Growth mechanism and atomic structure of group-IIA compound-promoted CVD-synthesized monolayer transition metal dichalcogenides.

Nanoscale

Science and Technology on Advanced Ceramic Fibers and Composites Laboratory, College of Aerospace Science and Engineering, National University of Defense Technology, Changsha 410073, P. R. China.

Published: August 2021

Developing promoters that can boost the growth quality, efficiency, and robustness of two-dimensional (2D) transition metal dichalcogenides is significant for their industrial applications. Herein a new group (group IIA) of promoters in the periodic table has been disclosed, whose chlorides (especially CaCl and SrCl) exhibit a versatile promoting effect on the CVD growth of various TMD monolayers, including hexagonal MoS, MoSe, Re doped MoS, and triclinic ReS. The promoting effect of group IIA promoters relies on the appropriate dose and is strongly substrate-dependent. The performances of five typical group IA-IIA metal chlorides are ranked by quantitative investigations, displaying periodic variations closely related to the electronegativities of the metal elements. A brand-new acid-base match model is proposed, attributing the promoting mechanism to an increase of the substrate basicity due to the usage of promoters, thus leading to the sufficient adsorption of the acidic precursor. Aberration-corrected annular dark field scanning transmission electron microscopy (ADF-STEM) was applied, unveiling anomalous grain boundaries (GBs) with a low density of coincident sites in the as-grown ReS and detailed atomic configurations of Re doped MoS. This work expands the promoter library and gives an insight into GB engineering for the CVD growth of 2D TMDs.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d1nr03273aDOI Listing

Publication Analysis

Top Keywords

transition metal
8
metal dichalcogenides
8
group iia
8
iia promoters
8
cvd growth
8
doped mos
8
growth
4
growth mechanism
4
mechanism atomic
4
atomic structure
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!