Low-grade heat is abundant, but its efficient recovery is still a great challenge. We report an asymmetric thermoelectrochemical cell using graphene oxide as a cathode and polyaniline as an anode with KCl as the electrolyte. This cell works under isothermal heating, exhibiting a high heat-to-electricity conversion efficiency in low-temperature regions.
Low-grade heat is abundantly available in the environment as waste heat. The efficient conversion of low-grade heat into electricity is very difficult. We developed an asymmetric thermoelectrochemical cell (aTEC) for heat-to-electricity conversion under isothermal operation in the charging and discharging processes without exploiting the thermal gradient or the thermal cycle. The aTEC is composed of a graphene oxide (GO) cathode, a polyaniline (PANI) anode, and 1M KCl as the electrolyte. The cell generates a voltage due to the pseudocapacitive reaction of GO when heating from room temperature (RT) to a high temperature (TH, ~40-90 °C), and then current is successively produced by oxidizing PANI when an external electrical load is connected. The aTEC demonstrates a remarkable temperature coefficient of 4.1 mV/K and a high heat-to-electricity conversion efficiency of 3.32%, working at a TH = 70 °C with a Carnot efficiency of 25.3%, unveiling a new promising thermoelectrochemical technology for low-grade heat recovery.
Ubiquitous low-grade heat energy (<100 °C) could be recycled and converted into electricity1,2 but is instead wasted. Unfortunately, heat recovery is still a great challenge, because converting low-grade heat to electricity is usually inefficient due to the low temperature differential and the distributed nature of the heat sources3. Intensive research has been conducted in solid-state thermoelectric (TE) materials and devices for the past decades, but the scalable application of TE devices in a low-grade heat regime is limited by the low energy conversion efficiency (ηE) of <2%4.
Alternative approaches based on the effect of temperature on electrochemical cells have been suggested as a solution to this problem, because the ionic Seebeck coefficient (α) of thermoelectrochemical cells (TECs) is much higher than that of TE semiconductors5,6. Thermogalvanic cells (TGC) utilize redox active electrolytes sandwiched between two identical electrodes to generate a voltage across the cell when a thermal gradient is applied. The commonly used aqueous Fe(CN)63-/Fe(CN)64- electrolyte in TGCs was reported to have an α of -1.4 mV/K and yield an ηE of <1%7,8,9,10,11. However, TGCs suffer the drawback of the poor ionic conductivity of the liquid electrolyte, which is around three orders of magnitude smaller than the electronic conductivity in TE materials. The electric conductivity could be improved, but this improvement is always accompanied by a higher thermal conductivity, which leads to a lower temperature gradient. Therefore, the ηE of TGCs is inherently limited due to the trade-off between the liquid electrolyte conductance and the temperature requirement for the desired redox reactions in each side of the electrode.
A thermally regenerative electrochemical cycle (TREC)12,13,14 based on a battery system using a solid copper hexacyanoferrate (CuHCF) cathode and a Cu/Cu+ anode was recently reported. TREC is configured as a pouch cell to improve the electrolyte conductance, showing an α of −1.2 mV/K and reaching a high ηE of 3.7% (21% of ηcarnot) when operated at 60 °C and 10 °C. Nevertheless, one limit of TREC is that external electricity is required at the start of the process to charge the electrodes in each thermal cycle, leading to complicated system designs14. A TREC without this limitation can be achieved, but it suffers from a poor conversion efficiency of <1%13. The TREC system demonstrates that a sodium-ion secondary battery (SIB)-type thermocell consisting of two types of Prussian blue analogues (PBA) with different α values can harvest waste heat. The thermal efficiency (η) increases proportionally with ΔT. Moreover, η reaches 1.08%, 3.19% at ΔT = 30 K, 56 K separately. The thermal cyclability is improved using Ni-substituted PBA15,16,17,18.
Alternatively, a thermally regenerative ammonia battery (TRAB) employs copper-based redox couples [Cu(NH3)42+/Cu and Cu(II)/Cu] that operate with the reverse temperature gradient by switching the temperature of electrolyte co-operated with positive and negative electrodes, which produces a ηE of 0.53% (13% of ηcarnot). However, this system is configured with two tanks full of liquid electrolyte, causing sluggish heating and cooling. Also, the ammonia stream in the system creates concerns regarding safety, leakage, and stability19,20,21.
