Bismuth-based metal–organic
frameworks (Bi-MOFs) have emerged
as important photocatalysts for pollutant degradation applications.
Understanding the photocatalytic degradation mechanism is key to achieving
technological advantage. Herein, we apply dark-field optical microscopy
(DFM) to realize in situ multicolor imaging of the photocatalytic
degradation process of permanganate (MnO4
–) on single CAU-17 Bi-MOFs. Three reaction kinetic processes such
as surface adsorption, photocatalytic reduction, and disproportionation
are revealed by combining the time-lapsed DFM images with optical
absorption spectra, indicating that the photocatalytic reduction of
purple MnO4
– first produces beige red
MnO4
2– through a one-electron pathway,
and then MnO4
2– disproportionates into
yellow MnO2 on CAU-17. Meanwhile, we observe that the deposition
of MnO2 cocatalysts enhances the surface adsorption reaction
and the photocatalytic reduction of MnO4
– to MnO4
2–. Unexpectedly, it is found
that isopropanol as a typical hole scavenger can stabilize MnO4
2–, avoiding disproportionation and causing
the alteration of the photocatalytic reaction pathway from a one-electron
avenue to a three-electron (1 + 2) process for producing MnO2 on CAU-17. This research opens up the possibility of comprehensively
tracking and understanding the photocatalytic degradation reaction
at the single MOF particle level.