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Peer-reviewedCC BY 4.0Nanomaterials

Region-Functionalized Laser-Induced Graphene Sensor Array for Flexible and Intelligent Multi-Gas Detection

  1. 1AVIC Chengdu Aircraft Industrial (Group) Co., Ltd., Chengdu 610092, China
  2. 2School of Instrument Science and Opto-Electronics Engineering, Beijing Information Science and Technology University, Beijing 100192, China
  3. 3Laboratory of Intelligent Microsystems, Beijing Information Science and Technology University, Beijing 100192, China

Abstract

Flexible multi-gas sensor array has promising applications in wearable monitoring, environmental safety and intelligent sensing systems. In this work, a flexible 2 × 2 multi-gas sensor array based on region-functionalized laser-induced graphene (LIG) was developed for room-temperature gas detection and intelligent identification. MXene, MoS2, TiO2 and CuO were selectively introduced into different regions of a polyimide substrate, followed by femtosecond pulsed-laser direct writing to form four functionally differentiated LIG-based sensing units. The porous LIG network simultaneously serves as the conductive pathway, gas-adsorption interface, and sensing electrode, enabling the integration of multiple sensing functions within a single flexible platform. The gas-sensing results show that the array exhibits differential response characteristics toward NH3, H2S, acetone, and ethanol. LIG@MXene exhibited a pronounced and repeatable response toward NH3, whereas LIG@MoS2, LIG@TiO2, and LIG@CuO showed preferential responses toward H2S, acetone, and ethanol, respectively. The distinct response amplitudes and polarities of the four sensing channels provide multidimensional features for gas-condition identification. The device also maintained relatively stable NH3 sensing performance under mechanical bending, with a response retention of approximately 84.2% at a bending angle of 120°. Based on the multidimensional response signals of the four-channel array, a backpropagation neural network (BPNN) was employed for gas-condition identification. The overall correlation coefficient between the network outputs and the numerically encoded target labels reached 0.99974 for the single-gas dataset and 0.94894 for the mixed-gas dataset. This study provides an effective strategy for integrating region-specific material functionalization, flexible laser fabrication, multi-channel sensing, and intelligent gas identification within a single LIG-based sensing platform.

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BibTeX
@article{wang2026regionfunctionalized,
  title = {{Region-Functionalized Laser-Induced Graphene Sensor Array for Flexible and Intelligent Multi-Gas Detection}},
  author = {Wengan Wang and Chaoqi Zhang and Guiyong Chen and Peihao Xu and Fan Wu and Misheng Liang and Rui You},
  journal = {Nanomaterials},
  year = {2026},
  month = oct,
  doi = {10.3390/nano16201321},
  url = {https://www.mdpi.com/2079-4991/16/20/1321},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Region-Functionalized Laser-Induced Graphene Sensor Array for Flexible and Intelligent Multi-Gas Detection
AU  - Wengan Wang
AU  - Chaoqi Zhang
AU  - Guiyong Chen
AU  - Peihao Xu
AU  - Fan Wu
AU  - Misheng Liang
AU  - Rui You
PY  - 2026
DA  - 2026/10/01
JO  - Nanomaterials
DO  - 10.3390/nano16201321
UR  - https://www.mdpi.com/2079-4991/16/20/1321
AB  - Flexible multi-gas sensor array has promising applications in wearable monitoring, environmental safety and intelligent sensing systems. In this work, a flexible 2 × 2 multi-gas sensor array based on region-functionalized laser-induced graphene (LIG) was developed for room-temperature gas detection and intelligent identification. MXene, MoS2, TiO2 and CuO were selectively introduced into different regions of a polyimide substrate, followed by femtosecond pulsed-laser direct writing to form four functionally differentiated LIG-based sensing units. The porous LIG network simultaneously serves as the conductive pathway, gas-adsorption interface, and sensing electrode, enabling the integration of multiple sensing functions within a single flexible platform. The gas-sensing results show that the array exhibits differential response characteristics toward NH3, H2S, acetone, and ethanol. LIG@MXene exhibited a pronounced and repeatable response toward NH3, whereas LIG@MoS2, LIG@TiO2, and LIG@CuO showed preferential responses toward H2S, acetone, and ethanol, respectively. The distinct response amplitudes and polarities of the four sensing channels provide multidimensional features for gas-condition identification. The device also maintained relatively stable NH3 sensing performance under mechanical bending, with a response retention of approximately 84.2% at a bending angle of 120°. Based on the multidimensional response signals of the four-channel array, a backpropagation neural network (BPNN) was employed for gas-condition identification. The overall correlation coefficient between the network outputs and the numerically encoded target labels reached 0.99974 for the single-gas dataset and 0.94894 for the mixed-gas dataset. This study provides an effective strategy for integrating region-specific material functionalization, flexible laser fabrication, multi-channel sensing, and intelligent gas identification within a single LIG-based sensing platform.
SN  - 2079-4991
ER  -