Here we present an asymmetric thermoelectrochemical cell (aTEC) for heat-to-electricity conversion that can be thermally charged and electrically discharged by continuous isothermal heating without maintaining a temperature gradient in a geometric configuration or switching temperatures in a thermal cycle. The aTEC uses asymmetric electrodes, including a graphene oxide (GO) cathode and a polyaniline (PANI) anode, and KCl as the electrolyte. It is thermally charged via the thermo-pseudocapacitive effect of GO and then discharged with the oxidation reaction of PANI. Notably, the aTEC exhibits a high α of 4.1 mV/K and attains a ηE of 3.32%, the highest ever achieved at 70 °C (25.3% of ηCarnot).
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1. Preparation of the graphene oxide electrode
- Synthesis of graphene oxide via the modified Hummer's method
- Steps 1.1.2 and 1.1.3 occur at a low temperature (<0 °C). Circulate ice water flowing through the external layer of a double wall glass beaker placed on a magnetic stirrer to create low temperature conditions for the reactants inside.
- Mix 1 g of sodium nitrate (NaNO3) with 100 mL of sulfuric acid (H2SO4, reagent grade, 95-98%) using slow stirring in the beaker.
- Add 1 g of flake graphite into the sulfuric acid and stir for 1 h in the cold bath. Add 6 g of potassium permanganate (KMnO4) gradually to the solution and stir the mixture for another 2 h.
- The next step of the reaction takes place at a middle temperature (~35 °C). Change the ice water to 35 °C water and continue the oxidation of the graphite by stirring for ½ h.
- The last step of the reaction takes place at a TH (80-90 °C). Add 46 mL of deionized (DI) water (70 °C) into the reaction tank drop by drop. Note that that the reaction is strong. Add 140 mL of DI water and 20 mL of hydrogen peroxide (30% H2O2) in the reaction tank as the last step of the reaction. Make sure that golden particles of GO appear as a result.
- Wash the product thoroughly with dilute hydrochloric acid (HCl) and DI water several times until the GO suspension reaches pH = 7.
- Freeze the washed GO suspension overnight and dry it in a freeze dryer until water evaporates completely.
- Preparation of the graphene oxide electrode
- Mix the graphene oxide, carbon black, and PVDF in a mass ratio of 75:15:10 and put them in a glass bottle. Drip the solvent N-methyl-2-pyrrolidone (NMP) into the solid mixture and ensure the weight ratio of solvent and solid mixture is 4:1.
- Prepare the paste by mixing at 2,000 rpm for 13 min and defoaming in 1,200 rpm for 2 min with a mixer.
- Brush coat the paste on carbon paper until the coat is ~8-15 mg/cm2 and dry it for 4 h at 40 °C.
2. Preparation of the polyaniline (PANI) electrode
- Prepare 1 wt% carboxymethyl cellulose (CMC) aqueous solution by dissolving CMC powder in DI water by stirring for 10 h.
- Mix 50 mg of leucoemeraldine-base PANI and 10 mg of carbon black in a beaker. Add 150 μL of 1 wt% CMC solution into the beaker and mix with a magnetic stirrer for 12 h.
- Add 6 μL of 40% styrene-butadiene (SBR) solution into the mixture and stir for another 15 min.
- Place a piece of carbon paper on the doctor blade coater and drop the mixed PANI slurry at the leading edge of the carbon paper.
- Blade coat the slurry to produce a film 400 μm thick on the carbon paper. Dry the coating for 4 h at 50 °C.
3. Assembling the pouch cell
- Cut titanium foil into the approproate size and then connect each piece to a nickel tab with a 20 kHz ultrasonic spot welding machine.
- Place the porous hydrophilic polypropylene-based separator between the GO electrode and the PANI electrode to avoid short circuits. Each electrode is paired with one current collector.
- Package the electrodes using aluminum laminated film. Seal the sides of the aluminum laminated film with a compact vacuum sealer for 4 s. Set the temperature of the top and bottom sealing parts as 180 °C and 160 °C separately.
- Inject 500 μL of the 1 M KCl electrolyte into the pouch cell and allow to equilibrate for 10 min.
- Extrude the excess electrolyte and seal the last side of the pouch cell in a -80 kPa vacuum chamber.
4. Setting up the temperature controlling system
- Stack the pouch cell between two thermoelectric modules. Place thermocouples on the top and bottom sides of the cell. Apply thermal paste to all the interfaces to ensure good thermal contact.
NOTE: The temperature is controlled with LabVIEW code. Temperatures measured from the thermocouples are compared with the setting temperatures and the output voltage is determined by the difference between the real time temperature and setting temperature via a PID control. The voltage signals are transmitted to the power supply and are connected to the thermoelectric module. The closed-loop control guarantees a temperature measurement accuracy within ± 0.5 °C.
