Entrapment of metal nanoparticles within nanocages of mesoporous silicas aided by co-surfactants

被引:18
|
作者
Li, Xiaobo [1 ,2 ]
Liu, Xiao [1 ,2 ]
Yang, Yan [1 ,2 ]
Zhao, Jiao [1 ,2 ]
Li, Can [1 ]
Yang, Qihua [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
关键词
FISCHER-TROPSCH SYNTHESIS; SELECTIVE HYDROGENATION; CATALYTIC-ACTIVITY; NANOCOMPOSITE CATALYSTS; GOLD NANOPARTICLES; ALCOHOL OXIDATION; PD NANOPARTICLES; HYBRID MATERIALS; SBA-15; SILICA; NANOCLUSTERS;
D O I
10.1039/c2jm33965j
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
We demonstrated an efficient approach for in situ encapsulation of metal nanoparticles (NPs) into nanocages of mesoporous silicas using a co-surfactant as the transportation medium. By using this approach, colloidal Pt and Au NPs were successfully encapsulated into the nanocages of cagelike mesoporous silicas (CMS) and FDU-12 using co-surfactants butanol and mesitylene (TMB) as the transportation medium, respectively. The prepared Pt/CMS catalysts are active and highly selective in the hydrogenation of chloronitrobenzene (CNB) to the corresponding chloroaniline (CAN). The catalyst prepared by the in situ method is superior to the catalyst prepared by the traditional solution impregnation method. This work provides a new approach for the synthesis of the mesoporous materials with encapsulated metal NPs.
引用
收藏
页码:21045 / 21050
页数:6
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