Detection of Trace Water Based on Electro-oxidation of Molybdenum Disulfide Nanomaterials to Form Molybdenum Oxysulfide

被引:10
|
作者
Liu, Di [1 ]
Bian, Yixuan [1 ]
Zhu, Zhiwei [1 ]
Shao, Yuanhua [1 ]
Li, Meixian [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
molybdenum disulfide; molybdenum oxysulfide; electro-oxidation; trace water detection; electrochemical sensors; REAL-TIME DETECTION; HYDROGEN EVOLUTION; ORGANIC-SOLVENTS; INDUCED EMISSION; IONIC LIQUIDS; MOS2; REDUCTION; FLUORESCENT; NANOPARTICLES; VOLTAMMETRY;
D O I
10.1021/acsami.2c02432
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Molybdenum disulfide nanomaterials nowadays are very popular in electrocatalysis field due to their outstanding catalytic performance toward many electrochemical reactions. However, the electrochemical oxidation reaction of molybdenum disulfide nanomaterials in the range of positive potential has not been studied thoroughly. Herein, we have investigated electro-oxidation of molybdenum disulfide nanomaterials and put forward a new reaction mechanism: molybdenum disulfide nanomaterials are electro-oxidized with water to form molybdenum oxysulfide (MoOS2) and hydrogen ions, leading to the release of hydrogen on the counter electrode. Various characterization methods such as contact angle measurement, scanning electron microscope (SEM), transmission electron microscope (TEM) with energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray absorption near edge structure (XANES) spectroscopy, time-of-flight secondary ion mass spectrometry (ToF-SIMS), and gas chromatography (GC) were applied to attest the doping of oxygen and the generation of hydrogen. Based on this reaction, we constructed a novel ultrasensitive electrochemical sensor for detecting trace water with the minimum detectable content of 0.0010% (v/v) in various organic solvents and ionic liquids, which is comparable to the Karl Fischer titration, but with much simpler reagent.
引用
收藏
页码:23850 / 23858
页数:9
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