Exploration of Electrochemical Reactions at Organic–Inorganic Halide Perovskite Interfaces via Machine Learning in In Situ Time-of-Flight Secondary Ion Mass Spectrometry

Kate Higgins, Matthias Lorenz, Maxim Ziatdinov, Rama K. Vasudevan, Anton V. Ievlev, Eric D. Lukosi, Olga S. Ovchinnikova, Sergei V. Kalinin, Mahshid Ahmadi

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

The instability of hybrid organic–inorganic perovskite (HOIP) devices is one of the significant challenges preventing commercialization. Exploring these phenomena is severely limited by the complexity of the intrinsic electrochemistry of HOIPs, the presence of multiple volatile and mobile ionic species, and the possible role of environmentally induced reactions at surfaces and triple-phase junctions. Here, in situ studies of the electrochemistry of methylammonium lead bromide perovskite with the Au electrode interface are reported via light- and voltage-dependent time-of-flight secondary ion mass spectrometry (ToF-SIMS) imaging of lateral perovskite heterostructures. While ToF-SIMS allows for the visualization of the chemical composition along the surface and its evolution with light and electrical bias, the interpretation of the multidimensional data obtained is often limited due to strong correlations between chemical signatures and the need to track multiple peaks at once. Here, a machine learning workflow combining the Hough transform and non-negative matrix factorization and non-negative tensor decomposition is developed to avoid this limitation and extract salient features of associated chemical changes and to separate the light- and voltage-dependent dynamics. Combining these in situ characterizations and the machine learning workflow provides comprehensive information on the chemical nature of moving species, ion accumulation, and interfacial electrochemical reactions in HOIP devices.

Original languageEnglish
Article number2001995
JournalAdvanced Functional Materials
Volume30
Issue number36
DOIs
StatePublished - Sep 1 2020

Funding

This material was based upon work supported by the U.S. Department of Homeland Security under Grant Award Number 16DNARI00018‐04‐0. K.H. acknowledges partial support from the Center for Materials Processing, a Center of Excellence at the University of Tennessee, Knoxville funded by the Tennessee Higher Education Commission (THEC). Time‐of‐flight secondary ion mass spectrometry (M.L., A.V.I., and O.S.O.) and data analysis workflow (R.K.V., M.Z., and S.V.K.) were conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility, using instrumentation within ORNL’s Materials Characterization Core provided by UT‐Battelle, LLC under Contract No. DE‐AC05‐00OR22725 with the U.S. Department of Energy. This material was based upon work supported by the U.S. Department of Homeland Security under Grant Award Number 16DNARI00018-04-0. K.H. acknowledges partial support from the Center for Materials Processing, a Center of Excellence at the University of Tennessee, Knoxville funded by the Tennessee Higher Education Commission (THEC). Time-of-flight secondary ion mass spectrometry (M.L., A.V.I., and O.S.O.) and data analysis workflow (R.K.V., M.Z., and S.V.K.) were conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility, using instrumentation within ORNL?s Materials Characterization Core provided by UT-Battelle, LLC under Contract No. DE-AC05-00OR22725 with the U.S. Department of Energy.

FundersFunder number
DOE Office of Science
Tennessee Higher Education Commission
UT-Battelle, LLCDE-AC05-00OR22725
U.S. Department of Energy
U.S. Department of Homeland Security16DNARI00018‐04‐0
Office of Science
University of Tennessee
Tennessee Higher Education Commission

    Keywords

    • MAPbBr
    • ToF-SIMS
    • electrochemical reaction
    • ion migration
    • machine learning
    • perovskite

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