期刊文献+

矿化剂浓度对水热法合成氧化锌晶体的影响 被引量:2

Effect of Mineralizer Concetration on ZnO Crystals Synthesized by Hydrothermal Method
下载PDF
导出
摘要 In this paper different shapes of ZnO crystals were synthesized by hydrotherma l method when different concentrations of mineralizer were used. When KOH was le ss than 2mol·L-1 and the fill factor was approximately 35%at 350℃, ZnO cryst als were synthesized with size of several hundred nanometer or several micron. T he shapes of crystals were hexagonal cones. When 3mol·L-1 KOH was used as mine ralize at 350℃and the fill factor was approximately 35%, the crystals with man y different sizes were synthesized, the size of maximal crystal was over 100 mic ron, the small-size crystals were only several micron. When mineralizer KOH was less than 1mol·L-1 and the fill factor was approximately 35%at 430℃, ZnO cr ystals were synthesized with size of several hundred nanometer or several micron . The shapes of crystals were hexagonal cones. When 1.5mol·L-1 KOH or 2mol·L -1 KOH was used as mineralize at 430℃and the fill factor was approximately 35 %, the high quality and hexagonal prism crystals were synthesized with many dif ferent sizes, the size of maximal crystal was over 100 micron, the small-size c rystal was only several micron. Especially when 3mol·L-1 KOH was used as miner alize at 430℃and the fill factor was approximately 35%, the high quality and h exagonal prism crystals were synthesized <IMG SRC="IMAGE/09150023.JPG" HEIGHT=11 WIDTH=23><IMG SRC="IMAGE/09150024.JPG" HEIGHT=11 WIDTH=23><IMG SRC="IMAGE/09150 025.JPG" HEIGHT=11 WIDTH=23><IMG SRC="IMAGE/09150026.JPG" HEIGHT=11 WIDTH=23><IM G SRC="IMAGE/09150027.JPG" HEIGHT=11 WIDTH=23>with size of 1mm along c axis. The exposed faces were hexagonal faces m{}, hexagonal cone faces p{}, negative pola r faces O{}. In addition, many crystals with the shape of hexagonal cone and in several micron to 50 μm of size were present. The exposed faces were hexagonal cone faces p{}, negative polar faces {}. In this paper different shapes of ZnO crystals were synthesized by hydrothermal method when different concentrations of mineralizer were used. When KOH was less than 2mol . L-1 and the fill factor was approximately 35% at 350degreesC, ZnO crystals were synthesized with size of several hundred nanometer or several micron. The shapes of crystals were hexagonal cones. When 3mol . L-1 KOH was used as mineralize at 350degreesC and the fill factor was approximately 35%, the crystals with many different sizes were synthesized, the size of maximal crystal was over 100 micron, the small-size crystals were only several micron. When mineralizer KOH was less than 1 mol . L-1 and the fill factor was approximately 35% at 430degreesC, ZnO crystals were synthesized with size of several hundred nanometer or several micron. The shapes of crystals were hexagonal cones. When 1. 5mol . L-1 KOH or 2mol L-1 KOH was used as mineralize at 430degreesC and the fill factor was approximately 35%, the high quality and hexagonal prism crystals were synthesized with many different sizes, the size of maximal crystal was over 100 micron, the small-size crystal was only several micron. Especially when 3mol . L-1 KOH was used as mineralize at 430degreesC and the fill factor was approximately 35%, the high quality and hexagonal prism crystals were synthesized with size of 1 mm along c axis. The exposed faces were hexagonal faces m{10(1) over bar 0}, hexagonal cone faces p{10(1) over bar 1}, negative polar faces O{000(1) over bar}. In addition, many crystals with the shape of hexagonal cone and in several micron to 50 mum of size were present. The exposed faces were hexagonal cone faces p{10(1) over bar 1}, negative polar faces {000(1) over bar}.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2003年第9期950-954,共5页 Chinese Journal of Inorganic Chemistry
基金 河北省自然科学基金资助项目(No.502123) 河北省科技攻关项目(No.2212204) 河北省教育厅资助项目(No.2002158)。
关键词 矿化剂浓度 氧化锌晶体 水热法合成 晶体生长 晶体形态 ZnO hydrothermal synthesis mineralize crystal shape
  • 相关文献

参考文献17

  • 1Bagnall D. M., Chen Y. F., Zhu Z. et al Appl. Phys. Lett.,1997, 70(17), 2230.
  • 2Tang Z. K., Wang G. K. L., Yu P. Appl. Phys. Lett., 1998,72(25), 3270.
  • 3Bagnall D. M., Chen Y. F., Zhu Z. et al Appl. Phys. Lett.,1998, 73(8), 1038.
  • 4GUO Chang-Xin(郭常新),FU Zhu-Xi(傅竹西),SHI Chao -Shu(施潮书)Faguang Xuebao(Chinese Journal of Luminescence),1998,19(3),293.
  • 5LU Shu-Chen(吕树臣),SONGGuo-Li(宋国利),XIAO Zhi -Yan(肖芝燕)Faguang Xuebao(Chinese Journal of Luminescence),2002,23(3),306.
  • 6Garces N. Y., Wang L., Bai L. et al Appl. Phys. Lett.,2002, 18(4), 622.
  • 7JING Li-Qiang(井立强), SUN Xiao-Jun(孙晓军), XU ZiLi(徐自力) et al Cuihua Xuebao( Chinese J. of Catalysis),2002, 23 ( 1 ), 37.
  • 8JING Li-Qiang(井立强),ZHENG Ying-Guang(郑莹光),XU Zi-Li(徐自力)et al Gaodeng Xuexiao Huaxue Xuebao (Chemical J of Chinese Universities),2001,22(11),1885.
  • 9DING Shi-Wen(丁士文),ZHANG Shao-Yan(张绍岩),LIU Shu-Juan(刘淑娟),DING Yu(丁宇)et al Wuji Huaxue Xuebao(Chinese J. of Inorganic Chemistry),2002,18(10),1015.
  • 10LI Dan-Zhen(李旦振),CHEN Yi-Lin(陈亦琳),LIN Xi(林熙),WANG Xu-Xu(王绪绪),FU Xian-Zhi(傅贤智)Wuji Huaxue Xuebao(Chinese J of Inorganic Chemistry),2002,18(12),1229.

同被引文献33

引证文献2

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部