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Review
. 2024 Jul 10;24(14):4465.
doi: 10.3390/s24144465.

Research Progress on Ammonia Sensors Based on Ti3C2Tx MXene at Room Temperature: A Review

Affiliations
Review

Research Progress on Ammonia Sensors Based on Ti3C2Tx MXene at Room Temperature: A Review

Kaixin Cheng et al. Sensors (Basel). .

Abstract

Ammonia (NH3) potentially harms human health, the ecosystem, industrial and agricultural production, and other fields. Therefore, the detection of NH3 has broad prospects and important significance. Ti3C2Tx is a common MXene material that is great for detecting NH3 at room temperature because it has a two-dimensional layered structure, a large specific surface area, is easy to functionalize on the surface, is sensitive to gases at room temperature, and is very selective for NH3. This review provides a detailed description of the preparation process as well as recent advances in the development of gas-sensing materials based on Ti3C2Tx MXene for room-temperature NH3 detection. It also analyzes the advantages and disadvantages of various preparation and synthesis methods for Ti3C2Tx MXene's performance. Since the gas-sensitive performance of pure Ti3C2Tx MXene regarding NH3 can be further improved, this review discusses additional composite materials, including metal oxides, conductive polymers, and two-dimensional materials that can be used to improve the sensitivity of pure Ti3C2Tx MXene to NH3. Furthermore, the present state of research on the NH3 sensitivity mechanism of Ti3C2Tx MXene-based sensors is summarized in this study. Finally, this paper analyzes the challenges and future prospects of Ti3C2Tx MXene-based gas-sensitive materials for room-temperature NH3 detection.

Keywords: Ti3C2Tx MXene; ammonia; gas sensors; room-temperature; sensitivity mechanism.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 4
Figure 4
(a) Dynamic response curves of TT8 h-, TT12 h-, TT16 h- and TT32 h-based sensors; (b) dynamic response curves with UV illumination on T-T-12 h and without UV illumination on TT12 h; (c) schematic illustration of band diagrams of Ti3C2Tx and (001) TiO2; (d) schematic illustration of ammonia gas-sensing mechanism under UV irradiation [64]. (e) The transient response curves of the composite sensors with different WO3 contents to 1 ppm NH3 at room temperature; (f) the dependence of the composite sensor response on the WO3 content; (g) schematic illustration of the gas-sensing mechanism and the energy band structure diagram of Ti3C2Tx/WO3 before and after exposed NH3 [70].
Figure 5
Figure 5
(a) SEM image of Ti3C2Tx MXene; (b) SEM image of PANI/Ti3C2Tx; (c) PANI/Ti3C2Tx composite nanofiber sensor for the detection of NH3 at room temperature; (d) UPS spectra of pure Ti3C2Tx sensor and (e) PANI/Ti3C2Tx composite sensors; (f) the PANI/Ti3C2Tx-based flexible sensor bent at different angles [82]. FESEM images of (g) Ti3C2Tx MXene (inset is Ti3C2Tx MXene on an AAO membrane) and (h) PEDOT:PSS/Ti3C2Tx MXene composites. The cross-sectional FESEM images of (i) Ti3C2Tx MXene films and (j) PEDOT:PSS/Ti3C2Tx MXene films, (k) effect of the Ti3C2Tx MXene content in PEDOT-PSS on the sensor response toward 100 ppm NH3 at room temperature (27 °C), and (l) gas response of the PEDOT:PSS/Ti3C2Tx MXene composite-based sensor against 100 ppm NH3 bent at different angles [94].
Figure 1
Figure 1
Ti3AlC2 is etched as Ti3C2Tx. (a) Structural schematic diagram of Ti3AlC2, (b) schematic of the process by which -OH replaces Al atoms after HF treatment, and (c) hydrogen bond breaking and nanolayer separation after sonication treatment [14].
Figure 2
Figure 2
(a) SEM image of the Ti3C2Tx MXene after HF treatment; (b) by comparing the single-layer band structures of Ti3C2(OH)2, Ti3C2F2, and Ti3C2, it can be seen that Ti3C2Tx exhibits a change from metal to semiconductor due to changes in surface functional groups [14]; (c) XRD pattern of Ti3AlC2 and as-prepared Ti3C2Tx; (d) SEM images of Ti3C2 nanoflakes after exfoliation by TMAOH [33].
Figure 3
Figure 3
Adsorption process of H2O and NH3 molecules on the surface of alkalized Ti3C2Tx [40].
Figure 6
Figure 6
The resistance variation curves of the SM-5 sensor to (a) ppm-level NH3 concentration from 2 to 100 ppm and (b) ppb-level NH3 concentration from 10 ppb to 1 ppm at 18 °C; (c) the long-term stability of the SM-5 sensor to 1 ppm NH3 for 20 days [56]. (d,e) Ti3C2Tx MXene@TiO2/MoS2; (f) dynamic sensing performance of the sensor-based Ti3C2Tx MXene to NH3 at a room temperature of 27 °C and an RH of 43%; (g) energy band diagrams of Ti3C2Tx MXene@TiO2/MoS2 sensors [30].
Figure 7
Figure 7
(a) Comparison of the gas response of MXene film, rGO fiber, and MXene/rGO hybrid fiber; (b) schematic illustration of the fiber bending test. The “M” stands for multimeter. (c) Cyclic bending fatigue versus resistance difference of the rGO fiber and MXene/rGO hybrid fiber [19]. (d) FE-SEM images of Ti3C2Tx MXene/GO/CuO/ZnO nanocomposite and (e) pristine Ti3C2Tx Mxene. (f) Schematic diagram of the energy band structure of the Ti3C2Tx MXene/GO/CuO/ZnO heterostructure [25].
Figure 8
Figure 8
(a) Schematic diagram of the possible gas-sensing mechanisms of the Ti3C2Tx MXene for NH3 [18]. (b) The gas-sensing mechanism diagram of the Ti3C2Tx/In2O3 composite materials. (c,d) Schematic diagram of the electron transfer at the interface of Ti3C2Tx/In2O3 composite materials in the air and NH3 [57].

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