Physics:Hyperpolarizability

From HandWiki

The hyperpolarizability, a nonlinear-optical property of a molecule, is the second order electric susceptibility per unit volume.[1] The hyperpolarizability can be calculated using quantum chemical calculations developed in several software packages.[2][3][4] See nonlinear optics.

Definition and higher orders

The linear electric polarizability α in isotropic media is defined as the ratio of the induced dipole moment 𝐩 of an atom to the electric field 𝐄 that produces this dipole moment.[5]

Therefore, the dipole moment is:

𝐩=α𝐄

In an isotropic medium 𝐩 is in the same direction as 𝐄, i.e. α is a scalar. In an anisotropic medium 𝐩 and 𝐄 can be in different directions and the polarisability is now a tensor.

The total density of induced polarization is the product of the number density of molecules multiplied by the dipole moment of each molecule, i.e.:

𝐏=ρ𝐩=ρα𝐄=ε0χ𝐄,

where ρ is the concentration, ε0 is the vacuum permittivity, and χ is the electric susceptibility.

In a nonlinear optical medium, the polarization density is written as a series expansion in powers of the applied electric field, and the coefficients are termed the non-linear susceptibility:

𝐏(t)=ε0(χ(1)𝐄(t)+χ(2)𝐄2(t)+χ(3)𝐄3(t)+),

where the coefficients χ(n) are the n-th-order susceptibilities of the medium, and the presence of such a term is generally referred to as an n-th-order nonlinearity. In isotropic media χ(n) is zero for even n, and is a scalar for odd n. In general, χ(n) is an (n + 1)-th-rank tensor. It is natural to perform the same expansion for the non-linear molecular dipole moment:

𝐩(t)=α(1)𝐄(t)+α(2)𝐄2(t)+α(3)𝐄3(t)+,

i.e. the n-th-order susceptibility for an ensemble of molecules is simply related to the n-th-order hyperpolarizability for a single molecule by:

α(n)=ε0ρχ(n).

With this definition α(1) is equal to α defined above for the linear polarizability. Often α(2) is given the symbol β and α(3) is given the symbol γ. However, care is needed because some authors[6] take out the factor ε0 from α(n), so that 𝐩=ε0nα(n)𝐄n and hence α(n)=χ(n)/ρ, which is convenient because then the (hyper-)polarizability may be accurately called the (nonlinear-)susceptibility per molecule, but at the same time inconvenient because of the inconsistency with the usual linear polarisability definition above.

See also

References