Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
Phys Rev Lett. 2018 Jan 26;120(4):046001. doi: 10.1103/PhysRevLett.120.046001.
The perovskite oxynitride LaTiO_{2}N is a promising material for photocatalytic water splitting under visible light. One of the obstacles towards higher efficiencies of this and similar materials stems from charge-carrier recombination, which could be suppressed by the surface charges resulting from the dipolar field in polar materials. In this study, we investigate the spontaneous polarization in epitaxially strained LaTiO_{2}N thin films via density functional theory calculations. The effect of epitaxial strain on the anion order, resulting out-of-plane polarization, energy barriers for polarization reversal, and corresponding coercive fields are studied. We find that for compressive strains larger than 4% the thermodynamically stable anion order is polar along the out-of-plane direction and has a coercive field comparable to other switchable ferroelectrics. Our results show that strained LaTiO_{2}N could indeed suppress carrier recombination and lead to enhanced photocatalytic activities.
钙钛矿氧氮化物 LaTiO_{2}N 是一种在可见光下光催化水分解的有前途的材料。提高这种材料和类似材料效率的一个障碍源于载流子复合,而通过在极性材料中偶极场产生的表面电荷可以抑制载流子复合。在这项研究中,我们通过密度泛函理论计算研究了外延应变 LaTiO_{2}N 薄膜中的自发极化。研究了外延应变对阴离子有序、产生的面外极化、极化反转的能垒以及相应的矫顽场的影响。我们发现,对于大于 4%的压缩应变,热力学稳定的阴离子有序沿面外方向具有极性,并且具有与其他可切换铁电体相当的矫顽场。我们的结果表明,应变 LaTiO_{2}N 确实可以抑制载流子复合并提高光催化活性。