Alkaline anion exchange membrane fuel cell

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An alkaline anion exchange membrane fuel cell (AAEMFC), also known as anion-exchange membrane fuel cells (AEMFCs), alkaline membrane fuel cells (AMFCs), hydroxide exchange membrane fuel cells (HEMFCs), or solid alkaline fuel cells (SAFCs) is a type of alkaline fuel cell that uses an anion exchange membrane to separate the anode and cathode compartments.

Contents

Alkaline fuel cells (AFCs) are based on the transport of alkaline anions, usually hydroxide OH−
, between the electrodes. Original AFCs used aqueous potassium hydroxide (KOH) as an electrolyte. The AAEMFCs use instead a polymer membrane that transports hydroxide anions.

Alkaline Anion Exchange Membrane Fuel Cell AAEMFC.png
Alkaline Anion Exchange Membrane Fuel Cell

Mechanism

In an AAEMFC, the fuel, hydrogen or methanol, is supplied at the anode and oxygen through air, and water are supplied at cathode. Fuel is oxidized at anode and oxygen is reduced at cathode. At cathode, oxygen reduction produces hydroxides ions (OH−) that migrate through the electrolyte towards the anode. At anode, hydroxide ions react with the fuel to produce water and electrons. Electrons go through the circuit producing current. [1]

Electrochemical reactions when hydrogen is the fuel

At Anode: H2 + 2OH− → 2H2O + 2e−

At cathode: O2 + 2H2O + 4e− → 4OH−

Electrochemical reactions when methanol is the fuel

At anode: CH3OH + 6OH− → CO2 + 5H2O + 6e-

At cathode: 3/2O2 + 3H2O + 6e− → 6OH−

Mechanical Properties

Measuring mechanical properties

The mechanical properties of anion exchange membranes are relevant for use in electrochemical energy technologies such as polymer electrolyte membranes in fuel cells. Mechanical properties of polymers include the elastic modulus, tensile strength, and ductility. Traditional tensile stress-strain test used to measure these properties are very sensitive to the experimental procedure because the mechanical properties of polymers are heavily dependent on the nature of the environment such as the presence of water, organic solvents, oxygen, and temperature. [2] [3] Increasing the temperature generally results in a decrease of elastic modulus, a reduction of tensile strength, and an increase of ductility, assuming there is no modification of the microstructure. Near the glass transition temperature, very significant changes in mechanical properties is observed. Dynamic Mechanical Analysis (DMA) is a widely used complimentary, characterization technique for measuring the mechanical properties of polymers including the storage modulus and loss modulus as functions of temperature.

Methods of Increasing Mechanical Properties

One method of increasing the mechanical properties of polymers used for anion exchange membranes (AEM) is substituting conventional ternary amine and anion exchange groups with grafted quaternary groups. [4] These ionomers results in large storage and Young's moduli, a high tensile strength, and high ductility. Exchanging the counterion from hydroxide to hydrogen carbonate, carbonate, and chloride ions further enhances the strength and elastic modulus of the membranes. Narducci and colleagues concluded that the water uptake, related to the type of anion, plays a very important role for the mechanical properties. [4] Zhang and colleagues prepared a series of robust and crosslinked poly(2,6-dimethyl-1,4-phenylene oxide)s (PPO) AEMs with chemically stable imidazolium cations through quaternization of C1, C3, C4-substituted imidazole and crosslinking them via "thiol-ene" chemistry. [5] These crosslinked AEMs showed excellent film forming properties and exhibited a higher tensile strength owing to the increased entanglement interactions in the polymer chains which in turn increased the water up take. This strong relation between water uptake and mechanical properties mirrors the findings of Narducci and colleagues. [5] The findings of Zhang et al. suggest that the crosslinking of anion conductive materials with stable sterically-protected organic cations is an effective strategy to produce robust AEMs for use in alkaline fuel cells.

