Advances in Dye Degradation

Volume: 2

UV, Visible, and Near-Infrared Responsive Photocatalyst for Dye Degradation

Author(s): Natarajan Prakash*, Subramanian Balachandran, Muhammad Y. Bashouti, Mukkanan Arivananthan and Yasuhiro Hayakawa

Pp: 54-76 (23)

DOI: 10.2174/9789815238150124020006

* (Excluding Mailing and Handling)

Abstract

 Environmental contamination has long been a big problem for the planet. One of the greatest ways to harness the massive amounts of sunshine available is photocatalysis, which may be used to remove dangerous organic pollutants from water and the air. Due to its large band gap (3.2 eV), the golden standard TiO2 catalyst only uses the UV area of the sun, or 5% of it, and cannot absorb all of the solar energy. To attain optimal photocatalytic effectiveness, the photocatalytic materials must efficiently harvest photons from sunlight's visible, NIR, and ultraviolet energies to form photocarriers. Several methods for efficiently forming and separating light-induced charge carriers and absorbing visible and near-infrared light photons from sunlight are compiled in this chapter to provide increased photocatalytic efficiency. Effective tactics, including doping and the fabrication of composite materials, are highlighted to emphasize the distinct physicochemical qualities and photocatalytic enhancement of changed materials that are impacted by band alignment, shape, and defect structures. Despite the discussion of an up-conversion method for NIR light absorption, multiphoton emission, continuous luminescence, photo carrier multiplication, and/or plasmonic processes, in addition to the control of photo-thermo effects, make it difficult to use NIR effectively. To fully use the solar spectrum for enhanced photocatalytic pollutant degradation, the chapter provides an overview of UV, Visible, and/or NIR active catalytic materials based on design, synthesis, and interface engineering.


Keywords: Dye degradation, NIR photocatalyst, Plasmonic nanoparticle, Visible photocatalyst, Z – scheme composites.

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