Mo2C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO2 reduction
Biotechnology for Biofuels volume 12, Article number: 71 (2019)
Microbial electrosynthesis (MES) is a biocathode-driven process, in which electroautotrophic microorganisms can directly uptake electrons or indirectly via H2 from the cathode as energy sources and CO2 as only carbon source to produce chemicals.
This study demonstrates that a hydrogen evolution reaction (HER) catalyst can enhance MES performance. An active HER electrocatalyst molybdenum carbide (Mo2C)-modified electrode was constructed for MES. The volumetric acetate production rate of MES with 12 mg cm−2 Mo2C was 0.19 ± 0.02 g L−1 day−1, which was 2.1 times higher than that of the control. The final acetate concentration reached 5.72 ± 0.6 g L−1 within 30 days, and coulombic efficiencies of 64 ± 0.7% were yielded. Furthermore, electrochemical study, scanning electron microscopy, and microbial community analyses suggested that Mo2C can accelerate the release of hydrogen, promote the formation of biofilms and regulate the mixed microbial flora.
Coupling a HER catalyst to a cathode of MES system is a promising strategy for improving MES efficiency.
Due to the fossil resources depletion, the population expansion and continuously economy prosperity, there are increasing demands for more clean, affordable, reliable and sustainable energy supplies . With the more competitive cost, additional engagement of the scientific, financial and public–policy communities, the renewable energy supply from hydropower, solar cells and wind turbines might power the global economic growth, increase energy security, as well as mitigate the risks of climate change . However, due to the energy intermittency of renewable sources, efficient energy storage is a prerequisite for a smooth transition to a clean energy economy . Among existing renewable energy storage technologies, microbial electrosynthesis (MES) is an emerging strategy . MES is a biocathode-driven process, in which the electroautotrophic microorganisms may use electrons generated from renewable energy on the cathode as energy sources and CO2 as only carbon source to produce chemicals [4, 5]. Thus, the hard-to-store energy generated from renewable sources is converted into high value-added chemicals [6, 7].
The operation efficiency of MES is highly affected by the activity of the biocatalysts and the supply of electrons from the cathode. Therefore, a large number of studies on MES have been focused on the screening and optimization of electroautotrophic microorganisms  or the improvement of the electron transfer capability from electrodes to biocatalysts by materials science [7, 9]. Biocatalysts used in MES systems can be classified into two major categories: pure bacterium [3, 10,11,12,13] and mixed microbial flora [8, 14,15,16,17,18,19,20]. Although biocatalysts used in MES were different, the dominant product in MES was acetate for early years of MES development. Recently, two independent research groups screened and obtained a large number of mixed bacterial populations that are capable of synthesizing isopropanol  and butyric acid , thereby enabling MES systems to synthesize C3 and C4 compounds. A lot more MES studies focused on the modification of electrode materials to improve the electron transfer rate and biocompatibility of the electrodes in the MES system [21, 22]. Decoration of conductive materials on both carbon cloth [10, 11] and three-dimensional scaffold [12,13,14, 16, 23], such as RVC or nickel foam, may increase the acetate production rate as well as CO2 to acetate conversion rates.
However, most of the existing electrode modification has been focused on direct electron transfer (DET). In DET, electroautotrophic microbes may obtain electrons that pass through membrane proteins, such as C-type cytochromes and H+-dependent Rnf complex or hydrogenase ; or electrons are directly obtained from the cathode via biological nanowires , i.e., conductive pili [9, 21, 26]. Different from the DET, which requires direct contact between microbes and the cathode, the mediated electron transfer (MET) is accomplished through the redox electron mediator secreted by the autotrophic microorganisms or extracellular H2, formate, Fe2+, NH3, etc. . However, the researches on MES system through MET were much less compared to DET. Liao’s group and Nocera’s group demonstrated examples of electrochemically converting electrons into electron mediators, such as formic acid and hydrogen, respectively [27, 28]. Therefore, the engineered Ralstonia eutropha, which cannot obtain electrons directly from electrodes, may biotransfer CO2 and electron mediators into biofuels [27, 28].
Most electroautotrophic microorganisms used in MES (either pure bacteria or the dominant strains in mixed microbial flora) are acetogens. Acetogens adopt the Wood–Ljungdahl pathway to fix CO2 with the reducing power provided by H2. In MES, H2 might be produced in the cathodic chamber by water electrolysis; however, the activation energy of hydrogen evolution reaction without catalyst is relatively high. Therefore, decorating H2 evolution catalysis on the cathode of MES and using hydrogen as an electron mediator to improve electron transfer from the electrode to the electroautotrophic microorganisms should be an effective strategy for improving MES efficiency .
The common method of producing hydrogen is to electrochemically split water into hydrogen and oxygen gases . Therefore, substantial research was applied to develop catalysis materials for hydrogen evolution reaction (HER), reduce kinetic barriers, and perform efficient electrolysis . The most active HER electrocatalysts are obtained from precious platinum group metals, but they are too expensive for large-scale deployment. Among the most frequently proposed HER electrocatalysts, transition metal carbides are considered as promising replacements for platinum cathode catalyst for HER due to their high catalytic activities, low cost, and high abundance . In this study, we coupled an active HER electrocatalyst, i.e., molybdenum carbide (Mo2C), to a microbial electrosynthesis system to demonstrate a highly effective CO2 reduction process through chemical and biological catalyses.
Characterization of electrocatalysts
X-ray diffraction (XRD) analysis was used to confirm the crystallinity and phase structure of the commercially available Mo2C powder. The XRD patterns (Additional file 1: Fig S1) showed that all the diffraction peaks of the Mo2C sample are unambiguously indexed based on the hexagonal of β-Mo2C phases (PDF#35-0787). No evident diffraction peaks of impurities were detected, and strong diffraction peaks were monitored at 2–θ angles of 39.3°, 69.5°, and 4.6°, which can be assigned to the (101), (103), and (112) diffraction planes, respectively, of Mo2C.
