Related Experiment Video
Updated: May 24, 2025

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Eco-friendly synthesis and stability analysis of CsPbBr3and poly(methyl methacrylate)-CsPbBr3films
You-Lin Huang1,2, Wei Li2, Fuqian Yang1,3
1Laboratory of Functional Materials, University of Kentucky, Lexington, KY 40506, United States of America.
Abstract:
This study presents an eco-friendly mechanochemical synthesis of cesium lead bromide (CsPbBr3), eliminating the need of organic solvents and high temperatures. The synthesized CsPbBr3powder is used to fabricate poly(methyl methacrylate) (PMMA)-CsPbBr3films and CsPbBr3nanocrystals (NCs). The photoluminescence (PL) peaks of the emission light are centered at 541 nm, 538 nm, and 514 nm for the CsPbBr3powder, PMMA-CsPbBr3films, and CsPbBr3NCs, respectively, correlating with crystal sizes of 0.96, 0.56, and 0.12μm, respectively. The PL lifetime analysis reveals decay times (τ1,τ2) of (4.18, 20.08), (5.7, 46.99), and (5.81, 23.14) in the units (ns, ns) for the CsPbBr3powder, PMMA-CsPbBr3films, and CsPbBr3NCs, respectively. The PL quantum yield of the CsPbBr3NCs in toluene is 61.3%. Thermal activation energies for thermal quenching are 217.48 meV (films) and 178.15 meV (powder), indicating improved thermal stability with the PMMA encapsulation. The analysis of the PL intensity decay from water diffusion in the PMMA-CsPbBr3films yields 1.70 × 10-12m2s-1for the diffusion coefficient of water, comparable to that for water diffusion in pure PMMA. This work demonstrates a scalable, sustainable strategy for CsPbBr3synthesis and stability enhancement for optoelectronic applications.
More Related Videos
08:56Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
10:42Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
Published on: December 29, 2016
Related Concept Videos
Radical Substitution: Allylic Bromination
Hybridization of Atomic Orbitals I
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Radical Reactivity: Steric Effects
Along with electronic...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...