MARATTO

article · Scientific Reports

Surface structural probing and photoelectrochemical characterization of electrodeposited MoS2 nanostructured thin film

20256 citationsOpen accessOsun State University

Abstract

Molybdenum disulfide (MoS2) has advantageous traits and characteristics that make it suitable for a diverse array of practical applications, such as optoelectronics and gas sensing. Enhancing the surface area of the adsorbent leads to a proportional increase in its performance. Hence, the synthesized two-electrode electrodeposited MoS2 (ED-MoS2) thin films were microstructurally characterized to investigate its surface modulation for suitable enhancement in its applicative properties. The characterization shows that the surface properties of the deposited film can easily be modulated to favor its needs and can be done by simply varying its electrodeposition parameters, such as growth period and voltage supplied. In addition, persistent n-type conductivity of intrinsic MoS2 makes it challenging to achieve p-type conductivity. By simply varying the cathodic potential, the challenge of obtaining p-type MoS2 thin films was solved. The photoelectrochemical cell measurements revealed that lower cathodic potentials (1.15–1.35 V) favored the growth of p-type MoS2 layers while the growth of n-type MoS layers was achieved at the higher cathodic potential.

Research topics

  • Chalcogenide Semiconductor Thin Films
  • 2D Materials and Applications
  • Copper-based nanomaterials and applications

Read the original research

This page summarises published work. The authoritative version sits with the publisher.

DOI: 10.1038/s41598-025-96930-7

Is something wrong with this record? Report it or request removal.

Discussion

Discuss this research

Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.

No discussion yet. Open the first thread.