As observed from the scanning electron microscope (SEM) image (Fig. 1), the morphology and structure of Mo2C–CF and CF were investigated. The surface of bare CF was smooth, whereas the CF samples with different amounts of Mo2C loading presented distinct morphology. CF with 12 mg cm−2 Mo2C (Fig. 1d) exhibited good particle distribution and loading conditions. Moreover, the elemental analysis of the selected region (Additional file 1: Table S1) showed the distribution of the elements on the cathode materials compared with that of the control group, which demonstrated that Mo2C was successfully adsorbed onto CF.
The electrocatalytic performance of Mo2C–CF for HER was then evaluated in a cathode medium using a three-electrode system. Bare CF was used as the control group. During the test, Fig. 2a shows that CF delivered poor performance for linear sweep voltammetry (LSV) curves shifting from 0.2 to − 1.2 V (vs. SHE). As expected, the HER performance of CF can be considerably enhanced by 12 mg cm−2 Mo2C modification with a large overpotential of only − 0.173 V at a representative current density of 1 mA cm−2 (η1). The overpotential of CF with 4 mg cm−2 and 2 mg cm−2 Mo2C modification was − 0.333 V and − 0.663 V at 1 mA cm−2 (η1), respectively. Tafel plots were also obtained from the LSV curves. As shown in Fig. 2b, the Tafel plots constructed from steady-state polarization measurements presented HER activity from a kinetic viewpoint. For comparison, the Tafel slope of 12 mg cm−2 Mo2C was 0.131 V dec−1, which was lower than those of 4 mg cm−2 Mo2C (0.215 V dec−1), 2 mg cm−2 Mo2C (0.279 V dec−1), and the control (0.325 V dec−1). Among the samples, CF with 12 mg cm−2 achieved the highest electrocatalytic performance for generating hydrogen from a cathode medium.
The hydrogen production by Mo2C–CF and CF in the MES system was experimentally quantified by gas chromatography (GC), which confirmed the same trend. The average H2 production rate of Mo2C–CF (12 mg cm−2) reached about 2.29 × 104 mol day−1, which was 12.7 times than that of CF (1.80 × 103 mol day−1) (Fig. 3b). It showed that the Mo2C modification significantly improved the hydrogen evolution in the MES system.
Furthermore, the stability of Mo2C–CF (12 mg cm−2) was evaluated after 1000 cycles of cyclic voltammograms (CV) scans in the cathodic medium. There was no significant difference between LSV curves before and after CV scans (Fig. 3a). The results indicated that the Mo2C-decorated CF was quite stable in this system.
MES of acetate from CO2
After inoculation, the OD600 of the cathodic medium represents microorganism growth in the solution to a certain extent. The OD600 values of the MES with Mo2C and the control were approximately 0.02 after inoculation (Fig. 4a). The OD600 value of the MES with 12 mg cm−2 Mo2C increased during the first 12 days of operation, and then increased slowly, and finally stabilized. The maximum OD600 value reached 0.07 ± 0.01, which was still higher than that of the control. However, the final OD600 values of the MES with 4 mg cm−2 and 2 mg cm−2 Mo2C were slightly lower than that of the control, reaching 0.05 ± 0.01 and 0.06 ± 0.01, respectively. In general, the growth rate of the OD600 of MES with Mo2C was higher than that of the control at the beginning of the experiment. However, the differences in the OD600 values became insignificant after the OD600 value had stabilized.
Acetate was the predominant product in all the MES reactors (Fig. 4b). Tiny amount of other products such as formate and ethanol was observed in the initial 7 days and gradually declined (Additional file 1: Fig S2). After 30 days, an increase in acetate production was observed in all the MES groups. However, the acetate production rate increased with an increase in Mo2C loading. After a 30-day operation, the MES with 12 mg cm−2 Mo2C obtained the highest maximum acetate titer of 5.72 ± 0.6 g L−1, followed by the MES with 4 mg cm−2 and 2 mg cm−2 Mo2C, which yielded a maximum acetate titer of 4.33 ± 0.5 g L−1 and 3.69 ± 0.3 g L−1, respectively. The maximum acetate titer of the control was only 2.75 ± 0.10 g L−1. Meanwhile, the average acetate production rate of the MES with 12 mg cm−2 Mo2C was the highest (0.19 ± 0.02 g L−1 day−1), i.e., 2.1 times higher than that of the control (0.09 ± 0.01 g L−1 day−1). The acetate production rates of the MES with 4 mg cm−2 and 2 mg cm−2 Mo2C were 0.14 ± 0.02 g L−1 day−1 and 0.12 ± 0.01 g L−1 day−1, respectively.
Current was generated immediately after inoculation (Fig. 5a). The current of the MES with 12 mg cm−2 Mo2C was stable for the first 22 days; however, those of the other MES systems started to decline after 7 days. By the end of the experiment, the current of the control was only 5.82 ± 0.2 mA, which was lower than those of the MES with 2, 4, and 12 mg cm−2 Mo2C (8.75 ± 0.3, 9.90 ± 0.2, and 13.1 ± 0.3 mA, respectively). The overall trend of the current in all the MES systems presented a slow decline. This phenomenon is similar to those in other reports [10, 11, 32, 33]. Furthermore, coulombic efficiency (CE) was calculated (Fig. 5b). The CEs of the control and MES with Mo2C were close and maintained a value of approximately 64 ± 0.7%.
