4.6 Article

Low Threshold Voltages Electrochemically Drive Gold Migration in Halide Perovskite Devices

Journal

ACS ENERGY LETTERS
Volume 5, Issue 11, Pages 3352-3356

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.0c01805

Keywords

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Funding

  1. ExxonMobil
  2. Princeton Center for Complex Materials, a National Science Foundation (NSF)-MRSEC program [DMR-1420541]
  3. ONR [N00014191P0005]
  4. U.S. Department of Energy (DOE) [DE-AC36-08GO28308]
  5. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Solar Energy Technologies Office (SETO) [DE-FOA-0000990]

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The constituent ions of halide perovskite materials are mobile in the solid state and known to participate in reduction/oxidation reactions. Yet few parameters related to electrochemical processes occurring within devices have been carefully determined. Here, we characterize such reactions in model MAPbI(3) perovskite devices, and we quantify threshold voltages for key reactions. Gold is oxidized and mobilized under nitrogen, in the dark, at the MAPbI(3)/Au interface at 0.8 V. When this interface is buffered with the organic hole transport material (HTM), 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamino)-9,9'-spirobifluorene, MAPbI(3) begins to degrade at 1.2 V; degradation liberates ions that subsequently enable Au migration. Thresholds are insensitive to MAPbI(3) thickness or choice of organic HTM or oxide cathode, which suggests that these reactions are driven electrochemically; the electric field across the device is less important. These results have profound implications for understanding in operando degradation pathways of optoelectronic perovskite devices that are varied in terms of interface structures, active material compositions, and ranges of external stressors.

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