Janković Ivana A, Saponjić Zoran V, Džunuzović Enis S, Nedeljković Jovan M
Nanoscale Res Lett. 2009 Oct 13;5(1):81-88. doi: 10.1007/s11671-009-9447-y.
Surface modification of nanocrystalline TiO(2) particles (45 A) with bidentate benzene derivatives (catechol, pyrogallol, and gallic acid) was found to alter optical properties of nanoparticles. The formation of the inner-sphere charge-transfer complexes results in a red shift of the semiconductor absorption compared to unmodified nanocrystallites. The binding structures were investigated by using FTIR spectroscopy. The investigated ligands have the optimal geometry for chelating surface Ti atoms, resulting in ring coordination complexes (catecholate type of binuclear bidentate binding-bridging) thus restoring in six-coordinated octahedral geometry of surface Ti atoms. From the Benesi-Hildebrand plot, the stability constants at pH 2 of the order 10(3) M(-1) have been determined.
研究发现,用双齿苯衍生物(儿茶酚、连苯三酚和没食子酸)对纳米晶TiO₂颗粒(45 Å)进行表面改性会改变纳米颗粒的光学性质。与未改性的纳米微晶相比,内球电荷转移络合物的形成导致半导体吸收发生红移。通过傅里叶变换红外光谱(FTIR)研究了结合结构。所研究的配体具有螯合表面Ti原子的最佳几何结构,形成环配位络合物(双核双齿结合桥连的儿茶酚盐类型),从而恢复表面Ti原子的六配位八面体几何结构。根据贝内西-希尔德布兰德图,已确定pH值为2时稳定性常数约为10³ M⁻¹。