Advanced Materials · 2021 · 99 citations · 51 references
EngineeringMaterials SciencePhysicsNanotechnologyPhotonicsSemiconductor MaterialsNanomaterial CharacterizationNanomechanicsSemiconductor NanomaterialsStrain EngineeringTwo-dimensional NanomaterialsTwo-dimensional SemiconductorsEnergy TransferExciton TransportNanostructured SemiconductorsPhotoluminescence SpectroscopyThin-film SemiconductorsTransition Metal DichalcogenidesTunable Photonic DevicesTwo-dimensional Materials
Abstract The tunability of the bandgap, absorption and emission energies, photoluminescence (PL) quantum yield, exciton transport, and energy transfer in transition metal dichalcogenide (TMD) monolayers provides a new class of functions for a wide range of ultrathin photonic devices. Recent strain‐engineering approaches have enabled to tune some of these properties, yet dynamic control at the nanoscale with real‐time and ‐space characterizations remains a challenge. Here, a dynamic nano‐mechanical strain‐engineering of naturally‐formed wrinkles in a WSe 2 monolayer, with real‐time investigation of nano‐spectroscopic properties is demonstrated using hyperspectral adaptive tip‐enhanced PL ( a ‐TEPL) spectroscopy. First, nanoscale wrinkles are characterized through hyperspectral a ‐TEPL nano‐imaging with <15 nm spatial resolution, which reveals the modified nano‐excitonic properties by the induced tensile strain at the wrinkle apex, for example, an increase in the quantum yield due to the exciton funneling, decrease in PL energy up to ≈10 meV, and a symmetry change in the TEPL spectra caused by the reconfigured electronic bandstructure. Then the local strain is dynamically engineered by pressing and releasing the wrinkle apex through an atomic force tip control. This nano‐mechanical strain‐engineering allows to tune the exciton dynamics and emission properties at the nanoscale in a reversible fashion. In addition, a systematic switching and modulation platform of the wrinkle emission is demonstrated, which provides a new strategy for robust, tunable, and ultracompact nano‐optical sources in atomically thin semiconductors.
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