Microbial fuel cells integrating photosynthetic microorganisms hold promise for sustainable bioelectricity generation but their operation in real matrices remains underexplored. Here, we report the development of a polydopamine-coated polyhydroxybutyrate-carbon nanofibers electrode colonized by the purple non-sulfur bacterium Rhodobacter capsulatus enabling simultaneous light-driven current production, CO2 sequestration, and long-term stability in real highly saline environments. Specifically, the artificial bioelectrode demonstrated high operational durability over one month of continuous fed-batch operation, maintaining stable current generation across repeated 6-day analytical cycles. Under stressful conditions (50:50 growth medium:seawater), the biophotoelectrode achieved a current density of 32±[jls-end-space/]1 μA cm−2 alongside a Coulombic efficiency of 7.2±[jls-end-space/]1.2%. Headspace gas chromatography analysis revealed CO2 depletion over time, with formate identified among the major products in the investigated conditions, particularly under moderate salinity (80:20 growth medium:seawater). In contrast, hydrogen evolution was detected only under high-salinity stress (50:50 growth medium:seawater), suggesting activation of alternative metabolic pathways. These findings demonstrate that R. capsulatus-modified electrodes can harness light energy and drive carbon conversion in complex saline environments. By leveraging stress-responsive metabolic flexibility and electroactive biofilm engineering, this platform paves the way for self-sustaining systems capable of simultaneous renewable electricity generation in highly saline environments, and production of value-added chemicals.

Phototrophic carbon dioxide reduction in highly saline microbial fuel cell

Lacalamita, Dario;Stufano, Paolo;Labarile, Rossella;Farinola, Gianluca Maria
;
Grattieri, Matteo
;
2026-01-01

Abstract

Microbial fuel cells integrating photosynthetic microorganisms hold promise for sustainable bioelectricity generation but their operation in real matrices remains underexplored. Here, we report the development of a polydopamine-coated polyhydroxybutyrate-carbon nanofibers electrode colonized by the purple non-sulfur bacterium Rhodobacter capsulatus enabling simultaneous light-driven current production, CO2 sequestration, and long-term stability in real highly saline environments. Specifically, the artificial bioelectrode demonstrated high operational durability over one month of continuous fed-batch operation, maintaining stable current generation across repeated 6-day analytical cycles. Under stressful conditions (50:50 growth medium:seawater), the biophotoelectrode achieved a current density of 32±[jls-end-space/]1 μA cm−2 alongside a Coulombic efficiency of 7.2±[jls-end-space/]1.2%. Headspace gas chromatography analysis revealed CO2 depletion over time, with formate identified among the major products in the investigated conditions, particularly under moderate salinity (80:20 growth medium:seawater). In contrast, hydrogen evolution was detected only under high-salinity stress (50:50 growth medium:seawater), suggesting activation of alternative metabolic pathways. These findings demonstrate that R. capsulatus-modified electrodes can harness light energy and drive carbon conversion in complex saline environments. By leveraging stress-responsive metabolic flexibility and electroactive biofilm engineering, this platform paves the way for self-sustaining systems capable of simultaneous renewable electricity generation in highly saline environments, and production of value-added chemicals.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/600900
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 1
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact