Strong Photoluminescence Enhancement of MoS2 through Defect Engineering and Oxygen Bonding
Haiyan Nan, Zilu Wang, Wenhui Wang, Zheng Liang, Yan Lu, Qian Chen,, Daowei He, Pingheng Tan, Feng Miao, Xinran Wang, Jinlan Wang, Zhenhua Ni

TL;DR
This study demonstrates that defect engineering and oxygen bonding significantly enhance the photoluminescence of monolayer MoS2, offering a new approach to modulate optical properties for optoelectronic applications.
Contribution
The paper introduces a novel method of defect engineering combined with oxygen bonding to achieve large PL enhancement in MoS2, supported by experimental and theoretical analysis.
Findings
PL enhancement up to thousands of times at defect sites
Oxygen adsorption induces heavy p doping and exciton conversion
Defect engineering via oxygen plasma is effective and stable
Abstract
We report on a strong photoluminescence (PL) enhancement of monolayer MoS2 through defect engineering and oxygen bonding. Micro- PL and Raman images clearly reveal that the PL enhancement occurs at cracks/defects formed during high temperature vacuum annealing. The PL enhancement at crack/defect sites could be as high as thousands of times after considering the laser spot size. The main reasons of such huge PL enhancement include: (1) the oxygen chemical adsorption induced heavy p doping and the conversion from trion to exciton; (2) the suppression of non-radiative recombination of excitons at defect sites as verified by low temperature PL measurements. First principle calculations reveal a strong binding energy of ~2.395 eV for oxygen molecule adsorbed on an S vacancy of MoS2. The chemical adsorbed oxygen also provides a much more effective charge transfer (0.997 electrons per O2)…
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