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Charge carrier density, also known as carrier concentration, denotes the number of charge carriers per volume. In SI units, it is measured in m −3. As with any density, in principle it can depend on position. However, usually carrier concentration is given as a single number, and represents the average carrier density over the whole material.
Density system unit unit-code symbol or abbrev. notes sample default conversion combination output units Metric: kilogram per cubic metre: kg/m3 kg/m 3: 1.0 kg/m 3 (1.7 lb/cu yd)
A unit can be defined as a ratio of two other units. For example, L/km can be defined as "liters per kilometer" by entering ==L/km as the symbol for the unit. A single "=" is used with an alias to specify that a unit code is an alternative name for another unit.
Crystalline solids and molecular solids are two opposite extreme cases of materials that exhibit substantially different transport mechanisms. While in atomic solids transport is intra-molecular, also known as band transport, in molecular solids the transport is inter-molecular, also known as hopping transport.
Unit name Symbol Base units E energy: joule: J = C⋅V = W⋅s kg⋅m 2 ⋅s −2: Q electric charge: coulomb: C A⋅s I electric current: ampere: A = C/s = W/V A J electric current density: ampere per square metre A/m 2: A⋅m −2: U, ΔV; Δϕ; E, ξ potential difference; voltage; electromotive force: volt: V = J/C kg⋅m 2 ⋅s −3 ⋅A ...
N dop is the net density of dopants (either donors or acceptors). When doping profiles exceed the Debye length, majority carriers no longer behave according to the distribution of the dopants. Instead, a measure of the profile of the doping gradients provides an "effective" profile that better matches the profile of the majority carrier density.
In the presence of a magnetic flux density B, the energy eigenvalues of this system are described by Landau levels. As shown in Fig 1, these levels are equidistant along the vertical axis. Each energy level is substantially flat inside a sample (see Fig 1). At the edges of a sample, the work function bends levels upwards.
Let ρ denote the number density of electrons, and φ the electric potential. At first, the electrons are evenly distributed so that there is zero net charge at every point. Therefore, φ is initially a constant as well. We now introduce a fixed point charge Q at the origin. The associated charge density is Qδ(r), where δ(r) is the Dirac ...