Abstract

The morphology of CVD-grown molybdenum disulfide (MoS2) is sensitive to the local precursor environment, which governs nucleation density, edge stability, and growth kinetics. In this work, we systematically investigate the effect of precursor ratio on the morphological evolution of MoS2 microstructures synthesized by atmospheric-pressure chemical vapor deposition on SiO2/Si substrates. By varying the relative amounts of MoO3 and sulfur precursors, distinct growth regimes were obtained, ranging from compact hexagonal and quasi-circular domains to multilayer hexagonal structures, triangular domains, and dendritic morphologies. At higher MoO3 loading, growth is dominated by dense nucleation, leading to isolated few-layer hexagonal domains. A moderate reduction in Mo precursor concentration promotes diffusion-assisted growth and secondary nucleation, resulting in multilayer hexagonal structures with aligned or slightly rotated stacked layers. Under sulfur-rich conditions, morphology evolves into triangular domains due to anisotropic edge stabilization, while further increase in sulfur concentration gives rise to branched dendritic structures through kinetically limited, diffusion-dominated growth. Cross-sectional FIB analysis reveals dense vertical stacking and lateral displacement of upper layers in the multilayer hexagonal domains. Raman and photoluminescence measurements confirm strong correlations between morphology, layer thickness, and optical response, with thinner regions exhibiting reduced Raman peak separation, enhanced photoluminescence intensity, and blue-shifted excitonic transitions. The results show that, under fixed APCVD reactor geometry, source positions, temperature profile, carrier-gas flow, and nominal growth duration, the nominal MoO3 to sulfur source-loading ratio reproducibly correlates with the transition between compact hexagonal, multilayer hexagonal, triangular, and dendritic MoS2 morphologies on amorphous SiO2/Si substrates. Because vapor-phase Mo- and S-containing partial pressures were not directly measured, this ratio is treated as a nominal source-inventory descriptor rather than as a direct vapor-phase stoichiometric ratio. The observed trends are interpreted using a qualitative thermodynamic and kinetic framework based on precursor fluence, nucleation density, edge stability, and diffusion-limited growth.

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