Generic MFCRepresentative model
Click to animate flow
loading 3D model…

Representative MFC — matched on the paper’s system type only, not its reactor or geometry.

Extraction

Reported parameters

No values extracted from this paper yet.

Open in lab for full controls, parameter editing, and template overlays.

Open in lab →

What they did

System
MFC

What worked

No outcome metrics extracted yet.

Abstract

In this work, the ferrous (Fe 2+ ) and graphitic N modified graphene-based composite cathode materials (N-rGO/Fe 3 O 4 ) were developed through an in-situ reduction method, aiming to facilitate the two-electron pathway in the oxidation-reduction process. This approach generated a specific concentration of H 2 O 2 , enabling the construction of a sediment bio-electro-Fenton system using Fe 2+ released from the cathode materials. Notably, this system operates without the need for proton exchange membranes. During the cathode material preparation, the utilization of Fe 2+ as a reduction agent for graphene oxide (GO), triggered ammonia water to form graphitic N in graphene sheets. This addition enhanced the two-electron pathway, resulting in increased H 2 O 2 production. Specifically, when the Fe 2+ concentration was maintained at 0.1 mol/L, precise preparation of N-rGO/Fe 3 O 4 occurred, leading to a maximum output voltage of 0.528 V and a maximum power density of 178.17 mW/m 2 . The degradation of methyl orange (MO) reached 68.91% within a 25-h period, a phenomenon contributed to the presence of graphitic N in the graphene sheets. H 2 O 2 , a byproduct of the two-electron pathway in cathode oxidation reduction reaction, played a crucial role in constructing the bio-electro-Fenton system. This system, in conjunction with Fe 2+ released from N-rGO/Fe 3 O 4 , facilitated the complete degradation process of MO.

Keywords

GrapheneMicrobial fuel cellCathodeFerrousOxideMethyl orange

Identifiers

PubMed
38333867
Journal
Heliyon
Year
2024