纳米团簇
反键分子轨道
光催化
材料科学
电子顺磁共振
催化作用
析氧
光化学
共沉淀
化学工程
纳米技术
无机化学
化学
电子
物理化学
有机化学
核磁共振
物理
电极
量子力学
原子轨道
电化学
工程类
作者
Fan Li,Taobo Huang,Fengbin Sun,Long Chen,Peishen Li,Feng Shao,Xudong Yang,Wen Liu
标识
DOI:10.1016/j.apcatb.2022.121725
摘要
Fe2O3, as an earth-abundant photocatalyst for water purification, has attracted great attention. However, the high-spin FeIII in traditional Fe2O3 restricts its catalytic performance. In this work, based on the nanocrystal size alteration strategy, cubic Fe2O3 nanoclusters (3–4 nm) with low-spin FeIII were successfully anchored on six-fold cavities of the supramolecular condensed g-C3N4 rod (FCN) through the impregnation-coprecipitation method. FCN showed high photocatalytic activity, as the d band center of Fe 3d orbital (−1.79 eV) in low-spin FeIII shifted closer to Femi level, generating a weaker antibonding state. Then, the enhanced bonding state strengthened the interaction between Fe and O, further accelerating the charge carrier separation and enhancing its ability to capture OH−. Thus, low-spin FeIII enhanced the production of dominant reactive oxygen species (•OH/•O2−), promoting diclofenac photocatalytic degradation under solar light, with a kinetic rate constant (0.206 min−1) of ~5 times compared with that of pristine g-C3N4.
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