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Title: Metal/Ion Interactions Induced p–i–n Junction in Methylammonium Lead Triiodide Perovskite Single Crystals

Journal Article · · Journal of the American Chemical Society
DOI:https://doi.org/10.1021/jacs.7b10416· OSTI ID:1422483
 [1];  [1];  [2];  [2];  [1]; ORCiD logo [3]; ORCiD logo [3];  [3];  [2];  [1]; ORCiD logo [1]
  1. Univ. of Tennessee, Knoxville, TN (United States). Dept. of Materials Science and Engineering
  2. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science (CNMS); Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Inst. for Functional Imaging of Materials
  3. Univ. of Tennessee, Knoxville, TN (United States). Dept. of Chemistry

Hybrid perovskites, as emerging multifunctional semiconductors, have demonstrated dual electronic/ionic conduction properties. Here, we report a metal/ion interaction induced p-i-n junction across slightly n-type doped MAPbI3 single crystals with Au/MAPbI3/Ag configuration based on interface dependent Seebeck effect, Hall effect and time-of-flight secondary ion mass spectrometry analysis. The organic cations (MA+) interact with Au atoms, forming positively charged coordination complexes at Au/MAPbI3 interface, whereas iodine anions (I) can react with Ag contacts, leading to interfacial ionic polarization. Such metal/ion interactions establish a p-doped region near the Au/MAPbI3 interface due to the formation of MA+ vacancies, and an n-doped region near the Ag/MAPbI3 interface due to formation of I vacancies, consequently forming a p-i-n junction across the crystal in Au/MAPbI3/Ag configuration. Therefore, the metal/ion interaction plays a role in determining the surface electronic structure and semiconducting properties of hybrid perovskites.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); US Air Force Office of Scientific Research (AFOSR); National Science Foundation (NSF); National Science Foundation of China
Grant/Contract Number:
AC05-00OR22725; FA 9550-15-1-0064; 21161160445
OSTI ID:
1422483
Journal Information:
Journal of the American Chemical Society, Vol. 139, Issue 48; ISSN 0002-7863
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 27 works
Citation information provided by
Web of Science

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Cited By (8)

When defects become ‘dynamic’: halide perovskites: a new window on materials? journal January 2019
Fundamental Thermoelectric Properties in Organic Heterojunctions from Molecular to Thin‐Film and Hybrid Designs journal August 2019
Charge Transport in Halide Perovskite Single Crystals: Experimental and Theoretical Perspectives journal January 2019
Giant current amplification induced by ion migration in perovskite single crystal photodetectors journal January 2018
Conductive metallic filaments dominate in hybrid perovskite-based memory devices journal May 2019
Dynamic Impact of Electrode Materials on Interface of Single-Crystalline Methylammonium Lead Bromide Perovskite journal June 2018
Enabling Self-passivation by Attaching Small Grains on Surfaces of Large Grains toward High-Performance Perovskite LEDs journal September 2019
Rapid Oxidation of the Hole Transport Layer in Perovskite Solar Cells by A Low-Temperature Plasma journal January 2019