欢迎登录材料期刊网

材料期刊网

高级检索

用化学方法制备了负载金的纳米管钛酸(Au/H2Ti2O4(OH)2)光催化剂,并用TEM,XPS,XRD和DRS等技术对催化剂进行了表征. 结果表明,经573 K处理后,纳米管钛酸表面及管内均有零价的金颗粒存在. 与纳米管钛酸(H2Ti2O4(OH)2)相比,Au/H2Ti2O4(OH)2具有明显的CO光催化氧化活性,但在暗态时无活性. 经分析认为,暗态时Au与纳米管相互接触的周界处不活泼,故催化剂无CO催化氧化活性; 紫外光照射下,纳米管激发产生e--h+对,e-从纳米管转移到Au0上, 使纳米管和Au-在接触周界处产生相互作用,形成活性位,导致CO催化氧化反应发生.

参考文献

[1] Haruta M .[J].Catalysis Today,1997,36(01):153.
[2] Haruta M;Yamada N;Kobayashi T;Iijima S .[J].Journal of Catalysis,1989,115(02):301.
[3] Valden M;Lai X;Goodman D W .[J].科学(上海),1998,281(5383):1647.
[4] Valden M.;Lai X.;Goodman DW.;Pak S. .Structure sensitivity of CO oxidation over model Au/TiO2 catalysts[J].Catalysis Letters,1998(1):7-10.
[5] Arrii S;Morfin F;Renouprez A J;Rousset J L .[J].Journal of the American Chemical Society,2004,126(04):1199.
[6] Yang J J;Jin Zh Sh;Wang X D;Li W,Zhang J W,Zhang Sh L,Guo X Y,Zhang Zh J.[J].Dalton Transactions,2003(20):3898.
[7] Zhang M;Jin Zh Sh;Zhang J W;Guo X Y, Yang J J, Li W, Wang X D, Zhang Zh J .[J].Journal of Molecular Catalysis A:Chemical,2004,217(1/2):203.
[8] Qian L;Jin Z S;Zhang J W .[J].Applied Physics A:Materials Science and Processing,2005,80(08):1801.
[9] Wagner C D;Riggs W M;Davis L E;Moulder J F.Handbook of X-Ray Photoelectron Spectroscopy[M].Eden Prairie(MN): Perkin-Elmer Corporation, Physical Electronics Division,1979:154.
[10] Ertl G.[A].Boca Raton (FL):CRC Press,1982:19.
[11] 张敏,金振声,王守斌,张顺利,张治军.在Pd/TiO2上CO的光催化增强效应[J].物理化学学报,2003(02):100-104.
[12] Mills G.;Gordon MS.;Metiu H. .The adsorption of molecular oxygen on neutral and negative Au-n clusters (n=2-5)[J].Chemical Physics Letters,2002(5-6):493-499.
[13] Salisbury B E;Wallace W T;Whetten R L .[J].Chemical Physics,2000,262(01):131.
[14] Okumura M.;Haruta M.;Yamaguchi K.;Kitagawa Y. .DFT studies of interaction between O-2 and Au clusters. The role of anionic surface Au atoms on Au clusters for catalyzed oxygenation[J].Chemical Physics Letters,2001(1/2):163-168.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%