Batteries
Further study: original battery types and explicitly specified circuit enrichment; a battery label alone does not determine current.
Before this connection: Cell processes, potential and current; A complete voltage, resistance and load model for circuit examples.
Supporting original reading. Follow the AP topic pathway for reviewed scope, worked reasoning and targeted practice.
Chemistry II · original Chapter 9 · combined Chapter 17
Section Breakdown
- Voltaic Pile
- Daniel Cell
- Battery Classification
- Modern Batteries
- Simple Circuits
- Slightly more complex circuits
Section 1
Batteries
We spoke a little about batteries before, but we didn’t get much further past the fact they were galvanic cells.
Of course, the original battery was a galvanic cell, but a single galvanic cell alone can be fairly limited in its current output, and it is at a set voltage. If you want in boost the battery’s power and voltage, then you need to start combining galvanic cells.
The original chain of galvanic cells actually preceded most single galvanic cells. It was known as the voltaic pile, and it was the first complex battery that generated useful electricity (though back then, it was mostly used for experiments with electricity.)
The voltaic pile was a series of zinc-copper cells stacked atop one another in a large pile, separated by a brine-soaked cloth, which acted as the electrolyte for the cell.
The output of this battery was fairly low voltage, and the lifetime was fairly short, due to corrosion of the zinc and short-circuiting across the electrolyte.
The Daniel cell was a good source of current, but it was still a fairly large device, especially when multiple were chained together to achieve a higher output.
The early Daniel cell and its first few derivatives were all in the similar vein of an electricity source which required a liquid electrolyte and would only work as long as the anode remained. Once the anode fully corroded, the battery would no longer function.
These types of batteries were known as both “Primary Cells” and “Wet Cells”. A primary cell is simply a galvanic cell that cannot be recharged. It’s opposite, the “Secondary Cell” is a rechargeable cell. After the reaction fully progresses, an outside source of electricity can provide a current in the opposite direction and reverse the reaction.
A common primary alkaline cell uses a zinc anode, manganese dioxide MnO₂ cathode material and a potassium-hydroxide electrolyte. The retained MgO₂ label is a source error. Rechargeable nickel–metal hydride cells use nickel oxyhydroxide/metal-hydride chemistry; they are one rechargeable technology, rather than a timeless description of the most typical rechargeable battery.
The other two prevalent, but less obvious batteries are car batteries, and laptop/electronics batteries. The car battery is a Lead-Acid battery, and has a electrode coupled with a electrode, interspersed with sulfuric acid as the electrolyte. This type of battery has changed little since its inception, except to improve the safety. It is a wet cell battery, but has a gel encasing the cells, keeping the electrolyte contained.
Typical lithium-ion cells use a nonaqueous electrolyte, often an organic liquid containing a lithium salt. “Nonaqueous” does not mean the electrolyte must be solid or dry. Different cell designs can use gels or solid electrolytes.
Okay, that’s been two and a half pages on history. What do I care?
Well, first off, the structure of batteries is a subject commonly referred to in electrochemistry, and as there are many varieties of cell types, that overview should have shown you most of them.
Also, by knowing what makes a battery operate, you can appreciate how important it is to handle batteries (especially car batteries) carefully. That acid is not the most skin-friendly substance.
As for the quantitative side of things, batteries are typically a source of electricity, and they are manufactured such to have a reliable output. This allows us to examine the effects of mixing together batteries in various ways to see the effects on the electrical output.
Depending on the type of battery, modern batteries can either be single cell or multi-cell batteries.
Remember that the cathode is marked with a () in galvanic cells. This holds true in batteries as well, and it is still the side of the battery where reduction occurs. The anode is the oxidized electrode, marked with a () on batteries and galvanic cells.
Anode (): Oxidized electrode
Cathode (): Reduced electrode
In a series setup, the batteries are connected in a line. In a parallel setup, batteries have each anode wired together and each cathode wired together.
Example Problem 9.1.1
Series voltages add in the stipulated polarity: V=4×1.50=6.00 V.
The load determines current: I=V/R=6.00/24.0=0.250 A. The same current passes through all four series cells.
This ideal enrichment model explicitly specifies the load and internal resistance. A battery’s marked current alone cannot determine circuit current.
Series voltages add in the stipulated polarity: V=4×1.50=6.00 V.
