Exploiting Photoinduced Atom Transfer Radical Polymerizations with Boron-Dopant and Nitrogen-Defect Synergy in Carbon Nitride Nanosheets.

Graphitic carbon nitrides (g-C 3 N 4 ) possess various benefits as heterogeneous photocatalysts, including tunable bandgaps, scalability and chemical robustness. However, their efficacy and ongoing advancement are hindered by challenges like limited charge carrier separation rates, insufficient driving force for photocatalysis, small specific surface area and inadequate absorption of visible light. In this study, we introduced boron dopants and nitrogen defects synergy into bulk g-C 3 N 4 through the calcination of a blend of nitrogen-defective g-C 3 N 4 and NaBH 4 under inert conditions, resulting in the formation of BCN nanosheets characterized by abundant porosity and increased specific surface area. These BCN nanosheets promoted intermolecular single electron transfer to the radical initiator, maintaining radical intermediates at a low concentration for better control of photoinduced atom transfer radical polymerization (photo-ATRP). Consequently, this method yielded polymers with low dispersity and tailorable molecular weights under mild blue light illumination, outperforming previous reports on bulk g-C 3 N 4 . The heterogeneity of BCN enabled easy separation and efficient reuse in subsequent polymerization processes. This study effectively showcases a simple method to alter the electronic and band structures of g-C 3 N 4 with simultaneously introducing dopants and defects, leading to high-performance photo-ATRP and providing valuable insights for designing efficient photocatalytic systems for solar energy harvesting. This article is protected by copyright. All rights reserved.