Electrical resistivity and conductivity
Electrical resistivity (also known as specific electrical resistance, or volume resistivity) is a fundamental property of a material that quantifies how strongly that material opposes the flow of electric current. A low resistivity indicates a material that readily allows the flow of electric current. Resistivity is commonly represented by the Greek letter ρ (rho). The SI unit of electrical resistivity is the ohm-metre (Ω⋅m).[1][2][3] As an example, if a 1 m × 1 m × 1 m solid cube of material has sheet contacts on two opposite faces, and the resistance between these contacts is 1 Ω, then the resistivity of the material is 1 Ω⋅m.
Electrical conductivity or specific conductance is the reciprocal of electrical resistivity, and measures a material's ability to conduct an electric current. It is commonly represented by the Greek letter σ (sigma), but κ (kappa) (especially in electrical engineering) or γ (gamma) are also occasionally used. Its SI unit is siemens per metre (S/m).
Contents
1 Definition
1.1 Ideal case
1.2 General scalar case
1.3 Tensor resistivity
2 Causes of conductivity
2.1 Band theory simplified
2.2 In metals
2.3 In semiconductors and insulators
2.4 In ionic liquids/electrolytes
2.5 Superconductivity
2.6 Plasma
3 Resistivity and conductivity of various materials
4 Temperature dependence
4.1 Linear approximation
4.2 Metals
4.3 Semiconductors
5 Complex resistivity and conductivity
6 Resistance versus resistivity in complicated geometries
7 Resistivity density products
8 See also
9 Notes
10 References
11 Further reading
12 External links
Definition
Ideal case
In an ideal case, cross-section and physical composition of the examined material are uniform across the sample, and the electric field and current density are both parallel and constant everywhere. Many resistors and conductors do in fact have a uniform cross section with a uniform flow of electric current, and are made of a single material, so that this is a good model. (See the adjacent diagram.) When this is the case, the electrical resistivity ρ (Greek: rho) can be calculated by:
- ρ=RAℓ,displaystyle rho =Rfrac Aell ,,!
where
Rdisplaystyle R is the electrical resistance of a uniform specimen of the material
ℓdisplaystyle ell is the length of the specimen
Adisplaystyle A is the cross-sectional area of the specimen
Both resistance and resistivity describe how difficult it is to make electrical current flow through a material, but unlike resistance, resistivity is an intrinsic property. This means that all pure copper wires (which have not been subjected to distortion of their crystalline structure etc.), irrespective of their shape and size, have the same resistivity, but a long, thin copper wire has a much larger resistance than a thick, short copper wire. Every material has its own characteristic resistivity. For example, rubber has a far larger resistivity than copper.
In a hydraulic analogy, passing current through a high-resistivity material is like pushing water through a pipe full of sand—while passing current through a low-resistivity material is like pushing water through an empty pipe. If the pipes are the same size and shape, the pipe full of sand has higher resistance to flow. Resistance, however, is not solely determined by the presence or absence of sand. It also depends on the length and width of the pipe: short or wide pipes have lower resistance than narrow or long pipes.
The above equation can be transposed to get Pouillet's law (named after Claude Pouillet):
- R=ρℓA.displaystyle R=rho frac ell A.,!
The resistance of a given material is proportional to the length, but inversely proportional to the cross-sectional area. Thus resistivity can be expressed using the SI unit "ohm metre" (Ω⋅m) (i.e ohms divided by metres (for the length) and then multiplied by square metres (for the cross-sectional area)}.
For example, if A = 7000100000000000000♠1 m2 ℓdisplaystyle ell = 7000100000000000000♠1 m (forming a cube with perfectly conductive contacts on opposite faces), then the resistance of this element in ohms is numerically equal to the resistivity of the material it is made of in Ω⋅m.
Conductivity, σ, is the inverse of resistivity:
- σ=1ρ.displaystyle sigma =frac 1rho .,!
Conductivity has SI units of "siemens per metre" (S/m).
General scalar case
For less ideal cases, such as more complicated geometry, or when the current and electric field vary in different parts of the material, it is necessary to use a more general expression in which the resistivity at a particular point is defined as the ratio of the electric field to the density of the current it creates at that point:
- ρ=EJ,displaystyle rho =frac EJ,,!
where
ρdisplaystyle rho is the resistivity of the conductor material,
Edisplaystyle E is the magnitude of the electric field,
Jdisplaystyle J is the magnitude of the current density,
in which Edisplaystyle E and Jdisplaystyle J are inside the conductor.
Conductivity is the inverse (reciprocal) of resistivity. Here, it is given by:
- σ=1ρ=JE.displaystyle sigma =frac 1rho =frac JE.,!
For example, rubber is a material with large ρ and small σ—because even a very large electric field in rubber makes almost no current flow through it. On the other hand, copper is a material with small ρ and large σ—because even a small electric field pulls a lot of current through it.
As shown below, this expression simplifies to a single number when the electric field and current density are constant in the material.
Derivation from general definition of resistivity There are three equations to be combined here. The first is the resistivity for parallel current and electric field: - ρ=EJ,displaystyle rho =frac EJ,,!