5. Electrochemical characterization
- Perform the electrochemical tests of the cell using a potentiostat. Conduct the thermal charging in open circuit mode while carrying out the electrical discharging process at a constant current.
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The aTEC pouch cell was configured with asymmetric electrodes consisting of a GO cathode, a PANI anode, and filled with the KCl electrolyte. The thickness of the pouch cell shown in Figure 1A is 1 mm, which facilitates isothermal conditions between the two electrodes as well as efficient heat conduction. The scanning electron microscopy (SEM) images of the GO cathode and the PANI anode coated on carbon paper are shown in Figure 1B and Figure 1C. The porous structure increases the contact area between the active electrode materials and the electrolyte, thus optimizing the discharging current and the output power.
With the different work functions of the asymmetric electrodes, a built-in voltage (ΔV0) was observed on the cell in open circuit conditions at RT (Figure 2A1). When aTEC was heated from RT to TH, heat triggered the pseudocapacitive reactions between functional groups containing oxygen (e.g., C=O bonds) and protons in the electrolyte at the GO-aqueous interface, thus the cell voltage (Voc) increased as electrons moved to the surface of the GO (Figure 2A2). When an external load was connected, the aTEC was discharged under the potential differential between electrodes at TH, where the discharge capacity was mainly due to the oxidation of the PANI anode and the reduction of functional groups (Figure 2A3), which can be presented as
The voltages of aTEC during thermal charging and electrical discharging at TH = 70 °C are shown in Figure 2B. The open circuit potential reached 0.185 V when the cell was heated from RT to TH = 70 °C, where aTEC exhibited a high temperature coefficient (α = ∂V/∂T, where V is the electrode voltage and T is the temperature) of 4.1 mV/K. The discharging of aTEC was conducted under a constant current of 0.1 mA. The specific gravimetric capacity of the GO was 10.43 mAh/g while that of the PANI was 103.4 mAh/g. The heat-to-electricity conversion efficiency of aTEC can be calculated as the output electrical work (W) divided by input thermal energy, which can be expressed as
The output electrical work was calculated from the integration of discharging voltage over charge capacity while the input thermal energy consisted of the QH for heating the cell up from RT to TH and Qiso for heat absorbed during discharging at TH. In the equation, q is the discharge capacity, ηHX is the efficiency of heat recovery, m is the mass of the active materials of electrodes and electrolyte, Cp is the specific heat, ΔT is the temperature difference between the operating temperature and RT, and ΔS is the reaction entropy change. Based on the discharging shown in Figure 2B, our aTEC attained a ηE of 3.32% at 70 °C, which is equivalent to 25.3% of ηCarnot (13.1%).
The isothermal operating of aTEC allows its use in many various scenarios. The aTEC can be charged by a hot pot with boiling water (Figure 3). The voltage of six aTECs connected in a series can reach >1 V. Our aTEC illustrated an excellent heat-to-electricity performance with a high temperature coefficient and energy conversion efficiency. The cell device performance and operating temperature window could be further improved by changing the composition of the electrolyte and using electrode materials with high α, low heat capacity, and robust functionalities. Our work sheds light on the design of thermoelectrochemical systems. With further research and development, aTEC has the potential to become a key technology for low-grade heat recovery.
Figure 1: aTEC pouch cell. (A) Pouch cell configuration. The GO cathode and the PANI anode are assembled with the titanium (Ti) foil current collector and separated by the hydrophilic polypropylene separator. SEM images of (B) the GO cathode and (C) the PANI anode both coated on carbon paper. Please click here to view a larger version of this figure.
Figure 2: aTEC charging and discharging. (A) Working principle of aTEC. (B) Open circuit voltage of the thermal charging process (red line) and electrical discharging curve (blue line) of the aTEC. Please click here to view a larger version of this figure.
