3D‐cavity‐confined CsPbBr3 quantum dots for visible‐light‐driven photocatalytic C(sp3)–H bond activation

Author:

Gao Yu‐Jie1ORCID,Jin Handong2,Esteban Daniel A.3ORCID,Weng Bo1ORCID,Saha Rafikul A.1ORCID,Yang Min‐Quan4ORCID,Bals Sara3ORCID,Steele Julian A.156ORCID,Huang Haowei1,Roeffaers Maarten B. J.1ORCID

Affiliation:

1. Centre for Membrane Separations, Adsorption, Catalysis and Spectroscopy for Sustainable Solutions (cMACS) KU Leuven Leuven Belgium

2. Department of Chemistry KU Leuven Leuven Belgium

3. Electron Microscopy for Materials Science (EMAT) University of Antwerp Antwerpen Belgium

4. Fujian Key Laboratory of Pollution Control and Resource Reuse, College of Environmental and Resource Sciences, College of Carbon Neutral Modern Industry Fujian Normal University Fuzhou China

5. Australian Institute for Bioengineering and Nanotechnology The University of Queensland Brisbane Queensland Australia

6. School of Mathematics and Physics The University of Queensland Brisbane Queensland Australia

Abstract

AbstractMetal halide perovskite (MHP) quantum dots (QDs) offer immense potential for several areas of photonics research due to their easy and low‐cost fabrication and excellent optoelectronic properties. However, practical applications of MHP QDs are limited by their poor stability and, in particular, their tendency to aggregate. Here, we develop a two‐step double‐solvent strategy to grow and confine CsPbBr3 QDs within the three‐dimensional (3D) cavities of a mesoporous SBA‐16 silica scaffold (CsPbBr3@SBA‐16). Strong confinement and separation of the MHP QDs lead to a relatively uniform size distribution, narrow luminescence, and good ambient stability over 2 months. In addition, the CsPbBr3@SBA‐16 presents a high activity and stability for visible‐light‐driven photocatalytic toluene C(sp3)–H bond activation to produce benzaldehyde with ∼730 µmol g−1 h−1 yield rate and near‐unity selectivity. Similarly, the structural stability of CsPbBr3@SBA‐16 QDs is superior to that of both pure CsPbBr3 QDs and those confined in MCM‐41 with 1D channels.

Publisher

Wiley

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