To investigate the electrochemical behavior of the biocathodes, CV was performed in the MES reactors on day 14 of MES operation (Fig. 6). The visualized maximum current of the control biocathode in forward (1.11 mA cm−2) and reverse (− 0.88 mA cm−2) scans was lower than that of the Mo2C biocathode. Apparently, the MES with 12 mg cm−2 Mo2C (13.53 mA cm−2 and − 12.78 mA cm−2) exhibited a higher cathodic current density than the other systems, whereas the control yielded the lowest cathodic current density. The results indicated that the electron transfer capability of the cathode was improved by Mo2C modification. In addition, the MES with 12 mg cm−2 Mo2C obtained the highest electron transfer ability.
On day 14 of MES operation, the average H2 production rates in MES with Mo2C-biofilm (12 mg cm−2) and CF biofilm were measured, respectively. The average H2 production rate of Mo2C biofilm reached about 4.94 × 102 mol day−1, while the H2 production was almost undetectable in the CF biofilm (Fig. 3b). The H2 production in MES with Mo2C-modified biocathode was significantly higher than that in MES without modification. The observation of lower hydrogen production rate in biocathode compared with the bare cathode might be due to the constant consumption of hydrogen by microorganisms in the MES system.
The surfaces of the biofilms were analyzed at the end of the experiment via SEM (Additional file 1: Fig. S3). The surface morphology of the cathode from the control group was relatively smooth, and thin biofilm could be observed on the carbon fiber. CF with Mo2C modification contained thick biofilm on the carbon fiber. An increasing number of microorganisms attached to the cathode with an increase in catalyst loading. The protein content of the cathode was measured at the end of experiments. The protein contents of the MES with 2, 4, and 12 mg cm−2 Mo2C were 220.53 ± 2.54 μg cm−2, 226.81 ± 2.11 μg cm−2, and 336.39 ± 0.42 μg cm−2, respectively. The MES with 12 mg cm−2 Mo2C obtained the highest protein content, which was approximately 2.1 times higher than that of the control (163.76 ± 6.08 μg cm−2). The protein content results are consistent with the SEM observation and indicated that the difference in biomass may be caused by acetate production change.
Furthermore, the microbial community of planktonic cells and biofilms in the control and MES with 12 mg cm−2 Mo2C groups were analyzed at the end of the experiments. At the phylum level (Fig. 7a), the relative abundance of Proteobacteria, Bacteroidetes, and Firmicutes was dominant. Proteobacteria was the most abundant phylum in planktonic cells and biofilms in the control and MES with 12 mg cm−2 Mo2C groups. Simultaneously, Proteobacteria accounted for over 98 ± 1% of the planktonic cells, which was higher than their proportion in biofilms. By contrast, the abundance of Firmicutes and Bacteroidetes in planktonic cells was lower than that in biofilms.
At the genus level (Fig. 7b), the predominant species mainly included Arcobacter, Sulfurospirillum, Acetobacterium, and Citrobacter. Remarkably, the relative abundance of Arcobacter in planktonic cells (91.8 ± 0.3%) for the control group was higher than those for the other groups, followed by Citrobacter (4.4 ± 0.3%), Sulfurospirillum (2.2 ± 0.4%), and Acetobacterium (0.9 ± 0.3%). Moreover, the relative abundance of Acetobacterium in biofilms was higher than that in planktonic cells. This phenomenon is consistent with previous reports . The dominant species in biofilms was also Arcobacter (65.4 ± 0.2%), followed by Sulfurospirillum (16.6 ± 0.6%), Acetobacterium (14.7 ± 1.7%), and Citrobacter (2.6 ± 0.1%).
Hydrogen is a well-recognized energy carrier that can be easily developed further . Lanchet et al.  reported that hydrogen produced on the cathode by water electrolysis is an essential mediator in the microbial electrochemical. Later, Jourdin et al.  found that bacterial modification of the electrode surface (possibly via synthesis of Cu nanoparticles) was directly involved in the significant enhancement of the hydrogen production. In MES, H2 might be produced in the cathodic chamber by water electrolysis. However, the activation energy of hydrogen evolution reaction without catalyst is relatively high. Therefore, coupling a HER catalyst to a cathode of a MES system to enhance hydrogen evolution might be a promising strategy to improve the MES performance, from the engineering perspective.
The HER electrocatalyst used in this study was Mo2C, which is an important member of early transition metal carbides. It has been proven to be a high-performing HER electrocatalyst because it exhibits an electronic structure similar to that of platinum group metals [29, 37]. For the cathode of our MES system, CF was used as the base material and commercially available β-Mo2C powder was selected as HER electrocatalyst. Consistent with our designation assumptions, the decoration of Mo2C considerably improved hydrogen evolution in our MES systems. The Tafel plot constructed from steady-state polarization measurements is believed to show HER activity from a kinetic point of view. The cathode with 12 mg cm−2 Mo2C loading achieved the best HER activity, whereas its Tafel slope yielded the lowest value of 0.131 V dec−1 (Fig. 2b), followed by the cathodes with 4 mg cm−2 (0.215 V dec−1) and 2 mg cm−2 (0.279 V dec−1) Mo2C loadings. The bare CF demonstrated the worst electrocatalytic performance in generating hydrogen from the cathode medium, and its Tafel slope reached as high as 0.325 V dec−1. The results of H2 production rate also further confirmed that the presence of Mo2C can improve the hydrogen evolution. The average H2 production rate of Mo2C–CF (2.29 × 104 mol day−1) was 12.7 times than that of CF (1.80 × 103 mol day−1) (Fig. 3b).
