U.S. flag

An official website of the United States government

PubAg

Main content area

Influence of the Substrate on the Optical and Photo-electrochemical Properties of Monolayer MoS₂

Author:
Wang, Li, Nilsson, Zach N., Tahir, Muhammad, Chen, Hua, Sambur, Justin B.
Source:
ACS applied materials & interfaces 2020 v.12 no.13 pp. 15034-15042
ISSN:
1944-8252
Subject:
Raman spectroscopy, atomic force microscopy, catalytic activity, electric current, electrochemistry, electrodes, iodides, light microscopy, molybdenum disulfide, optical properties, oxidation, photoluminescence, quartz, tin dioxide, transistors
Abstract:
Substrates influence the electrical and optical properties of monolayer (ML) MoS₂ in field-effect transistors and photodetectors. Photoluminescence (PL) and Raman spectroscopy measurements have shown that conducting substrates can vary the doping concentration and influence exciton decay channels in ML-MoS₂. Doping and exciton decay dynamics are expected to play a major role in the efficiency of light-driven chemical reactions, but it is unclear to what extent these factors contribute to the photo(electro)catalytic properties of ML-MoS₂. Here, we report spatially resolved PL, Raman, and photo-electrochemical current measurements of 5–10 μm-wide ML-MoS₂ triangles deposited on pairs of indium-doped tin oxide (ITO) electrodes that are separated by a narrow insulating quartz channel [i.e., an ITO interdigitated array (IDA) electrode]. Optical microscopy images and atomic force microscopy measurements revealed that the ML-MoS₂ triangles lie conformally on the quartz and ITO substrates. The PL spectrum of MoS₂ shifts and decreases in intensity in the ITO region, which can be attributed to differences in nonradiative and radiative exciton decay channels. Raman spectra showed no significant peak shifts on the two substrates that would have indicated a substrate-induced doping effect. We spatially resolved the photo-electrochemical current because of hole-induced iodide oxidation and observed that ML-MoS₂ produces lower photocurrents in the quartz region than in the ITO region. The correlated PL, Raman, and photocurrent mapping data show that the MoS₂/quartz interface diminishes fast nonradiative exciton decay pathways but the photocurrent response in the quartz region is likely limited by inefficient in-plane carrier transport to the ITO electrode because of carrier recombination with S vacancies in MoS₂ or charged impurities in the quartz substrate. Nonetheless, the experimental methodology presented herein provides a framework to evaluate substrate engineering strategies to tune the (photo)electrocatalytic properties of two-dimensional materials.
Agid:
6875620