review-StatusJa

Externe IDs

ORCID /0000-0003-3814-0378/work/159608602
PubMed 38355302

Schlagworte