journal article·2018-08-27

Insight into MoS2 Synthesis with Biophotoelectrochemical Engineering and Applications in Levofloxacin Elimination

Libin Zeng, Xinyong Li, Shiying Fan, Mingmei Zhang, Zhifan Yin, Moses Tadé, Shaomin Liu

ACS Applied Energy Materials· Volume 1· Issue 8
Publisher page

Abstract

Biosynthesis of nanomaterials is an emerging technology in recent decades ascribed to its unique “greener” route and higher energy efficiency. It is superior to the traditional physicochemical synthesis processes, in which hazardous intermediates or high energy-consumption are often inevitable and remain a significant obstacle. In this work, a coupling system based on a photodriven microbial fuel cell (MFC) was constructed to controllably synthesize different sizes of MoS2 nanomaterials in situ. By virtue of the MFC producing electricity as a driving force, the MoS42– ions could be reduced to MoS2 nanoparticles. Impressively, photoexcited electrons produced from a polydopamine coated TiO2 nanotube (PDA/TiO2 NT) electrode under visible light irradiation (>420 nm) could also be utilized online to facilitate MoS2 nanoparticle growth effectively. Interestingly, the MoS2 material was further cultivated on a PDA/TiO2 substrate and then biologically modified MoS2/PDA/TiO2 electrodes were easily obtained, which exhibited unique hydrophilic behavior (14.74°) and bioelectrocatalytic performance for effectively promoting the complete removal of antibiotics in the MFC and photoelectrocatalytic (PEC) cooperative system. Thus, we believe that such obvious advantages of the constructed photoboosted MFC system could provide an environmentally benign pathway to synthesize nanostructured electrode materials and create new opportunities for diverse pollutant removal in situ.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced Photocatalysis Techniques · Advanced biosensing and bioanalysis techniques

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

Affiliations

State Key Laboratory of Fine Chemicals, Key Laboratory of Industrial Ecology and Environmental Engineering (MOE), School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024, China

Department of Chemical Engineering, Curtin University, GPO Box U1987, Perth, WA 6845, Australia

Funding

State Administration of Foreign Experts Affairs · Ministry of Science and Technology of the People's Republic of China · Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Key Laboratory of Industrial Ecology and Environmental Engineering, Dalian University of Technology

References (53)

Show source-provided references
1. 10.1126/science.348.6239.1100-d10.1126/science.348.6239.1100-d ↗
2. 10.1021/am404774z10.1021/am404774z ↗
3. 10.1016/j.apcatb.2016.09.00310.1016/j.apcatb.2016.09.003 ↗
4. 10.1039/C5NR06121K10.1039/C5NR06121K ↗
5. 10.1016/j.apcatb.2016.09.02310.1016/j.apcatb.2016.09.023 ↗
6. 10.1021/acs.jpcc.5b0801610.1021/acs.jpcc.5b08016 ↗
7. 10.1039/C5TA10224C10.1039/C5TA10224C ↗
8. 10.1002/anie.20160167310.1002/anie.201601673 ↗
9. 10.1016/j.jpowsour.2016.11.04110.1016/j.jpowsour.2016.11.041 ↗
10. 10.1021/acsami.7b0510410.1021/acsami.7b05104 ↗
11. 10.1126/science.121586810.1126/science.1215868 ↗
12. 10.1021/nl403661s10.1021/nl403661s ↗
13. 10.1002/adma.20130268510.1002/adma.201302685 ↗
14. 10.1039/C5GC00272A10.1039/C5GC00272A ↗
15. 10.1038/nnano.2016.13810.1038/nnano.2016.138 ↗
16. 10.1038/nmat343910.1038/nmat3439 ↗
17. 10.1021/nn501479e10.1021/nn501479e ↗
18. 10.1038/nnano.2015.4010.1038/nnano.2015.40 ↗
19. 10.1039/C7EE01047H10.1039/C7EE01047H ↗
20. 10.1039/C5CC00106D10.1039/C5CC00106D ↗
21. 10.1039/C4EE01932F10.1039/C4EE01932F ↗
22. 10.1039/C5NR05595D10.1039/C5NR05595D ↗
23. 10.1021/ja201269b10.1021/ja201269b ↗
24. 10.1002/adma.20140272810.1002/adma.201402728 ↗
25. 10.1021/am302201510.1021/am3022015 ↗
26. 10.1039/C5TA02198G10.1039/C5TA02198G ↗
27. 10.1002/adma.20110479810.1002/adma.201104798 ↗
28. 10.1021/acsnano.5b0376410.1021/acsnano.5b03764 ↗
29. 10.1021/cm200837g10.1021/cm200837g ↗
30. 10.1039/C4NR02044H10.1039/C4NR02044H ↗
31. 10.1016/j.jcis.2010.11.00710.1016/j.jcis.2010.11.007 ↗
32. 10.1021/acs.chemrev.5b0004910.1021/acs.chemrev.5b00049 ↗
33. 10.1039/C4EE00654B10.1039/C4EE00654B ↗
34. 10.1016/j.bios.2016.02.05410.1016/j.bios.2016.02.054 ↗
35. 10.1016/j.biotechadv.2013.10.00110.1016/j.biotechadv.2013.10.001 ↗
36. 10.1039/b806498a10.1039/b806498a ↗
37. 10.1021/es060501610.1021/es0605016 ↗
38. 10.1016/j.watres.2014.08.01310.1016/j.watres.2014.08.013 ↗
39. 10.1016/j.biortech.2015.06.05810.1016/j.biortech.2015.06.058 ↗
40. 10.1039/C6GC00273K10.1039/C6GC00273K ↗
41. 10.1166/asl.2010.109910.1166/asl.2010.1099 ↗
42. 10.1038/srep1351510.1038/srep13515 ↗
43. 10.1016/j.cej.2015.02.02410.1016/j.cej.2015.02.024 ↗
44. 10.1016/j.bej.2015.09.02210.1016/j.bej.2015.09.022 ↗
45. 10.1039/C6RA17236A10.1039/C6RA17236A ↗
46. 10.1016/j.bios.2016.12.02110.1016/j.bios.2016.12.021 ↗
47. 10.1126/science.114148310.1126/science.1141483 ↗
48. 10.1016/j.electacta.2013.07.16810.1016/j.electacta.2013.07.168 ↗
49. 10.1088/0953-8984/21/39/39530110.1088/0953-8984/21/39/395301 ↗
50. 10.1016/j.elecom.2015.01.01110.1016/j.elecom.2015.01.011 ↗
51. 10.1039/C3TA14744D10.1039/C3TA14744D ↗
52. 10.1002/anie.20140293510.1002/anie.201402935 ↗
53. 10.1021/cr400407a10.1021/cr400407a ↗