Comparison with traditional alkaline fuel cell

The alkaline fuel cell used by NASA in 1960s for Apollo and Space Shuttle program generated electricity at nearly 70% efficiency using aqueous solution of KOH as an electrolyte. In that situation, CO2 coming in through oxidant air stream and generated as by product from oxidation of methanol, if methanol is the fuel, reacts with electrolyte KOH forming CO32−/HCO3−. Unfortunately as a consequence, K2CO3 or KHCO3− precipitate on the electrodes. However, this effect has found to be mitigated by the removal of cationic counterions from the electrode, and carbonate formation has been found to be entirely reversible by several industrial and academic groups, most notably Varcoe. Low-cost CO2 systems have been developed using air as the oxidant source. [6] In alkaline anion exchange membrane fuel cell, aqueous KOH is replaced with a solid polymer electrolyte membrane, that can conduct hydroxide ions. This could overcome the problems of electrolyte leakage and carbonate precipitation, though still taking advantage of benefits of operating a fuel cell in an alkaline environment. In AAEMFCs, CO2 reacts with water forming H2CO3, which further dissociate to HCO3− and CO32−. The equilibrium concentration of CO32−/HCO3− is less than 0.07% and there is no precipitation on the electrodes in the absence of cations (K+, Na+). [7] [8] The absence of cations is, however, difficult to achieve, as most membranes are conditioned to functional hydroxide or bicarbonate forms out of their initial, chemically stable halogen form, and may significantly impact fuel cell performance by both competitively adsorbing to active sites and exerting Helmholtz-layer effects. [9]

In comparison, against alkaline fuel cell, alkali anion exchange membrane fuel cells also protect the electrode from solid carbonate precipitation, which can cause fuel (oxygen/hydrogen) transport problem during start-up. [10]

The large majority of membranes/ionomer that have been developed are fully hydrocarbon, allowing for much easier catalyst recycling and lower fuel crossover. Methanol has an advantage of easier storage and transportation and has higher volumetric energy density compared to hydrogen. Also, methanol crossover from anode to cathode is reduced in AAEMFCs compared to PEMFCs, due to the opposite direction of ion transport in the membrane, from cathode to anode. In addition, use of higher alcohols such as ethanol and propanol is possible in AAEMFCs, since anode potential in AAEMFCs is sufficient to oxidize C-C bonds present in alcohols. [11] [8]

Challenges

The biggest challenge in developing AAEMFCs is the anion exchange membrane (AEM). A typical AEM is composed of a polymer backbone with tethered cationic ion-exchange groups to facilitate the movement of free OH− ions. This is the inverse of Nafion used for PEMFCs, where an anion is covalently attached to the polymer and protons hop from one site to another. The challenge is to fabricate AEM with high OH− ion conductivity and mechanical stability without chemical deterioration at elevated pH and temperatures. The main mechanisms of degradation are Hofmann elimination when β-hydrogens are present and direct nucleophilic attack by OH− ion at the cationic site. One approach towards improving the chemical stability towards Hofmann elimination is to remove all β-hydrogens at the cationic site. All these degradation reactions limit the polymer backbone chemistries and the cations that can be incorporated for developing AEM.

Another challenge is achieving OH− ion conductivity comparable to H+ conductivity observed in PEMFCs. Since the diffusion coefficient of OH− ions is half that of H+ (in bulk water), a higher concentration of OH− ions is needed to achieve similar results, which in turn needs higher ion exchange capacity of the polymer. [12] However, high ion exchange capacity leads to excessive swelling of polymer on hydration and concomitant loss of mechanical properties.

Management of water in AEMFCs has also been shown to be a challenge. Recent research has shown [13] that careful balancing of the humidity of the feed gases significantly improves fuel cell performance.

See also

Related Research Articles

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Electrolysis Technique in chemistry and manufacturing

In chemistry and manufacturing, electrolysis is a technique that uses direct electric current (DC) to drive an otherwise non-spontaneous chemical reaction. Electrolysis is commercially important as a stage in the separation of elements from naturally occurring sources such as ores using an electrolytic cell. The voltage that is needed for electrolysis to occur is called the decomposition potential. The word "lysis" means to separate or break, so in terms, electrolysis would mean either "breakdown of electricity" or "breakdown via electricity".

An electrolyte is a substance that produces an electrically conducting solution when dissolved in a polar solvent, such as water. The dissolved electrolyte separates into cations and anions, which disperse uniformly through the solvent. Electrically, such a solution is neutral. If an electric potential is applied to such a solution, the cations of the solution are drawn to the electrode that has an abundance of electrons, while the anions are drawn to the electrode that has a deficit of electrons. The movement of anions and cations in opposite directions within the solution amounts to a current. This includes most soluble salts, acids, and bases. Some gases, such as hydrogen chloride (HCl), under conditions of high temperature or low pressure can also function as electrolytes. Electrolyte solutions can also result from the dissolution of some biological and synthetic polymers, termed "polyelectrolytes", which contain charged functional groups. A substance that dissociates into ions in solution acquires the capacity to conduct electricity. Sodium, potassium, chloride, calcium, magnesium, and phosphate are examples of electrolytes.