The SEM images and Bradford assay indicated that the formation of biofilms was improved by Mo2C modification of the cathode. A comparison of the SEM images of biofilms on the cathodes with and without Mo2C modification showed that the distribution of biofilm on the cathode with 12 mg cm−2 Mo2C was more extensive (Additional file 1: Fig. S3). Meanwhile, Bradford assay demonstrated the same results. The protein content of the cathode with 12 mg cm−2 Mo2C was nearly twice as much as that of the control. It is probably due to that the more production of electron carrier, hydrogen, improved autotrophic microbial growth significantly. We evaluated the average H2 production rates in MES with Mo2C biofilm (12 mg cm−2) and CF biofilm on day 14 of MES operation. The average H2 production rate of Mo2C biofilm reduced to 4.94 × 102 mol day−1, while the H2 production was almost undetectable in the CF biofilm (Fig. 3b). Compared with the average H2 production rates in MES with bare Mo2C–CF (2.29 × 104 mol day−1) and CF (1.80 × 103 mol day−1), almost 98% and 100% of H2 produced in MES system with Mo2C-modified and unmodified cathode were consumed by autotrophic microorganisms, respectively. Therefore, the biocatalysts in biofilms and planktonic cells acquire electrons more easily from the Mo2C-modified MES systems because of the highly efficient electrocatalyzed hydrogen production.
The presence of Mo2C also regulates the mixed microbial flora of biofilms and planktonic cells in the MES system. The predominant species in the microbial community of MES systems include Arcobacter, Acetobacterium, Sulfurospirillum, and Citrobacter. Compared with the microbial community of the CF biofilm, the content of Arcobacter decreased, whereas that of Acetobacterium increased in the 12 mg cm−2 Mo2C biofilm. Arcobacter has been reported to be an electrochemically active bacterium that is responsible for electron transfer via an electrode [38, 39], whereas Acetobacterium was recognized as the main acetogen in bacterial flora that is responsible for acetate production through the Wood–Ljungdahl pathway [7, 16, 17, 39, 40]. As an electronic carrier, H2 played a dominant role in electron transport and considerably promoted electron transfer through a hydrogen-related metabolic pathway because of the decoration of HER catalyst in the MES system. Therefore, electron transfer through Arcobacter was relatively reduced, and acetate production depending on H2 was strengthened. A similar pattern was observed in planktonic cells. The content of Arcobacter in the planktonic cells of the CF group was lower than that in 12 mg cm−2 Mo2C group. Meanwhile, Acetobacterium, which was nearly undetectable in the planktonic cells of the CF group, significantly accumulated in the 12 mg cm−2 Mo2C group. We also observed that the abundance of Sulfurospirillum was increased in 12 mg cm−2 Mo2C in biofilm (16.7 ± 0.3%) and planktonic cells (6.5 ± 0.1%). Sulfurospirillum, which was reported as the microaerophilic bacterium in the cathodic microbial community , was responsible for expending the trace amounts of oxygen that diffused from the anode and for maintaining an anaerobic environment in the rest of the community. The abundance of Sulfurospirillum in MES with 12 mg cm−2 Mo2C was higher than that of MES with CF. This phenomenon suggested that more microaerobic bacteria might be needed to maintain anaerobic environment in the MES with 12 mg cm−2 Mo2C. In addition, Citrobacter had been reported as a hydrogen-producing bacterium . We observed that the abundance of Citrobacter in the planktonic cells of the 12 mg cm−2 Mo2C group was considerably lower than that of the CF group because of the electrochemical catalyzed hydrogen evolution. However, this pattern was not as significant as that in biofilm. This phenomenon may be explained by the dominant electron transfer mechanism being MET in planktonic cells and DET in biofilms. Therefore, when HER catalyst was used to enhance hydrogen production, its impact on MET was considerably higher than that on DET. In summary, the decoration of HER catalyst on the cathode remarkably enhanced indirect electron transfer through H2 and regulated the composition of microbial flora in a MES system, thereby causing a reduction in the abundance of the electron transfer bacterium Arcobacter and the hydrogen-producing bacterium Citrobacter and promoting microbial electrosynthesis through the Wood–Ljungdahl pathway, which caused Acetobacterium accumulation. The side effect of water electrolysis is the additional requirement of the microaerophilic bacterium, Sulfurospirillum, in a MES system with Mo2C decoration.
In the present study, coupling an active HER electrocatalyst to a cathode of MES system enhanced the electron transfer rate, thereby promoting an effective CO2 reduction process. Consequently, a relatively high maximum acetate concentration of 5.72 g L−1 was obtained from the MES with 12 mg cm−2 Mo2C decoration, which was 2.08 times higher than that of the control. The maximum acetate concentration between our study and those in the literature was incomparable due to the differences in mixed microbial cultures, operation days, and potentials. However, as the reaction goes on, due to the continuous accumulation of acetate, the activity of electroautotrophic bacteria might be inhibited. The volumetric production rate and CE are meaningful for practical industrial use. Therefore, a lot more researches focused on the acceleration of volumetric acetate production rate through material science [41, 42] or separation process of acetate , rather than the maximum acetate production. We summarized the key values in Table 1, which indicates that the efficiency that MES systems was obtained via mixed microbial cultures using different cathode materials and potentials. Our MES system with 12 mg cm−2 Mo2C demonstrated the outstanding production rate of 0.19 g L−1 day−1, which is higher than those of most reported MES systems but lower than that of the MES system reported by Marshall et al. (1.0 g L−1 day−1) . For their MES system, the high volumetric production rate might be due to the high packing density of graphite granules (400 g L−1) in their MES system, where the packed bed was fully clogged with biocatalysts. However, due to the increased internal resistance in their MES system, the volumetric acetate production rate for certain amount of biocatalysts might not be optimized. Our strategy is to improve hydrogen evolution by electrode modification, the volume rate of acetate production was effectively increased, and the autotrophic microorganism may gain electrons through hydrogen, which effectively reduced internal resistance caused by excessive microorganisms.
