Enhanced photoelectrochemical water splitting coupled with pharmaceutical pollutants degradation on Zr:BiVO4 photoanodes by synergetic catalytic activity of NiFeOOH nanostructures

Prabhakarn Arunachalam, Maged N. Shaddad, Mabrook S. Amer, Abdulhadi AL-Qadi

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Globally, the emergence of drug-resistant bacteria has created an urgent need for an effective method to remove antibiotics from pharmaceutical wastewater. Engineering Bismuth vanadate (BiVO4) with an oxygen evolution cocatalyst (OEC) holds a promising potential for enhancing water splitting efficiency in the production of hydrogen (H2) using free solar energy. Here, we successfully developed a Zr:BiVO4/NiFeOOH heterojunction by electrodeposition and photoelectrochemical transformation. Zr:BiVO4/NiFeOOH photoanodes exhibit 5 fold superior photocurrent response at 1.23 V compared with Zr:BiVO4 electrodes, since NiFeOOH acts as an oxygen-releasing catalyst. Furthermore, the attained heterojunctioned electrode can effectively degrade TCH, riboflavin, and streptomycin in PEC. The degradation rate of TCH acquired 96% within 1 h, which is 3 times superior than the efficiency reported for pristine Zr:BiVO4 photoelectrodes. By introducing NiFeOOH into BiVO4, electron life-time was increased and electron-hole recombination was suppressed. In this study, we present a solar-driven, sustainable and effective way of treating wastewater and provide new insights into the process.

Original languageEnglish
Pages (from-to)64-75
Number of pages12
JournalAlexandria Engineering Journal
Volume99
DOIs
StatePublished - Jul 2024

Keywords

  • BiVO
  • Electrodepostiion
  • Nickel Iron oxy hydroxide
  • Photoelectro transformation
  • Photoelectrocatalysis
  • Tetracylcine

Fingerprint

Dive into the research topics of 'Enhanced photoelectrochemical water splitting coupled with pharmaceutical pollutants degradation on Zr:BiVO4 photoanodes by synergetic catalytic activity of NiFeOOH nanostructures'. Together they form a unique fingerprint.

Cite this