Here, we report the protocol for the fabrication of a Nafion-coated, polyaniline-functionalized, electrochemically reduced graphene oxide chemiresistive micro pH sensor. This chemiresistor-based, solid-state micro pH sensor can detect pH changes in real-time during a Lactococcus lactis fermentation process.
Here, we report the engineering of a solid-state micro pH sensor based on polyaniline-functionalized, electrochemically reduced graphene oxide (ERGO-PA). Electrochemically reduced graphene oxide acts as the conducting layer and polyaniline acts as a pH-sensitive layer. The pH-dependent conductivity of polyaniline occurs by doping of holes during protonation and by the dedoping of holes during deprotonation. We found that an ERGO-PA solid-state electrode was not functional as such in fermentation processes. The electrochemically active species that the bacteria produce during the fermentation process interfere with the electrode response. We successfully applied Nafion as a proton-conducting layer over ERGO-PA. The Nafion-coated electrodes (ERGO-PA-NA) show a good sensitivity of 1.71 Ω/pH (pH 4 – 9) for chemiresistive sensor measurements. We tested the ERGO-PA-NA electrode in real-time in the fermentation of Lactococcus lactis. During the growth of L. lactis, the pH of the medium changed from pH 7.2 to pH 4.8 and the resistance of the ERGO-PA-NA solid-state electrode changed from 294.5 Ω to 288.6 Ω (5.9 Ω per 2.4 pH unit). The pH response of the ERGO-PA-NA electrode compared with the response of a conventional glass-based pH electrode shows that reference-less solid-state microsensor arrays operate successfully in a microbiological fermentation.
pH plays a vital role in many chemical and biological processes. Even small changes in the pH value alter the process and adversely affect the outcome of the process. Hence, it is necessary to monitor and control the pH value during every stage of experiments. The glass-based pH electrode has been successfully used to monitor pH in many chemical and biological processes, although the use of a glass electrode poses several limitations to measuring pH. The glass-based pH electrode is relatively large, fragile, and small leakages of the electrolyte into the sample are possible. Furthermore, the electrode and electronics are relatively expensive for applications in 96-well screening fermentation systems. Moreover, the electrochemical sensors are invasive and consume the sample. Hence, it is more advantageous to use non-invasive, reference-less sensors.
Nowadays, miniaturized reaction systems are favored in many chemical engineering and biotechnology applications as these microsystems provide enhanced process control, along with many other advantages over their macro system analogs. To monitor and control the parameters in a miniaturized system is a challenging task as the sizes of the sensor to measure, for instance, pH and O2, need to be minimized as well. The successful production of microreactors for biological systems require different kinds of analytical tools for process monitoring. Hence, the development of smart microsensors plays a significant role in carrying out biological processes in microreactors.
Recently, there have been several attempts to develop smart pH sensors using chemiresistive sensing materials like carbon nanotubes and conducting polymers1. These chemiresistive sensors require no reference electrode and are easy to integrate with electronic circuits. Successful chemiresistive sensors make it possible to produce smart sensors that are cost-effective and easy to manufacture, require a small volume for testing, and are non-invasive.
Here, we report a method to develop an electrode with polyaniline-functionalized, electrochemically reduced graphene oxide. The chemiresistive electrode operates as a pH sensor during an L. lactis fermentation. L. lactis is a lactic-acid-producing bacterium used in food fermentation and food preservative processes. During fermentation, the production of lactic acid lowers the pH, and the bacterium stops growing at a low pH2,3,4.
A fermentation medium is a complex chemical environment that contains peptides, salts, and redox molecules which tend to interfere with the sensor surface5,6,7,8,9. This study shows that a pH sensor based on chemiresistive material with a proper surface protection layer could be used to measure pH in this kind of complex fermentation media. In this study, we successfully use Nafion as the protection layer for polyaniline-coated, electrochemically reduced graphene oxide to measure the pH in real-time during an L. lactis fermentation.
1. Preparation of Graphite Oxide
NOTE: Graphite oxide is prepared according to Hummers' method10,11.
