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Enhanced Photovoltaic Performance and Thermal Stability of CH3NH3PbI3 Perovskite through Lattice Symmetrization

  • Feng Shao
    Feng Shao
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
    Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, China
    More by Feng Shao
  • Peng Qin*
    Peng Qin
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
    *E-mail: [email protected] (P.Q.).
    More by Peng Qin
  • Dong Wang
    Dong Wang
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
    More by Dong Wang
  • Guoqing Zhang
    Guoqing Zhang
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
  • Bo Wu
    Bo Wu
    Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371
    More by Bo Wu
  • Jianqiao He
    Jianqiao He
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
    More by Jianqiao He
  • Wei Peng
    Wei Peng
    State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China
    More by Wei Peng
  • Tze Chien Sum
    Tze Chien Sum
    Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371
  • Deliang Wang*
    Deliang Wang
    Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, China
    *E-mail: [email protected] (D.W.).
    More by Deliang Wang
  • , and 
  • Fuqiang Huang*
    Fuqiang Huang
    State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
    State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China
    *E-mail: [email protected] (F.H.).
Cite this: ACS Appl. Mater. Interfaces 2019, 11, 1, 740–746
Publication Date (Web):December 20, 2018
https://doi.org/10.1021/acsami.8b17068
Copyright © 2018 American Chemical Society
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Supporting Info (2)»

Abstract

Abstract Image

The organic–inorganic lead halide perovskites are attractive materials for photovoltaic application. The most widely studied perovskites based on methyl ammonium organic cation are less likely to form an ideal high-symmetry configuration at room temperature, leading to the appearance of local lattice strain. Herein, this study reports a strategy for the construction of thermally stable cubic perovskites at room temperature through the incorporation of the larger organic cation dimethyl ammonium. Detailed characterization on the single crystals and thin films reveals the formation of cubic phase with the addition of a certain amount of dimethyl ammonium at room temperature. With the presence of dimethyl ammonium, the nonradiative recombination in perovskite is suppressed, showing a longer PL lifetime and hole diffusion length. The more efficient charge extraction leads to an improvement in the photocurrent density, and then the device efficiency from 17.1% to 18.6%, together with an enhanced thermal stability at 85 °C. The influence of incorporating a larger organic cation on the structural configuration, optical properties, charge extraction, as well as the photovoltaic performance is systematically investigated, which offers an alternative way to improve the intrinsic stability of hybrid perovskites.

Supporting Information

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The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acsami.8b17068.

  • Characterization of the single crystals and thin films; elemental analysis; crystal data; X-ray diffraction patterns of the single crystals; SEM images of the perovskite films; time-resolved photoluminescent spectra; photovoltaic parameters of the devices; the light harvesting efficiency spectra (PDF)

  • Crystallographic data for MA0.91DMA0.09PbI3 (CIF)

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Cited By


This article is cited by 2 publications.

  1. Yutong Wang, Run Long. Rapid Decoherence Induced by Light Expansion Suppresses Charge Recombination in Mixed Cation Perovskites: Time-Domain ab Initio Analysis. The Journal of Physical Chemistry Letters 2020, 11 (4) , 1601-1608. https://doi.org/10.1021/acs.jpclett.0c00139
  2. Dibyajyoti Ghosh, Debdipto Acharya, Liujiang Zhou, Wanyi Nie, Oleg V. Prezhdo, Sergei Tretiak, Amanda J. Neukirch. Lattice Expansion in Hybrid Perovskites: Effect on Optoelectronic Properties and Charge Carrier Dynamics. The Journal of Physical Chemistry Letters 2019, 10 (17) , 5000-5007. https://doi.org/10.1021/acs.jpclett.9b02020

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