This study focuses on the synthesis and investigation
of ZnIn2S4 nanoparticle (NP) photocatalysts
treated with
different sulfur sources, thioacetamide (TAA), or thiourea (TU), to
explore their wavelength-dependent photocatalytic activity. The research
aims to understand the impact of Zn vacancies present on the surface
of ZnIn2S4 NPs. The investigation involves electron
spin resonance and in situ X-ray photoelectron spectroscopy to study
the photocatalytic activity of ZnIn2S4–TU
and ZnIn2S4–TAA NPs, following the characterization
of surface morphology and electronic properties using high-resolution
transmission electron microscopy and X-ray diffraction. Additionally,
the study delves into the wavelength-dependent photocatalytic degradation
(PCD) activity of the ZnIn2S4 NPs using 2,5-hydroxymethylfurfural
(HMF) across a wide range. Notably, the selective oxidation of HMF
using ZnIn2S4–TU NPs resulted in the
formation of 2,5-furandicarboxylic acid (FDCA) via 2,5-diformylfuran,
with an efficiency exceeding 40% over the broad wavelength range.
The research demonstrates that the irradiation wavelength for PCD
is influenced by the number of defect structures introduced into the
ZnIn2S4 NPs through the sulfur source.