摘要
Lead halide perovskite quantum dots (QDs) are promising electrochemiluminescence (ECL) nanoemitters due to their fascinating photophysical properties. However, due to their poor structural stability against the external environment, the trade-off between their colloidal stability and carrier injection/transport efficiency is a major challenge in the advancement of perovskite-based ECL technology. In this work, intense and stable ECL from CsPbBr 3 (CPB) QDs is achieved by simultaneously encapsulating CPB QDs and coreactant (CoR) into in situ generated SiO 2 matrix via hydrolysis of tetramethyl orthosilicate. The well-designed architecture of the as-obtained CPB-CoR@SiO 2 nanocomposites (NCs) guarantees not only greatly improved stability thanks to the peripheral SiO 2 protecting matrix, but also efficient self-enhanced ECL between CPB and the intra-coreactants. Consequently, by elaborately selecting the CoR molecules with different tertiary/secondary amines and functional groups, multifold higher (up to 10.2 times) ECL efficiencies are obtained for the CPB-CoR@SiO 2 NCs alone in reference to the standard Ru(bpy) 3 2+ /tri- n -propylamine system. This work provides an efficient design strategy for obtaining stable and highly efficient ECL from perovskite QDs, and offers a new perspective for the development and application of perovskite-based ECL system.
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