Key Laboratory for New Type of Functional Materials in Hebei Province, School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130, People's Republic of China.
Nanotechnology. 2016 Sep 2;27(35):355203. doi: 10.1088/0957-4484/27/35/355203. Epub 2016 Jul 25.
Although MoS2 based heterostructures have drawn increased attention, the van der Waals forces within MoS2 layers make it difficult for the layers to form strong chemical coupled interfaces with other materials. In this paper, we demonstrate the successful strong chemical attachment of MoS2 on TiO2 nanobelts after appropriate surface modifications. The etch-created dangling bonds on TiO2 surfaces facilitate the formation of a steady chemically bonded MoS2/TiO2 interface. With the aid of high resolution transmission electron microscope measurements, the in-plane structure registry of MoS2/TiO2 is unveiled at the atomic scale, which shows that MoS2[1-10] grows along the direction of TiO2[001] and MoS2[110] parallel to TiO2[100] with every six units of MoS2 superimposed on five units of TiO2. Electronically, type II band alignments are realized for all surface treatments. Moreover, the band offsets are delicately correlated to the surface states, which plays a significant role in their photocatalytic performance.
尽管基于 MoS2 的异质结构引起了越来越多的关注,但 MoS2 层内的范德华力使得层难以与其他材料形成强化学耦合界面。在本文中,我们证明了经过适当的表面修饰后,MoS2 可以成功地与 TiO2 纳米带进行强化学附着。TiO2 表面上的刻蚀产生的悬空键有助于形成稳定的化学键合 MoS2/TiO2 界面。借助高分辨率透射电子显微镜测量,在原子尺度上揭示了 MoS2/TiO2 的面内结构配准,表明 MoS2[1-10]沿着 TiO2[001]的方向生长,MoS2[110]与 TiO2[100]平行,每六个 MoS2 单元叠加在五个 TiO2 单元上。对于所有的表面处理,都实现了 II 型能带排列。此外,能带偏移与表面态精细相关,这对其光催化性能起着重要作用。