Intriguing electronic, optical and photocatalytic performance of BSe, M(2)CO(2) monolayers and BSe–M(2)CO(2) (M = Ti, Zr, Hf) van der Waals heterostructures

Using density functional (DFT) theory calculations, we have investigated the electronic band structure, optical and photocatalytic response of BSe, M(2)CO(2) (M = Ti, Zr, Hf) monolayers and their corresponding BSe–M(2)CO(2) (M = Ti, Zr, Hf) van der Waals (vdW) heterostructures. Optimized lattice constant, bond length, band structure and bandgap values, effective mass of electrons and holes, work function and conduction and valence band edge potentials of BSe and M(2)CO(2) (M = Ti, Zr, Hf) monolayers are in agreement with previously available data. Binding energies, interlayer distance and Ab initio molecular dynamic simulations (AIMD) calculations show that BSe–M(2)CO(2) (M = Ti, Zr, Hf) vdW heterostructures are stable with specific stacking and demonstrate that these heterostructures might be synthesized in the laboratory. The electronic band structure shows that all the studied vdW heterostructures have indirect bandgap nature – with the CBM and VBM at the Γ–K and Γ-point of BZ for BSe–Ti(2)CO(2), respectively; while for BSe–Zr(2)CO(2) and BSe–Hf(2)CO(2) vdW heterostructures the CBM and VBM lie at the K-point and Γ-point of BZ, respectively. Type-II band alignment in BSe–M(2)CO(2) (M = Ti, Zr, Hf) vdW heterostructures prevent the recombination of electron–hole pairs, and hence are crucial for light harvesting and detection. Absorption spectra are investigated to understand the optical behavior of BSe–M(2)CO(2) (M = Ti, Zr, Hf) vdW heterostructures, where the lowest energy transitions are dominated by excitons. Furthermore, BSe–M(2)CO(2) (M = Ti, Zr, Hf) vdW heterostructures are found to be potential photocatalysts for water splitting at pH = 0, and exhibit enhanced optical properties in the visible light zones.