Immobilizing Metal Nanoparticles to Metal-Organic Frameworks with Size and Location Control for Optimizing Catalytic Performance

被引:671
作者
Zhu, Qi-Long [1 ]
Li, Jun [1 ,2 ]
Xu, Qiang [1 ,2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Ikeda, Osaka 5638577, Japan
[2] Kobe Univ, Grad Sch Engn, Nada Ku, Kobe, Hyogo 657, Japan
关键词
CHEMICAL HYDROGEN STORAGE; POROUS COORDINATION POLYMER; AMMONIA-BORANE; SYNERGISTIC CATALYSIS; HYDROLYTIC DEHYDROGENATION; NICKEL NANOPARTICLES; ALLOY NANOPARTICLES; PD NANOPARTICLES; SEPARATION; OXIDATION;
D O I
10.1021/ja403330m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
AuNi alloy nanoparticles were successfully immobilized to MIL-101 with size and location control for the first time by double solvents method (DSM) combined with a liquid-phase concentration-controlled reduction strategy. When an overwhelming reduction approach was employed, the uniform 3D distribution of the ultrafine AuNi nanoparticles (NPs) encapsulated in the pores of MIL-101 was achieved, as demonstrated by TEM and electron tomographic measurements, which brings light to new opportunities in the fabrication of ultrafine non-noble metal-based NPs throughout the interior pores of MOFs. The ultrafine AuNi alloy NPs inside the mesoporous MIL-101 exerted exceedingly high activity for hydrogen generation from the catalytic hydrolysis of ammonia borane.
引用
收藏
页码:10210 / 10213
页数:4
相关论文
共 51 条
[1]   Immobilizing Highly Catalytically Active Pt Nanoparticles inside the Pores of Metal-Organic Framework: A Double Solvents Approach [J].
Aijaz, Arshad ;
Karkamkar, Abhi ;
Choi, Young Joon ;
Tsumori, Nobuko ;
Roennebro, Ewa ;
Autrey, Tom ;
Shioyama, Hiroshi ;
Xu, Qiang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (34) :13926-13929
[2]   Cellulose Hydrolysis by a New Porous Coordination Polymer Decorated with Sulfonic Acid Functional Groups [J].
Akiyama, George ;
Matsuda, Ryotaro ;
Sato, Hiroshi ;
Takata, Masaki ;
Kitagawa, Susumu .
ADVANCED MATERIALS, 2011, 23 (29) :3294-+
[3]   A class of non-precious metal composite catalysts for fuel cells [J].
Bashyam, Rajesh ;
Zelenay, Piotr .
NATURE, 2006, 443 (7107) :63-66
[4]   Metal-Organic Frameworks with Functional Pores for Recognition of Small Molecules [J].
Chen, Banglin ;
Xiang, Shengchang ;
Qian, Guodong .
ACCOUNTS OF CHEMICAL RESEARCH, 2010, 43 (08) :1115-1124
[5]   Multifunctional fourfold interpenetrating diamondoid network: Gas separation and fabrication of palladium nanoparticles [J].
Cheon, Young Eun ;
Suh, Myunghyun Paik .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (13) :3961-3967
[6]   Catalysis by metal nanoparticles embedded on metal-organic frameworks [J].
Dhakshinamoorthy, Amarajothi ;
Garcia, Hermenegildo .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (15) :5262-5284
[7]   Systematic design of pore size and functionality in isoreticular MOFs and their application in methane storage [J].
Eddaoudi, M ;
Kim, J ;
Rosi, N ;
Vodak, D ;
Wachter, J ;
O'Keeffe, M ;
Yaghi, OM .
SCIENCE, 2002, 295 (5554) :469-472
[8]   A chromium terephthalate-based solid with unusually large pore volumes and surface area [J].
Férey, G ;
Mellot-Draznieks, C ;
Serre, C ;
Millange, F ;
Dutour, J ;
Surblé, S ;
Margiolaki, I .
SCIENCE, 2005, 309 (5743) :2040-2042
[9]   Large breathing effects in three-dimensional porous hybrid matter: facts, analyses, rules and consequences [J].
Ferey, Gerard ;
Serre, Christian .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (05) :1380-1399
[10]   A dynamic, isocyanurate-functionalized porous coordination polymer [J].
Ghosh, Sujit K. ;
Bureekaew, Sareeya ;
Kitagawa, Susumu .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (18) :3403-3406