Paper-Based Disposable Molecular Sensor Constructed from Oxide Nanowires, Cellulose Nanofibers, and Pencil-Drawn Electrodes
Source abstract
Abstract
Progress toward the concept of “a trillion sensor universe” requires sensor devices to become more abundant, ubiquitous, and be potentially disposable. Here, we report a paper-based disposable molecular sensor device constructed from a nanowire sensor based on common zinc oxide (ZnO), a wood-derived biodegradable cellulose nanofiber paper substrate, and a low-cost graphite electrode. The ZnO nanowire/cellulose nanofiber composite structure is embedded in the surface of the cellulose nanofiber paper substrate via a two-step papermaking process. This structure provides a mechanically robust and efficiently bridged network for the nanowire sensor, while ensuring efficient access to target molecules and allowing reliable electrical contact with electrodes. The as-fabricated paper sensor device with pencil-drawn graphite electrodes exhibits efficient resistance change-based molecular sensing of NO2 as a model gas. The performance of our device is comparable to that of noble metal electrodes. Furthermore, we demonstrate cut-and-paste usability and easy disposal of the sensor device with its uniform in-plane sensing properties. Our strategy offers a disposable molecular sensing platform for use in future sensor network technologies.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gas Sensing Nanomaterials and Sensors · Advanced Chemical Sensor Technologies · Biosensors and Analytical Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga, Fukuoka 816-8580, Japan
Key Laboratory of Optoelectronic Technology and Systems of the Education Ministry of China, College of Optoelectronic Engineering, Chongqing University, Chongqing 400044, China
Funding
CAS-JSPS Joint Research Projects
References (33)
Show source-provided references
1. 10.3390/jsan103021710.3390/jsan1030217 ↗
2. 10.1021/acs.chemrev.6b0018710.1021/acs.chemrev.6b00187 ↗
3. 10.1108/SR-12-2013-75510.1108/SR-12-2013-755 ↗
4. Zhang J. · 2018
5. 10.3390/s1707160610.3390/s17071606 ↗
6. 10.1002/adfm.20160581710.1002/adfm.201605817 ↗
7. 10.2217/nnm.13.6410.2217/nnm.13.64 ↗
8. 10.1016/j.mseb.2007.01.04410.1016/j.mseb.2007.01.044 ↗
9. 10.3390/s1804105210.3390/s18041052 ↗
10. Umar A. · 2010
11. 10.3390/s1704068310.3390/s17040683 ↗
12. 10.1002/adma.20080317410.1002/adma.200803174 ↗
13. 10.1063/1.480436110.1063/1.4804361 ↗
14. 10.1039/C2EE23635D10.1039/C2EE23635D ↗
15. 10.1038/am.2014.910.1038/am.2014.9 ↗
16. 10.1021/nn304407r10.1021/nn304407r ↗
17. 10.1002/adfm.20130302410.1002/adfm.201303024 ↗
18. 10.1039/C4NR02036G10.1039/C4NR02036G ↗
19. 10.1002/adma.20140455510.1002/adma.201404555 ↗
20. 10.1038/srep0553210.1038/srep05532 ↗
21. 10.1038/srep3838910.1038/srep38389 ↗
22. 10.1021/acsnano.5b0241410.1021/acsnano.5b02414 ↗
23. 10.1021/acsami.7b1482710.1021/acsami.7b14827 ↗
24. 10.1038/ncomms817010.1038/ncomms8170 ↗
25. 10.1038/am.2016.14410.1038/am.2016.144 ↗
26. 10.1016/j.tsf.2009.03.22910.1016/j.tsf.2009.03.229 ↗
27. 10.1039/C4TA00387J10.1039/C4TA00387J ↗
28. 10.1016/j.snb.2015.04.03510.1016/j.snb.2015.04.035 ↗
29. 10.1103/PhysRevLett.96.07550510.1103/PhysRevLett.96.075505 ↗
30. 10.1021/jp311323210.1021/jp3113232 ↗
31. 10.1016/j.snb.2009.02.00810.1016/j.snb.2009.02.008 ↗
32. 10.1007/s40820-014-0023-310.1007/s40820-014-0023-3 ↗
33. 10.1038/srep0381210.1038/srep03812 ↗