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Progress in Chemistry 2021, Vol. 33 Issue (2): 232-242 DOI: 10.7536/PC200506 Previous Articles   Next Articles

• Review •

Application for Exhaled Gas Sensor Based on Novel Mxenes Materials*

Jixiu Zhu1, Qiaofen Chen2, Titong Ni1, Aimin Chen1,*(), Jianmin Wu2,*()   

  1. 1 College of Chemical Engineering, Zhejiang University of Technology,Hangzhou 310014, China
    2 Institute of Analytical Chemistry, Department of Chemistry, Zhejiang University, Hangzhou 310058, China
  • Received: Revised: Online: Published:
  • Contact: Aimin Chen, Jianmin Wu
  • About author:
    * Corresponding author e-mail: (Aimin Chen);
  • Supported by:
    National Natural Science Foundation of China(21575127); Natural Science Foundation of Zhejiang Province(LY19B050004)
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In order to detect, analyze, and identify exhaled gas, electronic-nose combined with artificial intelligence has become a hot spot in the field of non-invasive medical detection. However, gas sensing materials cannot meet the requirements of high sensitivity as well as high selectivity at room temperature, which seriously hinders the application of gas sensors in the field of health care. It is still challenging to find suitable materials for the electronic-nose. With many unique properties: a wide variety, large specific surface area, strong electrical conductivity, rich functional groups on the surface, and adjustable bandwidth, novel two-dimensional MXenes material has become a star candidate for the gas sensor of highly sensitive and low energy consumption. In this review, we summarize the latest research achievements of MXenes based materials with the special structure in gas sensing, focus on the gas sensing mechanism and modification methods, and probe into the problems and challenges still existing in the application of MXenes materials in gas sensing.

Contents

1 Introduction

2 Synthesis of MXenes

3 Structure and properties of MXenes

3.1 Structure of MXenes

3.2 MXenes electronic characteristics for gas sensing

4 Application of MXenes in gas sensing

4.1 Surface adsorption calculation of MXenes

4.2 Gas sensing performance of MXenes

4.3 Gas sensing mechanism of MXenes

5 Conclusion and outlook

Fig.1 Schematic crystal structures and electron microscopy images for MXenes.(a) Schematic illustrating evolution from MAX phases to MXenes;(b~d) SEM images of Ti2CTx, Ti3C2Tx and Ta4C3Tx[49]
Table 1 The preparation reaction conditions of HF etched MXenes were partly based on HF etched MXenes
Fig.2 Side views of pristine(a) M3X2,(b) M4X3,(c) M'2M″X2, and(d) M'2M″2X3 MXenes, where M, M', and M″ denote transition metals, and X represents C or N[71]
Table 2 Bandgap width for some MXenes
Fig.3 (a) Adsorption sites of different gases on Ti2CO2 MXene[81];(b) charge adsorbed density distribution[81];(c) predicted I-V characteristics of Ti2CO2 with NH3 and CO2 molecules[81];(d) predicted I-V characteristics of Sc2CO2 with SO2 molecules[83]
Fig.4 (a) A gas sensor made from Ti3C2Tx drop-cast on an interdigitated circuit[88];(b) Maximal SNR values of sensors upon exposure to 100 ppm of acetone, ethanol, ammonia, and propanal[89];(c) Maximal resistance change upon exposure to 100 ppm of acetone, ethanol, ammonia, propanal, NO2, SO2, and 10 000 ppm of CO2 at room temperature(25 ℃)[89];(d) Resistance variation versus time upon exposure to highly diluted acetone(top), ethanol(middle), and ammonia(bottom) in ppb concentration range(50~1000 ppb)[89]
Table 3 Gas sensing performance of MXene-based gas sensor
Fig.5 (a) Real-time sensing response of Ti3C2Tx and Ti3C2Tx/WSe2 gas sensors upon ethanol exposure with concentrations ranging from 1 to 40 ppm[94];(b) Enhanced sensing mechanism of Ti3C2Tx/WSe2 heterostructure[94];(c) A multielectrode chip with a film of partially oxidized MXenes flakes prepared by drop-casting[95];(d) LDA diagram of partially oxidized MXenes sensor[95]
Fig.6 (a) Schematic illustration of the spinning process for MXene/GO hybrid fiber;(b) The resistance change of MXene/rGO hybrid fiber exposed to 100 ppm of NH3 at room temperature during fiber cyclic bending;(c) MXene/rGO hybrid fibers were woven in a lab coat and connected to a multimeter;(d) Gas response of 100 ppm of NH3 molecules in MXene/rGO hybrid fibers woven into a lab coat[98]
Fig.7 (a) Minimum binding energies of acetone and ammonia on Ti3C2(OH)2, Ti3C2O2, Ti3C2F2, graphene, MoS2, and BP[89];(b) The(002) peak shift of Ti3C2Tx film during introduction of ethanol(0.1%) for 70 min, followed by N2 purging for 120 min to purge out target gases[106]
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Koh H J, Kim S J, Maleski K, Cho S Y, Kim Y J, Ahn C W, Gogotsi Y, Jung H T. ACS Sens., 2019, 4(5):1365. Gas molecules are known to interact with two-dimensional (2D) materials through surface adsorption where the adsorption-induced charge transfer governs the chemiresistive sensing of various gases. Recently, titanium carbide (Ti3C2T x) MXene emerged as a promising sensing channel showing the highest sensitivity among 2D materials and unique gas selectivity. However, unlike conventional 2D materials, MXenes show metallic conductivity and contain interlayer water, implying that gas molecules will likely interact in a more complex way than the typical charge transfer model. Therefore, it is important to understand the role of all factors that may influence gas sensing. Here, we studied the gas-induced interlayer swelling of Ti3C2T x MXene thin films and its influence on gas sensing performance. In situ X-ray diffraction was employed to simultaneously measure dynamic swelling behavior where Ti3C2T x MXene films displayed selective swelling toward ethanol vapor over CO2 gas. Results show that the controlling sodium ion concentration in the interlayers is highly important in tuning the swelling behavior and gas sensing performance. The degree of swelling matched well with the gas response intensity, and the highest gas selectivity toward ethanol vapor was achieved for Ti3C2T x sensing channels treated with 0.3 mM NaOH, which also displayed the largest amount of swelling. Our results demonstrate that controlling the interlayer transport of Ti3C2T x MXene is essential for enhancing the selective sensing of gas molecules.

doi: 10.1021/acssensors.9b00310 pmid: 31062965
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