Inorganic carbon (HCO3-) was efficiently converted into acetate (204.4 ± 0.5 mM with a coulombic efficiency of 96 ± 3% over 24 days operation) in a photo-assisted microbial electrosynthesis system (MES) using a urea-treated MnFe2O4/g-C3N4 cathode and the nonphotosynthetic bacteria Serratia marcescens Q1. The remarkable photocatalytic performance of MnFe2O4/g-C3N4 heterojunction was resulted from the charge transfer mechanism switch (from type II to Z-scheme) induced by the synergistic effect of oxygen vacancies and pyrrolic N after urea treatment. The increased pyrrolic N was conductive to photoinduced electron transfer while the oxygen vacancies provided a higher fraction of surface-active sites for H2 evolution, which was metabolized in-situ with bicarbonate by S. marcescens Q1 to yield acetate via the Wood–Ljungdahl pathway. This study provides a simple and feasible strategy for switching the photocatalytic charge transfer in a spinel-based heterojunction and offers new insights for ingeniously synthesizing photocatalysts with high CO2 conversion in MES.
Kong W., Huang L., Quan X., Li Puma G. (2022). Synergistic induced charge transfer switch by oxygen vacancy and pyrrolic nitrogen in MnFe2O4/g-C3N4 heterojunctions for efficient transformation of bicarbonate to acetate in photo-assisted MES. APPLIED CATALYSIS. B, ENVIRONMENTAL, 307 [10.1016/j.apcatb.2022.121214].
Synergistic induced charge transfer switch by oxygen vacancy and pyrrolic nitrogen in MnFe2O4/g-C3N4 heterojunctions for efficient transformation of bicarbonate to acetate in photo-assisted MES
Li Puma G.
2022-06-15
Abstract
Inorganic carbon (HCO3-) was efficiently converted into acetate (204.4 ± 0.5 mM with a coulombic efficiency of 96 ± 3% over 24 days operation) in a photo-assisted microbial electrosynthesis system (MES) using a urea-treated MnFe2O4/g-C3N4 cathode and the nonphotosynthetic bacteria Serratia marcescens Q1. The remarkable photocatalytic performance of MnFe2O4/g-C3N4 heterojunction was resulted from the charge transfer mechanism switch (from type II to Z-scheme) induced by the synergistic effect of oxygen vacancies and pyrrolic N after urea treatment. The increased pyrrolic N was conductive to photoinduced electron transfer while the oxygen vacancies provided a higher fraction of surface-active sites for H2 evolution, which was metabolized in-situ with bicarbonate by S. marcescens Q1 to yield acetate via the Wood–Ljungdahl pathway. This study provides a simple and feasible strategy for switching the photocatalytic charge transfer in a spinel-based heterojunction and offers new insights for ingeniously synthesizing photocatalysts with high CO2 conversion in MES.File | Dimensione | Formato | |
---|---|---|---|
1-s2.0-S0926337322001540-main.pdf
Solo gestori archvio
Tipologia:
Versione Editoriale
Dimensione
8.19 MB
Formato
Adobe PDF
|
8.19 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
revised manuscript_GLP1_deposited.pdf
Open Access dal 16/02/2024
Tipologia:
Post-print
Dimensione
1.93 MB
Formato
Adobe PDF
|
1.93 MB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.