TY - JOUR
T1 - Enhanced photoelectrochemical water splitting coupled with pharmaceutical pollutants degradation on Zr:BiVO4 photoanodes by synergetic catalytic activity of NiFeOOH nanostructures
AU - Arunachalam, Prabhakarn
AU - Shaddad, Maged N.
AU - Amer, Mabrook S.
AU - AL-Qadi, Abdulhadi
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/7
Y1 - 2024/7
N2 - 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.
AB - 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.
KW - BiVO
KW - Electrodepostiion
KW - Nickel Iron oxy hydroxide
KW - Photoelectro transformation
KW - Photoelectrocatalysis
KW - Tetracylcine
UR - http://www.scopus.com/inward/record.url?scp=85192484594&partnerID=8YFLogxK
U2 - 10.1016/j.aej.2024.05.012
DO - 10.1016/j.aej.2024.05.012
M3 - Article
AN - SCOPUS:85192484594
SN - 1110-0168
VL - 99
SP - 64
EP - 75
JO - Alexandria Engineering Journal
JF - Alexandria Engineering Journal
ER -