Electrostatic Self-Assembly of Heterostructured In2O3/Ti3C2Tx Nanocomposite for High-Selectivity NO2 Gas Sensing at Room Temperature

Owing to high electrical conductivity, layered structure, and abundant surface functional groups, transition metal carbides/nitrides (MXenes) have received enormous interest in the field of gas sensors at room temperature. In this work, we synthesize a heterostructured nanocomposite with indium oxid...

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Published inChemosensors Vol. 13; no. 7; p. 249
Main Authors Guo, Yongjing, Zhang, Zhengxin, Feng, Hangshuo, Dai, Qingfu, Zhao, Qiuni, Duan, Zaihua, Guo, Shenghui, Yang, Li, Hou, Ming, Xia, Yi
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 01.07.2025
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Summary:Owing to high electrical conductivity, layered structure, and abundant surface functional groups, transition metal carbides/nitrides (MXenes) have received enormous interest in the field of gas sensors at room temperature. In this work, we synthesize a heterostructured nanocomposite with indium oxide (In2O3) decorated on titanium carbide (Ti3C2Tx) nanosheets by electrostatic self-assembly and develop it for high-selectivity NO2 gas sensing at room temperature. Self-assembly formation of multiple heterojunctions in the In2O3/Ti3C2Tx composite provide abundant NO2 gas adsorption sites and high electron transfer activity, which is conducive to improving the gas-sensing response of the In2O3/Ti3C2Tx gas sensor. Assisted by rich adsorption sites and hetero interface, the as-fabricated In2O3/Ti3C2Tx gas sensor exhibits the highest response to NO2 among various interference gases. Meanwhile, a detection limit of 0.3 ppm, and response/recovery time (197.62/93.84 s) is displayed at room temperature. Finally, a NO2 sensing mechanism of In2O3/Ti3C2Tx gas sensor is constructed based on PN heterojunction enhancement and molecular adsorption. This work not only expands the gas-sensing application of MXenes, but also demonstrates an avenue for the rational design and construction of NO2-sensing materials.
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ISSN:2227-9040
2227-9040
DOI:10.3390/chemosensors13070249