D2O plays important roles
in a variety of fields (such
as the nuclear industry and bioorganic analysis), and thus its isotopic
purity (H2O contents) is highly concerned. Due to its highly
similar physical properties to H2O and large excess amounts
of H2O over D2O, it is challenging to distinguish
D2O from H2O. On the basis of the characteristic
NIR-II phosphorescence of singlet oxygen (1O2), and the fact that H2O is a more efficient quencher
for 1O2 than D2O, here, we proposed
to simply use the 1275 nm emission of 1O2 for
the analysis of the isotopic purity of D2O. In normal cases
(a xenon lamp for excitation), such steady-state emission is extremely
weak for valid analytical applications, we thus employed laser excitation
for intensification. To this goal, a series of photosensitizers were
screened, and eventually polythiophene PT10 was selected with high
singlet oxygen quantum yield (ΦΔ = 0.51), high
H2O/D2O contrast, and excellent photostability.
Upon excitation with a 445 nm laser, a limit of detection (LOD, 3σ)
of 0.1% for H2O in D2O was achieved. The accuracy
of the proposed method was verified by the analysis of the isotopic
purity of several D2O samples (with randomly added H2O). More interestingly, the hygroscopicity of D2O was sensitively monitored with the proposed probe in a real-time
manner; the results of which are important for strengthening the care
of D2O storage and the importance of humidity control during
related investigations. Besides D2O isotopic purity evaluation,
this work also indicated the potential usefulness of the NIR-II emission
of singlet oxygen in future analytical detection.