Formation and Properties of Stabilized Aluminum Nanoparticles

被引:129
作者
Meziani, Mohammed J. [2 ,3 ]
Bunker, Christopher E. [1 ]
Lu, Fushen [2 ,3 ]
Li, Heting [2 ,3 ]
Wang, Wei [2 ,3 ]
Guliants, Elena A. [4 ]
Quinn, Robert A. [2 ,3 ]
Sun, Ya-Ping [2 ,3 ]
机构
[1] USAF, Res Lab, Prop Directorate, Wright Patterson AFB, OH 45433 USA
[2] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
[3] Clemson Univ, Lab Emerging Mat & Technol, Clemson, SC 29634 USA
[4] Univ Dayton, Res Inst, Sensors Technol Off, Dayton, OH 45469 USA
关键词
aluminum nanoparticles; alanes; surface passivation; energetic nanomaterials; HYDROGEN STORAGE PROPERTIES; CARBOXYLIC-ACIDS; SURFACE; AL(111); POWDERS; NANOPOWDERS; ADSORPTION; DECOMPOSITION; PASSIVATION; REACTIVITY;
D O I
10.1021/am800209m
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The wet-chemical synthesis of aluminum nanoparticles was investigated systematically by using dimethylethylamine alane and 1-methylpyrrolidine alane as precursors and molecules with one or a pair of carboxylic acid groups as surface passivation agents. Dimethylethylamine alane was more reactive, capable of yielding well-defined and dispersed aluminum nanoparticles. 1-Methylpyrrolidine alane was less reactive and more complex in the catalytic decomposition reaction, for which various experimental parameters and conditions were used and evaluated. The results suggested that the passivation agent played dual roles of trapping aluminum particles to keep them nanoscale during the alane decomposition and protecting the aluminum nanoparticles postproduction from surface oxidation and that an appropriate balance between the rate of alane decomposition (depending more sensitively on the reaction temperature) and the timing in the introduction of the passivation agent into the reaction mixture was critical to the desired product mixes and/or morphologies. Some fundamental and technical issues on the alane decomposition and the protection of the resulting aluminum nanoparticles are discussed.
引用
收藏
页码:703 / 709
页数:7
相关论文
共 36 条
[1]   Sodium alanate nanoparticles -: Linking size to hydrogen storage properties [J].
Balde, Cornelis P. ;
Hereijgers, Bart P. C. ;
Bitter, Johannes H. ;
de Jong, Krijn P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (21) :6761-6765
[2]   Facilitated hydrogen storage in NaAlH4 supported on carbon nanoribers [J].
Balde, Cornelis P. ;
Hereijgers, Bart P. C. ;
Bitter, Johannes H. ;
de Jong, Krijn P. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (21) :3501-3503
[3]  
Brousseau P, 2002, PROPELL EXPLOS PYROT, V27, P300, DOI 10.1002/1521-4087(200211)27:5<300::AID-PREP300>3.0.CO
[4]  
2-#
[5]  
CLIFF M, 2001, 37 AIAA ASME SAE ASE, P1
[6]   THE ADSORPTION AND DECOMPOSITION OF CARBOXYLIC-ACIDS ON AL(111) [J].
CROWELL, JE ;
CHEN, JG ;
YATES, JT .
JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1986, 39 (1-4) :97-106
[7]   A VIBRATIONAL STUDY OF THE ADSORPTION AND DECOMPOSITION OF FORMIC-ACID AND SURFACE FORMATE ON AL(111) [J].
CROWELL, JE ;
CHEN, JG ;
YATES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1986, 85 (05) :3111-3122
[8]  
Eckert J., 1993, Nanostructured Materials, V2, P407, DOI 10.1016/0965-9773(93)90183-C
[9]   On the mechanism of low temperature oxidation for aluminum particles down to the nano-scale [J].
Eisenreich, N ;
Fietzek, H ;
Juez-Lorenzo, MD ;
Kolarik, V ;
Koleczko, A ;
Weiser, V .
PROPELLANTS EXPLOSIVES PYROTECHNICS, 2004, 29 (03) :137-145
[10]  
Fedotova TD, 2000, PROPELL EXPLOS PYROT, V25, P325, DOI 10.1002/1521-4087(200012)25:6<325::AID-PREP325>3.0.CO