Selective Synthesis of (9,8) Single Walled Carbon Nanotubes on Cobalt Incorporated TUD-1 Catalysts

被引:118
作者
Wang, Hong [1 ]
Wang, Bo [1 ,2 ]
Quek, Xian-Yang [1 ]
Wei, Li [1 ]
Zhao, Jianwen [3 ]
Li, Lain-Jong [4 ]
Chan-Park, Mary B. [1 ]
Yang, Yanhui [1 ]
Chen, Yuan [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[2] Inst Chem & Engn Sci, Singapore 627833, Singapore
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[4] Acad Sinica, Res Ctr Appl Sci, Taipei, Taiwan
基金
新加坡国家研究基金会;
关键词
CHIRALITY; CO-MCM-41;
D O I
10.1021/ja106937y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selective synthesis of single walled carbon nanotubes (SWCNTs) with specific (n,m) structures is desired for many potential applications. Current chirality control growth has only achieved at small diameter (6,5) and (7,5) nanotubes. Each (n,m) species is a distinct molecule with structure-dependent properties; therefore it is essential to extend chirality control to various (n,m) species. In this communication, we demonstrate the highly selective synthesis of (9,8) nanotubes on a cobalt incorporated TUD-1 catalyst are (Co-TUD-1). When catalysts were prereduced in H-2 at the optimized temperature of 500 degrees C, 59.1% of semiconducting nanotubes have the (9,8) structure. The uniqueness of Co-TUD-1 relies on its low reduction temperature (483 degrees C), large surface area, and strong metal-support interaction, which stabilizes Co clusters responsible for the growth of (9,8) nanotubes. SWCNT thin film field effect transistors fabricated using (9,8) nanotubes from our synthesis process have higher average device mobility and a higher fraction of semiconducting devices than those using (6,5) nanotubes. Combining with further postsynthetic sorting techniques, our selective synthesis method brings us closer to the ultimate goal of producing (n,m) specific nanotube materials.
引用
收藏
页码:16747 / 16749
页数:3
相关论文
共 18 条
[1]  
Aquino C, 2009, ORDERED POROUS SOLIDS: RECENT ADVANCES AND PROSPECTS, P3, DOI 10.1016/B978-0-444-53189-6.00001-9
[2]   Narrow (n,m)-distribution of single-walled carbon nanotubes grown using a solid supported catalyst [J].
Bachilo, SM ;
Balzano, L ;
Herrera, JE ;
Pompeo, F ;
Resasco, DE ;
Weisman, RB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (37) :11186-11187
[3]  
Chiang WH, 2009, NAT MATER, V8, P882, DOI [10.1038/NMAT2531, 10.1038/nmat2531]
[4]   X-ray absorption spectroscopic investigation of partially reduced cobalt species in Co-MCM-41 catalysts during synthesis of single-wall carbon nanotubes [J].
Ciuparu, D ;
Haider, P ;
Fernández-García, M ;
Chen, Y ;
Lim, S ;
Haller, GL ;
Pfefferle, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (34) :16332-16339
[5]   Uniform-diameter single-walled carbon nanotubes catalytically grown in cobalt-incorporated MCM-41 [J].
Ciuparu, D ;
Chen, Y ;
Lim, S ;
Haller, GL ;
Pfefferle, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (02) :503-507
[6]   Mechanism of cobalt cluster size control in Co-MCM-41 during single-wall carbon nanotubes synthesis by CO disproportionation [J].
Ciuparu, D ;
Chen, Y ;
Lim, S ;
Yang, YH ;
Haller, GL ;
Pfefferle, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (40) :15565-15571
[7]   The importance of strong carbon-metal adhesion for catalytic nucleation of single-walled carbon nanotubes [J].
Ding, Feng ;
Larsson, Peter ;
Larsson, J. Andreas ;
Ahuja, Rajeev ;
Duan, Haiming ;
Rosen, Arne ;
Bolton, Kim .
NANO LETTERS, 2008, 8 (02) :463-468
[8]   Dislocation theory of chirality-controlled nanotube growth [J].
Ding, Feng ;
Harutyunyan, Avetik R. ;
Yakobson, Boris I. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (08) :2506-2509
[9]   Raman spectroscopy of carbon nanotubes in 1997 and 2007 [J].
Dresselhaus, M. S. ;
Dresselhaus, G. ;
Jorio, A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (48) :17887-17893
[10]   Narrow-Chirality Distributed Single-Walled Carbon Nanotube Growth from Nonmagnetic Catalyst [J].
Ghorannevis, Zohreh ;
Kato, Toshiaki ;
Kaneko, Toshiro ;
Hatakeyama, Rikizo .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (28) :9570-9572