In situ thermolysis of Pt-carbonyl complex to form supported clean Pt nanoclusters with enhanced catalytic performance

被引:4
|
作者
Wei, Guijuan [1 ,2 ,3 ]
Zhao, Xixia [1 ,2 ]
An, Changhua [1 ,2 ,3 ]
Liu, Junxue [1 ,2 ]
Wang, Zhaojie [1 ,2 ]
Du, Kun [1 ,2 ]
Zhang, Jun [1 ,2 ]
机构
[1] China Univ Petr, Coll Sci, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] China Univ Petr, Coll Chem Engn, Qingdao 266580, Peoples R China
[3] Tianjin Univ Technol, Coll Chem & Chem Engn, Tianjin Key Lab Organ Solar Cells & Photochem Con, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrogenation; nanoclusters; reduced graphene oxide; platinum; catalyst; GRAPHENE OXIDE COMPOSITES; SELECTIVE HYDROGENATION; NITROBENZENE; PLATINUM; NANOPARTICLES; REDUCTION; NITRO; DEPOSITION; ULTRAFINE; ANILINE;
D O I
10.1007/s40843-016-5144-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Clean Pt nanoclusters with a diameter of 1.0-2.4 nm, supported on reduced graphene oxide (rGO) nanosheets, were successfully synthesized by simple in situ thermolysis of a Pt-carbonyl complex. The supported Pt nanoclusters are in an electron-deficient state because of the electron transfer between the nanoclusters and the rGO sheets. The as-prepared Pt-1 nm/rGO shows high catalytic activity for the 100% selective hydrogenation of nitrobenzene, with the turnover frequency (TOF) reaching 975.4 h(-1) at 25 degrees C and 1 atm. This number is higher than the previously reported value for the heterogeneously catalyzed hydrogenation of nitrobenzene. The proposed process follows a direct hydrogenation mechanism, as is revealed by the analyses of the intermediate products. This work presents a facile and effective synthetic approach for achieving highly efficient nanocatalysts, and can be extended to obtain other metal catalysts with ultra-small sizes and excellent performance.
引用
收藏
页码:131 / 140
页数:10
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