A Unique Platinum/Titania/Polymer Based Hybrid Organic-Inorganic Heterostructure for Enhanced Photocatalytic Activity

Author:

Ragsdale William1,Zanette Rikelli1,Electo Ana Paula1,Subramanian Vaidyanathan R.1ORCID,Gupta Satyajit2ORCID

Affiliation:

1. Chemical and Materials Engineering Department, University of Nevada, Reno, Reno– NV, 89557, United States

2. Department of Chemistry, Indian Institute of Technology, Bhilai, GEC Campus, Sejbahar, Old Dhamtari Rd., Chhattisgarh 492015, India

Abstract

This work delineates synthesis, characterization, and photocatalytic activity of a ‘hybrid organic-inorganic’ catalyst system, that consists of titanium dioxide (TiO<sub>2</sub>), platinum (Pt) and a conductive polymer (polypyrrole). The nanocomposite photocatalyst was developed to enhance exciton separation in the large band-gap oxide semiconductor (TiO<sub>2</sub>) by depositing a noble metal co-catalyst (Pt) at the surface. The hybrid nanocomposite was constructed through sequential sequestration of the building blocks i.e., the monomer (pyrrole) and the metal (Pt) salt, using a photo-deposition technique. At the same time, improvement for light absorbance as compared to pristine TiO<sub>2</sub> was realized through the deposition of a conducting polymer (polypyrrole) at the surface of the semiconductor. The polypyrrole provides a pathway for hole migration, thereby increasing the overall lifetime of the separated charges. The benefit of this architecture is demonstrated through an enhanced degradation (~40% increase) of an industrial dye, methyl orange as a representative example, under visible-light illumination compared to unmodified TiO<sub>2</sub>. Furthermore, photo(electro)chemical analysis of the composite offered valuable insights into the charge transport mechanism. It led to the conclusion that photo illumination results in the participating components to (a) enable visible light absorbance and, (b) facilitate charge separation and utilization at the hetero-interfaces leading to redox activity. Insights into the mechanism of charge separation and transport from chronopotentiometric analysis suggest that the assembly is successful and works as desired.

Funder

National Science Foundation

Publisher

Bentham Science Publishers Ltd.

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