Fuel CellsEssay title: Fuel CellsFuel CellsPetroleum, the worlds most prolific fuel, is becoming more scarce and its burning produces emissions which shoulder much of the responsibility for air pollution (Fig. 1). Contributions also come from deforestation, carbon dioxide from the burning of coal, and methane release. In order to reverse the trend of destroying the environment, a change to a more ecologically mundane resource, or method of producing energy such as hydrodynamic, wind, geothermal, solar and tidal is desirable. These methods are presently employed in a somewhat small scale, but require specific environments in order to work effectively. Fuel cells need no particular environment to work well (other than a heat sink) and is highly efficient both electrically and physically (without sound and with far fewer harmful air pollutants).
A fuel cell is an electrochemical device which brings together hydrogen and oxygen, or air in the midst of a catalyst to produce electricity, heat and water. (Fig. 2) or (Fig. 2a) The single cell fixture consists a single electrolyte sandwiched between electrodes. This inner sandwich is then placed in-between current collectors which usually serve as the poles of the cell. A fuel cell generates current by transforming (usually by using the catalyst in the electrodes) hydrogen gas into a mixture of hydrogen ions and electrons on the anode side of the cell. Because of the insulating nature of the electrolyte, the anions transfer through the electrolyte to the cathode side of the cell while the electrons are conducted to the current collectors and through a load to do work. The electrons then travel to the cathode side current collector where they disperse onto the electrodes to combine with incoming hydrogen anions, oxygen, or air in the presence of a catalyst to form water completing the circuit.
This process occurs in all types of fuel cells (alkaline, solid polymer, phosphoric acid and solid oxide) except for molten carbonate. The molten carbonate cell transfers the carbonate ions formed by the reaction of oxygen and carbon monoxide in the presence of electrons from the cathode side to the anode side to react with hydrogen and form water and two electrons for current. Thus the net flow of ions in the electrolyte is opposite of that in all other fuel cells, but since the current flows in the same direction as the other fuel cell types, the anode and cathode keep their polarity.
The fuel cell was first invented in 1839 by Sir William Grove, a professor of experimental philosophy at the Royal Institution in London. He tested what turned out to be the precursor to the phosphoric acid fuel cell by enclosing platinum in tubes of hydrogen and oxygen gas while submerging the tubes in sulfuric acid. (Fig. 3) Unfortunately, he was hampered by the inconsistency of cell performance (a common feature of cells today), but realized the importance of the three phase contact (gas, electrolyte and platinum) to energy generation. He spent most of his time searching for an electrolyte that would produce a more constant current. He found several electrolytes which produced current, but still struggled with consistent results. He also noted the potential of the energy production method commercially if hydrogen could replace coal and wood as energy sources (1).
Since that time, researchers world wide have attempted to increase cell performance electrically, chemically as well as physically. Their experiments ranged from an improved three phase contact to smart materials and the adoption of off gases from other power sources. After over 150 years of research, fuel cells can be divided into five major categories named after the electrolyte used in each; alkaline, solid polymer, phosphoric acid, molten carbonate and solid oxide. The five types resulted from the knowledge that heat accelerates chemical reaction rates and thus the electrical current. The materials used for electrolytes have their best conductance only within certain temperature ranges and thus other materials must be used in order to take advantage of the temperature increase (2).
Solid oxide fuel cells (SOFC) which operate at the highest temperature (1000 – 1100 degrees Celsius) are not the most reactive because of the low conductivity of its ionic conducting electrolyte (yttria-stabilized zirconia). (Fig. 4) Many advances have been made in solid oxide fuel cell (SOFC) research to increase the chemical to electrical efficiency to 50%, but because of the conductivity and the heat, it has been used mainly in large power plants which can use the cogeneration of steam for additional power. Because of the high temperature, the cell requires no expensive catalysts, or additional humidification and fuel treatment equipment which excludes the cost of these items.
The SOFC is extremely sensitive to various temperatures. A high pressure is needed to make the cell perform optimally in all conditions.
When you use liquid fuel cells, a low pressure is needed before they are truly capable of producing hydrogen. You could use solvents like naphthalene or fluoronium to obtain pure carbon dioxide. An alternative for building an ultra strong solid electrolyte (solid olivine) in your home would be a solid silicon dioxide (SI) solid (solid oxide) olivine hybrid. Another way to get this high temperature or higher temperature solid olivine oxide solvents is the use of a liquid oxygen and water (LOH) fuel cell.
With all the advances in solid oxide fuel cell technology, it seems that not all of them are to be able to control all of the temperatures at the moment. One such approach is for a very small temperature change in the electrolyte to have a very high current (a few thousandV) across the battery. The electrolyte will need a low input current as the battery must be cooled quickly, so the thermal efficiency of the electrolyte increase from about 1/4 to 8% or so.
One of the advantages of a solid hydrogen fuel cell electrolyte is the ability to operate low costly due to its low temperature and high reactivity (less friction for the electrolyte), and low power consumption (about 1.6 kWh/year), when operating at very low temperatures, especially in power stations, even when all of the electrolytes are not running at very low temperatures.