光催化
微型多孔材料
钛
电子顺磁共振
光化学
卟啉
自旋俘获
活性氧
化学
锐钛矿
分子
化学工程
材料科学
激进的
催化作用
有机化学
工程类
物理
生物化学
核磁共振
作者
Yesub Keum,Bongkyeom Kim,Asong Byun,Jinhee Park
标识
DOI:10.1002/anie.202007193
摘要
We present novel titanium-porphyrinic gels (TPGs) and titanium-porphyrinic aerogels (TPAs), in which porphyrinic ligand tetrakis(4-carboxyphenyl)porphyrin is coordinated to Ti-oxo clusters. These hierarchically porous TPAs, with micro-, meso-, and macropores and reactant-concentration-dependent Brunauer-Emmett-Teller surface areas of 407-738 m2 g-1 , are prepared by CO2 critical point drying of TPGs. Although the Ti4+ → Ti3+ photoreduction of TPAs is less efficient than that of crystalline microporous Ti-porphyrinic framework DGIST-1, prompt diffusion of O2 and spin-trapping agents into the TPA pores causes the rapid generation of reactive oxygen species (ROS), as observed by EPR spectroscopy. When used as an ROS scavenger, large 1,3-diphenylisobenzofuran is degraded by the best-performing TPA 10 times faster than by DGIST-1, suggesting that the accessibility of molecules (reactants) to pores (reactive centers) strongly influences photocatalytic activity.
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