Highly Photoluminescent Molybdenum Oxide Quantum Dots: One-Pot Synthesis and Application in 2,4,6-Trinitrotoluene Determination

As a well-studied transition-metal semiconductor material, MoO x has a wider band gap than molybdenum disulfide (MoS2), and its property varies dramatically for the existence of several different allotropes and suboxide phases of molybdenum oxides (MoO x , x < 3). In this manuscript, a one-pot me...

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Published inACS applied materials & interfaces Vol. 8; no. 12; pp. 8184 - 8191
Main Authors Xiao, Sai Jin, Zhao, Xiao Jing, Hu, Ping Ping, Chu, Zhao Jun, Huang, Cheng Zhi, Zhang, Li
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 30.03.2016
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Summary:As a well-studied transition-metal semiconductor material, MoO x has a wider band gap than molybdenum disulfide (MoS2), and its property varies dramatically for the existence of several different allotropes and suboxide phases of molybdenum oxides (MoO x , x < 3). In this manuscript, a one-pot method possessing the advantages of one pot, easily prepared, rapid, and environmentally friendly, has been developed for facile synthesis of highly photoluminescent MoO x quantum dots (MoO x QDs), in which commercial molybdenum disulfide (MoS2) powder and hydrogen peroxide (H2O2) are employed as the precursor and oxidant, respectively. The obtained MoO x QDs can be further utilized as an efficient photoluminescent probe, and a new turn-off sensor is developed for 2,4,6-trinitrotoluene (TNT) determination based on the fact that the photoluminescence of MoO x QDs can be quenched by the Meisenheimer complexes formed in the strong alkali solution through the inner filter effect (IFE). Under the optimal conditions, the decreased photoluminescence of MoO x QDs shows a good linear relationship to the concentration of TNT ranging from 0.5 to 240.0 μM, and the limit of detection was 0.12 μM (3σ/k). With the present turn-off sensor, TNT in river water samples can be rapidly and selectively detected without tedious sample pretreatment processes.
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ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.5b11316