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Structure-activity relationship of nanostructured ceria for the catalytic generation of hydroxyl radicals

机译:纳米结构二氧化碳的结构活性关系,用于催化羟基自由基的催化产生

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摘要

Reactive oxygen species (ROS) are powerful oxidants generated in both biological systems and natural environments. Though enzyme-mimic activity and Fenton-like reactions have been postulated to explain how ceria nanoparticles and ROS are involved in the catalytic decomposition of hydrogen peroxide (H2O2), the corresponding reaction kinetics for this reaction have not yet been completely resolved. Here we present our investigation of the structure-activity relationship of ceria nanostructures for the generation of hydroxyl radicals through the catalytic decomposition of H2O2. Different nanostructured ceria including nanorods (NR), nanocubes (NC), and nanooctahedra (NO), together with commercial ceria, were examined to elucidate the relationship between the morphology and reaction kinetics. The initial relative production rates of hydroxyl radicals over different ceria nanostructures were determined using fluorescence measurements and were applied to obtain the apparent activation energy for their intrinsic activity comparisons. The activity trend of the order: ceria NR > ceria NC > ceria NO > commercial ceria was observed. This trend was rationalized and assessed using activity descriptive factors including the intensity ratio of Raman bands of vibration modes due to atomic defects, the percentage of surface Ce3+ content, and the average coordination number of oxygen anions surrounding each cerium cation in the ceria samples.
机译:活性氧(ROS)是在生物系统和自然环境中产生的强大氧化剂。尽管已经假定酶模拟活性和芬顿样反应,以解释二氧化氢的催化分解(H2O2),但该反应的相应反应动力学尚未完全解析。在这里,我们介绍了通过H2O2的催化分解来生成二氧化碳纳米结构的结构活性关系。检查了包括纳米棒(NR),纳米管(NC)和纳米二十环(NO)的不同纳米结构化二氧化碳以及商业陶瓷,以阐明形态和反应动力学之间的关系。使用荧光测量确定羟基自由基的初始相对产生速率,并应用于获得其内在活性比较的明显活化能。该顺序的活动趋势:ceria nr> ceria nc> ceria no>商业陶瓷。使用活性描述性因素进行合理化并评估了这种趋势,包括由于原子缺陷而引起的振动模式的拉曼带的强度比,表面CE3+含量的百分比以及ceria样品中每个硫磺阳离子周围的氧阴离子的平均氧阴离子数量。

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