Lateral Etching of Core-Shell Au@Metal Nanorods to Metal-Tipped Au Nanorods with Improved Catalytic Activity

被引:135
作者
Guo, Xia [1 ]
Zhang, Qiao [1 ]
Sun, Yanghui [2 ,3 ]
Zhao, Qing [2 ,3 ]
Yang, Jian [1 ,4 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China
[2] Peking Univ, Dept Phys, State Key Lab Mesoscop Phys, Beijing 100871, Peoples R China
[3] Peking Univ, Dept Phys, Elect Microscopy Lab, Beijing 100871, Peoples R China
[4] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
关键词
hybrid materials; nanostructures; reaction mechanism; selective etching; catalysis; SEED-MEDIATED GROWTH; GOLD NANORODS; OPTICAL-PROPERTIES; SILVER; NANOSTRUCTURES; NANOPARTICLES; NANOCRYSTALS; OXIDATION; CONVERSION; CLUSTERS;
D O I
10.1021/nn203793k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selective growth/etching of hybrid materials is very important for the rational synthesis of hierarchical structures and precise modulation of their physical properties. Here, the lateral etching of the core-shell Au@Ag nanorods is achieved by FeCl3 at room temperature, producing a number of dumbbell-like Ag-tipped Au nanorods. This selective etching at the side of the core-shell nanorods is attributed to the increased reactivity of the side facets, due to less surface passivation of cetyltrimethylammonium bromide. The similar synthetic strategy has also been demonstrated to be successful for the Pd-tipped Au nanorods that have not been reported before, indicating the great potential of this selective etching. The Ag-tipped Au nanorods are examined as a catalyst for the reduction of p-nitrophenol at room temperature. The Ag-tipped Au nanorods exhibit a higher catalytic activity than Au nanorods and core-shell Au@Ag nanorods, which could be attributed to the electronic effect and the unique structure in the Ag-tipped Au nanorods.
引用
收藏
页码:1165 / 1175
页数:11
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