Photocatalysis for environmental
cleanup applications
has seen
an enormous increase in interest recently. This study aimed to examine
the in situ photoactivity of the photocatalyst BiOI/g-C3N4/Bi2WO6/Biochar for the photocatalytic
decomposition of the target pollutant methylene blue (MB). During
photocatalysis, biochar is utilized as a support material by using
light harvesting and electron-conductive qualities to hinder the quick
recombination of e–/h+ pairs. The BiOI/g-C3N4/Bi2WO6/Biochar composite
showed improved photoactivity and stability after adding biochar.
For MB degradation, the attained rate constant K was
found to be 0.04102 > 0.02446 > 0.01818 > 0.0119 > 0.00933
> 0.00705
min–1 for g-C3N4/Bi2WO6/BIOI/Biochar > g-C3N4/Bi2WO6/BIOI > g-C3N4/Bi2WO6 > BiOI > Bi2WO6 > g-C3N4, respectively. The degradation
efficiencies
of BiOI/g-C3N4/Bi2WO6/Biochar
photocatalysts for MB were 97.56% within 70 min. Scavenger and electron
spin resonance (ESR) studies further demonstrated that h+, •O2
–, and •OH are significant reactive species that aid in the photodegradation
of dyes. Additionally, the structural analyses of MB using DFT calculations
and the examination of the degraded products using GC-MS (gas chromatography–mass
spectrometry) allowed for a more insightful deduction of the photodegradation
pathways. Results showed that the degradation efficiencies of BiOI/g-C3N4/Bi2WO6 significantly improved
the degradation rate with the addition of biochar. The quaternary
composite improved light harvesting, absorption capacity, porosity,
and pore structure of the photocatalyst. This work suggests possible
applications and a novel technique for large-scale photocatalytic
degradation. It also suggests a straightforward and inexpensive strategy
for creating a stable semiconductor-based photocatalytic system.