2. GO-deposited Electrode Preparation
3. Reduction of GO to Electrochemically Reduced Graphene Oxide
4. Polyaniline Functionalization of the ERGO Electrode
5. ERGO-PA Electrode Testing at Different pH (Pre-calibration Before Nafion Coating)
6. Preparation of the Nafion-coated ERGO-PA Electrode
7. Preparation of L. lactis Culture Medium
8. Testing of the ERGO-PA-NA pH Response in an L. lactis Fermentation Experiment
The appearance of a strong reduction peak around -1.0 V (Figure 3) illustrated the reduction of GO to ERGO12,13,14,22. The intensity of the peak depends on the number of GO layers on the electrode. A thick black film completely covered the gold wires on the electrode. At that point, the two insulated gold electrodes were conductive because the GO connected the two gold electrode wires. Electropolymerization of aniline deposited a green film on the ERGO15,16,17,18,19,20,21,22. This green color is an indication of the formation of a conductive polyaniline layer on the ERGO. The conductivity of the ERGO electrode (resistance decrease) increased after the polyaniline functionalization.
When we put the ERGO-PA electrode in a solution with a pH between 4 and 9, the current value increased (Figure 5) due to the doping and dedoping of holes during the protonation/deprotonation process in ERGO-PA (Figure 2)22. The desired pH value for the measurement of the current value of the ERGO-PA electrode was obtained by titrating the Britton-Robinson buffer solution with 0.2 M NaOH. Hence, for every addition of 0.2 M NaOH, the current value of the electrode increased (Figure 5 and Figure 6). The response of the electrode was immediately stable when the addition of 0.2 M NaOH stopped at a particular pH.
A thin film of proton-conductive Nafion formed after the solvent evaporated at room temperature. The conductivity of the electrode was not affected much, but a few ohms of difference in the resistance value occurred and changed the base current value of the ERGO-PA electrode. Similar to the ERGO-PA electrode, the resistance of the ERGO-PA-NA electrode changed when the pH of the buffer solution changed from 4 to 9, as shown in Figure 618.
After placing the ERGO-PA-NA electrode inside the L. lactis culture, the current initially decreased and then took some time to reach a stable value. Once the growth of L. lactis started, the current of the ERGO-PA-NA decreased gradually. The decrease in current accelerated during the exponential growth-phase of L. lactis and reached a stable value at the end of the growth (Figure 7)18. The final value of the current (or resistance) is comparable to the current value of the ERGO-PA-NA electrode tested in buffer solution (pH 4 – 7), as shown in the inset of Figure 7.
Figure 1: Images of the bottom (left) and the top (right) part of the PDMS electrode holder. (A) The assembled cell with (B) reference and (C) counter electrode. (D) The interdigitated gold electrode with the scale bar in centimeters. Please click here to view a larger version of this figure.
Figure 2: Schematic of ERGO-PA-deposited interdigitated gold electrode with a graphical representation of ERGO and PA formation. The image also shows hole doping on ERGO-PA during protonation. Please click here to view a larger version of this figure.
Figure 3: Cyclic voltammetry of GO reduction with different GO concentrations at a scan rate of 50 mV/s. Please click here to view a larger version of this figure.
Figure 4: Cyclic voltammetry of polyaniline deposition at a scan rate of 50 mV/s. The first 10 scans from a total of 50 are shown. The vertical arrow marks the trend of the current increase during the scans, and the horizontal arrows mark the direction of the voltage scan. Please click here to view a larger version of this figure.
Figure 5: Resistance value of the ERGO-PA electrode against pH 4 to 9. Please click here to view a larger version of this figure.
Figure 6: Resistance value of the ERGO-PA-NA electrode against pH 4 to 9. Please click here to view a larger version of this figure.
Figure 7: Real-time continuous pH change of ERGO-PA-NA during L. lactis fermentation. The inset shows the expected resistance value of ERGO-PA-NA for pH 4 – 7 measured in Britton-Robinson buffer solution. Please click here to view a larger version of this figure.
