Fully printed flexible and disposable wireless cyclic voltammetry tag

A disposable cyclic voltammetry (CV) tag is printed on a plastic film by integrating wireless power transmitter, polarized triangle wave generator, electrochemical cell and signage through a scalable gravure printing method. By proximity of 13.56 MHz RF reader, the printed CV tag generates 320 mHz of triangular sweep wave from +500 mV to −500 mV which enable to scan a printed electrochemical cell in the CV tag. By simply dropping any specimen solution on the electrochemical cell in the CV tag, the presence of solutes in the solution can be detected and shown on the signage of the CV tag in five sec. 10 mM of N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD) was used as a standard solute to prove the working concept of fully printed disposable wireless CV tag. Within five seconds, we can wirelessly diagnose the presence of TMPD in the solution using the CV tag in the proximity of the 13.56 MHz RF reader. This fully printed and wirelessly operated flexible CV tag is the first of its kind and marks the path for the utilization of inexpensive and disposable wireless electrochemical sensor systems for initial diagnose hazardous chemicals and biological molecules to improve public hygiene and health.

C yclic voltammetry (CV) has been used as a powerful tool for the study of electrochemical redox reactions between the electrodes and the solutions of all kind of solutes such as metals 1 , organic molecules 2 , proteins 3 , bacteria 4 , viruses 5 , and DNA 6 . Because of the high sensitivity of the electron transfer redox reactions, CV could become a very promising ubiquitous electrochemical sensor protocol if the cost and size of the CV system were significantly reduced to commercially viable single-use disposable units for checking traces of hazardous materials such as lead 7 , mercury 8 , arsenic 9 , e-coli 10 , and pesticides 11 in water or to diagnose the level of glucose 12 , cholesterol 13 and specific enzymes 14 in blood. This single-use disposable CV would dramatically reduce the cost of maintaining the public health system 15 . Therefore, inexpensive and disposable CV measurement system that can be operated wirelessly using a smartphone or RF (radio frequency) reader without complicate operation processes is in high demand for the realization of an ubiquitous sensor network system (Figure 1a). They would mainly be used as ubiquitous diagnostic and testing tools for detecting and monitoring the level of target specimens. However, there is no technology that is advanced enough yet to build a wireless, inexpensive and disposable CV system. In this paper, as a form of RF-tag, an extremely inexpensive, disposable and fully printed CV system is demonstrated for the first time by mimicking and combining basic CV concepts and wireless power transmission technologies of RF devices. To realize the fully printed CV tag, a key issue of wirelessly generating triangular waveform (6500 mV) that can scan the electrochemical cell at a low frequency (,1 Hz) to set up a redox reaction needs to be addressed through a minimum number of printed thin film transistors (TFTs). Fully printed 13.56 MHz rectenna and a ring oscillator with large trap charges in the channels of printed TFTs were respectively utilized to wirelessly generate triangular waveform by using only 10 printed TFTs.

Results
Based on two key units of the wireless power transmitter (Figure 1b-) and the triangular wave generator (Figure 1b-), the circuit layout of the fully printed wireless CV tag was designed by using a minimum number of printed thin film transistors (TFTs) to alleviate the issue of V th shift and shown in Figure 1b as a platform of disposable CV system. The circuit of CV tag was fabricated using all scalable printing methods, a roll-to-roll gravure, a roll-to-plate gravure, a drop casting, and a screen printer ( Figure S1 in Supplementary Information).
