journal article·2017

Rapid Synthesis of ZIF-8 Nanocrystals for Electrochemical Detection of Dopamine

Ming Nie, Shun Lu, Dan Lei, Chi Yang, Zuzhen Zhao

Publisher page

Abstract

Zeolitic imidazolate framework-8 is obtained rapidly within 30 min via ultrasonic-assisted solvothermal method. The structure, elemental composition and morphology are investigated by X-ray diffraction, energy-dispersive X-ray detector, scanning electron microscopy, transmission electron microscopy and Brunauer-Emmett-Teller. The results show that Zeolitic imidazolate framework-8 nanocrystals possess cubic sodalite-related structure and provide more active sites for adsorption. Furthermore, the prepared Zeolitic imidazolate framework-8 nanocrystals have been examined for the electrochemical sensor of dopamine using cyclic voltammetry and differential pulse voltammetry techniques. The electrochemical studies demonstrate that the modified electrode displayed enhanced catalytic activity in the process of oxidation of dopamine when the working potential is −100 mV. Additionally, we use the sensor to detect dopamine linearly over a concentration range from 5.0 × 10 −8 to 2.0 × 10 −5 M with a lower detection limit of 1.95 × 10 −7 M (S/N = 3). Importantly, Zeolitic imidazolate framework-8 nanocrystals modified electrode showes favorable anti-interference ability and long-term stability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Electrochemical Analysis and Applications

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

References (31)

Show source-provided references
1. 10.1002/adfm.20130235910.1002/adfm.201302359 ↗
2. 10.1016/j.clinph.2008.03.01710.1016/j.clinph.2008.03.017 ↗
3. 10.1016/j.aca.2008.02.04210.1016/j.aca.2008.02.042 ↗
4. 10.1002/elan.20090057110.1002/elan.200900571 ↗
5. 10.1016/j.bios.2015.11.06310.1016/j.bios.2015.11.063 ↗
6. 10.1016/j.aca.2009.04.05010.1016/j.aca.2009.04.050 ↗
7. 10.1021/ac301835f10.1021/ac301835f ↗
8. 10.1039/b901273g10.1039/b901273g ↗
9. 10.1039/C4NR02399D10.1039/C4NR02399D ↗
10. 10.1073/pnas.060243910310.1073/pnas.0602439103 ↗
11. 10.1149/1.370196710.1149/1.3701967 ↗
12. 10.1016/j.trac.2014.02.01210.1016/j.trac.2014.02.012 ↗
13. 10.1016/j.trac.2015.07.01110.1016/j.trac.2015.07.011 ↗
14. Luche J.-L. , Synthetic organic sonochemistry, Springer Science & Business Media, 2013.
15. 10.1016/j.matlet.2008.09.01010.1016/j.matlet.2008.09.010 ↗
16. 10.1038/srep3164110.1038/srep31641 ↗
17. 10.1016/j.molliq.2016.06.02810.1016/j.molliq.2016.06.028 ↗
18. 10.1039/C5RA02557E10.1039/C5RA02557E ↗
19. 10.1016/j.molliq.2015.05.04010.1016/j.molliq.2015.05.040 ↗
20. 10.1021/cm900166h10.1021/cm900166h ↗
21. 10.1039/c3ta11054k10.1039/c3ta11054k ↗
22. 10.1360/N032015-0019710.1360/N032015-00197 ↗
23. 10.1016/j.electacta.2012.03.17710.1016/j.electacta.2012.03.177 ↗
24. 10.1039/C4NR01774A10.1039/C4NR01774A ↗
25. 10.1002/elan.20150113610.1002/elan.201501136 ↗
26. 10.1016/j.bios.2010.02.03110.1016/j.bios.2010.02.031 ↗
27. 10.1016/j.jelechem.2013.04.02010.1016/j.jelechem.2013.04.020 ↗
28. 10.1039/c4ra04046e10.1039/c4ra04046e ↗
29. 10.1016/j.snb.2014.05.09510.1016/j.snb.2014.05.095 ↗
30. 10.1021/ac302134s10.1021/ac302134s ↗
31. 10.1007/s00604-013-1028-110.1007/s00604-013-1028-1 ↗