Yuan Wentao, Chen Bingwei, Han Zhong-Kang, You Ruiyang, Jiang Ying, Qi Rui, Li Guanxing, Wu Hanglong, Ganduglia-Pirovano Maria Veronica, Wang Yong
Center of Electron Microscopy and State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, 310027, Hangzhou, China.
Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering, 030000, Taiyuan, China.
Nat Commun. 2024 Feb 22;15(1):1616. doi: 10.1038/s41467-024-46011-6.
The reconstruction of rutile TiO (110) holds significant importance as it profoundly influences the surface chemistry and catalytic properties of this widely used material in various applications, from photocatalysis to solar energy conversion. Here, we directly observe the asymmetric surface reconstruction of rutile TiO (110)-(1×2) with atomic-resolution using in situ spherical aberration-corrected scanning transmission electron microscopy. Density functional theory calculations were employed to complement the experimental observations. Our findings highlight the pivotal role played by repulsive electrostatic interaction among the small polarons -formed by excess electrons following the removal of neutral oxygen atoms- and the subsequent surface relaxations induced by these polarons. The emergence and disappearance of these asymmetric structures can be controlled by adjusting the oxygen partial pressure. This research provides a deeper understanding, prediction, and manipulation of the surface reconstructions of rutile TiO (110), holding implications for a diverse range of applications and technological advancements involving rutile-based materials.
金红石型TiO(110)的表面重构具有重要意义,因为它深刻影响着这种在从光催化到太阳能转换等各种应用中广泛使用的材料的表面化学性质和催化性能。在此,我们利用原位球差校正扫描透射电子显微镜,以原子分辨率直接观察了金红石型TiO(110)-(1×2)的不对称表面重构。采用密度泛函理论计算来补充实验观察结果。我们的研究结果突出了小极化子之间的排斥性静电相互作用——由中性氧原子去除后多余电子形成——以及这些极化子随后引起的表面弛豫所起的关键作用。这些不对称结构的出现和消失可以通过调节氧分压来控制。这项研究为金红石型TiO(110)的表面重构提供了更深入的理解、预测和调控方法,对涉及金红石基材料的各种应用和技术进步具有重要意义。