The need for high‐quality large‐scale monolayers of layered materials pushes the development of scalable gold‐mediated exfoliations. Gold proves to be a suitable adhesive for exfoliation of several 2D materials. However, the extension to other noble metals remains underwhelming as gold outperforms all previously studied metals by a large margin. This is attributed to compromised stability against oxidation and surface contamination of less noble metals, leading to nonideal interfaces for exfoliation. The closest competitor to gold is silver, where gold still leads by a factor 100 regarding exfoliated layer size. In this work, a silver‐mediated exfoliation process performing on par with gold is presented. The combination of freshly cleaved silver surfaces with a low‐temperature annealing is found to be crucial. The exfoliation yield shows a dependence with annealing temperature, leading to loss in exfoliation performance for higher temperature. Raman studies indicate inhomogeneous strain for the MoS2/Ag interface at these temperatures, which hints at the competing factors of thermal activation versus oxidation of silver. Finally, a transfer process is implemented to promote silver to a fully functional exfoliation substrate. Ultimately, heating up exfoliations tips the strict balance between interfacial interactions and surface contaminations toward robust high monolayer yield exfoliation as demonstrated for silver.
Abstract2D transition metal dichalcogenides (TMDCs) are atomically‐thick semiconductors with great potential for next‐generation optoelectronic applications, such as transistors and sensors. Their large surface‐to‐volume ratio makes them energy‐efficient but also extremely sensitive to the physical‐chemical surroundings. The latter must be carefully considered when predicting the electronic behavior, such as their energy level alignment, which ultimately affects the charge carrier injection and transport in devices. Here, local doping is demonstrated and thus adjusting the opto‐electronic properties of monolayer TMDCs (WSe2 and MoS2) by chemically engineering the surface of the supporting substrate. This is achieved by decorating the substrate by microcontact printing with patterns of two different self‐assembled monolayers (SAMs). The SAMs posses distinct molecular dipoles and dielectric constants, significantly influencing the TMDCs electronic and optical properties. By analyzing (on various substrtates), it is confirmed that these effects arise solely from the interaction between SAMs and TMDCs. Understanding the diverse dielectric environments experienced by TMDCs allows for a correlation between electronic and optical behaviours. The changes primarily involve alteration in the electronic band gap width, which can be calculated using the Schottky‐Mott rule, incorporating the dielectric screening of the TMDCs surroundings. This knowledge enables accurate prediction of the (opto‐)electronic behavior of monolayer TMDCs for advanced device design.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.