Photophysics behind highly luminescent two-dimensional hybrid perovskite (CH3(CH2)2NH3)2(CH3NH3)2Pb3Br10 thin filmsElectronic supplementary information (ESI) available: AFM and KPFM image of the 2D perovskite. Temperature dependent PL spectra. Explanatory note for the temperature dependent PL analysis. See DOI: 10.1039/c8tc01582a
Two-dimensional (2D) Ruddlesden-Popper perovskites have emerged as a new class of hybrid materials with high photoluminescence and improved stability compared to their three-dimensional (3D) counterparts. Studies of the photophysics of these new 2D perovskites are essential for the fast development...
Gespeichert in:
Hauptverfasser: | , , , , , |
---|---|
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Two-dimensional (2D) Ruddlesden-Popper perovskites have emerged as a new class of hybrid materials with high photoluminescence and improved stability compared to their three-dimensional (3D) counterparts. Studies of the photophysics of these new 2D perovskites are essential for the fast development of optoelectronic devices. Here, we study the power and temperature dependences of the photoluminescence properties of the (PA)
2
(MA)
2
Pb
3
Br
10
hybrid perovskite. High electron-phonon coupling near room temperature was found to be dominated by longitudinal optical (LO) phonons
via
the Fröhlich interaction. However, we show that the presence of free carriers is also possible, with lower trapping states and higher and more stable emission compared to the 3D MAPbBr
3
. These characteristics make the studied 2D material very attractive for optoelectronic applications, including solar cells and light emitting diodes (LEDs). Our investigation provides new fundamental insights into the emission characteristics of 2D lead halide perovskites.
Two-dimensional (2D) Ruddlesden-Popper perovskites have emerged as a new class of hybrid materials with high photoluminescence and improved stability compared to their three-dimensional (3D) counterparts. |
---|---|
ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/c8tc01582a |