Electrochemically Chlorinated Graphene for Ultrafast NO2 Detection at Room Temperature
Functionalization of two-dimensional (2D) materials is a key approach to enhancing the performance of gas sensors since it effectively modulates the intrinsic chemical properties. Various atoms have been exploited to change molecular interaction between sensing materials and target species. Especial...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
2025
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Online Access | Get full text |
ISSN | 2050-7488 2050-7496 |
DOI | 10.1039/D5TA05009J |
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Summary: | Functionalization of two-dimensional (2D) materials is a key approach to enhancing the performance of gas sensors since it effectively modulates the intrinsic chemical properties. Various atoms have been exploited to change molecular interaction between sensing materials and target species. Especially, chlorine has been widely studied due to its extremely high surface reactivity and high electronegativity. However, traditional chlorination methods have been conducted by hazardous processes. Herein, we report a non-toxic electrochemical chlorination of graphene that enables superior nitrogen dioxide (NO2) gas sensing properties at room temperature. Chlorinated graphene (Cl-Gr) was synthesized by an electrochemical reaction using an aqueous sodium chloride (NaCl) solution under an applied voltage. The Cl-Gr gas sensors exhibit enhanced sensitivity and improved reversibility upon exposure to NO2 at room temperature. The response and recovery time were dramatically decreased by 75.8% and 86.4%, respectively. The role of chlorine on the sensing performance is investigated by first-principles density functional theory (DFT) calculations, which are in agreemenet with experimental results. This work extends the potential use of functionalized 2D material-based gas sensors and deepens the understanding of their gas sensing mechanism. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/D5TA05009J |