If the electric field is constant, the electric field is given by the total voltage across the conductor, V, divided by length of the conductor, l:
- E=V/ldisplaystyle E=V/l
If the current density is constant, it is equal to the total current divided by the cross sectional area:
- J=I/Adisplaystyle J=I/A
Plugging in the values of E and J into the first expression, we obtain:
- ρ=VAIldisplaystyle rho =frac VAIl
Finally, we apply Ohm's law, V/I=R.
- ρ=RAldisplaystyle rho =Rfrac Al
Tensor resistivity
When the resistivity of a material has a directional component, the most general definition of resistivity must be used. It starts from the tensor-vector form of Ohm's law which relates the electric field inside a material to the electric current flow. This equation is completely general, meaning it is valid in all cases, including those mentioned above. However, this definition is the most complicated, so it is only directly used in anisotropic cases, where the more simple definitions cannot be applied. If the material is not anisotropic, it is safe to ignore the tensor-vector definition, and use a simpler expression instead.
Here, anisotropic means that the material has different properties in different directions. For example, a crystal of graphite consists microscopically of a stack of sheets, and current flows very easily through each sheet, but much less easily from one sheet to the adjacent one.[4] In such cases, the current does not flow in exactly the same direction as the electric field. Thus, the appropriate equations are generalized to the three-dimensional tensor form:[5][6]
- J=σE⇌E=ρJdisplaystyle mathbf J =boldsymbol sigma mathbf E ,,rightleftharpoons ,,mathbf E =boldsymbol rho mathbf J ,!
where the conductivity σ and resistivity ρ are rank-2 tensors, and electric field E and current density J are vectors. These tensors can be represented by 3×3 matrices, the vectors with 3x1 matrices, with matrix multiplication used on the right side of these equations. In matrix form, the resistivity relation is given by:
- [ExEyEz]=[ρxxρxyρxzρyxρyyρyzρzxρzyρzz][JxJyJz]displaystyle beginbmatrixE_x\E_y\E_zendbmatrix=beginbmatrixrho _xx&rho _xy&rho _xz\rho _yx&rho _yy&rho _yz\rho _zx&rho _zy&rho _zzendbmatrixbeginbmatrixJ_x\J_y\J_zendbmatrix
where
Edisplaystyle mathbf E is the electric field vector, with components (Ex, Ey, Ez).
ρdisplaystyle boldsymbol rho is the resistivity tensor, in general a three by three matrix.
Jdisplaystyle mathbf J is the electric current density vector, with components (Jx, Jy, Jz)
Equivalently, resistivity can be given in the more compact Einstein notation:
- Ei=ρijJjdisplaystyle mathbf E _i=boldsymbol rho _ijmathbf J _j
In either case, the resulting expression for each electric field component is:
Ex=ρxxJx+ρxyJy+ρxzJzdisplaystyle E_x=rho _xxJ_x+rho _xyJ_y+rho _xzJ_z.
Ey=ρyxJx+ρyyJy+ρyzJzdisplaystyle E_y=rho _yxJ_x+rho _yyJ_y+rho _yzJ_z.
Ez=ρzxJx+ρzyJy+ρzzJzdisplaystyle E_z=rho _zxJ_x+rho _zyJ_y+rho _zzJ_z.
Since the choice of the coordinate system is free, the usual convention is to simplify the expression by choosing an x-axis parallel to the current direction, so Jy=Jz=0. This leaves:
ρxx=ExJxdisplaystyle rho _xx=frac E_xJ_x, ρyx=EyJxdisplaystyle rho _yx=frac E_yJ_x, and ρzx=EzJxdisplaystyle rho _zx=frac E_zJ_x
Conductivity is defined similarly:[7]
- [JxJyJz]=[σxxσxyσxzσyxσyyσyzσzxσzyσzz][ExEyEz]displaystyle beginbmatrixJ_x\J_y\J_zendbmatrix=beginbmatrixsigma _xx&sigma _xy&sigma _xz\sigma _yx&sigma _yy&sigma _yz\sigma _zx&sigma _zy&sigma _zzendbmatrixbeginbmatrixE_x\E_y\E_zendbmatrix
or
- Ji=σijEjdisplaystyle mathbf J _i=boldsymbol sigma _ijmathbf E _j
Both resulting in:
- Jx=σxxEx+σxyEy+σxzEzdisplaystyle J_x=sigma _xxE_x+sigma _xyE_y+sigma _xzE_z
- Jy=σyxEx+σyyEy+σyzEzdisplaystyle J_y=sigma _yxE_x+sigma _yyE_y+sigma _yzE_z
- Jz=σzxEx+σzyEy+σzzEzdisplaystyle J_z=sigma _zxE_x+sigma _zyE_y+sigma _zzE_z
Looking at the two expressions, ρdisplaystyle boldsymbol rho and σdisplaystyle boldsymbol sigma are the matrix inverse of each other. However, in the most general case, the individual matrix elements are not necessarily reciprocals of one another; for example, σxx may not be equal to 1/ρxx. This can be seen in the Hall effect, where ρxydisplaystyle rho _xy is nonzero. In the Hall effect, due to rotational invariance about the z-axis, ρyy=ρxxdisplaystyle rho _yy=rho _xx and ρyx=−ρxydisplaystyle rho _yx=-rho _xy, so the relation between resistivity and conductivity simplifies to:[8]
σxx=ρxxρxx2+ρxy2displaystyle sigma _xx=frac rho _xxrho _xx^2+rho _xy^2, σxy=−ρxyρxx2+ρxy2displaystyle sigma _xy=frac -rho _xyrho _xx^2+rho _xy^2
If the electric field is parallel to the applied current, ρxydisplaystyle rho _xy and ρxzdisplaystyle rho _xz are zero. When they are zero, one number, ρxxdisplaystyle rho _xx, is enough to describe the electrical resistivity. It is then written as simply ρdisplaystyle rho , and this reduces to the simpler expression.