To provide a polarized DC voltage from the coupled 13.56 MHz AC signal of the reader, we modified our previously reported R2R gravure printed rectenna 16,17 , as shown in the layout in Figure 2a and Figure S2 in Supplementary Information). The polarized DC voltage was also decreased with decreasing load's resistance ( Figure 2d). To generate a cyclic waveform with a low frequency (,1 Hz) from the rectified polarized DC voltage, fully gravure printed p-type SWNT-based channel network thin film transistors (cnTFTs) were used to construct a five stage ring oscillator with p-type inverters. The cnTFTs can operate under less than 20 V and their mobility range (0.01 to 10 cm 2 /Vs) can be controlled through the loading concentration of SWNT in the ink [18][19][20][21] . To print the five stage ring oscillator, we used the same silver and BaTiO 3 inks as in the printing of the rectenna for reducing a number of printing steps while SWNT ink was used for printing the channel of the cnTFTs. To manufacture the ring oscillator, roll-to-plate (R2P) gravure was used to print 10 cnTFTs with a gate width of 300 mm and channel length of 160 mm for both the drive and load cnTFTs ( Figure S3 in Supplementary Information). The optimized cell depth of gravure plate was 37-40 mm with the cell wall thickness of 50-55 mm for the printing active layers of drive and load TFTs using low viscosity of SWNT based ink (,30 cp) ( Figure S4 in Supplementary Information). By repeating the printing of active layers on load TFTs, a higher SWNT network density can be achieved to generate higher current in the  Figure 1b). Polarized DC will operate the printed ring oscillator to generate a triangular voltage waveform ( in Figure 1b). The generated waveform will pass through the buffer to meet the impedance difference from the electrochemical cell ( in Figure 1b). The electrochemical cell will run the redox reaction with a single drop of specimen solution ( in Figure 1b) by the voltage triangular waveform. The output current of the electrochemical redox reaction will be amplified via an amplifier circuit ( in Figure b) and the signal will pass through the buffer to meet the impedance difference from the printed signage ( in Figure b). The signage will indicate the concentration level of specimen in the solution ( in Figure b). It will indicate whether the concentration is above or below a pre-determined value.
Their output and transfer characteristics are shown in Figure 3a and 3b respectively. Based on the attained transfer characteristics, the mobility (m), transconductance (g m ), on-off current ratios from I DS -V DS and threshold voltages (V th ) for both five drive cnTFTs and five load cnTFTs were extracted and shown in Table S1 (Supplementary Information). The shift range of V th from the fully gravure printed 10 cnTFTs were about 60.4 V for the drive cnTFTs and 60.6 V for load cnTFTs. Those shift ranges are narrow enough to run the printed ring oscillator for generating the triangular wave. Each inverter delivered a gain of 3 (Figure 3c), and the ring oscillator with five inverters generated a pseudo triangular waveform with a voltage amplitude of 7 V at 320 mHz ( Figure 3d). In fact, the pseudo triangular wave can be only generated by the printed cnTFTs based ring oscillator because of the parasitic and trapped channel capacitances due to carbon nanotube network structures in cnTFTs. Although we only showed the frequency of 320 mHz at here, the frequency can be varied from 0.3 Hz to 2 Hz based on the printed network density of SWNT of printed cnTFTs. This is an advantage of our printed cnTFTs for scanning electrochemical cell in CV tag over other technologies such as amorphous silicon TFTs where only a sine wave with a designed single frequency can be generated because of no trap capacitance in the channel ( Figure S6 in Supplementary Information). The frequency of the triangular waveform can be fine-tuned in the range of 0.3 Hz to 2 Hz as shown in the Figure  S7 (Supplementary Information) by simply changing loading concentration of SWNTs.
