Spatial-temporal spectroscopy characterizations and electronic structure of methylammonium perovskites
Author(s) -
Zhaoyu Liu,
K.C. Bhamu,
Liang Luo,
Satvik Shah,
Joong-Mok Park,
Di Cheng,
Long Men,
R. Biswas,
F. Fungara,
Ruth Shinar,
J. Shinar,
Javier Vela,
Jigang Wang
Publication year - 2018
Publication title -
mrs communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.751
H-Index - 31
eISSN - 2159-6859
pISSN - 2159-6867
DOI - 10.1557/mrc.2018.114
Subject(s) - materials science , spectroscopy , perovskite (structure) , exciton , photoluminescence , rydberg formula , molecular physics , dielectric , optical conductivity , binding energy , atomic physics , condensed matter physics , optoelectronics , physics , ion , crystallography , chemistry , quantum mechanics , ionization
Using time-resolved laser-scanning confocal microscopy and ultrafast optical pump/THz probe spectroscopy, we measure photoluminescence (PL) and THz-conductivity in perovskite micro-crystals and films. PL quenching and lifetime variations occur from local heterogeneity. Ultrafast THz-spectra measure sharp quantum transitions from excitonic Rydberg states, providing weakly bound excitons with a binding energy of ~13.5 meV at low temperatures. Ab-initio electronic structure calculations give a direct band gap of 1.64 eV, a dielectric constant of ~18, heavy electrons, and light holes, resulting in weakly bound excitons, consistent with the binding energies from the experiment. The complementary spectroscopy and simulations reveal fundamental insights into perovskite light-matter interactions.
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