材料科学
光敏剂
海绵
极化(电化学)
离子键合
聚合物
多孔性
联轴节(管道)
电子
多孔介质
化学工程
光电子学
纳米技术
光化学
复合材料
离子
有机化学
物理化学
化学
植物
物理
量子力学
工程类
生物
作者
Wuzi Zhao,Lixuan Kan,Danfeng Wang,Lu Zhai,Xiangming Li,Shiyuan Zhou,Guangfeng Liu,Lei Zhu,Peiyang Gu
标识
DOI:10.1002/adfm.202425137
摘要
Abstract Porous organic polymers (POPs) are emerging as up‐and‐coming photocatalysts for energy conversion, and environmental treatment. However, attention to simultaneously improving photoinduced charge separation, transfer, and interfacial reaction is markedly lagged. Herein, the strategy of coupling ionic polarization, electron sponge effect for enhancing the built‐in electric field (BIEF), and surface mass transfer process of the POPs is proposed, which can be realized by a one‐pot post‐pyridiniumnation, Friedel‐Craft reaction. This method endows the ionic polarization effect for elevating BIEF for boosting charge separation/migration. The pyridiniumnation not only induces the electron sponge effect to allow the shallow trap of free electrons but also effectively reduces the oxygen adsorption energy, the free energy of the pertinent reaction intermediates, thus leading to stronger BIEF in 2.73‐fold of the neutral polymer and strengthened O 2 activation. Additionally, the photothermal performance with up to 15 °C increment contributes to the enhancement of photocatalysis. Consequently, iBPyP‐33 exhibits an unprecedentedly efficient photodegradation of 100 ppm bisphenol A (BPA) in just 20 min, photosynthesis of H 2 O 2 with the rate of 3070 µmol g −1 h −1 in air, up to 6583 µmol g −1 h −1 aided by sodium ethylenediaminetetraacetic acid. This study provides fresh, valuable insights into the design of photocatalysts with high interfacial reaction efficiency.
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