When the generated triangular waveform is supplied directly into the printed electro-chemical cell ( Figure S8 in Supplementary Information), wherein printed silver and carbon electrodes were used with a poly(ethylene oxide) and LiCF 3 SO 3 gel type electrolyte, the output voltage range is reduced to zero because of improper impedance matching between the electrochemical cell (10 KV) and ring oscillator (1 MV). Therefore, a buffer unit is needed to match the impedance levels between the ring oscillator and electrochemical cell.  Table S1 (Supplementary Information). The 6 cnTFTs of buffer unit were printed using R2P gravure with high SWNT concentration in the semiconducting ink. Each cnTFTs exhibited oncurrents in the range of 400 , 500 mA with a very low on-off ratio due to the enhanced metallic percolation in the dense SWNT networks. The buffer units with low on-off ratio were employed to reduce the input voltage to 6500 mV ( Figure 3f) which is the appropriate scanning range of the electrochemical cell. The printed electrochemical cell with two electrodes was proven to be well operated under commercial CV ( Figure S9 in Supplementary Information). The resulting current after scanning printed electrochemical cell in the CV tag can be converted to voltage by connecting the printed resistor (Figure 1b-: ,5 3 10 3 ohm) which provides the output voltage for electrochromic indicator and re-plotted into the cyclic voltammogram.
Because these output voltage (670 mV) and current (,40 mA) were low after scanning the electrochemical cell, they need to be amplified to turn on the electrochromic indicator for showing predetermined concentration (10 mM) level of N,N,N9,N9-tetramethylp-phenylenediamine (TMPD, purchased from Aldrich) as a standard reference in this work (Figure 3g). After running the redox reaction of TMPD (Figure 3h) in the printed cell, the output voltage and current needed to be amplified to reach 1.5 V and 500 mA, respectively, to provide sufficient power to display the letters ''PE'' as an indicator of the presence of TMPD in the specimen. To construct the amplifier, cnTFTs based three inverters were printed with a gain of three to five ( Figure S10 in Supplementary Information) to amplify the output signal as shown in Figure 3i. The electrical characteristics of the 6 cnTFTs in the inverters with extracted mobility, transcon- ductance, on-off current ratios and threshold voltage are shown in Table S2 (Supplementary Information). As the impedance was matched between the ring oscillator and the electrochemical cell using the buffer unit, another buffer unit (Figure 1b-) is also needed between the electrochromic signage (20 KV) and the amplifier (1 MV) for impedance matching. The electrical parameters of the buffer are listed in Table S2 (Supplementary Information).
The amplified output signal was used to run the reduction and oxidation of the patterned conducting polymer in the electrochromic signage, and thus the blinking signage will be used to indicate the presence of chemicals in the specimens. The signage was fully printed and attached on printed CV tag. A clear concept of the printing sequence for the electrochromic signage was given in Figure S11 in Supplementary Information.

Discussion
The fully printed flexible CV tag was completed by assembling the printed circuits including ring oscillator, buffer, electrochemical cell, amplifier, and signage onto the previously R2R gravure printed rectenna. The resultant CV tag is shown in Figure 4a. The working concept of the wireless and flexible CV tag is demonstrated in the following sequences (watch the video file by clicking Figure S12 in Supplementary Information). After dropping 500 ml of TMPD solu-tion (10 mM) on the printed electrochemical cell, the CV tag was placed on the custom made RF (13.56 MHz) reader ( Figure S13 in Supplementary Information). The antenna was subsequently coupled to 13.56 MHz AC. The coupled AC was rectified into polarized DC (. 6 10 V) through two diodes and two capacitors which caused the ring oscillator to generate a pseudo triangular waveform with output voltage of 7 V at 320 mHz. This was then passed through the buffer unit to scan the electrochemical cell. The output signal after scanning the electrochemical cell was amplified to turn on the signage according to the concentration level of TMPD in the solution. In this work, whenever the concentration of TMPD was higher than 10 mM, the signage ''PE'' blinked ( Figure 4b) while it did not show anything (Figure 4c) when it was lower than 10 mM. Furthermore, clear cyclic voltammograms for scanning the electrochemical cell with and without 10 mM of TMPD were obtained by re-plotting the output triangular voltage waveform (Figure 4d). The attained half potential (E 1/2 , 0.05 V, oxidation potential is 0.22 V and reduction potential is 20.17 V) of TMPD from the CV tag was nearly identical to the value obtained from a commercial CV instrument, SP-240, Biologic, which uses the same frequency for the triangular voltage waveform and printed electrochemical cell (Figure 4e). However, when the generated triangle wave frequency is higher than 0.6 Hz in the CV tag, the clear redox peaks cannot be observed as shown in Figure S14 (Supplementary Information). Furthermore, as a typical example of testing a specimen in aqueous solution, 10 mM of K 3 (FeCN) 6 aqueous solution was checked using the CV tag, and results of converted cyclic voltammogram was shown in Figure S15 (Supplementary Information). Those results support that the CV tag can examine specimens not only in organic solution, but also in aqueous one.