Causes of conductivity
Band theory simplified
According to elementary quantum mechanics, an electron in an atom or crystal can only have certain precise energy levels; energies between these levels are impossible. When a large number of such allowed energy levels are spaced close together (in energy-space)—i.e. have similar (minutely differing) energies— we can talk about these energy levels together as an "energy band". There can be many such energy bands in a material, depending on the atomic number number of electrons (if the atom is neutral) and their distribution (besides the size of the crystal and external factors like environmental modification of the energy bands).
The material's electrons seek to minimize the total energy in the material by going to low energy states; however, the Pauli exclusion principle means that only one can exist in each such state. So the electrons "fill up" the band structure starting from the bottom. The characteristic energy level up to which the electrons have filled is called the Fermi level. The position of the Fermi level with respect to the band structure is very important for electrical conduction: only electrons in energy levels near the Fermi level are free to move around, since the electrons can easily jump among the partially occupied states in that region. In contrast, the low energy states are rigidly filled with a fixed number of electrons at all times, and the high energy states are empty of electrons at all times.
Electric current consists of a flow of electrons. In metals there are many electron energy levels near the Fermi level, so there are many electrons available to move. This is what causes the high electronic conductivity of metals.
An important part of band theory is that there may be forbidden bands of energy: energy intervals that contain no energy levels. In insulators and semiconductors, the number of electrons is just the right amount to fill a certain integer number of low energy bands, exactly to the boundary. In this case, the Fermi level falls within a band gap. Since there are no available states near the Fermi level, and the electrons are not freely movable, the electronic conductivity is very low.
In metals
A metal consists of a lattice of atoms, each with an outer shell of electrons that freely dissociate from their parent atoms and travel through the lattice. This is also known as a positive ionic lattice.[9] This 'sea' of dissociable electrons allows the metal to conduct electric current. When an electrical potential difference (a voltage) is applied across the metal, the resulting electric field causes electrons to drift towards the positive terminal. The actual drift velocity of electrons is typically small, on the order of magnitude of meters per hour. However, due to the sheer number of moving electrons, even a slow drift velocity results in a large current density.[10] The mechanism is similar to transfer of momentum of balls in a Newton's cradle[11] but the rapid propagation of an electric energy along a wire is not due to the mechanical forces, but the propagation of an energy-carrying electromagnetic field guided by the wire.
Most metals have electrical resistance. In simpler models (non quantum mechanical models) this can be explained by replacing electrons and the crystal lattice by a wave-like structure. When the electron wave travels through the lattice, the waves interfere, which causes resistance. The more regular the lattice is, the less disturbance happens and thus the less resistance. The amount of resistance is thus mainly caused by two factors. First, it is caused by the temperature and thus amount of vibration of the crystal lattice. The temperature causes bigger vibrations, which act as irregularities in the lattice. Second, the purity of the metal is relevant as a mixture of different ions is also an irregularity.[12][13]
In semiconductors and insulators
In metals, the Fermi level lies in the conduction band (see Band Theory, above) giving rise to free conduction electrons. However, in semiconductors the position of the Fermi level is within the band gap, about halfway between the conduction band minimum (the bottom of the first band of unfilled electron energy levels) and the valence band maximum (the top of the band below the conduction band, of filled electron energy levels). That applies for intrinsic (undoped) semiconductors. This means that at absolute zero temperature, there would be no free conduction electrons, and the resistance is infinite. However, the resistance decreases as the charge carrier density (i.e., without introducing further complications, the density of electrons) in the conduction band increases. In extrinsic (doped) semiconductors, dopant atoms increase the majority charge carrier concentration by donating electrons to the conduction band or producing holes in the valence band. (A "hole" is a position where an electron is missing; such holes can behave in a similar way to electrons.) For both types of donor or acceptor atoms, increasing dopant density reduces resistance. Hence, highly doped semiconductors behave metallically. At very high temperatures, the contribution of thermally generated carriers dominates over the contribution from dopant atoms, and the resistance decreases exponentially with temperature.
In ionic liquids/electrolytes
In electrolytes, electrical conduction happens not by band electrons or holes, but by full atomic species (ions) traveling, each carrying an electrical charge. The resistivity of ionic solutions (electrolytes) varies tremendously with concentration – while distilled water is almost an insulator, salt water is a reasonable electrical conductor. Conduction in ionic liquids is also controlled by the movement of ions, but here we are talking about molten salts rather than solvated ions. In biological membranes, currents are carried by ionic salts. Small holes in cell membranes, called ion channels, are selective to specific ions and determine the membrane resistance.
