Multiemitting Ultralong Phosphorescent Carbonized Polymer Dots via Synergistic Enhancement Structure Design

Abstract

Abstract Advancing a metal‐free room temperature phosphorescent (RTP) material that exhibits multicolor emission, remarkable RTP lifetime, and high quantum yield still faces the challenge of achieving intersystem crossing between singly and triplet excited states, as well as the rapid decay of triplet excited states due to nonradiative losses. In this study, a novel strategy is proposed to address these limitations by incorporating o‐phenylenediamine, which generates multiple luminescent centers, and long‐chain polyacrylic acid to synthesize carbonized polymer dots (CPDs). These CPDs are then embedded in a rigid B2O3 matrix, effectively limiting nonradiative losses through the synergistic effects of polymer cross‐linking and the rigid matrix. The resulting CPD‐based materials exhibit remarkable ultralong phosphorescence in shades of blue and lime green, with a visible lifetime of up to 49 s and a high phosphorescence quantum yield. Simultaneously, this study demonstrates the practical applicability of these excellent material properties in anti‐counterfeiting and information encryption.

Keywords

• carbon dots (CDs)
• carbonized polymer dots (CPDs)
• cross‐linking enhance emission (CEE)
• matrix
• room temperature phosphorescence (RTP)