Zeolite Y microspheres with perpendicular mesochannels and metal@Y heterostructures for catalytic and SERS applications

被引:21
作者
Chen, Zhuwen [1 ]
Chen, Chao [1 ]
Zhang, Jian [1 ]
Zheng, Guangchao [1 ]
Wang, Yanding [1 ]
Dong, Lei [1 ]
Qian, Wei [1 ]
Bai, Shan [1 ]
Hong, Mei [1 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Guangdong Prov Key Lab Nanomicro Mat Res, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLECULAR MODIFIERS; COUPLING REACTIONS; SHAPE SELECTIVITY; AMINO-ACIDS; CRYSTALLIZATION; ADSORPTION; MORPHOLOGY; CONVERSION; NANOCHANNELS; CHALLENGES;
D O I
10.1039/c7ta10444h
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
The control over particle shape and internal architecture offers promise to better realize catalytic activity and selectivity through structural optimization but remains a challenge for crystalline zeolite frameworks. This work describes a facile one-pot strategy to synthesize uniform zeolite Y microspheres through epitaxial hydrogen bonding and entropic hydrophobic interactions using simple mono-alcohols as zeolite growth modifiers with judicious adjustment of synthesis parameters. The internal architecture can be fine-tuned by the co-presence of L-carnitine which creates hidden defects. Unprecedented wheellike mesoporous channels are created within the microspheres by acid attack of the induced weak points. Moreover, the combination of zeolite Y microspheres with other materials is expected to impart additional properties due to the hybrid nature of the resulting nanocomposites and the perpendicular mesochannels for alleviated diffusion. As demonstrated, Pd2+-exchanged microspheres exhibit remarkably enhanced catalytic activity and recyclability for C-C coupling reactions, and metal doped Ag@Y microspheres allow for fast sensing by surface-enhanced Raman scattering (SERS), achieving orders of magnitude lower detection limit for water soluble molecules.
引用
收藏
页码:6273 / 6281
页数:9
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