期刊文献+

光催化制氢和制氧体系中的助催化剂研究进展 被引量:4

Progress of Cocatalysts in Systems of Photocatalytic Hydrogen and Oxygen Generation
原文传递
导出
摘要 利用太阳能半导体光催化制氢和制氧,是解决化石能源短缺和环境污染问题的有效途径之一。光催化制氢和制氧体系非常复杂,助催化剂是影响催化效率的一个关键因素。本文综述了光催化产氢助催化剂、光催化产氧助催化剂、光催化产氢和产氧双助催化剂的研究进展。结合光催化原理,介绍了助催化剂的作用,即:作为产氢和产氧的活性位时,催化产氢和产氧反应、降低过电位、促进光生电子和空穴的有效分离等。并对光催化体系中助催化剂的发展提出设想,认为采用二元和多元助催化剂结合的策略,和采用非贵金属型助催化剂的策略将是未来的发展方向。 It is an efficient way to use the solar energy for photocatalytic H2 and O2 evolutions on semiconductors to resolve the problems of fossil energy shortage and environmental pollution. The photocatalytic systems of H2 and O2 evolutions are very complex and involve a series of issues in science and technology for obtaining the efficient photocatalytic systems of Ha and O2 evolutions, among which the selection of co-catalyst is a crucial one. This paper focuses on the progresses of the co-catalysts of photocatalytic H2 and O2 evolutions, analyzes and introduces the roles of cocatalysts integrating with the principle of photocatalysis. The roles of the cocatalyst as the active sites for H2 and O2 evolutions include the catalysis in the reactions of H2 and O2 evolutions, the reduction of overpotentials and the efficient separation of photo-induced electrons and holes. This paper also introduces the idea of the development of cocatalyts in the photocatalytic systems in the future. It is believed that the efficient combination of dual and multiplex cocatalysts, and the exploration of the non-noble metal cocatalyst are the direction of development in the future.
出处 《科技导报》 CAS CSCD 北大核心 2013年第28期103-106,共4页 Science & Technology Review
基金 宁夏回族自治区自然科学基金项目(NZ1110)
关键词 光催化 助催化剂 产氢 产氧 photocatalysis cocatalyst H2 evolution O2 evolution
作者简介 林克英,讲师,研究方向为光催化,电子信箱lkymbj@126.com; 马保军(通信作者),副研究员,研究方向为光催化,电子信箱:bjma@nxu.edu.cn
  • 相关文献

参考文献42

  • 1Penner S S. Steps towards the hydrogen economy[J]. Energy, 2006, 31(1): 33-43.
  • 2Turner J A. Sustainable hydrogen production [J]. Science, 2004, 305 (5686): 972-974.
  • 3Turner J A. A realizable renewable energy future[J]. Science, 1999, 285 (5428): 687-689.
  • 4Bowker M, Millard L, Greaves J, et al. Photocatalysis by Au nanoparti- cles: reforming of methanol[J]. Gold Bulletin, 2004, 37(3-4): 170-173.
  • 5Chiarello G L, Aguirre M H, Selli E. Hydrogen production by photo- catalytic steam reforming of methanol on noble metal modified TiO2[J]. Journal of Catalysis, 2010, 273(2): 182-190.
  • 6Li Z G, Wang Y X, Liu J W, et al. Photoeatalytic hydrogen production from aqueous methanol solutions under visible light over Na (BixTal~)O3 solid-solution [J]. International Journal of Hydrogen Energy, 2009, 34(1): 147-152.
  • 7Miwa T, Kaneco S, Katsumata H, et al. Photocatalytic hydrogen produc- tion from aqueous methanol solution with CuO/Al2O3/TiO2 nanocomposite [J]. International Journal of Hydrogen Energy 2010, 35(13): 6554-6560.
  • 8A1-Mazroai L S, Bowker M, Davies P, et al. The photocatalytic reforming of methanol[J]. Catalysis Today, 2007, 122(1): 46-50.
  • 9Wu G P, Chen T, Zong X, et al. Suppressing CO formation by anion ad- sorption and Pt deposition on TiO2 in H2 production from photocatalytic reforming of methanol[J]. Journal of Catalysis, 2008, 253(1): 225-227.
  • 10Reece S Y, Hamel J A, Sung K, et al. Wireless solar water splitting us- ing silicon-based semiconductors and earth-abundant catalysts [J]. Sci- ence, 2011, 334(6056): 645-648.

二级参考文献9

  • 1V Balzani, A Credi, M Venturi. ChemSusChem, 2008, 1(1 -2): 26-58.
  • 2T JMeyer. Ace. Chem. Res., 1989, 22(3):163 -170.
  • 3T Sanada, K Yamamoto, N Wada et al. Thin Solid Films, 2006, 496(1) : 169 - 173.
  • 4J Sato, H kobayashi, K Ikarashi et al. J. Phys. Chem. B, 2004,108(14) : 4369 -4375.
  • 5J Sato, N Saito, Y Yamada et al. J. Am. Chem. Soc. , 2005, 127(12) : 4150 -4151.
  • 6Y Lee, H Terashima, Y Shimodairaet al. J. Phys. Chem. C, 2007, 111(2):1042-1048.
  • 7W J Chun, A Ishikawa, H Fujisawa et al. J. Phys. Chem. B, 2003, 107(8) : 1798 -1803.
  • 8N D McDaniel, F G Coughlin, L L Tinker et al. J. Am. Chem. Soc. , 2008, 130(1) : 210 -217.
  • 9M W Kanan, D G Nocera. Science, 2008, 321 : 1072 - 1075.

同被引文献18

引证文献4

二级引证文献19

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