Superconductivity
The electrical resistivity of a metallic conductor decreases gradually as temperature is lowered. In ordinary conductors, such as copper or silver, this decrease is limited by impurities and other defects. Even near absolute zero, a real sample of a normal conductor shows some resistance. In a superconductor, the resistance drops abruptly to zero when the material is cooled below its critical temperature. An electric current flowing in a loop of superconducting wire can persist indefinitely with no power source.[14]
In 1986, researchers discovered that some cuprate-perovskite ceramic materials have much higher critical temperatures, and in 1987 one was produced with a critical temperature above 90 K (−183 °C).[15] Such a high transition temperature is theoretically impossible for a conventional superconductor, so the researchers named these conductors high-temperature superconductors. Liquid nitrogen boils at 77 K, cold enough to activate high-temperature superconductors, but not nearly cold enough for conventional superconductors. In conventional superconductors, electrons are held together in pairs by an attraction mediated by lattice phonons.[clarification needed] The best available model of high-temperature superconductivity is still somewhat crude. There is a hypothesis that electron pairing in high-temperature superconductors is mediated by short-range spin waves known as paramagnons.[16][dubious ]
Plasma
Plasmas are very good conductors and electric potentials play an important role.
The potential as it exists on average in the space between charged particles, independent of the question of how it can be measured, is called the plasma potential, or space potential. If an electrode is inserted into a plasma, its potential generally lies considerably below the plasma potential, due to what is termed a Debye sheath. The good electrical conductivity of plasmas makes their electric fields very small. This results in the important concept of quasineutrality, which says the density of negative charges is approximately equal to the density of positive charges over large volumes of the plasma (ne = <Z>ni), but on the scale of the Debye length there can be charge imbalance. In the special case that double layers are formed, the charge separation can extend some tens of Debye lengths.
The magnitude of the potentials and electric fields must be determined by means other than simply finding the net charge density. A common example is to assume that the electrons satisfy the Boltzmann relation:
- ne∝eeΦ/kBTe.displaystyle n_textepropto e^ePhi /k_textBT_texte.
Differentiating this relation provides a means to calculate the electric field from the density:
- E=−kBTee∇nene.displaystyle mathbf E =-frac k_textBT_texteefrac nabla n_texten_texte.
(The "downward pointing triangle" is a vector gradient; see nabla symbol and gradient for more information.)
It is possible to produce a plasma that is not quasineutral. An electron beam, for example, has only negative charges. The density of a non-neutral plasma must generally be very low, or it must be very small. Otherwise, the repulsive electrostatic force dissipates it.
In astrophysical plasmas, Debye screening prevents electric fields from directly affecting the plasma over large distances, i.e., greater than the Debye length. However, the existence of charged particles causes the plasma to generate, and be affected by, magnetic fields. This can and does cause extremely complex behavior, such as the generation of plasma double layers, an object that separates charge over a few tens of Debye lengths. The dynamics of plasmas interacting with external and self-generated magnetic fields are studied in the academic discipline of magnetohydrodynamics.
Plasma is often called the fourth state of matter after solid, liquids and gases.[18][19] It is distinct from these and other lower-energy states of matter. Although it is closely related to the gas phase in that it also has no definite form or volume, it differs in a number of ways, including the following:
Property | Gas | Plasma |
---|---|---|
Electrical conductivity | Very low: air is an excellent insulator until it breaks down into plasma at electric field strengths above 30 kilovolts per centimeter.[20] | Usually very high: for many purposes, the conductivity of a plasma may be treated as infinite. |
Independently acting species | One: all gas particles behave in a similar way, influenced by gravity and by collisions with one another. | Two or three: electrons, ions, protons and neutrons can be distinguished by the sign and value of their charge so that they behave independently in many circumstances, with different bulk velocities and temperatures, allowing phenomena such as new types of waves and instabilities. |
Velocity distribution | Maxwellian: collisions usually lead to a Maxwellian velocity distribution of all gas particles, with very few relatively fast particles. | Often non-Maxwellian: collisional interactions are often weak in hot plasmas and external forcing can drive the plasma far from local equilibrium and lead to a significant population of unusually fast particles. |
Interactions | Binary: two-particle collisions are the rule, three-body collisions extremely rare. | Collective: waves, or organized motion of plasma, are very important because the particles can interact at long ranges through the electric and magnetic forces. |
Resistivity and conductivity of various materials
- A conductor such as a metal has high conductivity and a low resistivity.
- An insulator like glass has low conductivity and a high resistivity.
- The conductivity of a semiconductor is generally intermediate, but varies widely under different conditions, such as exposure of the material to electric fields or specific frequencies of light, and, most important, with temperature and composition of the semiconductor material.
