4.7 Article

Metalloporphyrin-Decorated Titanium Dioxide Nanosheets for Efficient Photocatalytic Carbon Dioxide Reduction

Journal

INORGANIC CHEMISTRY
Volume 60, Issue 23, Pages 18337-18346

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c02957

Keywords

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Funding

  1. Fundamental Research Funds for the Jiangsu Province Universities [20KJB430037]
  2. Fundamental Research Funds for the Central Universities [FRF-IDRY-20-004]

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The study focused on fabricating MTCPP/TiO2 composite materials using a self-assembly method to improve the efficiency of photocatalytic reactions. By regulating the electron density of the porphyrin ring with metal ions, the charge separation process was optimized to enhance the overall performance.
In photocatalysis, the most efficient way to separate photogenerated electron-hole pairs has been extensively studied. However, the methods to increase the quantities of free electrons are neglected. Herein, we used a self-assembly method to fabricate MTCPP/TiO2 composite materials with a series of metalloporphyrins (MTCPPs, M = Fe, Co, Zn) as sensitizers to modify TiO2 nanosheets. First, abundant carboxyl and hydroxyl on porphyrin were adsorbed by metal ions. Then, the remaining carboxyl and hydroxyl on porphyrin were anchored on the surface of TiO2 nanosheets. Finally, MTCPP/TiO2 was obtained by a layer-by-layer self-assembly process. MTCPP broadens the light response of TiO2 from ultraviolet light to visible light and enhances the CO2 adsorption ability. Moreover, metal ions coordinating with porphyrin regulate the electron density of the porphyrin ring and provide a stronger pi feedback bond, which promote charge separation. Consequently, by optimizing the type of metal ion, the yield of ZnTCPP/TiO2 composites reached 109.33 mu mol/(g h) of CO and 9.94 mu mol/(g h) of CH4, which was more than 50 times that of pure TiO2. This study proposes a possible visible-light-induced CO2 reduction mechanism of metal-ion-based photocatalysis, which provides great insights into optimizing the designation of efficient photocatalysis.

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