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离子掺杂与载体类型交互效应对纳米TiO_2薄膜光活性改性研究 被引量:2

The Research on Interaction Effect between Ion-doped and Substrates on the Photocatalytic Activity of Nanometer TiO_(2) thin Film
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摘要 采用溶胶-凝胶法在六种不同基体材料上制备了掺杂La3+的TiO2纳米复合材料.利用扫描电子显微镜(SEM),x射线衍射(XRD)及紫外-可见吸收光谱对其TiO2薄膜的TiO2颗粒形态和相组成进行了详细研究,并以甲基橙为模拟对象,研究了不同浓度的La3+掺杂对催化剂光活性的影响,结果表明:脱色率(η%)随载体、掺杂浓度不同而变.不锈钢载体掺杂浓度为0.604×1021/cm3La3+的二氧化钛薄膜对甲基橙有最高的降解效率,陶瓷载体掺杂0.604×1017/cm3La3+的降解效率最高,玻璃载体最佳La3+掺杂浓度为6.04×1017/cm3,而钛片载体最佳La3+掺杂浓度为0.604×1023/cm3. Nanometer TiO2 composite materials doped La^3+ , which deposited on the surface of six kinds of substrates , were prepared by Sol-Gel method. A thorough study on the morphology and phase composition of TiO2 film were conducted through scanning electron microcopy , X-ray diffraction and ultraviolet-visual absorption spectrum. Meanwhile, the effects of the La^3+ concentration of various levels on the activity of the TiO2 catalysts were studied with methyl orange as the simulation object. The results showed that the degradation rate(η% ) is dependent with the doping concentration and substrates. When the optimum concentration of La^3+ is 0. 604 × 10^21 La^3+/cm^3 on Stainless steel substrates, 0. 604 ×10^17/cm^3 on the the degradation rate of the TiO2 ceramic, 6.04 ×10^17/cm^3 on film is the largest, but the optimum concentration is glass and 0. 604 × 10^23/cm^3 on the Titanium slices respectively.
出处 《分子催化》 EI CAS CSCD 北大核心 2006年第1期62-66,共5页 Journal of Molecular Catalysis(China)
基金 黑龙江科技学院青年科学基金项目(04-29)
关键词 镧掺杂 二氧化钛薄膜 载体 光催化活性 Doped- La^3+ Nanometer TiO2 thin films Substrates Photocatalytic activity
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参考文献14

  • 1Fujishima A,Honda K,Kikuchi S.Kogyo Kagaku Zasshi[J],1969,72:108 ~ 113.
  • 2Jaegermann W.Mod.Asp.Electro.[J],Plenum Press,New York,1996,30:1 ~ 185.
  • 3Peter L M.Appl.Kinetic Mod.[J],Elsevier,Amsterdam,1999,37:223~279.
  • 4Khaselev O,Turner J A.Science[J],1998,280:425 ~427.
  • 5ChenFei-li(陈非力) WangLiang-yi(王良焱) YangBaoShan(杨宝山) etal.太阳能学报,1994,20(4):471-474.
  • 6JiangWei-chuan(蒋伟川) TanXian-Ping(谭湘萍) etal.环境科学,1995,16(2).
  • 7于向阳,程继健.铁、铬离子掺杂对TiO_2薄膜光催化活性的影响[J].无机材料学报,2001,16(4):742-746. 被引量:47
  • 8PengXiao-chun(彭晓春) ChenXin-geng(陈新庚) etal.环境污染治理技术与设备,2002,(3).
  • 9Andrew Mills,Sian Morris.J.Photochem.Photobiol.[J],A:Chemistry,1993,71:285~289.
  • 10Choi W,et al.J.Phys.Chem.[J],1994,98(51):13669~13679.

二级参考文献26

  • 1FUJISHIMA A, HONDA K. Electrochemical photolysis of water at a semicoductor electrode[J]. Nature, 1972,238: 37-38.
  • 2HOFFMANN M R, MARTIN S T, CHOI W, et al. Environmental applications of semiconductor photocatalysis[ J ].Chemical Review, 1995, 95(1): 69-85.
  • 3ASAHI R, MORIKAWA T, OHWAKI T, et al. Visible- light photocatalysis in nitrogen- doped titanium oxides[J]. Science, 2000, 293: 269-271.
  • 4SHAHED U M K, MOFAREH A, WILLIAM B, et al. Efficient photochemical water splitting by a chemically modified n-TiO2[J]. Science, 2002, 297: 2243-2245.
  • 5AMAL K G, PAUL M H. Photoelectrolysis of water in sunlight with sensitized semiconductor electrode[J]. Journal of Electrochem Society: Electrochem Science and Technology, 1977, 124(10): 1516-1522.
  • 6CHOI W, TERMIN A, HOFFMANN M R. The role of metal ion dopants n quantum- sized TiO2: correlation beween photoreactivity and charger carrier recombination dynamics[J]. Journal of Physical Chemistry, 1994, 98(51): 13669- 13679.
  • 7TOSHIAKI O, FUJIO I, YOSHINORI F. Raman spectrum of anatase TiO2 [ J]. Journal of Raman Spectroscopy ,1978, 7(6) : 321 - 324.
  • 8CAFWELL R J, SPAGNOLD F, DESESA M A. A Rapid Determination of low Concentrations of Anatase in Rutile TiO2 Pigments by Raman Spectroscopy[J]. Applied Spectroscopy, 1972, 26(5) : 537 - 539.
  • 9MA Y, QIU J B, CAO Y A, et al. Photocatlaytic Activity of TiO2 films grown on different substrates[J]. Chemosphere, 2001, 44: 1087-1092.
  • 10EDELSON L H, GLAESER A M. Role of particle substructure in the sintering of monosized titania [ J]. Journal of Amercan Ceramic Society, 1988, 71: 225235.

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