光催化
材料科学
磁性
催化作用
可见光谱
纳米技术
化学工程
光电子学
化学
有机化学
凝聚态物理
物理
工程类
作者
Júlio C. S. Terra,Ariane Desgranges,Cyrille Monnereau,Elena H. Sánchez,J. A. De Toro,Zacharias Amara,Audrey Moores
标识
DOI:10.1021/acsami.0c06126
摘要
While magnetic supports have been widely used to immobilize homogeneous catalysts in organic chemistry, this strategy has so far found very little application in photocatalysis. Indeed, magnetic supports are dark colored, and thus compete for photon absorption with photocatalysts themselves. We have developed a series of core-shell Fe(0)-silica nanoparticles as supports for immobilizing the photosensitizer Ru(bpy)32+, featuring various silica shell thicknesses-16-34 nm SiO2-on 9 nm Fe cores. The supports and the resulting photocatalytic systems were studied for their magnetic, optical, and catalytic properties in the context of the photooxidation of citronellol, and we found that thicker silica shells lead to higher catalytic activity. We correlated this effect as well as Ru(bpy)32+ fluorescence and singlet oxygen generation to the absorption properties of the supports. We were able to reuse our optimal system three times with minimal loss of activity and achieved turnover numbers largely surpassing the performance of homogeneous Ru(bpy)32+. This work highlights the role of material design in the conception of new supports for applications in heterogeneous photocatalysis.
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