In general, the development of Mo2C–CF cathode is a simple, rapid and effective approach to improve MES efficiency. From the perspective of hydrogen evolution catalysts, we need to develop highly efficient hydrogen evolution catalysts under neutral conditions. However, Mo2C, the HER catalyst used in this study, always presents the advantage of hydrogen evolution in acidic conditions in previous reports . A catalyst with a large load is required because the hydrogen evolution effect of Mo2C is not optimal under neutral conditions. When we increase the loading of Mo2C to 24 mg cm−2, we find that Mo2C is not strongly adsorbed onto the surface of CF. This condition causes the catalyst to fall off and the detached Mo2C was suspended in the MES reaction solution (Additional file 1: Fig. S4), which considerably inhibits the growth of microorganisms, Moreover, the decoration methodology may also be improved, and an in situ growth of HER catalyst may be applied in the future to optimize its catalytic efficiency .
In this study, the Mo2C-modified electrode was constructed to demonstrate that decorating HER catalyst on cathode is a promising strategy to improve MES process efficiency. When the loading of Mo2C was 12 mg cm−2, the volumetric acetate production was twofold of the control (0.19 ± 0.02 g L−1 day−1) and the acetate concentration reached 5.72 ± 0.6 g L−1, within 30 days. The presence of Mo2C accelerates the release of hydrogen, regulates the mixed microbial flora and benefits the biofilm growth, and thus improves the CO2 reduction rate in the MES system.
Mo2C-modified carbon felt (CF) preparation
In accordance with previous reports , CF was immersed in 1 mol L−1 HCl and 1 mol L−1 NaOH for 24 h to remove metal impurities and organics, respectively. Then, CF was washed several times with deionized water to ensure that its surface was clean. Mo2C powder (99%; Zhongxin, China) was used as the cathodic catalyst in this study. For catalyst ink preparation, 50 mg, 100 mg, 300 mg and 600 mg of Mo2C powder were, respectively, mixed with 5 wt% Nafion solution (DuPont, USA) and ethanol (95%, AR) (VNafion:Vethanol = 1:10). The mixture was ultrasonically agitated for 30 min to obtain a homogenous cathodic catalyst ink. Then, the as-prepared CF was fully soaked in the ink for 12 h and dried at 80 °C in an oven. This process was repeated four times until the ink was adsorbed completely. From the preceding method, the loading of Mo2C on the electrode was 2, 4, 12, and 24 mg cm−2. CF without modification was used as control.
Microbial electrosynthesis experiment
The cathodic chamber was filled with a growth medium, which contained 50 mL PETC salt solution, 10 mL trace element solution, 0.5 g Cys-HCl, 1 g NaHCO3, and 10 mL Wolfe’s vitamin solution per liter of deionized water. The PETC salt solution was comprised of the following (per liter of deionized water): 1 g NH4Cl, 0.1 g KCl, 0.2 g MgSO4·7H2O, 0.8 g NaCl, 0.1 g KH2PO4, 0.02 g CaCl2. The trace elements solution was comprised in the following manner: (per liter of deionized water): 2 g Nitrilotriacetic acid, 1.3 g MnCl2·4H2O, 0.4 g FeSO4·7H2O, 0.2 g CoCl2·2H2O, 0.2 g ZnSO4·7H2O, 0.02 g CuCl2·2H2O, 0.02 g NiCl2·6H2O, 0.02 g Na2MoO4·2H2O, 0.02 g Na2SeO3, 0.025 g Na2WO4·2H2O. The Wolfe’s vitamin solution composed of the following (per liter of deionized water): 2.0 mg Biotin, 2.0 mg Folic acid, 10.0 mg Pyridoxine hydrochloride, 5.0 mg Thiamine·HCl, 5.0 mg Riboflavin, 5.0 mg Nicotinic acid, 5.0 mg Calcium d-(+)-pantothenate, 0.1 mg Vitamin B12, 5.0 mg p-aminobenzoic acid, 5.0 mg Thioctic acid. The final pH was adjusted to 7.0. The anodic medium consists of 50 mL L−1 PETC salt solution, 6 g L−1 NaCl, and 2 g L−1 KCl L−1 of deionized water. The PETC salt solution, trace element solution, and Wolfe’s vitamin solution were prepared by following previous reports .
The H-shaped reactors, with an internal volume of 280 mL in both anode and cathode chambers, were made of glass. A proton exchange membrane (Nafion 117; Dupont Co., USA) was selected to separate the anode and cathode chambers. A titanium mesh with iridium and ruthenium coating (50 mm × 25 mm × 1 mm, length × width × thickness; Baoji Longsheng Nonferrous Metal Co., Ltd., China) was used as a dimensionally stable anode in all the reactors. The Mo2C-modified CF (Mo2C–CF, 5 cm × 5 cm × 0.5 cm, length × width × thickness) and CF (5 cm × 5 cm × 0.5 cm, length × width × thickness) were used as cathodes in duplicate reactors. A multichannel potentiostat (CHI 1000C, Shanghai Chen Hua Instrument Co. Ltd., China) was used for all the experiments. The cathode was poised with a potentiostat setting of − 0.85 V (vs. SHE). The anodic chamber was continually gassed with N2. A magnetic stir plate was installed into the cathodic chamber to ensure homogeneous mixing, and 100% CO2 (3 mL min−1) was continually gassed into the cathodic chamber. The inoculation mix was enriched as previously reported . Then, 5% (V/V) inoculation was added to each cathodic chamber of all the MES systems used in this study. All the reactors were run for 30 days and maintained at room temperature (25 ± 2 °C).
