Bouri Maria, Aschauer Ulrich
University of Bern, Department of Chemistry and Biochemistry, Bern, Switzerland.
Phys Chem Chem Phys. 2018 Jan 24;20(4):2771-2776. doi: 10.1039/c7cp06791g.
Oxynitrides with the perovskite structure are promising candidates for photocatalysis under visible light due to their appropriate optical and electronic properties. Recently, layered perovskites have attracted attention for their improved performance with respect to bulk perovskites in photocatalytic water splitting. In this paper, we investigate the structural and electronic properties of the layered Ruddlesden-Popper oxynitride SrTaON and its (001) and (100) surfaces using density functional theory (DFT) calculations. We find that the energetically favoured configuration of the bulk has an in-plane cis anion order and exhibits rotations of the TaON octahedra. Furthermore, we show that the TaON-terminated (001) surface suppresses exciton recombination due to higher-energy surface states, giving a potential explanation for the good photocatalytic performance.
具有钙钛矿结构的氮氧化物因其合适的光学和电子性质而成为可见光下光催化的有前途的候选材料。最近,层状钙钛矿因其在光催化水分解方面相对于块状钙钛矿的性能改进而受到关注。在本文中,我们使用密度泛函理论(DFT)计算研究了层状Ruddlesden-Popper氮氧化物SrTaON及其(001)和(100)表面的结构和电子性质。我们发现块状材料能量上有利的构型具有面内顺式阴离子有序排列,并表现出TaON八面体的旋转。此外,我们表明TaON终止的(001)表面由于高能表面态而抑制了激子复合,这为良好的光催化性能提供了一个潜在的解释。