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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

  1. Voltaic Pile
  2. Daniel Cell
  3. Battery Classification
  4. Modern Batteries
  5. Simple Circuits
  6. 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.

Interactive 9.1.1 Voltaic Pile

Interactive 9.1.1 Voltaic Pile
Read all original figure notes

After the voltaic pile came the prototypical galvanic cell we were looking at before, the zinc-copper set-up. This was called a Daniel cell, and alone, it typically produced about 1.1V, and was quite a bit more reliable. It was prone to copper sealing its salt-bridge (which was a clay pot), thus cutting short its life.

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 “wet cell” is an electrochemical cell which uses a liquid electrolyte. These are much easier to design and manufacture in the laboratory setting, and as such, most early batteries were wet cells. It wasn’t until the late 1800s that the liquid electrolyte was replaced. The first “dry cell” used a paste to form the electrolyte. The paste allowed for ionic transfer between the cells, but it wasn’t as mobile as aqueous electrolytes, so the batteries didn’t need to be held upright and still during use. Shortly after their invention they were re-designed using cardboard as the electrolyte, which allowed the batteries to be mass produced for use in the recently invented flashlight

Gallery 9.1.1 Development of the Modern Battery

The source gallery placement has no frames.

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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 PbPb electrode coupled with a PbO2PbO_2 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.

For our investigation, we will look at the 9V battery. The alkaline battery cell is only a 1.5V setup, so in order to create a 9V battery, manufacturers use a set of 6 alkaline batteries. Each of these alkaline cells is connected in series, which ramps up the voltage of the cells

Gallery 9.1.2 The 9V Battery

The source gallery placement has no frames.

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Gallery 9.1.3 Series and Parallel Connections

The source gallery placement has no frames.

What do I mean, series? Basically, it just means that the batteries are hooked end-to-end, with cathode on anode.

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.

Gallery 9.1.4 Series and Parallel Voltage and

The source gallery placement has no frames.

A battery supplies a voltage associated with its chemistry and current conditions. Its delivered current depends on the external load and internal cell behavior. A capacity rating tells you about available charge under specified test conditions; it is not a fixed output current.

Example Problem 9.1.1

Reviewed circuit enrichment: four ideal 1.50 V cells are connected in series in the same polarity across a 24.0 Ω load. Each cell has zero internal resistance. Find the load voltage and current. This complete task replaces the underspecified source drawing and fixed-current rule.

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

Reviewed circuit enrichment: two identical ideal 3.00 V cells are connected in parallel with like-polarity terminals together across a 12.0 Ω load. Specify equal current sharing, zero internal resistance and no other loads. Find total current and each cell’s current.

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.

Review 9.1.1 Batteries

Question 1 of 5 · 0 correct

Two 9V batteries are placed in series. Each battery supplies 3A. What is the overall current?

Select one answer.

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.

  • 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.

    Read more: Galvanic (Voltaic) and Electrolytic Cells →

  • 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.

    Read more: Representations of Solutions →

  • 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.

    Read more: Oxidation-Reduction (Redox) Reactions →

  • 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.

    Read more: Galvanic (Voltaic) and Electrolytic Cells →

  • 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.

    Read more: Representations of Solutions →

  • 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.

    Read more: Galvanic (Voltaic) and Electrolytic Cells →

  • 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.

    Read more: Valence Electrons and Ionic Compounds →

  • 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.

    Read more: Oxidation-Reduction (Redox) Reactions →

  • 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.

    Read more: Oxidation-Reduction (Redox) Reactions →

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