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Jan-Niklas Heidkamp

Publications and source records attributed to Jan-Niklas Heidkamp.

3 recordsLinked to original sources

Mismatch between Raman shear modes and ferroelectric polarization in 3R-MoS$_{2}$

Sliding ferroelectricity in parallel-stacked two-dimensional van der Waals materials enables a broad range of novel device concepts, but exploiting it requires reliable, non-destructive assignment of the underlying stacking order and polarization state. Here, we combine Kelvin-probe force microscopy (KPFM) with low-frequency Raman spectroscopy to probe the polarization domains and stacking configurations of a exfoliated trilayer 3R-MoS$_{2}$ flake on a hBN substrate. We find that ABA and BAB - both stackings with zero net polarization - are indistinguishable in KPFM, yet show drastically different low-frequency shear modes. This observation is reproduced across multiple flakes and is corroborated by low-temperature photoluminescence. Notably, the standard bond-polarizability model does not account for the difference in shear-mode activity between the ABA and BAB configurations, indicating that the interlayer Raman response of these stackings is governed by physics beyond a simple polarizability picture. Our results show that none of the here-used individual techniques alone is sufficient to assign sliding-ferroelectric stacking order and motivate a combined spectroscopic-scanning-probe approach.

cond-mat.mes-hall

Ferroelectric Control of Interlayer Excitons in 3R-MoS$_{2}$ / MoSe$_{2}$ Heterostructures

We investigate the interaction between interlayer excitons and ferroelectric domains in hBN-encapsulated 3R-MoS$_2$/MoSe$_2$ heterostructures, combining photoluminescence experiments with density functional theory and many-body Green's function calculations. Low-temperature photoluminescence spectroscopy reveals a strong redshift of the interlayer exciton energy with increasing MoS$_2$ layer thickness, attributed to band renormalization and dielectric effects. We observe local variations in exciton energy that correlate with local ferroelectric domain polarization of the 3R-MoS$_2$ layer, showcasing distinct domain-dependent interlayer exciton transition energies. Gate voltage experiments demonstrate that the interlayer exciton energy can be tuned by electrically induced domain switching. These results highlight the potential for interlayer exciton control by local ferroelectric order and establish a foundation for future ferroelectric optoelectronic devices based on van der Waals heterostructures.

cond-mat.mtrl-sci

Investigating the Ferroelectric Potential Landscape of 3R-MoS$_2$ through Optical Measurements

In recent years, sliding ferroelectricity has emerged as a topic of significant interest due to its possible application in non-volatile, reconfigurable storage devices. This phenomenon is unique to two-dimensional van der Waals materials, where out-of-plane ferroelectric polarization switching is induced by relative in-plane sliding of adjacent layers. The intrinsic stacking order influences the resulting polarization, creating distinct polarization regions separated by domain walls. These regions and the domain walls can be manipulated using an applied vertical electric field, enabling a switchable system that retains the environmental robustness of van der Waals materials under ambient conditions. This study investigates 3R-MoS$_2$ using various optical measurement techniques at room temperature. The spatially resolved optical measurements reveal apparent signal changes corresponding to different ferroelectric stacking orders and variations in layer count. Our findings demonstrate that fast optical mapping at room temperature is a reliable method for probing ferroelectric potential steps in 3R-stacked MoS$_2$ samples, thereby facilitating the identification of the ferroelectric configuration. This approach does not require a conductive substrate or an electrical contact to the sample, making it more versatile than traditional atomic force probe techniques.

cond-mat.mtrl-sci