Topotactical growth of thick perovskite oxynitride layers by nitridation of single crystalline oxides

被引：42

作者：

Ebbinghaus, Stefan G. ^{[1
]}

Aguiar, Rosiana ^{[1
]}

Weidenkaff, Anke ^{[2
]}

Gsell, Stefan ^{[3
]}

Reller, Armin ^{[1
]}

机构：

[1] Univ Augsburg, Inst Phys, Lehrstuhl Festkorperchem, D-86159 Augsburg, Germany

[2] Abt Festkorperchem & Katalyse, CH-8600 Dubendorf, Switzerland

[3] Univ Augsburg, Inst Phys, Lehrstuhl Expt Phys 4, D-86159 Augsburg, Germany

来源：

SOLID STATE SCIENCES | 2008年 / 10卷 / 06期

关键词：

oxynitrides; perovskites; single crystal growth; ammonolysis; topotactical reaction;

D O I：

10.1016/j.solidstatesciences.2007.03.011

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Thick films of the perovskite-related oxynitrides LaTiO2N, NdTiO2N, SrNbO2N and SrTaO2N were synthesised by nitridation of single crystals of the corresponding oxides with general composition ABO(3.5). The oxide crystals were obtained by optical floating zone growth. They correspond to n = 4 member of the A(n)B(n)O3(n+2) family of layered perovskites and were reacted at temperatures between 900 degrees C and 1050 degrees C to form the oxynitrides. Electron probe microanalysis proved the presence of nitrogen in a surface layer of a few micrometer thickness. Cross-section SEM revealed additional thin stripes of oxynitride within the bulk of the crystals, indicating that nitrogen is incorporated preferably parallel to the perovskite-type layers, which in turn are connected in a zipper-type mechanism. The formation of the desired perovskite-type oxynitrides was confirmed by X-ray diffraction. Pole figure measurements proved an epitaxial orientation ABO(2)N (110)[001] parallel to ABO(3.5) (001)[100]. The mosaicity of the oxynitrides both in polar and azimuthal direction was very small (< 2 degrees) indicating a nearly single crystalline quality of the surface layer. The nitridation of the crystals results in a dramatic change in colour. Optical spectroscopy revealed shifts of the absorption edge by more than 200 nm to longer wavelengths with respect to the parent oxides, corresponding to a reduction of the band gap energies by 1.4-1.8 eV. (c) 2007 Elsevier Masson SAS. All rights reserved.

引用

页码：709 / 716

页数：8