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A biocompatible graphitic carbon nitride (g-C3N4) was prepared on the surface of carbon brush fiber (CB) via a facile one-step preparation method. The prepared g-C3N4 formed a composite with the carbon brush's fibers (g-C3N4@CB), as shown from the XRD analysis. The g-C3N4@CB was used as an anode in a yeast-based microbial fuel cell (MFC), and demonstrated an outstanding performance compared to plain CB. An anode potential of −0.27 V “vs. Ag/AgCl” and an open-circuit voltage of 0.77 V was obtained in the case of the composite electrode, compared to −0.1 V vs. Ag/AgCl and 0.62 V, respectively, in the case of the CB. The cell using the composite electrode demonstrated a maximum power of 772 mWm−2, which is twelve times that obtained using the CB. The outstanding performance of the composite electrode can be credited to the biocompatibility of the composite anode and its roughness, which improved the yeast biofilm formation and decreased the ohmic resistance. This is the first report involving the application of g-C3N4 in a yeast-based MFC, and it demonstrated promising results which can be used for other types of MFCs.

A biocompatible graphitic carbon nitride (g-C3N4) was prepared on the surface of carbon brush fiber (CB) via a facile one-step preparation method. The prepared g-C3N4 formed a composite with the carbon brush's fibers (g-C3N4@CB), as shown from the XRD analysis. The g-C3N4@CB was used as an anode in a yeast-based microbial fuel cell (MFC), and demonstrated an outstanding performance compared to plain CB. An anode potential of −0.27 V “vs. Ag/AgCl” and an open-circuit voltage of 0.77 V was obtained in the case of the composite electrode, compared to −0.1 V vs. Ag/AgCl and 0.62 V, respectively, in the case of the CB. The cell using the composite electrode demonstrated a maximum power of 772 mWm−2, which is twelve times that obtained using the CB. The outstanding performance of the composite electrode can be credited to the biocompatibility of the composite anode and its roughness, which improved the yeast biofilm formation and decreased the ohmic resistance. This is the first report involving the application of g-C3N4 in a yeast-based MFC, and it demonstrated promising results which can be used for other types of MFCs.

In this work, Cu2O nanoparticles were successfully prepared onto the surface of two-dimensional graphitic carbon nitride (g-C3N4) by using a simple solution chemistry approach. An environment-friendly reducing agent, glucose, was used for the synthesis of Cu2O NPs onto the surface of g-C3N4 without using any surfactant or additives. The surface composition, crystalline structure, morphology, as well as other properties have been investigated using XPS, XRD, SEM, FTIR, FESEM, EDS, etc. The electrochemical measurements of the prepared materials demonstrated that Cu2O exhibited a weak oxidation activity towards urea, while g-C3N4 has no activity towards urea oxidation. The Cu2O supported on the surface of g-C3N4 (Cu2O-g-C3N4) demonstrated a significant activity towards urea oxidation that reached two times that of the unsupported one. The significant increase in the performance was related to the synergetic effect between the Cu2O and g-C3N4 support. The prepared composite materials demonstrated high stability towards urea oxidation as confirmed from the stable current discharge for around 3 h without any noticeable degradation performance.

In this work, Cu2O nanoparticles were successfully prepared onto the surface of two-dimensional graphitic carbon nitride (g-C3N4) by using a simple solution chemistry approach. An environment-friendly reducing agent, glucose, was used for the synthesis of Cu2O NPs onto the surface of g-C3N4 without using any surfactant or additives. The surface composition, crystalline structure, morphology, as well as other properties have been investigated using XPS, XRD, SEM, FTIR, FESEM, EDS, etc. The electrochemical measurements of the prepared materials demonstrated that Cu2O exhibited a weak oxidation activity towards urea, while g-C3N4 has no activity towards urea oxidation. The Cu2O supported on the surface of g-C3N4 (Cu2O-g-C3N4) demonstrated a significant activity towards urea oxidation that reached two times that of the unsupported one. The significant increase in the performance was related to the synergetic effect between the Cu2O and g-C3N4 support. The prepared composite materials demonstrated high stability towards urea oxidation as confirmed from the stable current discharge for around 3 h without any noticeable degradation performance.

