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RESEARCH PRODUCT

Quantum size confinement in gallium selenide nanosheets: band gap tunability versus stability limitation

Juan F. Sánchez-royoJuan P. Martínez-pastorDaniel Andres-penaresAna Cros

subject

Materials scienceBand gapBioengineering02 engineering and technology010402 general chemistrymedicine.disease_cause01 natural sciencesDesorptionmedicineGeneral Materials ScienceElectrical and Electronic EngineeringNanosheetbusiness.industryMechanical EngineeringRelaxation (NMR)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSemiconductorMechanics of MaterialsQuantum dotOptoelectronics0210 nano-technologyLuminescencebusinessUltraviolet

description

Abstract Gallium selenide is one of the most promising candidates to extend the window of band gap values provided by existing two-dimensional semiconductors deep into the visible potentially reaching the ultraviolet. However, the tunability of its band gap by means of quantum confinement effects is still unknown, probably due to poor nanosheet stability. Here, we demonstrate that the optical band gap band of GaSe nanosheets can be tuned by ∼120 meV from bulk to 8 nm thick. The luminescent response of very thin nanosheets (<8 nm) is strongly quenched due to early oxidation. Oxidation favors the emergence of sharp material nanospikes at the surface attributable to strain relaxation. Simultaneously, incorporated oxygen progressively replaces selenium giving rise to Ga2O3, with a residual presence of Ga2Se3 that tends to desorb. These results are relevant for the development and design of visible/ultraviolet electronics and optoelectronics with tunable functionalities based on atomically thin GaSe.

https://doi.org/10.1088/1361-6528/aa669e