journal article·2017-04-26

Defect-Mediated Molecular Interaction and Charge Transfer in Graphene Mesh–Glucose Sensors

Sun Sang Kwon, Jae Hyeok Shin, Jonghyun Choi, SungWoo Nam, Won Il Park

Publisher page

Abstract

We report the role of defects in enzymatic graphene field-effect transistor sensors by introducing engineered defects in graphene channels. Compared with conventional graphene sensors (Gr sensors), graphene mesh sensors (GM sensors), with an array of circular holes, initially exhibited a higher irreversible response to glucose, involving strong chemisorption to edge defects. However, after immobilization of glucose oxidase, the irreversibility of the responses was substantially diminished, without any reduction in the sensitivity of the GM sensors (i.e., -0.53 mV/mM for the GM sensor vs -0.37 mV/mM for Gr sensor). Furthermore, multiple cycle operation led to rapid sensing and improved the reversibility of GM sensors. In addition, control tests with sensors containing a linker showed that sensitivity was increased in Gr sensors but decreased in GM sensors. Our findings indicate that edge defects can be used to replace linkers for immobilization of glucose oxidase and improve charge transfer across glucose oxidase-graphene interfaces.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Graphene research and applications · Advanced biosensing and bioanalysis techniques

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

Affiliations

Division of Materials Science and Engineering, Hanyang University, Seoul 04763, Korea

Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States

Funding

National Research Foundation of Korea · Air Force Office of Scientific Research

References (39)

Show source-provided references
1. 10.1038/nnano.2008.19910.1038/nnano.2008.199 ↗
2. 10.1021/nn304007x10.1021/nn304007x ↗
3. 10.1016/j.ssc.2008.02.02410.1016/j.ssc.2008.02.024 ↗
4. 10.1039/c3tc32264e10.1039/c3tc32264e ↗
5. 10.1021/ja805090z10.1021/ja805090z ↗
6. 10.1021/nl100633g10.1021/nl100633g ↗
7. 10.1021/nn301974u10.1021/nn301974u ↗
8. 10.1016/j.mee.2016.04.00310.1016/j.mee.2016.04.003 ↗
9. 10.1021/nl901596m10.1021/nl901596m ↗
10. 10.1016/S1369-7021(11)70160-210.1016/S1369-7021(11)70160-2 ↗
11. 10.1039/C5NR00414D10.1039/C5NR00414D ↗
12. 10.1088/0022-3727/43/34/34530310.1088/0022-3727/43/34/345303 ↗
13. 10.1039/c1jm11436k10.1039/c1jm11436k ↗
14. 10.1021/nn103043v10.1021/nn103043v ↗
15. 10.1021/nn402702w10.1021/nn402702w ↗
16. 10.1039/C4RA08811E10.1039/C4RA08811E ↗
17. 10.1021/ja205693t10.1021/ja205693t ↗
18. 10.1021/nl803279t10.1021/nl803279t ↗
19. 10.1038/nmat196710.1038/nmat1967 ↗
20. 10.1021/acsami.5b1018310.1021/acsami.5b10183 ↗
21. 10.1088/0022-3727/48/47/47510310.1088/0022-3727/48/47/475103 ↗
22. 10.1186/s40580-016-0075-910.1186/s40580-016-0075-9 ↗
23. 10.1021/jz400940d10.1021/jz400940d ↗
24. 10.1038/srep0831110.1038/srep08311 ↗
25. 10.1021/acsnano.5b0570910.1021/acsnano.5b05709 ↗
26. 10.1016/j.bios.2012.04.04210.1016/j.bios.2012.04.042 ↗
27. 10.3390/s12050599610.3390/s120505996 ↗
28. 10.1021/cr068123a10.1021/cr068123a ↗
29. 10.1021/nn100315s10.1021/nn100315s ↗
30. 10.1021/jp906348x10.1021/jp906348x ↗
31. 10.1039/c3nr33708a10.1039/c3nr33708a ↗
32. 10.1016/j.electacta.2015.06.03510.1016/j.electacta.2015.06.035 ↗
33. 10.1038/ncomms202210.1038/ncomms2022 ↗
34. 10.1038/nnano.2008.6710.1038/nnano.2008.67 ↗
35. Childres I. · 2013 · 1
36. 10.1021/nn800459e10.1021/nn800459e ↗
37. 10.1103/PhysRevB.20.39210.1103/PhysRevB.20.392 ↗
38. 10.1021/jp205261810.1021/jp2052618 ↗
39. 10.1021/jp100603h10.1021/jp100603h ↗