Hydrogen peroxide (HP) plays an indispensable
role in living organisms,
being both an intracellular messenger and a substrate or byproduct
of a number of enzymes. In this way, HP sensing is important for monitoring
the activity of various cell systems and assessing the redox balance
of the cell as whole. HP sensors based on luminescent inorganic nanoparticles
can be considered as a prospective alternative to traditional dye-
and enzyme-based sensors, which usually are unstable and nonreversible.
The undoped (CeO2–x
) and Eu3+-doped (CeO2–x
:Eu3+) colloidal ceria nanoparticles studied in the paper provide
HP detection by reversible quenching of Eu3+ (590 nm) and
Ce3+ (430 nm) luminescence bands. The dynamics of Eu3+ and Ce3+ luminescence quenching and recovery
during HP-nanoceria interaction provides an insight into the microscopic
mechanisms of HP sensing by CeO2–x
and CeO2–x
:Eu3+ nanoparticles.
Both CeO2–x
and CeO2–x
:Eu3+ luminescent sensors are reversible
and their recovery rates can be sufficiently increased by temperature
and continuous UV irradiation. At the same time, Eu3+ ions
deteriorate the catalase-mimetic activity of CeO2–x
NPs and worsen their antioxidant properties, which
should be kept in mind while using these sensors in biological media.