journal article·2019-01-30

Chemical Detection Using a Metal–Organic Framework Single Crystal Coupled to an Optical Fiber

Chen Zhu, Jason A. Perman, Rex E. Gerald, Shengqian Ma, Jie Huang

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Abstract

The quantitative detection and real-time monitoring of target chemicals in the liquid phase are made possible by combining the tailored adsorption properties of metal-organic framework (MOF) material and the precise measuring capabilities of an optical fiber (OF) Fabry-Pérot interferometer (FPI) device. As the single-crystal MOF host adsorbs target analyte guests from the environment, its dielectric properties change causing the reflection spectrum derived from the FPI device to shift. A single crystal of HKUST-1 was attached to the end-face of an OF to form the sensor OF∪MOF (∪, union). The sensor's response curve was accurately measured using low concentrations of the target analyte nitrobenzene, an explosive simulant. Additionally, the uptake rate of nitrobenzene into the MOF single crystal was characterized. The experimental results show that the sensor achieved quantitative and real-time adsorption measurements of a target analyte.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Gas Sensing Nanomaterials and Sensors · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Electrical and Computer Engineering, Missouri University of Science and Technology, Rolla, Missouri 65409 United States

Department of Chemistry, University of South Florida, 4202 East Flower Avenue, Tampa, Florida 33620, United States

Funding

University of South Florida · Division of Materials Research · Materials Research Center, Missouri University of Science and Technology · Office of Research, Graduate Studies and Economic Development, University of Missouri

References (38)

Show source-provided references
1. 10.1021/cr068102g10.1021/cr068102g ↗
2. 10.1021/acs.chemrev.6b0018710.1021/acs.chemrev.6b00187 ↗
3. 10.1039/C4CS00010B10.1039/C4CS00010B ↗
4. 10.1002/anie.20120888510.1002/anie.201208885 ↗
5. 10.1016/j.snb.2008.06.01810.1016/j.snb.2008.06.018 ↗
6. 10.1109/LPT.2018.288172110.1109/LPT.2018.2881721 ↗
7. 10.1016/j.snb.2017.04.01410.1016/j.snb.2017.04.014 ↗
8. 10.1021/cr300014x10.1021/cr300014x ↗
9. 10.1039/b903811f10.1039/b903811f ↗
10. MacGillivray L. R. · 201010.1002/9780470606858 ↗
11. Farrusseng D. · 201110.1002/9783527635856 ↗
12. Ma S. · 201810.1142/10616 ↗
13. 10.1039/C7CS90049J10.1039/C7CS90049J ↗
14. 10.1021/ac500235510.1021/ac5002355 ↗
15. 10.1002/ange.20090204510.1002/ange.200902045 ↗
16. 10.1016/j.snb.2015.07.02710.1016/j.snb.2015.07.027 ↗
17. 10.1039/C6CS00930A10.1039/C6CS00930A ↗
18. 10.1021/cr200324t10.1021/cr200324t ↗
19. 10.1021/ja101415b10.1021/ja101415b ↗
20. 10.1021/ac102127p10.1021/ac102127p ↗
21. 10.3390/s9030157410.3390/s90301574 ↗
22. 10.1021/ja805235k10.1021/ja805235k ↗
23. 10.1039/B927601G10.1039/B927601G ↗
24. 10.1039/c3cc44546a10.1039/c3cc44546a ↗
25. 10.1016/j.snb.2016.03.13510.1016/j.snb.2016.03.135 ↗
26. 10.1364/CLEO_AT.2016.JTu5A.13810.1364/CLEO_AT.2016.JTu5A.138 ↗
27. 10.1021/acssensors.7b0080810.1021/acssensors.7b00808 ↗
28. 10.1364/OL.41.00169610.1364/OL.41.001696 ↗
29. 10.1364/OE.16.00576410.1364/OE.16.005764 ↗
30. 10.1021/la051496710.1021/la0514967 ↗
31. 10.1039/c3ce40137e10.1039/c3ce40137e ↗
32. Lichtfouse E. · 201310.1007/978-3-319-02387-8 ↗
33. 10.1107/S160053680400877310.1107/S1600536804008773 ↗
34. 10.1021/cg034034510.1021/cg0340345 ↗
35. 10.1002/1521-3773(20020802)41:15<2821::AID-ANIE2821>3.0.CO;2-Y10.1002/1521-3773(20020802)41:15<2821::AID-ANIE2821>3.0.CO;2-Y ↗
36. 10.1063/1.481983610.1063/1.4819836 ↗
37. 10.1002/anie.20140836910.1002/anie.201408369 ↗
38. Auerbach S. M. · 2013