Effects of formamidinium and bromide ion substitution in methylammonium lead triiodide toward high-performance perovskite solar cells
Creators
- 1. Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195-2120 (United States)
- 2. Department of Chemistry, University of Washington, Seattle, WA 98195-2120 (United States)
Description
Highlights: • The roles of FA+ and Br- ions in MAxFA1-xPb(IyBr1-y)3 perovskite were revealed. • An average PCE of 17.34% was realized in the optimized MA0.7FA0.3Pb(I0.9Br0.1)3-based PVSC. • A perovskite with a large bandgap of 1.69 eV yields a high PCEAVG over 15%. Compositional engineering of organic-inorganic hybrid perovskite has attracted great research interests recently for seeking a better perovskite system to address existed challenges, such as the thermal and moisture instability, anomalous hysteresis, and toxic lead contamination, etc. In this study, we systematically investigated the structural, optophysical, and photovoltaic properties of the compositional MAxFA1−xPb(IyBr1−y)3 perovskite by sequentially introducing FA+ and Br- ions into the parental MAPbI3 to elucidate their respective roles when they were inserted into the perovskite lattice. We unraveled that such dual compositional tuning in perovskite can improve the crystallinity of the resultant film and thus reduce its density of defect states as evidenced by admittance spectroscopy, resulting in a prolonged carrier lifetime over 500 ns. As a result, a promising average PCE (PCEAVG) of 17.34% was realized in the optimized MA0.7FA0.3Pb(I0.9Br0.1)3-based PVSC with little hysteresis and stable photocurrent output. More significantly, another compositional MA0.7FA0.3Pb(I0.8Br0.2)3 perovskite with a large bandgap of 1.69 eV can yield an impressively high PCEAVG over 15%. To the best of our knowledge, this performance is among the state-of-the-art large bandgap (~1.7 eV) PVSCs reported so far, which paves the way for the development of high-performance tandem cells using efficient large bandgap PVSCs as the top subcells. This study not only manifests the pivotal roles of dual compositional tuning in MAxFA1−xPb(IyBr1−y)3 perovskites but also highlights the importance of compositional engineering for developing an even more efficient perovskite.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.nanoen.2016.02.033Additional details
Identifiers
- DOI
- 10.1016/j.nanoen.2016.02.033;
- PII
- S2211285516000847;
Publishing Information
- Journal Title
- Nano Energy (Print)
- Journal Volume
- 22
- Journal Page Range
- p. 328-337
- ISSN
- 2211-2855
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51106832
- Subject category
- S36: MATERIALS SCIENCE; S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- BROMINE IONS; CARRIER LIFETIME; IODINE COMPOUNDS; NICKEL OXIDES; PERFORMANCE; PEROVSKITE; PHOTOVOLTAIC EFFECT; SOLAR CELLS
- Descriptors DEC
- CHALCOGENIDES; CHARGED PARTICLES; DIRECT ENERGY CONVERTERS; EQUIPMENT; HALOGEN COMPOUNDS; IONS; LIFETIME; MINERALS; NICKEL COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PEROVSKITES; PHOTOELECTRIC CELLS; PHOTOELECTRIC EFFECT; PHOTOVOLTAIC CELLS; SOLAR EQUIPMENT; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Ltd. All rights reserved.