Kang Jianxin, Zhang Yan, Chai Ziwei, Qiu Xiaoyi, Cao Xingzhong, Zhang Peng, Teobaldi Gilberto, Liu Li-Min, Guo Lin
School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology, Beihang University, Beijing, 100191, China.
Beijing Computational Science Research Center, Beijing, 100193, China.
Adv Mater. 2021 Jun;33(23):e2100407. doi: 10.1002/adma.202100407. Epub 2021 Apr 28.
Although oxygen vacancies (O s) play a critical role for many applications of metal oxides, a controllable synthetic strategy for anisotropic O s remains a great challenge. Here, a novel strategy is proposed to achieve the regional dual structure with anisotropic O s at both the surface and in the interior of TiO by constructing amorphous domains. The as-prepared black TiO with amorphous domains exhibits superior activity in degrading rhodamine B (RhB) solutions, which can instantly decompose RhB with just a shake. First-principle simulations reveal that subsurface O s in TiO are energetically favored, resulting in the formation of amorphous domains in the interior region via diffusion of surface-formed O s into the subsurface. The stable O -induced amorphous domains in TiO with enhanced catalytic performances provide a scalable strategy to practical O engineering in functional metal oxides.
尽管氧空位(Os)在金属氧化物的许多应用中起着关键作用,但实现各向异性氧空位的可控合成策略仍然是一个巨大的挑战。在此,提出了一种新颖的策略,通过构建非晶域在TiO的表面和内部实现具有各向异性氧空位的区域双结构。所制备的具有非晶域的黑色TiO在降解罗丹明B(RhB)溶液中表现出优异的活性,只需摇晃就能立即分解RhB。第一性原理模拟表明,TiO中的次表面氧空位在能量上是有利的,导致通过表面形成的氧空位扩散到次表面而在内部区域形成非晶域。TiO中由稳定氧诱导的具有增强催化性能的非晶域为功能性金属氧化物中的实际氧工程提供了一种可扩展的策略。