The Mo2C structures were investigated via X-ray diffraction (XRD; Rigaku Smartlab 3 kW) analysis with filtered Cu Kα radiation (λ = 1.5406 Å) operating at a tube voltage of 40 kV and a current of 40 mA. Diffraction patterns were collected via step scanning within the 2θ range of 10°–80° with intervals of 0.02°. HER measurements were conducted at room temperature in a standard three-electrode electrochemical cell with a potentiostat (Zennium, Germany). All the tests were performed in the aforementioned cathodic medium (pH = 6.8) using Mo2C–CF or CF (1 cm × 1 cm × 0.5 cm) as working electrode, while platinum sheet and saturated calomel electrode (SCE) were used as the counter and reference electrode. The system was deoxygenated via continuous purging with ultrapure argon gas (99.999% purity) for 30 min before each measurement. The polarization curves were recorded using linear sweep voltammetry (LSV), shifting from 0.2 to − 1.2 V (vs. SHE), at a scan rate of 0.005 V s−1. Subsequently, the polarization curves were replotted as overpotential (η) versus the logarithm of current density (log |j|) to obtain Tafel plots. The linear portions of the Tafel plots were then fitted to the Tafel equation to obtain the Tafel slope (b):
HER catalyst stability of the Mo2C–CF was evaluated by LSV before and after 1000 continuous sweeps of CV between 0.2 and − 1.2 V (vs. SHE), at a scan rate of 0.1 V s−1 after stabilization. The H2 production rate of bare Mo2C–CF, CF, Mo2C biofilm (on day 14) and CF biofilm (on day 14) was measured by gas chromatography (GC) apparatus (Hope 9860, China) in the cathode compartment of MES reactors with a potentiostat setting of − 0.85 V (vs. SHE). GC analysis was carried out with thermal conductivity detector and ultrapure carbon dioxide gas (99.999% purity). The Faradaic efficiency was calculated by comparing the amount of hydrogen generated by potentiostatic cathodic electrolysis with calculated hydrogen (assuming 100% FE). On the day 14 of MES operation, the CV of all the reactors was scanned, ranging from 0 to − 1.2 V (vs. SHE), at a scan rate of 0.005 V s−1. For CV measurement, the cathode (5 cm × 5 cm × 0.5 cm) was used as the working electrode, whereas the anode and Ag/AgCl were used as the counter and reference electrodes, respectively.
The surface morphologies of the cathode surfaces were studied via scanning electron microscopy with coupled energy-dispersive spectroscopy (SEM–EDS; JSM–5900, Japan). The bacteria attached to the cathode were stabilized following previously described procedures at the end of the experiments . Volatile fatty acid (VFA) was measured using a high-performance liquid chromatography (HPLC) apparatus (Agilent Technologies 1260, USA). Alcohols were detected by a gas chromatography (GC) apparatus (Shimadzu 2010 Plus, Japan). To evaluate the biofilm, protein content was quantified via Bradford assay . The currents were continuously monitored using a precision multimeter and a data acquisition system (Keithley Instruments 2700, USA). Coulombic efficiencies (CE) were calculated as CE = CP/CT × 100%, where CT is the total coulombs consumed calculated by integrating the area under the current-versus-time curve (i–t curve). CP is the coulombs found in the product calculated as CP = b × n × F, where b is the number of electrons in the product (8 eqmol−1), n is the number of moles, and F is Faraday’s constant (96,485 C mol−1).
DNA extraction for 16S rDNA illumina sequencing and microbial community structure analysis
Samples from the inoculum, planktonic cells, and biofilm on the Mo2C–CF and CF cathodes were collected and preserved at − 80 °C until the extraction of the genomic DNA. Genomic DNA was extracted using PowerSoil® DNA Isolation Kit (MO BIO Laboratories Inc., Carlsbad, CA, USA) following the manufacturer’s protocol. DNA quality was assessed at a ratio of 260/280 nm, using a Nano Drop ND-2000 spectrophotometer (Nano Drop Technologies Inc., Wilmington, USA), and a highly pure genomic DNA (A260/A280 ≈ 1.8) was used only for Illumina high-throughput sequencing by Majorbio (Shanghai, China).
Richness and biodiversity indices were obtained using the mothur software package. Similar sequences were clustered into operational taxonomic units (OTUs) based on 3% dissimilarity. On the basis of these clusters, rarefaction curves, OTUs, Chao1 richness estimations, Shannon diversity indexes, and Good’s coverage were generated in mothur version 1.30.0 for each sample (http://www.mothur.org/wiki/Main_Page) at a cut-off of 0.03 by randomly selecting the minimum sequences of all the samples. BLAST reports of taxonomic classification down to the phylum, class, order, family, and genus levels were performed using mothur based on sequences from the ribosomal database project (RDP) with a bootstrap cutoff of 50%.
hydrogen evolution reaction
reticulated vitreous carbon
direct electron transfer
mediated electron transfer
scanning electron microscope
scanning electron microscopy with energy-dispersive spectroscopy
linear sweep voltammetry
volatile fatty acid
high-performance liquid chromatography
operational taxonomic unit
Chu S, Majumdar A. Opportunities and challenges for a sustainable energy future. Nature. 2012;488:294–303.
Suberu MY, Mustafa MW, Bashir N. Energy storage systems for renewable energy power sector integration and mitigation of intermittency. Renew Sust Energ Rev. 2014;35:499–514.
Nevin KP, Woodard TL, Franks AE, Summers ZM, Lovley DR. Microbial electrosynthesis: feeding microbes electricity to convert carbon dioxide and water to multicarbon extracellular organic compounds. Mbio. 2010;1(2):e00103–10.
