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

被引:14
作者
Gao, Yu-Jie [1 ]
Jin, Handong [2 ]
Esteban, Daniel A. [3 ]
Weng, Bo [1 ]
Saha, Rafikul A. [1 ]
Yang, Min-Quan [4 ]
Bals, Sara [3 ]
Steele, Julian A. [1 ,5 ,6 ]
Huang, Haowei [1 ]
Roeffaers, Maarten B. J. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Membrane Separat Adsorpt Catalysis & Spect Sus, Celestijnenlaan 200F, B-3001 Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Chem, Leuven, Belgium
[3] Univ Antwerp, Electron Microscopy Mat Sci EMAT, Antwerp, Belgium
[4] Fujian Normal Univ, Coll Environm & Resource Sci, Coll Carbon Neutral Modern Ind, Fujian Key Lab Pollut Control & Resource Reuse, Fuzhou, Peoples R China
[5] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld, Australia
[6] Univ Queensland, Sch Math & Phys, Brisbane, Qld, Australia
基金
澳大利亚研究理事会;
关键词
3D cavity silica; C(sp(3))-H bond activation; perovskite quantum dots; photocatalysis; stability; HALIDE PEROVSKITE NANOCRYSTALS; CSPBX3;
D O I
10.1002/cey2.559
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metal 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(sp(3))-H bond activation to produce benzaldehyde with similar to 730 mu mol 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.
引用
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页数:10
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