A biocompatible graphitic carbon nitride (g-C3N4) was prepared on the surface of carbon brush fiber (CB) via a facile one-step preparation method. The prepared g-C3N4 formed a composite with the carbon brush's fibers (g-C3N4@CB), as shown from the XRD analysis. The g-C3N4@CB was used as an anode in a yeast-based microbial fuel cell (MFC), and demonstrated an outstanding performance compared to plain CB. An anode potential of −0.27 V “vs. Ag/AgCl” and an open-circuit voltage of 0.77 V was obtained in the case of the composite electrode, compared to −0.1 V vs. Ag/AgCl and 0.62 V, respectively, in the case of the CB. The cell using the composite electrode demonstrated a maximum power of 772 mWm−2, which is twelve times that obtained using the CB. The outstanding performance of the composite electrode can be credited to the biocompatibility of the composite anode and its roughness, which improved the yeast biofilm formation and decreased the ohmic resistance. This is the first report involving the application of g-C3N4 in a yeast-based MFC, and it demonstrated promising results which can be used for other types of MFCs.

In this work, Cu2O nanoparticles were successfully prepared onto the surface of two-dimensional graphitic carbon nitride (g-C3N4) by using a simple solution chemistry approach. An environment-friendly reducing agent, glucose, was used for the synthesis of Cu2O NPs onto the surface of g-C3N4 without using any surfactant or additives. The surface composition, crystalline structure, morphology, as well as other properties have been investigated using XPS, XRD, SEM, FTIR, FESEM, EDS, etc. The electrochemical measurements of the prepared materials demonstrated that Cu2O exhibited a weak oxidation activity towards urea, while g-C3N4 has no activity towards urea oxidation. The Cu2O supported on the surface of g-C3N4 (Cu2O-g-C3N4) demonstrated a significant activity towards urea oxidation that reached two times that of the unsupported one. The significant increase in the performance was related to the synergetic effect between the Cu2O and g-C3N4 support. The prepared composite materials demonstrated high stability towards urea oxidation as confirmed from the stable current discharge for around 3 h without any noticeable degradation performance.

A biocompatible graphitic carbon nitride (g-C3N4) was prepared on the surface of carbon brush fiber (CB) via a facile one-step preparation method. The prepared g-C3N4 formed a composite with the carbon brush's fibers (g-C3N4@CB), as shown from the XRD analysis. The g-C3N4@CB was used as an anode in a yeast-based microbial fuel cell (MFC), and demonstrated an outstanding performance compared to plain CB. An anode potential of −0.27 V “vs. Ag/AgCl” and an open-circuit voltage of 0.77 V was obtained in the case of the composite electrode, compared to −0.1 V vs. Ag/AgCl and 0.62 V, respectively, in the case of the CB. The cell using the composite electrode demonstrated a maximum power of 772 mWm−2, which is twelve times that obtained using the CB. The outstanding performance of the composite electrode can be credited to the biocompatibility of the composite anode and its roughness, which improved the yeast biofilm formation and decreased the ohmic resistance. This is the first report involving the application of g-C3N4 in a yeast-based MFC, and it demonstrated promising results which can be used for other types of MFCs.

In this work, Cu2O nanoparticles were successfully prepared onto the surface of two-dimensional graphitic carbon nitride (g-C3N4) by using a simple solution chemistry approach. An environment-friendly reducing agent, glucose, was used for the synthesis of Cu2O NPs onto the surface of g-C3N4 without using any surfactant or additives. The surface composition, crystalline structure, morphology, as well as other properties have been investigated using XPS, XRD, SEM, FTIR, FESEM, EDS, etc. The electrochemical measurements of the prepared materials demonstrated that Cu2O exhibited a weak oxidation activity towards urea, while g-C3N4 has no activity towards urea oxidation. The Cu2O supported on the surface of g-C3N4 (Cu2O-g-C3N4) demonstrated a significant activity towards urea oxidation that reached two times that of the unsupported one. The significant increase in the performance was related to the synergetic effect between the Cu2O and g-C3N4 support. The prepared composite materials demonstrated high stability towards urea oxidation as confirmed from the stable current discharge for around 3 h without any noticeable degradation performance.