scholarly journals Performance Analysis of Biocathode in Bioelectrochemical CO2 Reduction

Catalysts ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 683 ◽  
Author(s):  
Nelabhotla ◽  
Bakke ◽  
Dinamarca

Microbial electrosynthesis (MES) biogas upgrading is done via reduction of carbon dioxide to methane through electroactive microbial catalysis. The baseline MES mode of operation showed about a 39% increase in the methane production rate compared to the open circuit mode of operation. MES is capable of producing acetic acid at relatively more negative potential (−0.80 to –0.90 V vs. Standard Hydrogen Electrode (SHE)) than the potential at which it produces methane (−0.65 V vs. SHE). The optimum pH for enhancing the electroactive acetogens is found to be around 6.8–7.0 while a pH of around 7.0–7.5 enhances the electroactive methanogens performance. The biocathode adaptation test reveals that 45% of the methane was produced through the electrochemical pathway with a coulombic efficiency of 100% while maintaining heterotrophic efficiency above 99%.

2019 ◽  
Vol 19 (6) ◽  
pp. 3232-3236 ◽  
Author(s):  
Mingyue Peng ◽  
Suqin Ci ◽  
Ping Shao ◽  
Pingwei Cai ◽  
Zhenhai Wen

Exploiting effective electrocatalysts toward electrochemical conversion of CO2 into valued-added chemicals is highly desirable for achieving the global carbon cycle. In this work, we report the synthesis of Cu3P/C nanocomposites by phosphatizing the copper-based metal organic framework precursor. Systematic electrochemical characterizations demonstrate the Cu3P/C nanocomposites hold high activity and favorable selectivity towards CO2 reduction reaction (CO2RR) into CO, as manifested by an onset potential is about −0.25 V versus reversible hydrogen electrode (RHE) and a faradic efficiency (FE) of 47% for CO production at a relatively low potential (−0.3 V). The attractive catalytic properties might be attributed to the synergistic effect of cooper and phosphorus elements, as well as the unique structure of Cu3P. Furthermore, we propose an asymmetrical-electrolyte Zn–CO2 battery with the Cu3P/C as cathode catalyst, demonstrating a decent performance with an open-circuit voltage of 1.5 V and a power density of 2.6 mW cm−2 (at 10 mA cm−2).


2000 ◽  
Vol 65 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Tomáš Loučka

The aim of this research was to study the oxidation and reduction of the adsorbed thiosulfate on the platinum electrode in a slightly alkaline medium. The adsorption was performed at the open circuit conditions. The reduction of the adsorbed layer in the hydrogen region is slower in a slightly alkaline medium than in acid. The mechanism of reduction and oxidation of adsorbed molecules is probably the same. The nonstationary currents measured in presence of thiosulfates showed that the change in the oxidation number does not take place during the adsorption in the double layer region. In the hydrogen region, thiosulfate replaces the adsorbed hydrogen while beeing reduced. Nonstationary currents at higher concentrations of thiosulfate indicate the presence of more layers on the electrode. Upon reaching higher concentrations of thiosulfate the oxidation reaction takes place between thiosulfate in solution and adsorbed product of its reduction. The open circuit potential of the platinum electrode measured in a thiosulfate solution was 0.780 and 0.783 V against the hydrogen electrode in the same solution.


mBio ◽  
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Joseph Oram ◽  
Lars J. C. Jeuken

ABSTRACTExoelectrogenic bacteria are defined by their ability to respire on extracellular and insoluble electron acceptors and have applications in bioremediation and microbial electrochemical systems (MESs), while playing important roles in biogeochemical cycling.Shewanella oneidensisMR-1, which has become a model organism for the study of extracellular respiration, is known to display taxis toward insoluble electron acceptors, including electrodes. Multiple mechanisms have been proposed for MR-1’s tactic behavior, and, here, we report on the role of electrochemical potential by video microscopy cell tracking experiments in three-electrode electrochemical cells. MR-1 trajectories were determined using a particle tracking algorithm and validated with Shannon’s entropy method. Tactic response by MR-1 in the electrochemical cell was observed to depend on the applied potential, as indicated by the average velocity and density of motile (>4 µm/s) MR-1 close to the electrode (<50 µm). Tactic behavior was observed at oxidative potentials, with a strong switch between the potentials −0.15 to −0.25 V versus the standard hydrogen electrode (SHE), which coincides with the reduction potential of flavins. The average velocity and density of motile MR-1 close to the electrode increased when riboflavin was added (2 µM), but were completely absent in a ΔmtrC/ΔomcAmutant of MR-1. Besides flavin’s function as an electron mediator to support anaerobic respiration on insoluble electron acceptors, we propose that riboflavin is excreted by MR-1 to sense redox gradients in its environment, aiding taxis toward insoluble electron acceptors, including electrodes in MESs.IMPORTANCEPrevious hypotheses of tactic behavior of exoelectrogenic bacteria are based on techniques that do not accurately control the electrochemical potential, such as chemical-in-plug assays or microscopy tracking experiments in two-electrode cells. Here, we have revisited previous experiments and, for the first time, performed microscopy cell-tracking experiments in three-electrode electrochemical cells, with defined electrode potentials. Based on these experiments, taxis toward electrodes is observed to switch at about −0.2 V versus standard hydrogen electrode (SHE), coinciding with the reduction potential of flavins.


