Affiliations 

  • 1 Center for Frontier Materials Research, School of Materials Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis, Malaysia
  • 2 Center for Frontier Materials Research, School of Materials Engineering, Universiti Malaysia Perlis, 02600, Arau, Perlis, Malaysia. Electronic address: [email protected]
  • 3 Water Research Group (WAREG), School of Environmental Engineering, Universiti Malaysia, Perlis, 02600, Arau, Perlis, Malaysia
Chemosphere, 2019 Jan;214:614-622.
PMID: 30292044 DOI: 10.1016/j.chemosphere.2018.09.144

Abstract

The hybrid system of photocatalytic fuel cell - peroxi-coagulation (PFC-PC) is a sustainable and green technology to degrade organic pollutants and generate electricity simultaneously. In this study, three different types of photocatalysts: TiO2, ZnO and α-Fe2O3 were immobilized respectively on carbon cloth (CC), and applied as photoanodes in the photocatalytic fuel cell of this hybrid system. Photocatalytic fuel cell was employed to drive a peroxi-coagulation process by generating the external voltage accompanying with degrading organic pollutants under UV light irradiation. The degradation efficiency of Amaranth dye and power output in the hybrid system of PFC-PC were evaluated by applying different photoanode materials fabricated in this study. In addition, the effect of light on the photocurrent of three different photoanode materials was investigated. In the absence of light, the reduction of photocurrent percentage was found to be 69.7%, 17.3% and 93.2% in TiO2/CC, ZnO/CC and α-Fe2O3/CC photoanodes, respectively. A maximum power density (1.17 mWcm-2) and degradation of dye (93.8%) at PFC reactor were achieved by using ZnO/CC as photoanode. However, the different photoanode materials at PFC showed insignificant difference in dye degradation trend in the PC reactor. Meanwhile, the degradation trend of Amaranth at PFC reactor was influenced by the recombination rate, electron mobility and band gap energy of photocatalyst among different photoanode materials.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.