Trap states in lead iodide perovskites

Xiaoxi Wu, M. Tuan Trinh, Daniel Niesner, Haiming Zhu, Zachariah Norman, Jonathan S. Owen, Omer Yaffe, Bryan J. Kudisch, X. -Y. Zhu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

840 Citations (Scopus)

Abstract

Recent discoveries of highly efficient solar cells based on lead iodide perovskites have led to a surge in research activity on understanding photo carrier generation in these materials, but little is known about trap states that may be detrimental to solar cell performance. Here we provide direct evidence for hole traps on the surfaces of three-dimensional (3D) CH3NH3PbI3 perovskite thin films and excitonic traps below the optical gaps in these materials. The excitonic traps possess weak optical transition strengths, can be populated from the relaxation of above gap excitations, and become more significant as dimensionality decreases from 3D CH3NH3PbI3 to two-dimensional (2D) (C4H9NH3I)2(CH3NH3I)n-1(PbI2)n (n = 1, 2, 3) perovskites and, within the 2D family, as n decreases from 3 to 1. We also show that the density of excitonic traps in CH3NH3PbI3 perovskite thin films grown in the presence of chloride is at least one-order of magnitude lower than that grown in the absence of chloride, thus explaining a widely known mystery on the much better solar cell performance of the former. The trap states are likely caused by electron-phonon coupling and are enhanced at surfaces/interfaces where the perovskite crystal structure is most susceptible to deformation.

Original languageEnglish
Pages (from-to)2089-2096
Number of pages8
JournalJournal of the American Chemical Society
Volume137
Issue number5
DOIs
Publication statusPublished - 11 Feb 2015
Externally publishedYes

Funding

The preparation of vapor-deposited perovskite samples, UPS measurements, and fluorescence measurements were supported by the US Department of Energy under Grant No. ER46980. The transient absorption measurements were supported by the US National Science Foundation under Grant Number DMR-1125845. Research carried out in part at the Center for Functional Nanomaterials, Brookhaven National Laboratory, which is supported by the U.S. Department of Energy, Office of Basic Energy Sciences, under Contract Number DE-AC02-98CH10886. D. N. acknowledges support by the Deutsche Forschungsgemeinschaft (DFG Forschungsstipendium). We thank Matthew Y. Sfeir for technical help with transient absorption measurements, Joshua Choi for providing solution based 3D perovskite samples, and Prakriti Joshi for help with vapor deposition of 3D perovskite samples. Author Contributions X.W., T.T., D.N., and H.Z. contributed equally.

All Science Journal Classification (ASJC) codes

  • Catalysis
  • General Chemistry
  • Biochemistry
  • Colloid and Surface Chemistry

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