Kumar Ram, Venardi V, Helal Y, Song Chengyu, Katz Alexander
Department of Chemical and Biomolecular Engineering, University of California Berkeley California 94720-1462 USA
National Center for Electron Microscopy, Molecular Foundry, Lawrence Berkeley National Laboratory Berkeley California 94720 USA.
RSC Adv. 2023 Jul 31;13(33):23030-23037. doi: 10.1039/d3ra03801g. eCollection 2023 Jul 26.
We report the synthesis of uniform 2.5 ± 0.4 nm diameter Ce(iii) carbonate clusters deposited on the surface of TiO nanoparticles and characterize them using HAADF-STEM and EELS, as well as UV-Vis and FTIR spectroscopies. This material is a highly proficient catalytic antioxidant for the degradation of photocatalytically generated reactive oxygen species (ROS). We observed an unusual U-shaped pH-dependence in its photoprotection catalytic activity, with an optimum function in the near-neutral pH range of 7.7 ± 0.7. This sharp pH dependence is not observed in previously reported bulk Ce(iii) carbonate materials, and it is also not a consequence of Ce(iii) carbonate cluster decomposition. However, it is consistent with a tandem reaction sequence consisting of a biomimetic superoxide dismutase and catalase function, which is dependent on a balance of protons and hydroxide anions for function. Our dissolution-deposition approach for synthesizing nanoscale Ce(iii) carbonate clusters on TiO should be generalizable to other carbonates and metal-oxide supports.
我们报道了沉积在TiO纳米颗粒表面的直径为2.5±0.4 nm的均匀碳酸铈(iii)簇的合成,并使用高角度环形暗场扫描透射电子显微镜(HAADF-STEM)、电子能量损失谱(EELS)以及紫外可见光谱和傅里叶变换红外光谱对其进行了表征。这种材料是一种高效的催化抗氧化剂,用于光催化产生的活性氧(ROS)的降解。我们观察到其光保护催化活性呈现出不寻常的U形pH依赖性,在7.7±0.7的近中性pH范围内具有最佳功能。在先前报道的块状碳酸铈(iii)材料中未观察到这种强烈的pH依赖性,这也不是碳酸铈(iii)簇分解的结果。然而,这与由仿生超氧化物歧化酶和过氧化氢酶功能组成的串联反应序列一致,该序列的功能依赖于质子和氢氧根阴离子的平衡。我们在TiO上合成纳米级碳酸铈(iii)簇的溶解-沉积方法应该可以推广到其他碳酸盐和金属氧化物载体。