Figure 3: Demonstration of aTEC charged by a hot pot. Please click here to view a larger version of this figure.
|Operating mode||TEC system||Structure and Materials||a||ηE||Ref|
(continuous operation based on the temperature-dependent redox potentials at the hot and cold sides)
|TGC||Electrode: Multi-walled carbon nanotubes (MWCNT) based electrode||1.4||0.24%||9|
|Electrode: Carbon-based material||1.85||0.11%||6|
|Electrolyte: K3[Fe(CN)6]/(NH4)4[Fe(CN)6] or Fe2(SO4)3/FeSO4||-0.40%|
|Electrode: CNT aerogel sheets||1.43||0.55%||8|
|Temperature gradient||RFB||Electrode: carbon cloth||3||1.80%||10|
|Flow electrolyte: [Fe(CN)6]3-/[Fe(CN)6]4- and V3+/V2+||-15%|
|Temperature cycle||TREC||Electrode: CuHCF and Cu||1.2||3.70%||14|
|Electrolyte: NaNO3 and Cu(NO3)2||-25%|
|Electrode: NiHCF and Ag/AgCl||0.74||1.60%||12|
|Electrode: KFeIIFeIII(CN)6 and K3Fe(CN)6/K4Fe(CN)6 with carbon cloth||1.45||0.72%||13|
|Flow electrolyte: Cu(NO3)2/NH4NO3||-5.00%|
|Temperature cycle||aTEC||Electrode: GO and PANI||4.1||3.32% (25.3%)||This work|
Table 1: Comparison of different TEC technologies for low-grade heat-to-electricity conversion.
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The aTEC converts thermal energy into electricity via a thermal charging process when heating from RT to TH and a successive electrical discharging process at TH. Getting rid of the dependence on a temperature gradient or a temperature cycle like the TGC and TREC, aTEC allows isothermal heating operation during the entire charging and discharging processes. Thermal induced voltage is based on the pseudocapacitive effect of GO because heating facilitates the chemisorption of protons on the oxygen functional groups of GO, causing the pseudocapacitive reaction at the GO-aqueous interface. PANI contributes little to the increased voltage but provides electrons in the discharging process. The utilization of the KCl electrolyte keeps the charge of the electrode-electrolyte interface balanced during the reaction and improves the conductivity of the whole cell. The system is nontoxic and environmentally friendly, which makes it ideal for commercial applications. Other alternatives for the electrolyte can be chloride salt, such as NaCl, because chloride ions play an essential role in the oxidation reaction of PANI in the discharging process.
Unlike technologies based on thermal gradients or thermal cycles, aTEC is unique and has potential for practical applications due to its low cost, flexibility, light weight, its isothermal and continuous thermal charge/electrical discharge process, and the ability to form stacks of cells. The aTEC achieves a high α of 4.1 mV/K and a high ηE of 3.32% (equivalent to 25.3% of ηcarnot) at 70 °C, which is superior to existing techniques for low-grade heat harvesting. A comparison of aTEC and other TEC techniques is shown in Table 1.
The cyclability performance of aTEC is still unsatisfactory. This may be improved by adding a redox couple into the electrolyte or changing the electrode materials. Prussian blue analogs (PBA) are likely to make a better anode electrode for aTEC, because the negative temperature coefficient of some PBAs can help enhance the efficiency of aTEC. An aTEC with improved cyclability has great potential for commercial use, such as recovering waste heat from an air conditioner.
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The authors declare no competing financial interests.
The authors acknowledge constructive discussion with Prof. D.Y.C. Leung and Dr. Y. Chen (The University of Hong Kong), Prof. M.H.K. Leung (City University of Hong Kong), Dr. W. S. Liu (Southern University of Science and Technology), and Mr. Frank H.T. Leung (Techskill [Asia] Limited). The authors acknowledge the financial support of General Research Fund of the Research Grants Council of Hong Kong Special Administrative Region, China, under Award Number 17204516 and 17206518, and Innovation and Technology Fund (Ref: ITS/171/16FX).
|Alumina laminated film||Showa Denko||SPALF C4|
|Carbon black||Alfa Aesar||H30253.22|
|Carbon paper||CeTech Co. Ltd||W0S1009|
|Carboxymethyl cellulose (CMC)||Guidechem company|
|DC Power supply||B&K Precision||Model 913-B|
|Doctor blade coater||Shining Energy Co. Ltd|
|Gamry||Gamry Instruments||Reference 3000|
|Nickel tab||Tianjin Iversonchem company||4 mm width|
|Polyaniline (leucoemeraldine base)||Sigma-Aldrich||530670-5G|
|potassium permanganate (KMnO4)||Sigma-Aldrich||223468-500G|
|Separator||CLDP||25 um thickness|
|Sodium nitrate (NaNO3)||Sigma-Aldrich||S5506-250G|
|Styrene butadiene||Tianjin Iversonchem company||BM400|
|Thermoelectric modules||CUI Inc.||CP455535H|
|Titanum foil||Qingyuan metal||0.03 mm thickness|
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