The degree of doping in semiconductors makes a large difference in conductivity. To a point, more doping leads to higher conductivity. The conductivity of a solution of water is highly dependent on its concentration of dissolved salts, and other chemical species that ionize in the solution. Electrical conductivity of water samples is used as an indicator of how salt-free, ion-free, or impurity-free the sample is; the purer the water, the lower the conductivity (the higher the resistivity). Conductivity measurements in water are often reported as specific conductance, relative to the conductivity of pure water at 7002298150000000000♠25 °C. An EC meter is normally used to measure conductivity in a solution. A rough summary is as follows:
Material | Resistivity, ρ (Ω·m) |
---|---|
Superconductors | 0 |
Metals | 10−8 |
Semiconductors | Variable |
Electrolytes | Variable |
Insulators | 1016 |
Superinsulators | ∞ |
This table shows the resistivity (ρ), conductivity and temperature coefficient of various materials at 20 °C (68 °F, 293 K)
Material | Resistivity ρ (Ω·m) at 7002293150000000000♠20 °C | Conductivity σ (S/m) at 7002293150000000000♠20 °C | Temperature coefficient[a] (K−1) | Reference |
---|---|---|---|---|
Silver | 6992159000000000000♠1.59×10−8 | 7007630000000000000♠6.30×107 | 0.0038 | [21][22] |
Copper | 6992167999999999999♠1.68×10−8 | 7007596000000000000♠5.96×107 | 0.00404 | [23][24] |
Annealed copper[b] | 6992172000000000000♠1.72×10−8 | 7007580000000000000♠5.80×107 | 0.00393 | [25] |
Gold[c] | 6992244000000000000♠2.44×10−8 | 7007410000000000000♠4.1×107 | 0.0034 | [21] |
Aluminium[d] | 6992265000000000000♠2.65×10−8 | 7007377000000000000♠3.77×107 | 0.0039 | [21] |
Calcium | 6992335999999999999♠3.36×10−8 | 7007298000000000000♠2.98×107 | 0.0041 | |
Tungsten | 6992560000000000000♠5.60×10−8 | 7007179000000000000♠1.79×107 | 0.0045 | [21] |
Zinc | 6992590000000000000♠5.90×10−8 | 7007169000000000000♠1.69×107 | 0.0037 | [26] |
Nickel | 6992699000000000000♠6.99×10−8 | 7007143000000000000♠1.43×107 | 0.006 | |
Lithium | 6992928000000000000♠9.28×10−8 | 7007108000000000000♠1.08×107 | 0.006 | |
Iron | 6992970000000000000♠9.7×10−8 | 7007100000000000000♠1×107 | 0.005 | [21] |
Platinum | 6993106000000000000♠1.06×10−7 | 7006943000000000000♠9.43×106 | 0.00392 | [21] |
Tin | 6993109000000000000♠1.09×10−7 | 7006917000000000000♠9.17×106 | 0.0045 | |
Gallium | 6993139999999999999♠1.40×10−7 | 7006710000000000000♠7.1×106 | 0.004 | |
Niobium | 6993139999999999999♠1.4×10−7 | 7006700000000000000♠7×106 | [27] | |
Carbon steel (1010) | 6993143000000000000♠1.43×10−7 | 7006699000000000000♠6.99×106 | [28] | |
Lead | 6993220000000000000♠2.20×10−7 | 7006455000000000000♠4.55×106 | 0.0039 | [21] |
Titanium | 6993420000000000000♠4.20×10−7 | 7006238000000000000♠2.38×106 | 0.0038 | |
Grain oriented electrical steel | 6993459999999999999♠4.60×10−7 | 7006217000000000000♠2.17×106 | [29] | |
Manganin | 6993482000000000000♠4.82×10−7 | 7006206999999999999♠2.07×106 | 0.000002 | [30] |
Constantan | 6993489999999999999♠4.90×10−7 | 7006204000000000000♠2.04×106 | 0.000008 | [31] |
Stainless steel[e] | 6993690000000000000♠6.90×10−7 | 7006145000000000000♠1.45×106 | 0.00094 | [32] |
Mercury | 6993979999999999999♠9.80×10−7 | 7006102000000000000♠1.02×106 | 0.0009 | [30] |
Manganese | 6994144000000000000♠1.44×10−6 | 7005694000000000000♠6.94×105 | ||
Nichrome[f] | 6994110000000000000♠1.10×10−6 | 7005670000000000000♠6.7×105 [citation needed] | 6996400000000000000♠0.0004 | [21] |
Carbon (amorphous) | 6996500000000000000♠5×10−4 to 6996800000000000000♠8×10−4 | 7003125000000000000♠1.25×103 to 7003200000000000000♠2×103 | −0.0005 | [21][33] |
Carbon (graphite) parallel to basal plane[g] | 6994249999999999999♠2.5×10−6 to 6994499999999999999♠5×10−6 | 7005200000000000000♠2×105 to 7005300000000000000♠3.00×105 [citation needed] | [4] | |
Carbon (graphite) perpendicular to basal plane[h] | 6997300000000000000♠3.0×10−3 | 7002330000000000000♠3.3×102 | [4] | |
GaAs | 6997100000000000000♠1.00×10−3 to 7008100000000000000♠1×108 | 6992100000000000000♠1.00×10−8 to 7003100000000000000♠103 | [34] | |
Germanium[i] | 6999459999999999999♠4.6×10−1 | 2.17 | −0.048 | [21][22] |
Sea water[j] | 6999200000000000000♠2.00×10−1 | 7000480000000000000♠4.8 | [35] | |
