4.6 Article

Metal-Organic Framework Photosensitized TiO2 Co-catalyst: A Facile Strategy to Achieve a High Efficiency Photocatalytic System

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 23, Issue 16, Pages 3931-3937

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201605282

Keywords

charge transfer; mechanical mixing; metal-organic frameworks; photocatalysis; sensitization

Funding

  1. National Natural Science Foundation of China [21301149, 21401160, 11474246]
  2. research fund of Jiangsu Collaborative Innovation Center for Ecological Building Materials and Environmental Protection Equipments [GX2015104, CP201502]
  3. Talent Project of Yancheng Institute of Technology [KJC 2013001, KJC2014034]
  4. Program for the Outstanding Young Talents of Yancheng Institute
  5. Qing Lan Project
  6. Natural Science Foundation of Jiangsu Province [BK20160061]
  7. College Natural Science Research Project of Jiangsu Province [13KJ430007]

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A 3D metal-organic framework (ADA-Cd=[Cd2L2(DMF)(2)]3H(2)O where H2L is (2E,2E)-3,3-(anthracene-9,10-diyl)diacrylic acid) constructed from diacrylate substituted anthracene, sharing structural characteristics with some frequently employed anthraquinone-type dye sensitizers, was introduced as an effective sensitizer for anatase TiO2 to achieve enhanced visible light photocatalytic performance. A facile mechanical mixing procedure was adopted to prepare the co-catalyst denoted as ADA-Cd/TiO2, which showed enhanced photodegradation ability, as well as sustainability, towards several dyes under visible light irradiation. Mechanistic studies revealed that ADA-Cd acted as the antenna to harvest visible light energy, generating excited electrons, which were injected to the conduction band (CB) of TiO2, facilitating the separation efficiency of charge carriers. As suggested by the results of control experiments, combined with the corresponding redox potential of possible oxidative species, O-.(2)-, generated from the oxygen of ambient air at the CB of TiO2 was believed to play a dominant role over (OH)-O-. and h(+). UV/Vis and photoluminescence technologies were adopted to monitor the generation of O-.(2)- and (OH)-O-., respectively. This work presents a facile strategy to achieve a visible light photocatalyst with enhanced catalytic activity and sustainability; the simplicity, efficiency, and stability of this strategy may provide a promising way to achieve environmental remediation.

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