journal article·2019-10-23

Conjugated Polymer Enhanced Photoelectric Response of Self-Circulating Photosynthetic Bioelectrochemical Cell

Xin Zhou, Panpan Gai, Pengbo Zhang, Han Sun, Fengting Lv, Libing Liu, Shu Wang

ACS Applied Materials & Interfaces· Volume 11· Issue 42
Publisher page

Abstract

A water–oxygen–water photosynthetic bioelectrochemical cell (PBEC) comprising hybrid poly(fluorene-alt-phenylene) (PFP)/PSII-enriched membranes (BBY) photoanode and bilirubin oxidase (BOD) biocathode has been designed and fabricated. In the PBEC, water is split into oxygen, protons, and electrons through light-dependent reaction of PSII at the photoanode, and oxygen is converted into water catalyzed by BOD at the biocathode, forming the electronic circuit and generating current. At the photoanode, PFP can simultaneously accelerate the photosynthetic water oxidation and the electron transfer between BBY and electrode. Interestingly, the photocurrent density produced by PBEC after the introduction of PFP reaches 1.05 ± 0.01 μA/cm2, which is 2.5 times more than that of the BBY electrode, indicating that conjugated polymer can enhance the photoelectric response of PBEC.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Microbial Fuel Cells and Bioremediation · Analytical Chemistry and Sensors

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

Affiliations

Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing 100049, P. R. China

College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao 266109, P. R. China

Funding

National Natural Science Foundation of China

References (30)

Show source-provided references
1. Halan, B.; Tschörtner, J.; Schmid, A. Generating Electric Current by Bioartificial Photosynthesis; Springer: Germany, 2018; Vol. 167, pp 361–393.10.1007/10_2017_44 ↗
2. 10.1002/celc.20140213310.1002/celc.201402133 ↗
3. 10.1002/adma.20180229010.1002/adma.201802290 ↗
4. 10.1002/anie.20130367110.1002/anie.201303671 ↗
5. 10.1039/c3cp51813b10.1039/c3cp51813b ↗
6. 10.1016/j.coelec.2017.09.01310.1016/j.coelec.2017.09.013 ↗
7. 10.1039/C5EE01707F10.1039/C5EE01707F ↗
8. 10.1039/C6EE01363E10.1039/C6EE01363E ↗
9. 10.1039/c3ee40634b10.1039/c3ee40634b ↗
10. 10.1039/c1ee02531g10.1039/c1ee02531g ↗
11. 10.1021/ja301488d10.1021/ja301488d ↗
12. 10.1039/c4cp00494a10.1039/c4cp00494a ↗
13. 10.1016/j.electacta.2017.03.12410.1016/j.electacta.2017.03.124 ↗
14. 10.1002/adma.20170407310.1002/adma.201704073 ↗
15. 10.1002/adfm.20170368910.1002/adfm.201703689 ↗
16. 10.1039/C8SC03058H10.1039/C8SC03058H ↗
17. 10.1021/cr200263w10.1021/cr200263w ↗
18. 10.1039/b909065g10.1039/b909065g ↗
19. 10.1073/pnas.01258139910.1073/pnas.012581399 ↗
20. 10.1021/acsnano.8b0171510.1021/acsnano.8b01715 ↗
21. 10.1016/j.nanoen.2018.04.00210.1016/j.nanoen.2018.04.002 ↗
22. 10.1002/adma.20170546310.1002/adma.201705463 ↗
23. Wang S. · 2013
24. 10.1002/aelm.20180078910.1002/aelm.201800789 ↗
25. 10.1007/978-1-60761-925-3_110.1007/978-1-60761-925-3_1 ↗
26. 10.1021/jacs.7b0856310.1021/jacs.7b08563 ↗
27. 10.1038/ncomms174110.1038/ncomms1741 ↗
28. 10.1002/anie.20170237610.1002/anie.201702376 ↗
29. Cooper G. M. · 2000
30. 10.1007/BF0292178410.1007/BF02921784 ↗