Size buys hours, chemistry buys volts
A battery is a chemical reaction with a wall down the middle. One electrode gives up electrons, the other takes them, and the material between them is a poor road for electrons. They leave by the wire instead, and that detour is the whole device.
A reaction held apart
Take a reaction that hands electrons from one substance to another and split it. One half runs at one electrode, the other half at the other, an electrolyte between them. Electrons freed on the giving side cannot cross that gap, so they travel out through the metal, around the outside circuit doing work, and back in at the other electrode. Section 17.5 draws the two half-cells and the bridge between them; the electron-blocking picture is standard cell chemistry rather than its wording. The Daniell cell, among the first successful batteries, bridged its two halves with a porous clay pot in the 1904 design the source shows.
For a dry cell, chemistry buys volts, material buys hours
The dry cell shows the split cleanly. The same components built at four sizes — D, C, AA and AAA — give the same voltage in every size. Size changes something else: a larger cell holds more of the reacting material, so it can transfer a correspondingly greater amount of charge. For a dry cell of one chemistry, the volts come from it and the hours from how much you packed in. A small high-voltage pack and a fat low-voltage cell can both be the right answer to the same job.
Interactive Grow the cell material slider and watch the cell get bigger while its voltage stays put: what grows is how long the lamp burns. Then stack cells in series and watch only the volts move — the chemistry in each cell never changes.
Inside a dry cell
The dry cell uses a zinc can that is both container and anode, the “–” terminal, and a graphite rod as the cathode, the “+” terminal. The can is packed with an electrolyte paste of manganese(IV) oxide, zinc(II) chloride, ammonium chloride and water, and the rod sits in the paste to complete the cell. Zinc is oxidised and manganese(IV) is reduced. The reaction does not conveniently run backwards, so the cell is a primary one: spent, then replaced.
The one that bites back
Alkaline batteries were developed in the 1950s as improved replacements, built around the same redox couples with an alkaline electrolyte, often potassium hydroxide, and can deliver about three to five times the energy of a zinc-carbon dry cell of similar size. Most are not rechargeable, and trying to recharge one that is not often ruptures it and leaks that electrolyte; it also leaks in storage, so cells are worth removing from anything left idle long. Where a cell must be recharged, lithium ion is among the most popular types, used in many portable devices, and its voltage varies with the cell reaction, sitting near 3.7 V in typical conditions.
Stacking cells in a row
When one cell's voltage is not enough, cells go in series: connected end to end, their voltages add, and every cell keeps the chemistry it started with. The lead-acid battery in a car does exactly this — each cell produces 2 V, and six in a row give 12 V; what a starter motor needs is high current. As a worked example, four dry cells in series give 4 × 1.5 V ≈ 6 V, and none of the four has changed its chemistry.
In short
A battery is a redox reaction held apart, so its electrons must take the long way round. For one chemistry the reaction fixes the voltage, whatever the cell's size, and the material fixes how long it lasts; and chemistry buys more than volts, as the alkaline cell above shows. Stacking cells in series lifts the voltage without touching the chemistry, and a secondary cell runs its reaction backwards when an outside source pushes current the other way.
Where this comes from
- Chemistry 2e, §17.5 Batteries and Fuel Cells linked only, not reproduced
openstax.org/books/chemistry-2e/pages/17-5-batteries-and-fuel-cells