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制备方法对Cd_(0.1)Cu_(0.01)Zn_(0.89)S光催化剂产氢性能的影响 被引量:2

Study on Photocatalytic Activity for Hydrogen Evolution over Cd_(0.1)Cu_(0.01)Zn_(0.89)S Catalysts by Different Synthesis Methods
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摘要 通过共沉淀法、水热法以及高温硫化法分别合成了Cd0.1Cu0.01Zn0.89S新型光催化剂,并通过XRD、SEM和UV-vis吸收光谱等技术对催化剂进行了表征.从UV-vis吸收光谱可以发现,Cu2+的加入都引起了催化剂吸收边不同程度的红移.在产氢测试中发现,高温合成的催化剂产氢能力反而下降.在3种催化剂中,共沉淀法合成的催化剂具有最高的产氢活性,无负载时在可见光照射下产氢速率为350μmol/h,而水热法和高温硫化法合成的催化剂的产氢速率分别只有120μmol/h和13μmol/h. CdxCuyZn1-x-y S photocatalysts were prepared by coprecipitation, hydrothermal and thermal sulfidation methods. They were characterized by XRD, SEM, BET and UV-vis spectra. The UV-vis spectra showed that the absorption edge of the photocatalysts which contained Cu^2+ had a red shift compared with that of Cd0.1Zn0.9 S. It was found that the photoactivity decreased when the temperature in the preparing process increased. The photocatalyst prepared by coprecipitation method had the highest photoactivity. Its rate of hydrogen production without any cocatalysts was 350 μmol/h under visible light irradiation. Moreover, the rates of the photocatalysts prepared by hydrothermal and thermal sulfidation methods were only 120 μmol/h and 13 μmol/h, respectively.
出处 《西安交通大学学报》 EI CAS CSCD 北大核心 2008年第3期381-384,共4页 Journal of Xi'an Jiaotong University
基金 国家重点基础研究发展计划资助项目(2003CB214500) 国家自然科学基金资助项目(90610022 50521604)
关键词 光催化剂 可见光 氢气 photocatalyst visible light hydrogen
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  • 1DOMEN K, KUDO A, OHNISHI T. Mechanism of photocatalytic decomposition of water into H2 and O2 over NiO-SrTiO3[J]. J Catal, 1986, 102(1): 92-98.
  • 2KATO H, ASAKURA K, KUDO A. Highly efficient water splitting into H2 and O2 over lanthanum-doped NaTaO3 photocatalysts with high crystallinity and surface nanostructure[J]. J Am Chem Soc, 2003, 125 (10) : 3082-3089.
  • 3ZOU Zhigang, YE Jinhua, SAYAMA K, et al. Direct splitting of water under visible light irradiation with an oxide semiconductor photocatalyst[J]. Nature, 2001, 414(6864): 625-627.
  • 4HITOKI G, TAKATA T, KONDO J, et al. An oxynitride, TaON, as an efficient water oxidation photocatalyst under visible light irradiation (λ≤ 500 nm) [J]. Chem Commun, 2002(16): 1698-1699.
  • 5NIISHIRO R, KATO H, KUDO A. Nickel and either tantalum or niobium-codoped TiO2 and SrTiO3. photocatalysts with visible-light response for H2 or O2 evolution from aqueous solutions[J]. Phys Chem Chem Phys, 2005, 7(10):2241-2245.
  • 6KUDO A, SEKIZAWA M. Photocatalytic H2 evolution under visible light irradiation on Zn1-x Cux S solid solution[J]. Catal Lett, 1999, 58(4): 241-243.
  • 7KUDO A, SEKIZAWA M. Photocatalytic H2 evolution under visible light irradiation on Ni-doped ZnS [J]. Chem Commun, 2000(15): 1371-1372.
  • 8REBER J F, RUSEK M. Phtotchemical hydrogen production with platinized suspensions of cadmium sulfide and cadmium zinc sulfide modified by silver sulfide[J]. J Phys Chem, 1986, 90(5): 824-834.
  • 9YOUN H C, BARAL S, FENDLER J. Dihexadecyl phosphate, vesicle-stabilized and in situ generated mixed CdS and ZnS semiconductor particles: preparation and utilization for photosensitized charge separation and hydrogen generation[J]. J Phys Chem, 1988, 92(22) : 6320-6327.
  • 10XING Chanjuan, ZHANG Vaojun, YAN Wei, et al. Band structure-controlled solid solution of Cd1-x Znx S photocatalyst for hydrogen production by water splitting[J]. Int J Hydrogen Energy, 2006, 31(14):2018- 2024.

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