journal article·2024-11

Photoelectrocatalytic‐Microbial Biohybrid for Nitrogen Reduction

Yingjie Zhang, Tianhang Feng, Xue Zhou, Zhonghai Zhang

Advanced Materials· Volume 36· Issue 44
Publisher page

Abstract

Abstract Nitrogen (N 2 ) conversion to ammonia (NH 3 ) in a mild condition is a big chemical challenge. The whole‐cell diazotrophs based biological NH 3 synthesis is one of the most promising strategies. Herein, the first attempt of photoelectrochemical‐microbial (PEC‐MB) biohybrid is contributed for artificial N 2 fixation, where Azotobacter vinelandii ( A. vinelandii ) is interfaced directly with polydopamine encapsulated nickel oxide (NiO) nanosheets (NiO@PDA). By virtue of excellent bio‐adhesive activity, high conductivity, and good biocompatibility of PDA layer, abundant A. vinelandii are effectively adsorbed on NiO@PDA to form NiO@PDA/ A. vinelandii biohybrid, and the rationally designed biohybrid achieved a record‐high NH 3 production yield of 1.85 µmol h −1 /10 8 cells (4.14 µmol h −1 cm −2 ). In addition, this biohybrid can operate both under illumination with a PEC model or in dark with an electrocatalytic (EC) model to implement long‐term and successional NH 3 synthesis. The enhancement mechanism of NH 3 synthesis in NiO@PDA/ A. vinelandii biohybrid can be ascribed to the increase of nicotinamide adenine dinucleotide‐hydrogen (NADH) and adenosine 5‐triphosphate (ATP) concentrations and over expression of nitrogen‐fixing genes of nif H, nif D and nif K in nitrogenase. This innovative PEC‐MB biohybrid strategy sheds light on the fundamental mechanism and establishes proof of concept of biotic‐abiotic photosynthetic systems for sustainable chemical production.
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Research context

OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Advanced Photocatalysis Techniques · Microbial Fuel Cells and Bioremediation

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

Affiliations

Shanghai Key Laboratory of Green Chemistry and Chemical Processes School of Chemistry and Molecular Engineering East China Normal University Shanghai 200241 China

Funding

National Natural Science Foundation of China

References (52)

Show source-provided references
1. 10.1038/s44160-023-00321-710.1038/s44160-023-00321-7 ↗
2. 10.1126/science.113667410.1126/science.1136674 ↗
3. 10.1002/anie.20161250010.1002/anie.201612500 ↗
4. 10.1039/D2EE03132A10.1039/D2EE03132A ↗
5. 10.1038/s41467-018-05758-510.1038/s41467-018-05758-5 ↗
6. 10.1002/anie.20210439410.1002/anie.202104394 ↗
7. 10.1021/acscatal.9b0324610.1021/acscatal.9b03246 ↗
8. 10.1002/anie.20201235710.1002/anie.202012357 ↗
9. 10.1016/j.chempr.2021.08.02110.1016/j.chempr.2021.08.021 ↗
10. 10.1038/s41564-019-0631-210.1038/s41564-019-0631-2 ↗
11. 10.1039/C9EE00705A10.1039/C9EE00705A ↗
12. 10.1016/j.joule.2023.08.00610.1016/j.joule.2023.08.006 ↗
13. 10.1021/cr400641x10.1021/cr400641x ↗
14. 10.1126/science.aaf209110.1126/science.aaf2091 ↗
15. 10.1039/C8SC01638K10.1039/C8SC01638K ↗
16. 10.1021/jacs.9b0254910.1021/jacs.9b02549 ↗
17. 10.1002/anie.20230710110.1002/anie.202307101 ↗
18. 10.1002/anie.20230387710.1002/anie.202303877 ↗
19. 10.1021/jacs.2c0188610.1021/jacs.2c01886 ↗
20. 10.1021/acs.nanolett.5b0125410.1021/acs.nanolett.5b01254 ↗
21. 10.1021/acs.nanolett.2c0157610.1021/acs.nanolett.2c01576 ↗
22. 10.1073/pnas.212236411910.1073/pnas.2122364119 ↗
23. 10.1016/j.joule.2020.03.00110.1016/j.joule.2020.03.001 ↗
24. 10.1021/acsami.2c0241010.1021/acsami.2c02410 ↗
25. 10.1016/j.apsusc.2021.15169710.1016/j.apsusc.2021.151697 ↗
26. 10.1002/aelm.20200014010.1002/aelm.202000140 ↗
27. 10.1016/j.jpowsour.2017.11.07110.1016/j.jpowsour.2017.11.071 ↗
28. 10.1016/j.cej.2019.12340810.1016/j.cej.2019.123408 ↗
29. 10.1021/acsnano.5b0043510.1021/acsnano.5b00435 ↗
30. 10.1021/acs.analchem.5b0264410.1021/acs.analchem.5b02644 ↗
31. 10.1021/am402869p10.1021/am402869p ↗
32. 10.1002/anie.20120712910.1002/anie.201207129 ↗
33. 10.1039/D1TA07303F10.1039/D1TA07303F ↗
34. 10.1021/la500225v10.1021/la500225v ↗
35. 10.1007/s10562-022-04022-210.1007/s10562-022-04022-2 ↗
36. 10.1016/j.ces.2016.08.02610.1016/j.ces.2016.08.026 ↗
37. 10.1016/j.cej.2019.12303610.1016/j.cej.2019.123036 ↗
38. 10.1021/cm300739y10.1021/cm300739y ↗
39. 10.1021/am507138b10.1021/am507138b ↗
40. 10.1021/acs.jpclett.7b0191110.1021/acs.jpclett.7b01911 ↗
41. 10.1021/acs.jpcc.1c0355310.1021/acs.jpcc.1c03553 ↗
42. 10.1016/j.memsci.2019.11764110.1016/j.memsci.2019.117641 ↗
43. 10.1042/bj072020410.1042/bj0720204 ↗
44. 10.1128/aem.01049-2210.1128/aem.01049-22 ↗
45. 10.1002/anie.20200719810.1002/anie.202007198 ↗
46. 10.1128/aem.00378-2310.1128/aem.00378-23 ↗
47. 10.1111/j.1472-765X.2008.02407.x10.1111/j.1472-765X.2008.02407.x ↗
48. 10.1021/cr00106a00210.1021/cr00106a002 ↗
49. 10.1007/s00239001006110.1007/s002390010061 ↗
50. 10.1126/sciadv.abm509110.1126/sciadv.abm5091 ↗
51. 10.1038/nmat369610.1038/nmat3696 ↗
52. 10.1021/ac60072a04410.1021/ac60072a044 ↗