Department of Chemistry, Oregon State University, Corvallis, Oregon 97330-4003, USA.
J Am Chem Soc. 2009 Dec 2;131(47):17084-6. doi: 10.1021/ja9080666.
We show that trivalent manganese, Mn(3+), imparts an intense blue color to oxides when it is introduced at dilution in trigonal bipyramidal coordination. Our optical measurements and first-principles density functional theory calculations indicate that the blue color results from an intense absorption in the red/green region. This absorption is due in turn to a symmetry-allowed optical transition between the valence-band maximum, composed of Mn 3d(x(2)-y(2),xy) states strongly hybridized with O 2p(x,y) states, and the narrow Mn 3d(z(2))-based conduction-band minimum. We begin by demonstrating and explaining the effect using a well-defined prototype system: the hexagonal YMnO(3)-YInO(3) solid solution. We then show that the behavior is a general feature of diluted Mn(3+) in this coordination environment.
我们表明,三价锰(Mn(3+))在以三角双锥配位形式稀释时,会使氧化物呈现强烈的蓝色。我们的光学测量和第一性原理密度泛函理论计算表明,蓝色是由于在红色/绿色区域的强烈吸收所致。这种吸收反过来是由于价带最大值(由强烈杂化的 Mn 3d(x(2)-y(2),xy)态和 O 2p(x,y)态组成)和狭窄的 Mn 3d(z(2))基导带最小值之间的对称性允许的光学跃迁所致。我们首先使用一个明确定义的原型系统:六方 YMnO(3)-YInO(3)固溶体,来证明和解释这一效应。然后,我们表明,这种行为是这种配位环境中稀释的 Mn(3+)的一般特征。