Spatial separation of oxidation and reduction co-catalysts for efficient charge separation: Pt@TiO2@MnOx hollow spheres for photocatalytic reactions† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc04163e Click here for additional data file.

نویسندگان

  • Ang Li
  • Tuo Wang
  • Xiaoxia Chang
  • Weiting Cai
  • Peng Zhang
  • Jijie Zhang
  • Jinlong Gong
چکیده

Efficient charge separation is a critical factor for solar energy conversion by heterogeneous photocatalysts. This paper describes the complete spatial separation of oxidation and reduction cocatalysts to enhance the efficacy of charge separation and surface reaction. Specifically, we design Pt@TiO2@MnOx hollow spheres (PTM-HSs) with Pt and MnOx loaded onto the inner and outer surface of TiO2 shells, respectively. Pt favours electron trapping, while MnOx tends to collect holes. Upon generation from TiO2, electrons and holes flow inward and outward of the spherical photocatalyst, accumulating on the corresponding cocatalysts, and then take part in redox reactions. Combined with other advantages, such as the large surface area and appropriate pore size, the PTM-HSs exhibit high efficiency for the photocatalytic oxidation of water and benzyl alcohol. The mechanism of the oxidation process of benzyl alcohol over the photocatalyst is also presented.

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Spatial separation of oxidation and reduction co-catalysts for efficient charge separation: Pt@TiO2@MnO x hollow spheres for photocatalytic reactions.

Efficient charge separation is a critical factor for solar energy conversion by heterogeneous photocatalysts. This paper describes the complete spatial separation of oxidation and reduction cocatalysts to enhance the efficacy of charge separation and surface reaction. Specifically, we design Pt@TiO2@MnO x hollow spheres (PTM-HSs) with Pt and MnO x loaded onto the inner and outer surface of TiO2...

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Distance dependent charge separation and recombination in semiconductor/molecular catalyst systems for water splitting† †Electronic supplementary information (ESI) available: Experimental details, DFT calculations and additional transient absorption measurements. See DOI: 10.1039/c4cc05143b Click here for additional data file.

The photoinduced reduction of three Co electrocatalysts immobilised on TiO2 is 10(4) times faster than the reverse charge recombination. Both processes show an exponential dependence on the distance between the semiconductor and the catalytic core.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016