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焙烧室温条件固相反应制备前驱物合成SnO2纳米棒的研究(英文) 被引量:2

Synthesis of SnO_2 nanorods via annealing precursor produced bysolid-state reaction at roomtemperature
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摘要 室温条件下通过固相反应合成了SnO2纳米颗粒前驱物.在600~780℃对前驱物进行焙烧,在NaCl、KCl和KCl+NaCl的熔盐介质中SnO2前驱物纳米颗粒自组装生长形成SnO2 纳米棒.利用TEM、XRD和XPS对SnO2纳米棒结构、形貌和成分进行了研究.结果表明SnO2纳米棒直径为20~80nm,长度从几百纳米到十几微米.分析了SnO2 纳米颗粒前驱体熔盐介质中的生长,利用固相转变生长可以解释SnO2纳米棒在熔盐介质中的生长机制. SnO2 nanorods were prepared via annealing precursor powders produced by solid- state reaction at room temperature. The precursor grows into SnO2 nanorods via self assembly annealing at 600~780℃ in NaCl,KCl and KCl+NaCl flux medium respectively. The structure and morpho1ogy of SnO2 nanorods were studied by means of X-ray diffraction (XRD),transmission electron microscopy (TEM) and X-ray photoelectron spectrum (XPS). The results show that diameter and length of the as-made nanorods are in the range of 20nm to 80nm and several micrometers respectively.The solid-state transformation explains the formation mechanism of SnO2 nanorods.
出处 《功能材料》 EI CAS CSCD 北大核心 2005年第10期1634-1637,1644,共5页 Journal of Functional Materials
基金 Thisworkwasfinanciallysupportedbythe"863"FoundationofChina(2002AA327090) NaturalScienceFoundationofEducationDepartmentofYunnanprovince(04Z205A) NaturalScienceFoundationofYunnanUniversity(2003Q003A)
关键词 固相反应 SNO2 纳米棒 熔盐介质 固相转变 solid state reaction SnO2 nanorods flux medium solid-state transformation
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  • 1Hu J, Odom T W, Lieber C M.[J]. Acc Chem Res, 1999, 32: 435.
  • 2Seeger T, Redlich P, Ruhle M.[J]. Adv Mater, 2000, 12:279.
  • 3Zang Y, Suenaga K, Colliex C, et al. [J].Science, 1998, 281:937.
  • 4Martin C R. [J].Science, 1994, 266:1961.
  • 5Martin B, Dermody D J, Reiss B D,et al. [J].Adv Mater, 1999, 11:1021.
  • 6Li Y, Ding Y, Wang Z. [J].Adv Mater, 1999, 11: 847.
  • 7Holmes J D, Johnston K P, Doty R C,et al. [J].Science, 2000, 287:1471.
  • 8Givargizov E I. [J].J Crystal Growth, 1975, 32: 20.
  • 9Morales A M, et al. [J].Science, 1998, 279:208.
  • 10Han W, Fan S, Li Q,et al.[J]. Science, 2000, 277:1287.

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