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Oxygen Exchange Processes between Oxide Memristive Devices and Water Molecules
Author(s) -
Heisig Thomas,
Baeumer Christoph,
Gries Ute N.,
Mueller Michael P.,
Torre Camilla,
Luebben Michael,
Raab Nicolas,
Du Hongchu,
Menzel Stephan,
Mueller David N.,
Jia ChunLin,
Mayer Joachim,
Waser Rainer,
Valov Ilia,
Souza Roger A.,
Dittmann Regina
Publication year - 2018
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201800957
Subject(s) - oxidizing agent , oxygen , materials science , water vapor , oxide , molecule , chemical physics , atmosphere (unit) , resistive touchscreen , redistribution (election) , resistive random access memory , humidity , nanotechnology , chemical engineering , electrode , photochemistry , chemistry , organic chemistry , thermodynamics , electrical engineering , physics , politics , political science , law , metallurgy , engineering
Resistive switching based on transition metal oxide memristive devices is suspected to be caused by the electric‐field‐driven motion and internal redistribution of oxygen vacancies. Deriving the detailed mechanistic picture of the switching process is complicated, however, by the frequently observed influence of the surrounding atmosphere. Specifically, the presence or absence of water vapor in the atmosphere has a strong impact on the switching properties, but the redox reactions between water and the active layer have yet to be clarified. To investigate the role of oxygen and water species during resistive switching in greater detail, isotope labeling experiments in a N 2 /H 2 18 O tracer gas atmosphere combined with time‐of‐flight secondary‐ion mass spectrometry are used. It is explicitly demonstrated that during the RESET operation in resistive switching SrTiO 3 ‐based memristive devices, oxygen is incorporated directly from water molecules or oxygen molecules into the active layer. In humid atmospheres, the reaction pathway via water molecules predominates. These findings clearly resolve the role of humidity as both oxidizing agent and source of protonic defects during the RESET operation.