Chen Xing, Zhao Cuihua, Wu Hao, Shi Yong, Chen Cuiting, Zhou Xi
School of Resources, Environment and Materials, School of Chemistry & Chemical Engineering, Guangxi University, Nanning 530004, China.
Guangxi Key Laboratory of Processing for Non-Ferrous Metal and Featured Materials, Guangxi University, Nanning 530004, China.
Materials (Basel). 2022 May 26;15(11):3786. doi: 10.3390/ma15113786.
Direct Z-scheme photocatalysts have attracted extensive attention due to their strong redox ability and efficient separation of photogenerated electron-hole pairs. In this study, we constructed two types of ZnS/SnS heterojunctions with different stacking models of ZnS and SnS layers, and investigated their structures, stabilities, and electronic and optical properties. Both types of heterojunctions are stable and are direct Z-scheme photocatalysts with band gaps of 1.87 eV and 1.79 eV, respectively. Furthermore, their oxidation and reduction potentials straddle the redox potentials of water, which makes them suitable as photocatalysts for water splitting. The built-in electric field at the heterojunction interface improves the separation of photogenerated electron-hole pairs, thus enhancing their photocatalytic efficiency. In addition, ZnS/SnS heterojunctions have higher carrier mobilities and light absorption intensities than ZnS and SnS monolayers. Therefore, the ZnS/SnS heterojunction has a broad application prospect as a direct Z-scheme visible-light-driven photocatalyst for overall water splitting.
直接Z型光催化剂因其强大的氧化还原能力和光生电子-空穴对的有效分离而受到广泛关注。在本研究中,我们构建了两种具有不同ZnS和SnS层堆叠模型的ZnS/SnS异质结,并研究了它们的结构、稳定性以及电子和光学性质。两种类型的异质结都很稳定,并且是直接Z型光催化剂,带隙分别为1.87 eV和1.79 eV。此外,它们的氧化和还原电位跨越了水的氧化还原电位,这使得它们适合作为光解水的光催化剂。异质结界面处的内建电场提高了光生电子-空穴对的分离效率,从而提高了它们的光催化效率。此外,ZnS/SnS异质结比ZnS和SnS单层具有更高的载流子迁移率和光吸收强度。因此,ZnS/SnS异质结作为直接Z型可见光驱动的全解水光催化剂具有广阔的应用前景。