Ultrastable Au nanoparticles on titania through an encapsulation strategy under oxidative atmosphere

被引:175
作者
Liu, Shaofeng [1 ,2 ,3 ]
Xu, Wei [4 ,5 ]
Niu, Yiming [6 ]
Zhang, Bingsen [6 ]
Zheng, Lirong [4 ]
Liu, Wei [1 ]
Li, Lin [1 ]
Wang, Junhu [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] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[5] Rome Int Ctr Mat Sci Superstripes, Via Sabelli 119A, I-00185 Rome, Italy
[6] Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-SUPPORT INTERACTION; GOLD NANOPARTICLES; METHANOL SYNTHESIS; THERMAL-STABILITY; CARBON-MONOXIDE; CO OXIDATION; ACTIVE GOLD; CATALYSTS; HYDROGENATION; SIZE;
D O I
10.1038/s41467-019-13755-5
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
Supported gold catalysts play a crucial role in the chemical industry; however, their poor on-stream stability because of the sintering of the gold nanoparticles restricts their practical application. The strong metal-support interaction (SMSI), an important concept in heterogeneous catalysis, may be applied to construct the structure of catalysts and, hence, improve their reactivity and stability. Here we report an ultrastable Au nanocatalyst after calcination at 800 degrees C, in which Au nanoparticles are encapsulated by a permeable TiOx thin layer induced by melamine under oxidative atmosphere. Owning to the formed TiOx overlayer, the resulting Au catalyst is resistant to sintering and exhibits excellent activity and stability for catalytic CO oxidation. Furthermore, this special strategy can be extended to colloidal Au nanoparticles supported on TiO2 and commercial gold catalyst denoted as RR2Ti, providing a universal way to engineer and develop highly stable supported Au catalysts with tunable activity.
引用
收藏
页数:9
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