Swimming pool water[k] | 6999330000000000000♠3.3×10−1 to 6999400000000000000♠4.00×10−1 | 6999250000000000000♠0.25 to 6999300000000000000♠0.30 | [36] | |
Drinking water[l] | 7001200000000000000♠2×101 to 7003200000000000000♠2×103 | 6996500000000000000♠5×10−4 to 6998500000000000000♠5×10−2 | [citation needed] | |
Silicon[i] | 7002640000000000000♠6.4×102 | 6997156000000000000♠1.56×10−3 | 3001250000000000000♠−0.075 | [21] |
Wood (damp) | 7003100000000000000♠1×103 to 7004100000000000000♠1×104 | 6996100000000000000♠10−4 to 6997100000000000000♠10−3 | [37] | |
Deionized water[m] | 7005180000000000000♠1.80×105 | 6994550000000000000♠5.50×10−6 | [38] | |
Glass | 7011100000000000000♠1×1011 to 7015100000000000000♠1×1015 | 6985100000000000000♠10−15 to 6989100000000000000♠10−11 | ? | [21][22] |
Carbon (diamond) | 7012100000000000000♠1×1012 | ~6987100000000000000♠10−13 | [39] | |
Hard rubber | 7013100000000000000♠1×1013 | 6986100000000000000♠10−14 | ? | [21] |
Air | 7009100000000000000♠109 to 7015100000000000000♠1015 | ~6985100000000000000♠10−15 to 6991100000000000000♠10−9 | [40][41] | |
Wood (oven dry) | 7014100000000000000♠1×1014 to 7016100000000000000♠1×1016 | 6984100000000000000♠10−16 to 6986100000000000000♠10−14 | [37] | |
Sulfur | 7015100000000000000♠1×1015 | 6984100000000000000♠10−16 | ? | [21] |
Fused quartz | 7017750000000000000♠7.5×1017 | 6982130000000000000♠1.3×10−18 | ? | [21] |
PET | 7021100000000000000♠1×1021 | 6979099999999999999♠10−21 | ? | |
Teflon | 7023100000000000000♠1×1023 to 7025100000000000000♠1×1025 | 6975100000000000000♠10−25 to 6977099999999999999♠10−23 | ? |
The effective temperature coefficient varies with temperature and purity level of the material. The 20 °C value is only an approximation when used at other temperatures. For example, the coefficient becomes lower at higher temperatures for copper, and the value 0.00427 is commonly specified at 7002273149999999999♠0 °C.[42]
The extremely low resistivity (high conductivity) of silver is characteristic of metals. George Gamow tidily summed up the nature of the metals' dealings with electrons in his popular science book One, Two, Three...Infinity (1947):
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The metallic substances differ from all other materials by the fact that the outer shells of their atoms are bound rather loosely, and often let one of their electrons go free. Thus the interior of a metal is filled up with a large number of unattached electrons that travel aimlessly around like a crowd of displaced persons. When a metal wire is subjected to electric force applied on its opposite ends, these free electrons rush in the direction of the force, thus forming what we call an electric current.
More technically, the free electron model gives a basic description of electron flow in metals.
Wood is widely regarded as an extremely good insulator, but its resistivity is sensitively dependent on moisture content, with damp wood being a factor of at least 7010100000000000000♠1010 worse insulator than oven-dry.[37] In any case, a sufficiently high voltage – such as that in lightning strikes or some high-tension powerlines – can lead to insulation breakdown and electrocution risk even with apparently dry wood.
Temperature dependence
Linear approximation
The electrical resistivity of most materials changes with temperature. If the temperature T does not vary too much, a linear approximation is typically used:
- ρ(T)=ρ0[1+α(T−T0)]displaystyle rho (T)=rho _0[1+alpha (T-T_0)]
where αdisplaystyle alpha is called the temperature coefficient of resistivity, T0displaystyle T_0 is a fixed reference temperature (usually room temperature), and ρ0displaystyle rho _0 is the resistivity at temperature T0displaystyle T_0. The parameter αdisplaystyle alpha is an empirical parameter fitted from measurement data. Because the linear approximation is only an approximation, αdisplaystyle alpha is different for different reference temperatures. For this reason it is usual to specify the temperature that αdisplaystyle alpha was measured at with a suffix, such as α15displaystyle alpha _15, and the relationship only holds in a range of temperatures around the reference.[43] When the temperature varies over a large temperature range, the linear approximation is inadequate and a more detailed analysis and understanding should be used.