Electrolytic cell Cell that uses electrical energy to drive a non-spontaneous redox reaction

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Proton-exchange membrane fuel cell

Proton-exchange membrane fuel cells (PEMFC), also known as polymer electrolyte membrane (PEM) fuel cells, are a type of fuel cell being developed mainly for transport applications, as well as for stationary fuel-cell applications and portable fuel-cell applications. Their distinguishing features include lower temperature/pressure ranges and a special proton-conducting polymer electrolyte membrane. PEMFCs generate electricity and operate on the opposite principle to PEM electrolysis, which consumes electricity. They are a leading candidate to replace the aging alkaline fuel-cell technology, which was used in the Space Shuttle.

Alkaline fuel cell

The alkaline fuel cell (AFC), also known as the Bacon fuel cell after its British inventor, Francis Thomas Bacon, is one of the most developed fuel cell technologies. Alkaline fuel cells consume hydrogen and pure oxygen, to produce potable water, heat, and electricity. They are among the most efficient fuel cells, having the potential to reach 70%.

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References

  1. ↑ Winter, M; Brodd, R. J. (2004). "What are batteries, fuel cells, and supercapacitors?". Chemical Reviews. 104 (10): 4245–4269. doi: 10.1021/cr020730k . PMID   15669155.
  2. ↑ Knauth, Philippe; Di Vona, Maria Luisa, eds. (2012-01-27). "Solid State Proton Conductors". doi:10.1002/9781119962502.Cite journal requires |journal= (help)
  3. ↑ Majsztrik, Paul W.; Bocarsly, Andrew B.; Benziger, Jay B. (2008-11-18). "Viscoelastic Response of Nafion. Effects of Temperature and Hydration on Tensile Creep". Macromolecules. 41 (24): 9849–9862. doi:10.1021/ma801811m. ISSN   0024-9297.
  4. 1 2 Narducci, Riccardo; Chailan, J.-F.; Fahs, A.; Pasquini, Luca; Vona, Maria Luisa Di; Knauth, Philippe (2016). "Mechanical properties of anion exchange membranes by combination of tensile stress–strain tests and dynamic mechanical analysis". Journal of Polymer Science Part B: Polymer Physics. 54 (12): 1180–1187. doi:10.1002/polb.24025. ISSN   1099-0488.
  5. 1 2 "Enhancement of the mechanical properties of anion exchange membranes with bulky imidazolium by "thiol-ene" crosslinking". Journal of Membrane Science. 596: 117700. 2020-02-15. doi:10.1016/j.memsci.2019.117700. ISSN   0376-7388.
  6. ↑ "US8628889 B2 - Operating method of anion-exchange membrane-type fuel cell".
  7. ↑ Adams, L. A.; Varcoe, J. R. (2008). ChemSusChem(PDF). 1 (1–2): 79–81. doi:10.1002/cssc.200700013. PMID   18605667 http://epubs.surrey.ac.uk/1686/1/fulltext.pdf |url= missing title (help).CS1 maint: untitled periodical (link)
  8. 1 2 Shen, P. K.; Xu, C. (2005). Adv. Fuel Cells: 149–179.CS1 maint: untitled periodical (link)
  9. ↑ Mills, J. N.; McCrum, I. T.; Janik, M. J. (2014). Phys. Chem. Chem. Phys. 16 (27): 13699–13707. Bibcode:2014PCCP...1613699M. doi:10.1039/c4cp00760c. PMID   24722828.CS1 maint: untitled periodical (link)
  10. ↑ Anion Exchange Membrane and Ionomer for Alkaline Membrane Fuel Cells Archived December 7, 2008, at the Wayback Machine
  11. ↑ Varcoe, J. R.; Slade, R. C. T. (2005). "Prospects for Alkaline Anion-Exchange Membranes in Low Temperature Fuel Cells" (PDF). Fuel Cells. 5 (2): 187–200. doi:10.1002/fuce.200400045.
  12. ↑ Agel, E; Bouet, J.; Fauvarque, J.F (2001). "Characterization and use of anionic membranes for alkaline fuel cells". Journal of Power Sources. 101 (2): 267–274. Bibcode:2001JPS...101..267A. doi:10.1016/s0378-7753(01)00759-5.
  13. ↑ Omasta, T.J.; Wang, L.; Peng, X.; Lewis, C.A.; Varcoe, J.R.; Mustain, W.E. (2017). "Importance of balancing membrane and electrode water in anion exchange membrane fuel cells" (PDF). Journal of Power Sources. 375: 205–213. doi:10.1016/j.jpowsour.2017.05.006.
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