TY - JOUR
T1 - Photoelectrocatalytic Surfactant Pollutant Degradation and Simultaneous Green Hydrogen Generation
AU - Davies, Katherine Rebecca
AU - Allan, Michael G.
AU - Nagarajan, Sanjay
AU - Townsend, Rachel
AU - Asokan, Vijayshankar
AU - Watson, Trystan
AU - Godfrey, A. Ruth
AU - Maroto-Valer, M. Mercedes
AU - Kuehnel, Moritz F.
AU - Pitchaimuthu, Sudhagar
N1 - Funding Information:
S.P. acknowledges European Regional Development Fund for providing Ser Cymru-II Rising Star Fellowship through Welsh Government (80761-SU-102-West) and supports this work. Also, S.P. thanks Heriot-Watt University for start-up grant support. S.P. and M.F.K. acknowledge support from the Welsh Government (Sêr Cymru III – Tackling Covid-19, Project 076 ReCoVir). EPSRC partially supported this work through a DTA studentship to M.A. (EP/R51312 X/1) and a capital investment grant to M.K. (EP/S017925/1). M.F.K. thanks Swansea University for providing start-up funds.
Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/11/15
Y1 - 2023/11/15
N2 - For the first time, we demonstrate a photoelectrocatalysis technique for simultaneous surfactant pollutant degradation and green hydrogen generation using mesoporous WO3/BiVO4 photoanode under simulated sunlight irradiation. The materials properties such as morphology, crystallite structure, chemical environment, optical absorbance, and bandgap energy of the WO3/BiVO4 films are examined and discussed. We have tested the anionic type (sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants (benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants. A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min, respectively, by applying 1.75 V applied potential vs RHE to the circuit, under 1 sun was achieved. An interesting competitive phenomenon for photohole utilization was observed between surfactants and adsorbed water. This led to the formation of H2O2 from water alongside surfactant degradation (anode) and hydrogen evolution (cathode). No byproducts were observed after the direct photohole mediated degradation of surfactants, implying its advantage over other AOPs and biological processes. In the cathode compartment, 82.51 μmol/cm2 and 71.81 μmol/cm2 of hydrogen gas were generated during the BAC-C12 and S2NS surfactant degradation process, respectively, at 1.75 V RHE applied potential.
AB - For the first time, we demonstrate a photoelectrocatalysis technique for simultaneous surfactant pollutant degradation and green hydrogen generation using mesoporous WO3/BiVO4 photoanode under simulated sunlight irradiation. The materials properties such as morphology, crystallite structure, chemical environment, optical absorbance, and bandgap energy of the WO3/BiVO4 films are examined and discussed. We have tested the anionic type (sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants (benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants. A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min, respectively, by applying 1.75 V applied potential vs RHE to the circuit, under 1 sun was achieved. An interesting competitive phenomenon for photohole utilization was observed between surfactants and adsorbed water. This led to the formation of H2O2 from water alongside surfactant degradation (anode) and hydrogen evolution (cathode). No byproducts were observed after the direct photohole mediated degradation of surfactants, implying its advantage over other AOPs and biological processes. In the cathode compartment, 82.51 μmol/cm2 and 71.81 μmol/cm2 of hydrogen gas were generated during the BAC-C12 and S2NS surfactant degradation process, respectively, at 1.75 V RHE applied potential.
KW - Industrial and Manufacturing Engineering
KW - General Chemical Engineering
KW - General Chemistry
UR - http://www.scopus.com/inward/record.url?scp=85163298887&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.3c00840
DO - 10.1021/acs.iecr.3c00840
M3 - Article
C2 - 38020790
SN - 0888-5885
VL - 62
SP - 19084
EP - 19094
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 45
ER -