Carbonyl-modified solid-state carbon nitrogen quantum
dots (m-OCNQDs) have emerged as promising
room-temperature
phosphorescent (RTP) materials close to commercialization. However,
high-crystallinity m-OCNQDs are insensitive
to external stimuli such as water and heat due to strong stacking
interactions between layers, restricting their applications in stimulus
responsive fields. Here, a polymer template space-confined growth
strategy is established for the large-scale synthesis of water stimulus
responsive polyvinylpyrrolidone-functionalized m-OCNQDs
with ultralong room-temperature phosphorescence (181 ms) using urea
and PVP as precursors. Theoretical and experimental results indicate
that the PVP template linked at the rim of m-OCNQDs
formed by in situ self-polymerization of urea inhibits interactions
between layers and increases their affinity for water, which is the
key to increasing their sensitivity with water. This strategy offers
a new path for developing commercial stimulus responsive RTP materials