Khaoula Chaoui, Zaari Halima, Benyoussef Abdelilah, El Kenz Abdellah, Loulidi Mohammed, Moatassim Hajar, Boujnah Mourad, Espinosa-Faller Francisco Javier, Caballero-Briones Felipe
Laboratory of Condensed Matter and Interdisciplinary Sciences (LaMCScI), "Unité de Recherche Labellisée CNRST URL-CNRST-17" Physics Department, Faculty of Sciences, Mohammed V University B.P. 1014 Rabat Morocco
Hassan II Academy of Science and Technology Rabat Morocco.
RSC Adv. 2024 Dec 11;14(53):39122-39130. doi: 10.1039/d4ra08172b. eCollection 2024 Dec 10.
CdS(Se)/graphene oxide (GO) heterostructures have received significant attention due to their potential application in optoelectronic devices with tunable bandgap, efficient charge transfer, and enhanced photocatalytic and photovoltaic activity. In this work, Density Functional Theory (DFT) calculations of the photocatalytic properties of CdS(Se)/GO heterostructures were performed. The results of work function, band gap, optical absorption, and band edges of CdS and CdSe in the (001) and (110) directions on graphene oxide are presented. Various approaches to simulate graphene oxide with a different concentration of oxygen, and their subsequent integration into CdS (Se)-GO heterostructures are discussed. DFT calculations were employed to determine the equilibrium value and adhesion energy for various compositions of layers at the interface, as well as different stacking arrangements between graphene oxide and CdS slabs. The results revealed that some oxygen atoms migrate to the CdS matrix and form bonds with Cd atoms. It was observed that the semiconductor band gap can be controlled by the oxidation degree in graphene oxide, and the electronic properties of CdS(Se) depend on the semiconductor orientation and slab number. Notably, surface states are found to be responsible for the negative part of the dielectric function at low frequencies, significantly influencing the electronic properties and charge transfer dynamics. The results show that both structures form type II heterostructures, which is promising for photocatalytic hydrogen generation.
硫化镉(硒)/氧化石墨烯(GO)异质结构因其在具有可调带隙、高效电荷转移以及增强光催化和光伏活性的光电器件中的潜在应用而受到了广泛关注。在这项工作中,对硫化镉(硒)/氧化石墨烯异质结构的光催化性能进行了密度泛函理论(DFT)计算。给出了氧化石墨烯上硫化镉和硒化镉在(001)和(110)方向上的功函数、带隙、光吸收和带边的计算结果。讨论了模拟不同氧浓度氧化石墨烯的各种方法,以及它们随后整合到硫化镉(硒)-氧化石墨烯异质结构中的情况。利用DFT计算确定了界面处各层不同组成的平衡值和粘附能,以及氧化石墨烯与硫化镉平板之间不同的堆叠排列。结果表明,一些氧原子迁移到硫化镉基体中并与镉原子形成键。观察到半导体带隙可由氧化石墨烯中的氧化程度控制,硫化镉(硒)的电子性质取决于半导体取向和平板数量。值得注意的是,表面态被发现是低频下介电函数负部分的原因,对电子性质和电荷转移动力学有显著影响。结果表明,两种结构均形成II型异质结构,这对于光催化产氢具有前景。