Salt-assisted deposition of SnO2 on α-MoO3 nanorods and fabrication of polycrystalline SnO2 nanotubes

被引:117
作者
Liu, B
Zeng, HC
机构
[1] Natl Univ Singapore, Fac Engn, Dept Environm Chem & Engn, Singapore 119260, Singapore
[2] Natl Univ Singapore, Chem & Proc Engn Ctr, Singapore 119260, Singapore
关键词
D O I
10.1021/jp037822d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Rutile-like tin dioxide (SnO2; tetragonal symmetry) is a strategic material for a wide range of important applications. Although numerous methods have been developed for preparations of SnO2 nanoparticles, nanowires, and nanorods, there has been no rational synthetic method reported to prepare this functional material into tubular nanostructures. In this article, we describe a facile template method for synthesis of free-standing polycrystalline SnO2 nanotubes in aqueous solution. With soluble alpha-MoO3 nanorod templates, polycrystalline SnO2 can be first deposited under normal atmospheric pressure (room temperature to 100 degreesC) or hydrothermal conditions (180 degreesC). In particular, salt additives such as Na2SO4 have been proven to be indispensable for the deposition of Sno(2) skins. Various preparative parameters have been examined in detail, and dissolution modes Of alpha-MoO3 have also been investigated to address the formation mechanism. The optical band gap determined for the nanotubes is 3.92 eV (for crystallites with an average size of similar to4 nm). This salt-assisted "one-pot" method promises large-scale production of polycrystalline SnO2 nanotubes with both structural engineering and crystallite size control.
引用
收藏
页码:5867 / 5874
页数:8
相关论文
共 62 条
[1]   TIN OXIDE THIN FILM TRANSISTORS [J].
AOKI, A ;
SASAKURA, H .
JAPANESE JOURNAL OF APPLIED PHYSICS, 1970, 9 (05) :582-&
[2]   Nanoparticles of SnO produced by sonochemistry as anode materials for rechargeable lithium batteries [J].
Aurbach, D ;
Nimberger, A ;
Markovsky, B ;
Levi, E ;
Sominski, E ;
Gedanken, A .
CHEMISTRY OF MATERIALS, 2002, 14 (10) :4155-4163
[3]   Synthesis of nanocrystalline SnO2 powder by amorphous citrate route [J].
Bhagwat, M ;
Shah, P ;
Ramaswamy, V .
MATERIALS LETTERS, 2003, 57 (9-10) :1604-1611
[4]   SAXS study of formation and growth of tin oxide nanoparticles in the presence of complexing ligands [J].
Broussous, L ;
Santilli, CV ;
Pulcinelli, SH ;
Craievich, AF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (11) :2855-2860
[5]  
Cotton F.A., 1980, ADV INORG CHEM, P852
[6]   Tin oxide nanowires, nanoribbons, and nanotubes [J].
Dai, ZR ;
Gole, JL ;
Stout, JD ;
Wang, ZL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (06) :1274-1279
[7]   Growth and structure evolution of novel tin oxide diskettes [J].
Dai, ZR ;
Pan, ZW ;
Wang, ZL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (29) :8673-8680
[8]   Ultra-long single crystalline nanoribbons of tin oxide [J].
Dai, ZR ;
Pan, ZW ;
Wang, ZL .
SOLID STATE COMMUNICATIONS, 2001, 118 (07) :351-354
[9]   Synthesis of tin oxide nanocrystalline phases via use of tin(II) halide precursors [J].
Deng, HM ;
Lamelas, FJ ;
Hossenlopp, JM .
CHEMISTRY OF MATERIALS, 2003, 15 (12) :2429-2436
[10]   LARGE-SCALE SYNTHESIS OF CARBON NANOTUBES [J].
EBBESEN, TW ;
AJAYAN, PM .
NATURE, 1992, 358 (6383) :220-222