Up to present, there has been no commercial success in fully printed TFT-based electronic devices due to some kind of difficulties in integrating a number of printed TFTs through a scalable printing method. As increasing a number of integrated TFTs, the range of threshold voltage shits of TFTs needs to be controlled as narrow as possible to properly operate designed function of printed devices. However, the scalable printing method is not fully understood to integrate a number of TFTs on plastic foils while keeping the constant range of threshold voltage shifts because of difficulty in controlling a constant charge transport through the printed channels. Therefore, the printed TFT-based devices should be constructed by using a minimum number of printed TFTs while a function of printed device needs to be competitive over Si based one. Since the fully printed CV tag required the integration of only 26 cnTFTs, the acceptable range of threshold voltage shits of cnTFTs is controllable and achievable by using a scalable printing method such as a roll-toroll gravure. Furthermore, the unique function of printed CV tags cannot be simply reproduced using a Si technology with a comparable cost to the R2R printing process. Therefore, the fully printed CV tag will be the first leading model to show a way of how printed TFTbased electronic devices should go for the successful launching in the IT markets.
In the core of the printed CV tag, fully gravure-printed cnTFTs were employed for constructing a circuit consisting of a ring oscillator to generate triangular waveforms, buffer units for an impedance matching, and an amplifier for enhancing output signal to turn on the signage. Those simple units can be combined with a variety of printable sensors and RF devices to create novel devices with an extremely low cost. In other words, the printed rectenna, ring oscillator, buffer and amplifier units in the printed CV tag will be key elements for the construction of variety of printed RF-sensors, this CV tag will be used as a platform for the further construction of a variety of RF based electrochemical sensors.
In conclusion, we have presented a fully printed flexible CV tag with the size of 9.5 3 5.5 cm 2 that can operate wirelessly using a 13.56 MHz RF reader. However, for the practical purpose, the size of the CV tag can be reduced up to the half (4 3 2 cm 2 ) of the current one by optimizing spaces between cnTFTs in the circuit of the CV tag and reducing the operation power to less than DC 5 V as the current size of 13.56 MHz antenna is designed to provide maximum coupled AC power using a sufficient length of printed antenna pattern (higher inductance). Furthermore, although we utilized R2P gravure, screen printer and drop casting method for the convenience of fabricating the CV tag in the Lab, the whole fabricating process can be repeated by R2R gravure because the rectenna, ring oscillator, buffers, electrochemical cell, amplifier and signage in the CV tag were all designed to compromise the limit (620 mm) of a registration accuracy of a current R2R gravure system. Therefore, this technology could be used as a platform for disposable wireless electrochemical sensors to a variety of specimens in aqueous and organic solutions to monitor or diagnose pathogens and hazardous materials by modifying the electrodes of the electrochemical cells.

Methods
Roll-to-roll (R2R) gravure printed antenna, bottom electrodes, gate electrodes and wires. Two color units of R2R gravure system (Taejin Co. Korea: Figure S1 in the Supplementary Information)   thickness of 100 mm, purchased from SKC, Korea) with silver nanoparticle based conducting ink (PG-007 BB type, Paru Co. Korea) and the web transfer speed of 8 m/min under roll pressure of 0.5 MPa and web tension of 60 N. The silver ink was further formulated to meet the viscosity of 500 cp and surface tension of 47 mN/m using respectively ethylene glycol (Aldrich) and Dipropylene glycol methyl ether (Aldrich). The curing time of printed silver layer was 10 sec by passing through a heating chamber of 150uC, installed in R2R gravure system. The resulting printed silver patterns on PET roll showed the thickness of 450 (650) nm without any defects and were shown in Figure S16a (Supplementary Information).