It is essential that the GO layers completely cover the gold electrode wires after the deposition of GO. If the gold electrodes are not covered with GO, polyaniline will not only deposit on ERGO but also on the visible gold electrode wires directly. Deposition of polyaniline on the gold electrode wires may have implications on the performance of the electrode. After the reduction of GO to ERGO, the electrode is dried at 100 °C to strengthen the bonding between the ERGO layer and the gold electrode wires. The resistance of each electrode varies based on the number of GO layers that are deposited on the gold electrodes. Therefore, it is important to have the same concentration of GO for each electrode, and it is difficult to manufacture the electrode with a resistance in a predetermined specified range that is compatible with the measuring circuit. This limits the easy mass production of the electrodes.
The preparation of reduced graphene oxide/polyaniline by an electrochemical method has some advantages over other reported preparation methods. The electrochemical method presented here does not require strong reducing and oxidizing agents (e.g., hydrazine and ammonium persulfate)23,26. In addition, the material is directly deposited on the electrode and no further processing is required, making the fabrication process faster and easier. As GO is electrochemically reduced in situ, a good connection between the gold and the graphene is achieved, making the pH electrode more robust.
Equilibrating the ERGO-PA electrode in a buffer with a pH between 3 and 9 before applying the Nafion improved the sensitivity of the electrode (data not shown). Omitting this step requires a soaking of the ERGO-PA-NA electrode in a buffer pH 5 for more than 24 h before use.
Furthermore, the ERGO-PA electrode must be dry before applying Nafion. A wet ERGO-PA electrode resulted in an aqueous layer between the ERGO-PA and Nafion and increased the response time of the pH sensor. The resistance or measured current of ERGO-PA-NA in solutions with a different pH varied between electrodes. This variation in resistance or current for each electrode is, most likely, caused by the difference in the number of GO layers deposited on the gold electrode wires. Just like with other pH electrodes, proper calibration of the ERGO-PA-NA electrode is necessary to obtain reliable pH values.
After placing the electrode inside the L. lactis culture, an initial stabilization time is necessary to obtain a constant current. In the L. lactis fermentation, the initial pH is 7.2. During the growth of L. lactis, glucose is converted into biomass and into lactic acid that acidifies the fermentation liquid. The growth stops when the pH of the fermentation medium becomes too low to support proper growth or when there is no glucose left. The current (or resistance) value of ERGO-PA-NA before and after growth are equal to the current (or resistance) value of ERGO-PA-NA previously calibrated in different buffer solutions. The initial pH and end pH of the L. lactis fermentation medium was confirmed using a conventional glass pH electrode.
The pH sensor can be easily manufactured in-house using cheap chemicals. The low manufacturing costs allow researchers to use this electrode in applications were a large number of pH electrodes are necessary (e.g., in a bacterial fermentation screening platform). Another application of the pH electrode is envisioned in situations where the diffusion of KCl from a conventional glass pH electrode into the measuring solution is not wanted. The pH electrode of this protocol has no internal liquids that can diffuse into the sample.
Compatibility of the chemiresistive sensor with currently available wireless electronic circuits1,27 makes it possible to easily develop applications using wireless pH sensors.
The authors have nothing to disclose.
The authors acknowledge the University of Groningen for financial support.
Graphite flakes | Sigma Aldrich | ||
Sulfuric acid (H2SO4) | Merck | ||
Sodium nitrite (NaNO2) | Sigma Aldrich | ||
Potassium permanganate (KMnO4) | Sigma Aldrich | ||
30 % H2O2 | Sigma Aldrich | ||
HCL | Merck | ||
Aniline | Sigma Aldrich | ||
5wt % Nafion | Sigma Aldrich | ||
M17 powder | BD Difco | ||
Phosphoric acid (H3PO4) | Sigma Aldrich | ||
Boric acid (HBO3) | Merck | ||
Acetic acid | Merck | ||
Sodium Hydroxide | Sigma Aldrich | ||
Potassium dihydrogen phosphate | Sigma Aldrich | ||
Dipostassium hydrogen phosphate | Sigma Aldrich | ||
Au Interdigitated electrodes | BVT technology – CC1 W1 | ||
Potentiostat | CH Instruments Inc (CH-600, CH-700) |