Templated synthesis of atomically-thin Ag nanocrystal catalysts in the interstitial space of a layered silicate

被引:42
作者
Doustkhah, Esmail [1 ,2 ]
Rostamnia, Sadegh [1 ,2 ]
Tsunoji, Nao [3 ]
Henzie, Joel [1 ]
Takei, Toshiaki [1 ]
Yamauch, Yusuke [4 ,5 ,6 ]
Ide, Yusuke [1 ]
机构
[1] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitechton MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[2] Univ Maragheh, Fac Sci, Dept Chem, Maragheh 5518183111, Iran
[3] Hiroshima Univ, Grad Sch Engn, Dept Appl Chem, 1-4-1 Kagamiyama, Higashihiroshima 7398527, Japan
[4] Kyung Hee Univ, Dept Plant & Environm New Resources, 1732 Deogyeong Daero, Yongin 446701, Gyeonggi Do, South Korea
[5] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
[6] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
AQUEOUS AMMONIA-BORANE; SILVER NANOPARTICLES; HYDROGEN GENERATION; MONTMORILLONITE; INTERCALATION; HYDROLYSIS; CLUSTERS; RELEASE; FILMS;
D O I
10.1039/c8cc00275d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enclosing functional nanoparticles in stable inorganic supports is important for generating ultra-stable catalytic active sites with good performance and material utilization efficiency. Here we describe a simple method to synthesize ultra-thin Ag nanocrystals with dimensions that are defined by the similar to 1.4 nm 2D interlayer separating a layered silicate nanostructure. We call the particles "nanoplates" because they are <1.4 nm thick in one direction and their in-plane dimensions are defined by reaction time. The layered silicate is pillared with dialkylurea, which serves both as a reducing agent for the Ag precursor and immobilizes the Ag nanoplates in the interstitial nanospace. The supported Ag nanoplates showed catalytic activity for hydrolysis of NH3BH3 and generation of H-2 at room temperature. These supported Ag nanocatalysts had performance much higher than spherical Ag nanoparticles. They, moreover, had performance and stability comparable to costly supported Pt nanoparticles.
引用
收藏
页码:4402 / 4405
页数:4
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