Roll-to-plate (R2P) gravure printed ring oscillator, buffer, and amplifier. Full R2P gravure system ( Figure S1 in the Supplementary Information) was employed to print single walled carbon nanotube network based thin film transistors (cnTFTs), used as a building block to construct all the integrated circuit of printed cyclic voltammetry (CV) tag (Figure 1). 26 cnTFTs for the integration of circuit in printed CV tag were printed on the previously R2R gravure printed film (printed antenna, bottom electrodes and wires with thickness of 450 nm; Figure S16b in Supplementary Information) following printing sequences. First, BaTiO 3 nanoparticle based dielectric ink (PD-100, Paru Co., Korea) was further formulated to meet viscosity (75 cP) and surface tension (31.8 mN/m) using the ethyl 2-cynoacrylate (Aldrich). As shown in R2P gravure printing scheme ( Figure S17 in Supplementary  Information), the homogeneous and defect free dielectric layers were first R2P gravure printed with a printing speed of 200 mm/s and roll pressure 7.5 kg f on previously printed gate electrodes and bottom electrodes (for capacitors) with a thickness of 2.3 (60.1) mm and width of 940 (62) mm ( Figure S5 in Supplementary  Information). The printed dielectric layers were cured for 1 min 20 sec at 150uC. Second, single walled carbon nanotube (SWNT) based semiconducting ink (PR-040, Paru Co., Korea) was diluted by diethylene glycol monobutyl ether (Daejung Co., Korea) to 151 volume ratio for printing active layers using R2P gravure on the printed dielectric layers with a printing speed of 350 mm/s and a roll pressure of 4 kg f . The viscosity and surface tension of diluted SWNT ink were respectively 30 cP and 29 mN/m. The resulting SWNT printed films were dried 1 min at 150uC. For using cnTFTs in the buffer unit, we used the dilution volume ratio of 551 between SWNT ink (PR-040, Paru Co., Korea) and diethylene glycol monobutyl ether for printing only on the TFTs in the buffer unit to increase SWNT network density for providing the high current ( Figure S5 in Supplementary Information). Finally, drain-source electrodes were R2P gravure printed using silver nanoparticle based ink (PG-007 AA type, Paru Co., Korea) on SWNT printed film with a viscosity of 800 cP and a surface tension of 42 mN/m. The R2P gravure printing was carried out under a printing speed of 200 mm/s and a role pressure of 5 kg f . Diode fabrication. Although Shottky diodes were able to print using R2R gravure based on our previous reported process 16,17 , the drop casting method was used for the convenience in this work. First, dropping ZnO based hybrid semiconducting ink (PD-070, Paru Co., Korea) on printed silver electrode and then, Al ink (PA-009, Paru Co., Korea) was dropped on the top of ZnO ink. The resulting diodes were further cured for 5 min at 120uC.
Measurements. Formulated and diluted inks were characterized using DCAT21 (Dataphysics Co., Germany) and SV-10 Vibro viscometer (AND Co., Japan) for respectively measure surface tension and viscosity. All measurements in this work were carried out under ambient condition if there are no other comments. Resistance of printed antenna, bottom electrodes, gate electrodes and wires were measured using two probe methods with HP3457A multimeter. Both surface morphology and thickness of printed layers was characterized using surface profiler (NV-2200, Nanosystem, Korea). LCR meter (E4980A, Agilent, USA), semiconductor parameter analyzer (4155C, Agilent, USA) and digital phosphor oscilloscope (DPO 4054, Tektronix, USA) were respectively used to characterize printed cnTFT based circuits.