Gram‐Scale Room‐Temperature Synthesis of Solid‐State Fluorescent Carbon Nanodots for Bright Electroluminescent Light Emitting Diodes

Abstract The reaction conditions of high temperature and high pressure will introduce structural defects, high energy consumption, and security risks, severely hindering the industrial application of organic carbon nanodots (CDs). Moreover, the aggregation caused quenching effect also fundamentally limits the CDs based electroluminescent light emitting diodes (LEDs). Herein, for the first time, a rapid one‐step room temperature synthetic strategy is introduced to prepare highly emissive solid‐state‐fluorescent CDs (RT‐CDs). A strong oxidizing agent, potassium periodate (KIO 4 ), is adopted as a catalyst to facilitate the cyclization of o ‐phenylenediamine and 4‐dimethylamino phenol in aqueous solution at room temperature for only 5 min. The resultant organic molecule, 2‐(dimethylamino) phenazine, will self‐assemble kinetically to generate supramolecular‐structure CDs during crystallization. The elaborately arranged supramolecular structure (J aggregates) endows CDs with intense solid‐state‐fluorescence. Density functional theory (DFT) calculation shows that the excited state of RT‐CDs exhibits charge transfer characteristic owing to the unique donor‐Π‐acceptor structure. A high‐performance monochrome RT‐CDs based electroluminescent LEDs (2967 cd m −2 and 1.38 cd A −1 ) were fabricated via systematic optimizations of device engineering. This work provides a concrete and feasible avenue for the rapid and massive preparation of CDs, advancing the commercialization of CDs based optoelectronic devices.