TY - JOUR
T1 - Effects of Polymer Matrix and Atmospheric Conditions on Photophysical Properties of a Cesium Lead Bromide (CsPbBr3) Perovskite Quantum Dot
AU - Yu, Jaesang
AU - Jo, Jinwoong
AU - Joung, Hyeyoung
AU - Kim, Chanwoo
AU - Sung, Yunmo
AU - Oh, Juwon
AU - Yang, Jaesung
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2025/1/9
Y1 - 2025/1/9
N2 - Understanding the environment-dependent stability and photoluminescence (PL) properties of advanced perovskite materials remains a challenge with conflicting views. Herein, we investigated the influence of the host matrix (poly(methyl methacrylate) (PMMA) and polystyrene (PS)) and atmospheric conditions (ambient and N2) on the PL properties of a CsPbBr3 perovskite quantum dot (PQD) using single-particle spectroscopy. Despite the same PL blinking mechanism, the PL properties of the PQD were considerably affected by the environmental conditions. The charge trapping and detrapping rates of the PQD were lower and higher, respectively, under ambient atmosphere than under N2 owing to surface defect passivation by oxygen. The frequency and rate of PQD decomposition were higher in the PMMA matrix than in the PS matrix under an ambient atmosphere. PS achieved superior PQD encapsulation owing to its higher affinity toward hydrophobic surface ligands because of its aromatic rings, thereby protecting the PQD surface from moisture and thus inhibiting decomposition.
AB - Understanding the environment-dependent stability and photoluminescence (PL) properties of advanced perovskite materials remains a challenge with conflicting views. Herein, we investigated the influence of the host matrix (poly(methyl methacrylate) (PMMA) and polystyrene (PS)) and atmospheric conditions (ambient and N2) on the PL properties of a CsPbBr3 perovskite quantum dot (PQD) using single-particle spectroscopy. Despite the same PL blinking mechanism, the PL properties of the PQD were considerably affected by the environmental conditions. The charge trapping and detrapping rates of the PQD were lower and higher, respectively, under ambient atmosphere than under N2 owing to surface defect passivation by oxygen. The frequency and rate of PQD decomposition were higher in the PMMA matrix than in the PS matrix under an ambient atmosphere. PS achieved superior PQD encapsulation owing to its higher affinity toward hydrophobic surface ligands because of its aromatic rings, thereby protecting the PQD surface from moisture and thus inhibiting decomposition.
UR - http://www.scopus.com/inward/record.url?scp=85214686494&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.4c02780
DO - 10.1021/acs.jpclett.4c02780
M3 - Article
C2 - 39780717
AN - SCOPUS:85214686494
SN - 1948-7185
VL - 16
SP - 384
EP - 395
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 1
ER -