Pt3Co Octapods as Superior Catalysts of CO2 Hydrogenation

被引:189
作者
Khan, Munir Ullah [1 ,2 ]
Wang, Liangbing [1 ,2 ]
Liu, Zhao [1 ,2 ]
Gao, Zehua [1 ,2 ]
Wang, Shenpeng [1 ,2 ]
Li, Hongliang [1 ,2 ]
Zhang, Wenbo [1 ,2 ]
Wang, Menglin [1 ,2 ]
Wang, Zhengfei [1 ,2 ]
Ma, Chao [1 ,2 ]
Zeng, Jie [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei Sci Ctr, Natl Synchrotron Radiat Lab, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Synerget Innovat Ctr Quantum Informat & Quantum P, Dept Chem Phys, Hefei 230026, Anhui, Peoples R China
关键词
carbon dioxide; charge transfer; cobalt; hydrogenation; platinum; CARBON-DIOXIDE; ELECTROCATALYTIC REDUCTION; PHOTOCHEMICAL REDUCTION; OXIDE CATALYST; CONVERSION; METHANOL; NANOCRYSTALS; SURFACES; LIGHT;
D O I
10.1002/anie.201602512
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As the electron transfer to CO2 is a critical step in the activation of CO2, it is of significant importance to engineer the electronic properties of CO2 hydrogenation catalysts to enhance their activity. Herein, we prepared Pt3Co nanocrystals with improved catalytic performance towards CO2 hydrogenation to methanol. Pt3Co octapods, Pt3Co nanocubes, Pt octapods, and Pt nanocubes were tested, and the Pt3Co octapods achieved the best catalytic activity. Both the presence of multiple sharp tips and charge transfer between Pt and Co enabled the accumulation of negative charges on the Pt atoms in the vertices of the Pt3Co octapods. Moreover, infrared reflection absorption spectroscopy confirmed that the high negative charge density at the Pt atoms in the vertices of the Pt3Co octapods promotes the activation of CO2 and accordingly enhances the catalytic activity.
引用
收藏
页码:9548 / 9552
页数:5
相关论文
共 52 条
[1]  
[Anonymous], 2013, ANGEW CHEM INT ED
[2]  
Behrens M., 2014, ANGEW CHEM-GER EDIT, V126, P12216, DOI [10.1002/ange.201409282, DOI 10.1002/ANGE.201409282]
[3]   Heterogeneous Catalysis of CO2 Conversion to Methanol on Copper Surfaces [J].
Behrens, Malte .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (45) :12022-12024
[4]   Enhanced wetting of Cu on ZnO by migration of subsurface oxygen vacancies [J].
Beinik, Igor ;
Hellstrom, Matti ;
Jensen, Thomas N. ;
Broqvist, Peter ;
Lauritsen, Jeppe V. .
NATURE COMMUNICATIONS, 2015, 6
[5]  
Calaza F., 2015, ANGEW CHEM, V127, P12661
[6]   Carbon Dioxide Activation and Reaction Induced by Electron Transfer at an Oxide-Metal Interface [J].
Calaza, Florencia ;
Stiehler, Christian ;
Fujimori, Yuichi ;
Sterrer, Martin ;
Beeg, Sebastian ;
Ruiz-Oses, Miguel ;
Nilius, Niklas ;
Heyde, Markus ;
Parviainen, Teemu ;
Honkala, Karoliina ;
Hakkinen, Hannu ;
Freund, Hans-Joachim .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (42) :12484-12487
[7]   COLLISIONAL IONIZATION OF NA, K, AND CS BY CO2, COS, AND CS2 - MOLECULAR ELECTRON AFFINITIES [J].
COMPTON, RN ;
REINHARDT, PW ;
COOPER, CD .
JOURNAL OF CHEMICAL PHYSICS, 1975, 63 (09) :3821-3827
[8]   Mechanistic Insights into CO2 Activation via Reverse Water-Gas Shift on Metal Surfaces [J].
Dietz, Luca ;
Piccinin, Simone ;
Maestri, Matteo .
JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (09) :4959-4966
[9]   Surface chemistry of carbon dioxide [J].
Freund, HJ ;
Roberts, MW .
SURFACE SCIENCE REPORTS, 1996, 25 (08) :225-273
[10]   Size-Dependent Electrocatalytic Reduction of CO2 over Pd Nanoparticles [J].
Gao, Dunfeng ;
Zhou, Hu ;
Wang, Jing ;
Miao, Shu ;
Yang, Fan ;
Wang, Guoxiong ;
Wang, Jianguo ;
Bao, Xinhe .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (13) :4288-4291