Rojas MDA, Zaiat M, Gonzalez ER, De Wever H, Pant D. Effect of the electric supply interruption on a microbial electrosynthesis system converting inorganic carbon into acetate. Bioresour Technol. 2018;266:203–10.
Rojas MDA, Mateos R, Sotres A, Zaiat M, Gonzalez ER, Escapa A, De Wever H, Pant D. Microbial electrosynthesis (MES) from CO2 is resilient to fluctuations in renewable energy supply. Energ Convers Manage. 2018;177:272–9.
Logan BE, Rabaey K. Conversion of wastes into bioelectricity and chemicals by using microbial electrochemical technologies. Science. 2012;337:686–90.
Patil SA, Gildemyn S, Pant D, Zengler K, Logan BE, Rabaey K. A logical data representation framework for electricity-driven bioproduction processes. Biotechnol Adv. 2015;33:736–44.
Patil SA, Arends JBA, Vanwonterghem I, van Meerbergen J, Guo K, Tyson GW, Rabaey K. Selective enrichment establishes a stable performing community for microbial electrosynthesis of acetate from CO2. Environ Sci Technol. 2015;49:8833–43.
Tremblay PL, Zhang T. Electrifying microbes for the production of chemicals. Front Microbiol. 2015;6:201.
Zhang T, Nie HR, Bain TS, Lu HY, Cui MM, Snoeyenbos-West OL, Franks AE, Nevin KP, Russell TP, Lovley DR. Improved cathode materials for microbial electrosynthesis. Energ Environ Sci. 2013;6:217–24.
Chen LF, Tremblay PL, Mohanty S, Xu K, Zhang T. Electrosynthesis of acetate from CO2 by a highly structured biofilm assembled with reduced graphene oxide-tetraethylene pentamine. J Mater Chem A. 2016;4:8395–401.
Aryal N, Tremblay PL, Lizak DM, Zhang T. Performance of different Sporomusa species for the microbial electrosynthesis of acetate from carbon dioxide. Bioresource Technol. 2017;233:184–90.
Cui M, Nie H, Zhang T, Lovley D, Russell TP. Three-dimensional hierarchical metal oxide-carbon electrode materials for highly efficient microbial electrosynthesis. Sustain Energ Fuels. 2017;1:1171–6.
Jourdin L, Grieger T, Monetti J, Flexer V, Freguia S, Lu Y, Chen J, Romano M, Wallace GG, Keller J. High acetic acid production rate obtained by microbial electrosynthesis from carbon dioxide. Environ Sci Technol. 2015;49:13566–74.
Song T, Zhang H, Zhang H, Yuan H, Yang Y, Ouyang P, Xie J. High efficiency microbial electrosynthesis of acetate from carbon dioxide using a novel graphene–nickel foam as cathode. J Chem Technol Biot. 2018;93:457–66.
Song TS, Zhang H, Liu H, Zhang D, Wang H, Yang Y, Yuan H, Xie J. High efficiency microbial electrosynthesis of acetate from carbon dioxide by a self-assembled electroactive biofilm. Bioresour Technol. 2017;243:573–82.
Marshall CW, Ross DE, Fichot EB, Norman RS, May HD. Long-term operation of microbial electrosynthesis systems improves acetate production by autotrophic microbiomes. Environ Sci Technol. 2013;47:6023–9.
Gildemyn S, Verbeeck K, Slabbinck R, Andersen SJ, Prevoteau A, Rabaey K. Integrated production, extraction, and concentration of acetic acid from CO2 through microbial electrosynthesis. Environ Sci Tech Let. 2015;2:325–8.
Arends JBA, Patil SA, Roume H, Rabaey K. Continuous long-term electricity-driven bioproduction of carboxylates and isopropanol from CO2 with a mixed microbial community. J CO2 Util. 2017;20:141–9.
Batlle-Vilanova P, Ganigué R, Ramió-Pujol S, Bañeras L, Jiménez G, Hidalgo M, Balaguer MD, Colprim J, Puig S. Microbial electrosynthesis of butyrate from carbon dioxide: production and extraction. Bioelectrochemistry. 2017;117:57–64.
Aryal N, Ammam F, Patil SA, Pant D. An overview of cathode materials for microbial electrosynthesis of chemicals from carbon dioxide. Green Chem. 2017;19:5748–60.
Katuri KP, Kalathil S, Ragab A, Bian B, Alqahtani MF, Pant D, Saikaly PE. Dual-function electrocatalytic and macroporous hollow-fiber cathode for converting waste streams to valuable resources using microbial electrochemical systems. Adv Mater. 2018;30:18.
Jourdin L, Freguia S, Donose BC, Chen J, Wallace GG, Keller J, Flexer V. A novel carbon nanotube modified scaffold as an efficient biocathode material for improved microbial electrosynthesis. J Mater Chem A. 2014;2:13093–102.
Shin HJ, Jung KA, Nam CW, Park JM. A genetic approach for microbial electrosynthesis system as biocommodities production platform. Bioresource Technol. 2017;245:1421–9.
Reguera G, McCarthy KD, Mehta T, Nicoll JS, Tuominen MT, Lovley DR. Extracellular electron transfer via microbial nanowires. Nature. 2005;435:1098.
Kalathil S, Pant D. Nanotechnology to rescue bacterial bidirectional extracellular electron transfer in bioelectrochemical systems. Rsc Adv. 2016;6:30582–97.
Li H, Opgenorth PH, Wernick DG, Rogers S, Wu TY, Higashide W, Malati P, Huo YX, Cho KM, Liao JC. Integrated electromicrobial conversion of CO2 to higher alcohols. Science. 2012;335:1596.
Liu C, Colon BC, Ziesack M, Silver PA, Nocera DG. Water splitting–biosynthetic system with CO2 reduction efficiencies exceeding photosynthesis. Science. 2016;352:1210–3.
