Interfacial Effects in Iron-Nickel Hydroxide-Platinum Nanoparticles Enhance Catalytic Oxidation

被引:605
作者
Chen, Guangxu [1 ,2 ]
Zhao, Yun [1 ,2 ]
Fu, Gang [1 ,2 ]
Duchesne, Paul N. [4 ]
Gu, Lin [3 ]
Zheng, Yanping [1 ,2 ]
Weng, Xuefei [1 ,2 ]
Chen, Mingshu [1 ,2 ]
Zhang, Peng [4 ]
Pao, Chih-Wen [5 ]
Lee, Jyh-Fu [5 ]
Zheng, Nanfeng [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Collaborat Innovat Ctr Chem Energy Mat, Natl Engn Lab Green Chem Prod Alcohols Ethers & E, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[4] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4R2, Canada
[5] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
基金
加拿大自然科学与工程研究理事会;
关键词
WATER; OXIDE; SURFACES; TRENDS; GOLD; CO;
D O I
10.1126/science.1252553
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hybrid metal nanoparticles can allow separate reaction steps to occur in close proximity at different metal sites and accelerate catalysis. We synthesized iron-nickel hydroxide-platinum (transition metal-OH-Pt) nanoparticles with diameters below 5 nanometers and showed that they are highly efficient for carbon monoxide (CO) oxidation catalysis at room temperature. We characterized the composition and structure of the transition metal-OH-Pt interface and showed that Ni2+ plays a key role in stabilizing the interface against dehydration. Density functional theory and isotope-labeling experiments revealed that the OH groups at the Fe3+-OH-Pt interfaces readily react with CO adsorbed nearby to directly yield carbon dioxide (CO2) and simultaneously produce coordinatively unsaturated Fe sites for O-2 activation. The oxide-supported PtFeNi nanocatalyst rapidly and fully removed CO from humid air without decay in activity for 1 month.
引用
收藏
页码:495 / 499
页数:5
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