Metals
In general, electrical resistivity of metals increases with temperature. Electron–phonon interactions can play a key role. At high temperatures, the resistance of a metal increases linearly with temperature. As the temperature of a metal is reduced, the temperature dependence of resistivity follows a power law function of temperature. Mathematically the temperature dependence of the resistivity ρ of a metal is given by the Bloch–Grüneisen formula:
- ρ(T)=ρ(0)+A(TΘR)n∫0ΘRTxn(ex−1)(1−e−x)dxdisplaystyle rho (T)=rho (0)+Aleft(frac TTheta _Rright)^nint _0^frac Theta _RTfrac x^n(e^x-1)(1-e^-x)dx
where ρ(0)displaystyle rho (0) is the residual resistivity due to defect scattering, A is a constant that depends on the velocity of electrons at the Fermi surface, the Debye radius and the number density of electrons in the metal. ΘRdisplaystyle Theta _R is the Debye temperature as obtained from resistivity measurements and matches very closely with the values of Debye temperature obtained from specific heat measurements. n is an integer that depends upon the nature of interaction:
- n=5 implies that the resistance is due to scattering of electrons by phonons (as it is for simple metals)
- n=3 implies that the resistance is due to s-d electron scattering (as is the case for transition metals)
- n=2 implies that the resistance is due to electron–electron interaction.
If more than one source of scattering is simultaneously present, Matthiessen's Rule (first formulated by Augustus Matthiessen in the 1860s)[44][45] states that the total resistance can be approximated by adding up several different terms, each with the appropriate value of n.
As the temperature of the metal is sufficiently reduced (so as to 'freeze' all the phonons), the resistivity usually reaches a constant value, known as the residual resistivity. This value depends not only on the type of metal, but on its purity and thermal history. The value of the residual resistivity of a metal is decided by its impurity concentration. Some materials lose all electrical resistivity at sufficiently low temperatures, due to an effect known as superconductivity.
An investigation of the low-temperature resistivity of metals was the motivation to Heike Kamerlingh Onnes's experiments that led in 1911 to discovery of superconductivity. For details see History of superconductivity.
Semiconductors
In general, intrinsic semiconductor resistivity decreases with increasing temperature. The electrons are bumped to the conduction energy band by thermal energy, where they flow freely, and in doing so leave behind holes in the valence band, which also flow freely. The electric resistance of a typical intrinsic (non doped) semiconductor decreases exponentially with temperature:
- ρ=ρ0e−aTdisplaystyle rho =rho _0e^-aT,
An even better approximation of the temperature dependence of the resistivity of a semiconductor is given by the Steinhart–Hart equation:
- 1T=A+Bln(ρ)+C(ln(ρ))3displaystyle frac 1T=A+Bln(rho )+C(ln(rho ))^3,
where A, B and C are the so-called Steinhart–Hart coefficients.
This equation is used to calibrate thermistors.
Extrinsic (doped) semiconductors have a far more complicated temperature profile. As temperature increases starting from absolute zero they first decrease steeply in resistance as the carriers leave the donors or acceptors. After most of the donors or acceptors have lost their carriers, the resistance starts to increase again slightly due to the reducing mobility of carriers (much as in a metal). At higher temperatures, they behave like intrinsic semiconductors as the carriers from the donors/acceptors become insignificant compared to the thermally generated carriers.[46]
In non-crystalline semiconductors, conduction can occur by charges quantum tunnelling from one localised site to another. This is known as variable range hopping and has the characteristic form of
ρ=Aexp(T−1n)displaystyle rho =Aexp left(T^-frac 1nright),
where n = 2, 3, 4, depending on the dimensionality of the system.
Complex resistivity and conductivity
When analyzing the response of materials to alternating electric fields (dielectric spectroscopy),[47] in applications such as electrical impedance tomography,[48] it is convenient to replace resistivity with a complex quantity called impedivity (in analogy to electrical impedance). Impedivity is the sum of a real component, the resistivity, and an imaginary component, the reactivity (in analogy to reactance). The magnitude of impedivity is the square root of sum of squares of magnitudes of resistivity and reactivity.
Conversely, in such cases the conductivity must be expressed as a complex number (or even as a matrix of complex numbers, in the case of anisotropic materials) called the admittivity. Admittivity is the sum of a real component called the conductivity and an imaginary component called the susceptivity.
An alternative description of the response to alternating currents uses a real (but frequency-dependent) conductivity, along with a real permittivity. The larger the conductivity is, the more quickly the alternating-current signal is absorbed by the material (i.e., the more opaque the material is). For details, see Mathematical descriptions of opacity.
Resistance versus resistivity in complicated geometries
Even if the material's resistivity is known, calculating the resistance of something made from it may, in some cases, be much more complicated than the formula R=ρℓ/Adisplaystyle R=rho ell /A above. One example is spreading resistance profiling, where the material is inhomogeneous (different resistivity in different places), and the exact paths of current flow are not obvious.
In cases like this, the formulas
- J=σE⇌E=ρJdisplaystyle J=sigma E,,rightleftharpoons ,,E=rho J,!
must be replaced with
- J(r)=σ(r)E(r)⇌E(r)=ρ(r)J(r),displaystyle mathbf J (mathbf r )=sigma (mathbf r )mathbf E (mathbf r ),,rightleftharpoons ,,mathbf E (mathbf r )=rho (mathbf r )mathbf J (mathbf r ),,!
where E and J are now vector fields. This equation, along with the continuity equation for J and the Poisson's equation for E, form a set of partial differential equations. In special cases, an exact or approximate solution to these equations can be worked out by hand, but for very accurate answers in complex cases, computer methods like finite element analysis may be required.