Ma FX, Wu HB, Xia BY, Xu CY, Lou XW. Hierarchical beta-Mo2C nanotubes organized by ultrathin nanosheets as a highly efficient electrocatalyst for hydrogen production. Angew Chem Int Edit. 2015;54:15395–9.
Zou XX, Zhang Y. Noble metal-free hydrogen evolution catalysts for water splitting. Chem Soc Rev. 2015;44:5148–80.
Chen WF, Muckerman JT, Fujita E. Recent developments in transition metal carbides and nitrides as hydrogen evolution electrocatalysts. Chem Commun. 2013;49:8896–909.
Bajracharya S, ter Heijne A, Dominguez Benetton X, Vanbroekhoven K, Buisman CJN. Strik DPBTB, Pant D: Carbon dioxide reduction by mixed and pure cultures in microbial electrosynthesis using an assembly of graphite felt and stainless steel as a cathode. Bioresource Technol. 2015;195:14–24.
Kazemi M, Biria D, Rismani-Yazdi H. Modelling bio-electrosynthesis in a reverse microbial fuel cell to produce acetate from CO2 and H2O. Phys Chem Chem Phys. 2015;17:12561–74.
Singh A, Sevda S, Abu Reesh IM, Vanbroekhoven K, Rathore D, Pant D. Biohydrogen production from lignocellulosic biomass: technology and sustainability. Energies. 2015;8:13062–80.
Blanchet E, Duquenne F, Rafrafi Y, Etcheverry L, Erable B, Bergel A. Importance of the hydrogen route in up-scaling electrosynthesis for microbial CO2 reduction. Energ Environ Sci. 2015;8:3731–44.
Jourdin L, Lu Y, Flexer V, Keller J, Freguia S. Biologically induced hydrogen production drives high rate/high efficiency microbial electrosynthesis of acetate from carbon dioxide. Chemelectrochem. 2016;3:581–91.
Vrubel H, Hu XL. Molybdenum boride and carbide catalyze hydrogen evolution in both acidic and basic solutions. Angew Chem Int Edit. 2012;51:12703–6.
Fedorovich V, Knighton MC, Pagaling E, Ward FB, Free A, Goryanin I. Novel electrochemically active bacterium phylogenetically related to arcobacter butzleri, isolated from a microbial Fuel Cell. Appl Environ Microb. 2009;75:7326–34.
Marshall CW, Ross DE, Handley KM, Weisenhorn PB, Edirisinghe JN, Henry CS, Gilbert JA, May HD, Norman RS. Metabolic reconstruction and modeling microbial electrosynthesis. Sci Rep UK. 2017;7:8391.
Blaser MB, Dreisbach LK, Conrad R. Carbon isotope fractionation of 11 acetogenic strains grown on H2 and CO2. Appl Environ Microb. 2013;79:1787–94.
Mohanakrishna G, Vanbroekhoven K, Pant D. Impact of dissolved carbon dioxide concentration on the process parameters during its conversion to acetate through microbial electrosynthesis. React Chem Eng. 2018;3:371–8.
Bajracharya S, van den Burg B, Vanbroekhoven K, De Wever H, Buisman CJN, Pant D, Strik D. In situ acetate separation in microbial electrosynthesis from CO2 using ion-exchange resin. Electrochim Acta. 2017;237:267–75.
Xie S, Liang P, Chen Y, Xia X, Huang X. Simultaneous carbon and nitrogen removal using an oxic/anoxic-biocathode microbial fuel cells coupled system. Bioresour Technol. 2011;102:348–54.
Song TS, Tan WM, Wu XY, Zhou CC. Effect of graphite felt and activated carbon fiber felt on performance of freshwater sediment microbial fuel cell. J Chem Technol Biot. 2012;87:1436–40.
Yang YG, Xiang YB, Xia CY, Wu WM, Sun GP, Xu MY. Physiological and electrochemical effects of different electron acceptors on bacterial anode respiration in bioelectrochemical systems. Bioresour Technol. 2014;164:270–5.
Su M, Jiang Y, Li D. Production of acetate from carbon dioxide in bioelectrochemical systems based on autotrophic mixed culture. J Microbiol Biotechn. 2013;23:1140–6.
Dong Z, Wang H, Tian S, Yang Y, Yuan H, Huang Q, Song TS, Xie J. Fluidized granular activated carbon electrode for efficient microbial electrosynthesis of acetate from carbon dioxide. Bioresour Technol. 2018;269:203–9.
Bajracharya S, Vanbroekhoven K, Buisman CJN, Strik DP, Pant D. Bioelectrochemical conversion of CO2 to chemicals: CO2 as a next generation feedstock for electricity-driven bioproduction in batch and continuous modes. Faraday Discuss. 2017;202:433–49.
TS and JX designed the experiments. ST, HW and YY conducted the experiments. ST and JX wrote the manuscript. TS, HW, ZD, YY, HY, QH and JX provided advices on the experimental design and data analysis. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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This work was supported by the National Natural Science Foundation of China (Grant No.: 21878150); the Major projects of natural science research in Jiangsu Province (Grant No.: 15KJA530002); the technology supporting program of Jiangsu Province (Grant No.: BE2015167); Fund from the State Key Laboratory of Materials-Oriented Chemical Engineering (ZK201605) and the Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture.
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Tian, S., Wang, H., Dong, Z. et al. Mo2C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO2 reduction. Biotechnol Biofuels 12, 71 (2019). https://doi.org/10.1186/s13068-019-1413-z
- Microbial electrosynthesis
- Carbon dioxide
- Indirect electron transfer
- Hydrogen evolution reaction
- Molybdenum carbide