2020 ◽  
Vol 12 (8) ◽  
pp. 3081 ◽  
Author(s):  
Vasan Sivalingam ◽  
Carlos Dinamarca ◽  
Gamunu Samarakoon ◽  
Dietmar Winkler ◽  
Rune Bakke

Biogas upgrading to biomethane with microbial electrosynthesis (MES) is receiving much attention due to increasing biomethane demands and surplus renewable energy. Research has demonstrated the feasibility of MES to increase methane yield by reducing CO2 in anaerobic digestion (AD). Such CO2 reduction occurs at the cathode and requires the supply of both protons and electrons. The most studied sources of protons and electrons are oxidation of organic substances and water, generated at the anode. These anodic reactions, however, also imply the production of CO2 and O2, respectively, both with negative implications for the AD process. A source of protons and electrons without CO2 and O2 as by-products would be beneficial for MES-enhanced biomethane production. This opinion article discusses the possibility of ammonium to serve as a sustainable proton and electron source.


1989 ◽  
Vol 264 (1) ◽  
pp. 265-273 ◽  
Author(s):  
F A Armstrong ◽  
S J George ◽  
R Cammack ◽  
E C Hatchikian ◽  
A J Thomson

Desulfovibrio africanus ferredoxin III is a monomeric protein (Mr 6585) containing seven cysteine residues and 7-8 iron atoms and 6-8 atoms of acid-labile sulphur. It is shown that reversible unmediated electrochemistry of the two iron-sulphur clusters can be obtained by using a pyrolytic-graphite-‘edge’ carbon electrode in the presence of an appropriate aminoglycoside, neomycin or tobramycin, as promoter. Cyclic voltammetry reveals two well-defined reversible waves with E0′ = -140 +/- 10 mV and -410 +/- 5 mV (standard hydrogen electrode) at 2 degrees C. Bulk reduction confirms that each of these corresponds to a one-electron process. Low-temperature e.p.r. and magnetic-c.d. spectroscopy identify the higher-potential redox couple with a cluster of core [3Fe-4S]1+.0 and the lower with a [4Fe-4S]2+.1+ centre. The low-temperature magnetic-c.d. spectra and magnetization properties of the three-iron cluster show that it is essentially identical with that in Desulfovibrio gigas ferredoxin II. We assign cysteine-11, -17 and -51 as ligands of the [3Fe-4S] core and cysteine-21, -41, -44 and -47 to the [4Fe-4S] centre.


2021 ◽  
Author(s):  
Akansha Shrivastava ◽  
Mamta Pal ◽  
Rakesh Kumar Sharma

Abstract Production of bioethanol and bioelectricity is a promising approach through microbial electrochemical technology. Sugars are metabolized by yeast to produces ethanol, CO2 and energy. Surplus electrons produced during the fermentation can be transferred through the circuit to generate electricity in a Microbial fuel cell (MFC). In the present study, a membrane less single chambered microbial fuel cell was developed for simultaneous production of bioethanol and bioelectricity. Pichia fermentans along with a well-known ethanol producing yeast Saccharomyces cerevisiae was allowed to ferment glucose. S. cerevisiae demonstrated maximum open circuit voltage (OCV) 0.287 ± 0.009 V and power density 4.473 mW m− 2 on 15th day, with a maximum ethanol yield of 5.6% (v/v) on 12th day. P. fermentans demonstrated a maximum OCV of 0.318 ± 0.0039 V and power density of 8.299 mW m− 2 on 15th day with ethanol yield of 4.7 % (v/v) on 12th day. Coulombic efficiency (CE) increased gradually from 0.002–0.471 % and 0.012–0.089 % in the case of S. cerevisiae and P. fermentans, respectively, during 15 days of experiment. Thus, the result indicated that Single chambered fuel cell can be explored for its potential applications for ethanol production along with clean energy generation.


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