The load determines current: I=V/R=6.00/24.0=0.250 A. The same current passes through all four series cells.
This ideal enrichment model explicitly specifies the load and internal resistance. A battery’s marked current alone cannot determine circuit current.
Series voltages add in the stipulated polarity: V=4×1.50=6.00 V.
The load determines current: I=V/R=6.00/24.0=0.250 A. The same current passes through all four series cells.
This ideal enrichment model explicitly specifies the load and internal resistance. A battery’s marked current alone cannot determine circuit current.
Series cells carry the same circuit current, determined by the complete voltage/resistance/load model. Parallel-cell currents add at a node, but the current contributed by each cell depends on its behavior and connections. A battery label is not a universal fixed-current source. The following circuit tasks are explicitly stipulated retained enrichment.
Series and parallel battery arrangements require a circuit model that includes the source voltages, internal resistances and load. A universal rule based on the minimum marked current or voltage is insufficient. Circuit design is retained enrichment; AP electrochemistry can use a separately specified constant current for Q=It.
Example Problem 9.1.2
Parallel identical ideal sources keep the terminal voltage at 3.00 V. The two voltages do not add.
I(total)=V/R=3.00/12.0=0.250 A. Under the stipulated equal-sharing model, each cell supplies 0.125 A.
Real sharing depends on source voltages and internal resistances. The source’s 4.5 V at 2 A result does not solve this newly authored task.
Parallel identical ideal sources keep the terminal voltage at 3.00 V. The two voltages do not add.
I(total)=V/R=3.00/12.0=0.250 A. Under the stipulated equal-sharing model, each cell supplies 0.125 A.
Real sharing depends on source voltages and internal resistances. The source’s 4.5 V at 2 A result does not solve this newly authored task.
Parallel identical ideal sources keep the terminal voltage at 3.00 V. The two voltages do not add.
I(total)=V/R=3.00/12.0=0.250 A. Under the stipulated equal-sharing model, each cell supplies 0.125 A.
Real sharing depends on source voltages and internal resistances. The source’s 4.5 V at 2 A result does not solve this newly authored task.
Glossary and deeper reading · 9 refreshers
These editorial refreshers supplement the reading. Definitions and examples are added guidance; original source wording and recorded answers remain in their original context.
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Electrochemical cell
An electrochemical cell separates oxidation and reduction into electrode processes. A galvanic cell delivers electrical energy from a favored reaction, while an electrolytic cell uses supplied electrical energy to drive an unfavored direction. For example, a zinc–copper galvanic model transfers electrons through the external wire while ions carry charge through the solutions.
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Electrolyte
An electrolyte forms mobile ions when dissolved and can allow a solution to conduct electric current. Strong and weak electrolytes differ in the extent to which dissolved species form ions under the stated conditions. For example, dissolved sodium chloride supplies sodium and chloride ions to water.
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Corrosion
Corrosion is deterioration of a material through chemical or electrochemical reactions with its environment. Metal corrosion commonly involves oxidation coupled to a reduction process. For example, rust formation involves iron oxidation together with reactions involving oxygen and water.
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Anode
The anode is the electrode where oxidation occurs. This definition applies to both galvanic and electrolytic cells. For example, a zinc electrode releasing zinc ions and electrons is an anode in the zinc–copper galvanic model.
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Aqueous solution
An aqueous solution is a solution in which water is the solvent. The dissolved substance may originate as a solid, liquid, or gas, so aqueous does not mean that a solid has melted. For example, sodium chloride dissolved in water is aqueous even though the pure salt is solid.
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Cathode
The cathode is the electrode where reduction occurs. It may deposit metal or host another reduction without necessarily gaining mass. For example, a copper electrode receiving electrons that reduce dissolved copper ions is a cathode.
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Ion
An ion is an atom or group of atoms with a net electric charge. Ordinary ion formation changes electron count without changing the element's proton count. For example, a sodium atom losing one electron becomes a sodium ion with charge +1.
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Reduction
Reduction is electron gain, represented by a decrease in oxidation number. It is paired with oxidation in an electron-transfer reaction. For example, a copper ion with charge +2 gaining two electrons to form copper metal undergoes reduction.
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Oxidation
Oxidation is electron loss, represented by an increase in oxidation number. It occurs together with reduction so that electrons are conserved in the overall reaction. For example, a zinc atom becoming a zinc ion with charge +2 undergoes oxidation.
