Ultrastable Hydroxyapatite/Titanium-Dioxide-Supported Gold Nanocatalyst with Strong Metal-Support Interaction for Carbon Monoxide Oxidation

被引:218
|
作者
Tang, Hailian [1 ,2 ,3 ]
Liu, Fei [1 ]
Wei, Jiake [4 ]
Qiao, Botao [1 ]
Zhao, Kunfeng [5 ]
Su, Yang [1 ]
Jin, Changzi [1 ,2 ]
Li, Lin [1 ]
Liu, Jingyue [4 ]
Wang, Junhu [1 ,2 ]
Zhang, Tao [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Mossbauer Effect Data Ctr, Dalian 116023, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[5] Natl Engn Res Ctr Nanotechnol, Shanghai 200241, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
gold; heterogeneous catalysis; metal-support interactions; nanoparticles; surface chemistry; CO OXIDATION; NANOPARTICLE CATALYSTS; CARBOXYLATE CEMENTS; AU NANOPARTICLES; TEMPERATURE; AU/TIO2; TIO2; ADSORPTION; PLATINUM; ADHESION;
D O I
10.1002/anie.201601823
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supported Au nanocatalysts have attracted intensive interest because of their unique catalytic properties. Their poor thermal stability, however, presents a major barrier to the practical applications. Here we report an ultrastable Au nanocatalyst by localizing the Au nanoparticles (NPs) in the interfacial regions between the TiO2 and hydroxyapatite. This unique configuration makes the Au NP surface partially encapsulated due to the strong metal-support interaction and partially exposed and accessible by the reaction molecules. The strong interaction helps stabilizing the Au NPs while the partially exposed Au NP surface provides the active sites for reactions. Such a catalyst not only demonstrated excellent sintering resistance with high activity after calcination at 800 degrees C but also showed excellent durability that outperforms a commercial three-way catalyst in a simulated practical testing, suggesting great potential for practical applications.
引用
收藏
页码:10606 / 10611
页数:6
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