Jiang Jingjie, Ye Gang, Lorandi Francesca, Liu Zeyu, Liu Yanqi, Hu Tongyang, Chen Jing, Lu Yuexiang, Matyjaszewski Krzysztof
Collaborative Innovation Center of Advanced Nuclear Energy Technology, Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing, 100084, China.
Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA, 15213, USA.
Angew Chem Int Ed Engl. 2019 Aug 26;58(35):12096-12101. doi: 10.1002/anie.201906194. Epub 2019 Jul 25.
The photophysical process of localized surface plasmon resonance (LSPR) is, for the first time, exploited for broadband photon harvesting in photo-regulated controlled/living radical polymerization. Efficient macromolecular synthesis was achieved under illumination with light wavelengths extending from the visible to the near-infrared regions. Plasmonic Ag nanostructures were in situ generated on Ag PO photocatalysts in a reversible addition-fragmentation chain transfer (RAFT) system, thereby promoting polymerization of various monomers following a LSPR-mediated electron transfer mechanism. Owing to the LSPR-enhanced broadband photon harvesting, high monomer conversion (>99 %) was achieved under natural sunlight within 0.8 h. The deep penetration of NIR light enabled successful polymerization with reaction vessels screened by opaque barriers. Moreover, by trapping active oxygen species generated in the photocatalytic process, polymerization could be implemented without pre-deoxygenation.
局部表面等离子体共振(LSPR)的光物理过程首次被用于光调控可控/活性自由基聚合中的宽带光子捕获。在从可见光到近红外区域的光波长照射下实现了高效的大分子合成。在可逆加成-断裂链转移(RAFT)体系中,等离子体银纳米结构在Ag₃PO₄光催化剂上原位生成,从而按照LSPR介导的电子转移机制促进各种单体的聚合。由于LSPR增强的宽带光子捕获,在自然阳光下0.8小时内实现了高单体转化率(>99%)。近红外光的深度穿透使得在有不透明屏障屏蔽的反应容器中成功进行聚合。此外,通过捕获光催化过程中产生的活性氧物种,可以在不预先脱氧的情况下进行聚合。