Resistivity density products
In some applications where the weight of an item is very important, resistivity density products are more important than absolute low resistivity – it is often possible to make the conductor thicker to make up for a higher resistivity; and then a low resistivity density product material (or equivalently a high conductivity to density ratio) is desirable. For example, for long distance overhead power lines, aluminium is frequently used rather than copper (Cu) because it is lighter for the same conductance.
Silver, although it is the least resistive metal known, has a high density and performs similarly to copper by this measure, but is much more expensive. Calcium and the alkali metals have the best resistivity-density products, but are rarely used for conductors due to their high reactivity with water and oxygen (and lack of physical strength). Aluminium is far more stable. Two other important attributes, price and toxicity, exclude the (otherwise) best choice[citation needed]: beryllium. (Pure beryllium is also brittle.) Thus, aluminium is usually the metal of choice when the weight or cost of a conductor is the driving consideration.
Material | Resistivity (nΩ·m) | Density (g/cm3) | Resistivity × density product | Relative volume required to give same conductance as Cu | Relative weight (mass) required to give same conductance as Cu | Approx price (USD per kg) (12/9/2018) | Relative cost versus Cu | |
---|---|---|---|---|---|---|---|---|
(g.Ω.m−1) | Relative to Cu | |||||||
Sodium | 47.7 | 0.97 | 46 | 31% | 2.843 | 0.31 | ||
Lithium | 92.8 | 0.53 | 49 | 33% | 5.531 | 0.33 | ||
Calcium | 33.6 | 1.55 | 52 | 35% | 2.002 | 0.35 | ||
Potassium | 72.0 | 0.89 | 64 | 43% | 4.291 | 0.43 | ||
Beryllium | 35.6 | 1.85 | 66 | 44% | 2.122 | 0.44 | ||
Aluminium | 26.50 | 2.70 | 72 | 48% | 1.5792 | 0.48 | 2.0 | 0.16 |
Magnesium | 43.90 | 1.74 | 76 | 51% | 2.616 | 0.51 | ||
Copper | 16.78 | 8.96 | 150 | 100% | 1 | 1 | 6.0 | 1 |
Silver | 15.87 | 10.49 | 166 | 111% | 0.946 | 1.11 | 456 | 84 |
Gold | 22.14 | 19.30 | 427 | 285% | 1.319 | 2.85 | 39,000 | 19,000 |
Iron | 96.1 | 7.874 | 757 | 505% | 5.727 | 5.05 |
See also
- Charge transport mechanisms
- Chemiresistor
- Classification of materials based on permittivity
- Conductivity near the percolation threshold
- Contact resistance
- Electrical impedance
- Electrical resistivities of the elements (data page)
- Electrical resistivity tomography
- Ohm's law
- Sheet resistance
- SI electromagnetism units
- Skin effect
- Spitzer resistivity
Notes
^ The numbers in this column increase or decrease the significand portion of the resistivity. For example, at 30 °C (303 K), the resistivity of silver is 6992165000000000000♠1.65×10−8. This is calculated as Δρ = α ΔT ρo where ρo is the resistivity at 7002293150000000000♠20 °C (in this case) and α is the temperature coefficient.
^ Referred to as 100% IACS or International Annealed Copper Standard. The unit for expressing the conductivity of nonmagnetic materials by testing using the eddy-current method. Generally used for temper and alloy verification of aluminium.
^ Gold is commonly used in electrical contacts because it does not easily corrode.
^ Commonly used for high voltage power lines
^ 18% chromium and 8% nickel austenitic stainless steel
^ Nickel-iron-chromium alloy commonly used in heating elements.
^ Graphite is strongly anisotropic.
^ Graphite is strongly anisotropic.
^ ab The resistivity of semiconductors depends strongly on the presence of impurities in the material.
^ Corresponds to an average salinity of 35 g/kg at 7002293150000000000♠20 °C.
^ The pH should be around 8.4 and the conductivity in the range of 2.5–3 mS/cm. The lower value is appropriate for freshly prepared water. The conductivity is used for the determination of TDS (total dissolved particles).
^ This value range is typical of high quality drinking water and not an indicator of water quality
^ Conductivity is lowest with monatomic gases present; changes to 6996120000000000000♠1.2×10−4 upon complete de-gassing, or to 6995750000000000000♠7.5×10−5 upon equilibration to the atmosphere due to dissolved CO2
References
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Further reading
Paul Tipler (2004). Physics for Scientists and Engineers: Electricity, Magnetism, Light, and Elementary Modern Physics (5th ed.). W. H. Freeman. ISBN 978-0-7167-0810-0.- Measuring Electrical Resistivity and Conductivity
External links
Wikibooks has a book on the topic of: A-level_Physics_(Advancing_Physics)/Resistivity_and_Conductivity |
"Electrical Conductivity". Sixty Symbols. Brady Haran for the University of Nottingham. 2010.
Electrical Resistivity and conductivity-Wikipedia article spoken for the blind "Audiopedia as of July 17, 2014"- Comparison of the electrical conductivity of various elements in WolframAlpha